- 1Institute of Infection & Immunity, St George’s University of London, London, United Kingdom
- 2Clinical Academic Group in Infection and Immunity, St. George’s University Hospital National Health Service (NHS) Foundation Trust, London, United Kingdom
Candida species are the leading cause of invasive fungal infections worldwide and are associated with acute mortality rates of ~50%. Mortality rates are further augmented in the context of host immunosuppression and infection with drug-resistant Candida species. In this review, we outline antifungal drugs already in clinical use for invasive candidiasis and candidaemia, their targets and mechanisms of resistance in clinically relevant Candida species, encompassing not only classical resistance, but also heteroresistance and tolerance. We describe novel antifungal agents and targets in pre-clinical and clinical development, including their spectrum of activity, antifungal target, clinical trial data and potential in treatment of drug-resistant Candida. Lastly, we discuss the use of combination therapy between conventional and repurposed agents as a potential strategy to combat the threat of emerging resistance in Candida.
1 Introduction
Candida species are commensal yeasts of the skin, gastrointestinal tract, and other mucosal surfaces of healthy humans. These opportunistic pathogens do not pose a risk to healthy individuals yet have the potential to cause invasive infections in the context of local or generalised reduction in host immune defences or antibiotic-induced overgrowth. Invasive candidiasis (IC) refers to a group of diseases initiated by Candida species that comprises candidaemia (bloodstream infection), disseminated and deep-seated (abdominal) candidiasis (Pappas et al., 2018). Increasing use of broad-spectrum antibiotics, an ever-expanding range of immunosuppressive disease states (e.g. HIV/AIDS) and treatments (e.g. for cancer and following solid organ transplantation), and advances in intensive care medicine have led to rising incidence of IC over the past two decades. IC now represents the fourth most common cause of nosocomial bloodstream infections and the most common invasive fungal infection in the UK (Pegorie et al., 2017). IC is associated with a high mortality rate (40-60%) leading to an estimated 400,000 deaths globally each year (Zaoutis et al., 2005; Pappas et al., 2018).
Candida albicans, Candida glabrata, Candida parapsilosis and Candida tropicalis are the four Candida species most frequently isolated from IC cases (Toda et al., 2019). Although variation exists based on age and geography, most likely due to differences in antifungal usage and species background, C. albicans remains the most frequently clinically isolated species, however the past decade has witnessed an increase in the proportion of IC caused by non-albicans species (Pfaller et al., 2011b; Castanheira et al., 2016).
Just three classes of antifungals targeting two unique pathways only are used as first-line treatment of IC (Pappas et al., 2015). The polyenes (e.g. amphotericin B) and the azoles (e.g. fluconazole) both target the major fungal sterol ergosterol, whilst the echinocandins (e.g. anidulafungin) disrupt the fungal cell wall through inhibition of β-1,3-glucan synthase (Table 1; Figure 1). In contrast to bacteria where 15 new antibiotics representing 5 novel drug classes were approved for use in the past two decades (Hutchings et al., 2019), just one new antifungal class has been clinically deployed during this timeframe: the echinocandins have been the only new antifungal drug class approved for use in IC since the early 2000s (Letscher-Bru and Herbrecht, 2003) and the azole isavuconazole is the only antifungal approved for IC in the past decade (Miceli and Kauffman, 2015). Due to their fungicidal activity and favourable safety profile in clinical trials, the echinocandins are now the first-line antifungal treatment for IC in clinical guidelines (Pappas et al., 2015).
The emergence of antifungal resistance remains an ever-present threat to the limited antifungal armamentarium. The paucity of antifungal drug classes, coupled with the intrinsic plasticity of the fungal genome promotes fungal adaptation and survival under antifungal drug stress. An increasing number of Candida species that are resistant to first line antifungal treatments (azoles or echinocandins) are being identified (Pfaller et al., 2011b; Castanheira et al., 2016), particularly in high antifungal use settings thereby almost eliminating all current treatment options (Healey et al., 2016). This trend is paralleled by increased clinical prevalence of multi-drug resistant isolates (e.g. azole and echinocandin resistant C. glabrata).
Candida auris has emerged as a global pathogen over the past decade, reported from all continents except Antarctica, with the majority of cases associated with ICU outbreaks and high mortality rates (Chowdhary et al., 2014; Sears and Schwartz, 2017; Vallabhaneni et al., 2017; Lamoth and Kontoyiannis, 2018). C. auris is usually intrinsically resistant to fluconazole (93%) with varying resistance to the echinocandins (7%) and polyenes (35%), with 41% of isolates reported as multidrug resistant (Chowdhary et al., 2013; Calvo et al., 2016; Lockhart et al., 2017; Vallabhaneni et al., 2017) and 4% of strains pan-resistant to azoles, polyenes and echinocandins (Lockhart et al., 2017). Unusually for Candida species, C. auris can spread through person-to-person contact, persisting on surfaces and medical devices for months, potentially due to its ability to form biofilms (Schelenz et al., 2016; Eyre et al., 2018). The high transmissibility of this pathogen is highlighted in reports of hospital outbreaks with clonal isolates (Ruiz-Gaitán et al., 2018).
The increasing clinical prevalence of multidrug resistant Candida species such as C. glabrata and C. auris highlights the potential for fungi to pose a serious future threat if we fail to steward and deploy existing and novel antifungal treatments in a manner that prevents the emergence of resistance. In this review, we discuss mechanisms whereby Candida species evade antifungals and identify promising novel drugs and therapeutic strategies to tackle this.
2 Mechanisms of Antifungal Resistance
2.1 Antifungal Susceptibility Testing
The susceptibility of fungal isolates to antifungal drugs is quantified by determining the minimum inhibitory concentration (MIC) through established CLSI (CLSI, 2017) or EUCAST methods (Arendrup et al., 2012). To guide clinicians with treatment selection, the MIC is compared to predetermined clinical breakpoints specific for a drug-species combination and classifies the isolate as susceptible, intermediate/susceptible, dose-dependent, or resistant. Despite the high mortality rate of IC, resistance in C. albicans remains relatively rare to the echinocandins and azoles (~1%) (Pfaller et al., 2019) highlighting the fact that the MIC is one of many factors that govern treatment success or failure in IC. Risk factors such as source control (e.g. removal of prosthetic material/devices associated with biofilm formation), fungal burden, extent and reversibility of host immunosuppression, penetration of antifungals into the site of infection, and the potential for pathogen growth at high MICs that is missed by conventional MIC methods are all important considerations that have been extensively covered in other reviews (Pappas et al., 2018; Berman and Krysan, 2020; Perfect and Ghannoum, 2020).
2.2 Routes to Resistance
Resistance has been reported against all antifungal drug classes, however the extent of resistance varies between classes and fungal species. Resistance can be classified as either intrinsic (resistance without prior antifungal exposure, e.g. C. krusei and fluconazole) or acquired (developing following antifungal exposure in a previously susceptible isolate, e.g. C. albicans and fluconazole) (Dagi et al., 2016). Although the overall rates of resistance remain low, the frequency at which both intrinsically and acquired resistant strains are isolated is increasing.
Resistance can occur through any single or concurrent mechanism (Figure 2).
![www.frontiersin.org](https://www.frontiersin.org/files/Articles/759408/fcimb-11-759408-HTML/image_m/fcimb-11-759408-g002.jpg)
Figure 2 Mechanisms of resistance of currently licensed antifungal drugs. Echinocandin resistance is almost exclusively due to point mutations in three hot spot regions in FKS1 or less frequently due to mutations in FKS2. The most frequently observed mechanism of azole resistance is reduced intracellular accumulation of drug through over-expression of efflux pumps (e.g. ABC or MFS transporters). Polyene resistance is due to incorporation of non-ergosterol sterols into cell membranes. 5FC resistance is mediated by point mutations in enzymes controlling its cellular uptake and conversion to 5FU: cytosine permease (FCY), cytosine deaminase (FCA1), and phosphoribosyl transferase (FUR1).
2.2.1 Increased Activity of Drug Efflux Pumps
Increased activity of drug efflux pumps is the most frequently observed mechanism of azole resistance in clinical Candida isolates (Sasse et al., 2012; Prasad et al., 2016). Two major efflux families are associated with resistance, the ATP-binding cassette (ABC) transporters and the major facilitator super family (MFS) pumps. Gain-of-function mutations in transcriptional regulators for both families, such as TAC1 (C. albicans) and PDR1 (C. glabrata) increase efflux pump expression and therefore lower intracellular accumulation of drug. These transcriptional regulators have additional non-protein pump targets that further contribute to the development of resistance, such as GPX1, a glutathione peroxidase that enhances oxidative stress responses (Rogers and Barker, 2002; Liu et al., 2007) and CaCHK1, a histidine kinase which regulates cell wall biosynthesis (Liu et al., 2007; Sasse et al., 2012). A significant portion of the C. auris genome is devoted to the ABC and MFS efflux pump families which is consistent with its lack of response to azoles at typical therapeutic doses (Sharma et al., 2016; Ben-Ami et al., 2017; Chowdhary et al., 2018).
2.2.2 Overexpression of Target Protein
Overexpression of target protein due to gain-of-function mutations in transcriptional regulators or gene duplication overwhelms the inhibitory capacity of the drug. Azole resistance in C. albicans can be mediated by gain-of-function mutations in key ERG11 transcriptional regulators, for example A643V in Upc2, resulting in the constitutive overexpression of Erg11 and reduced sensitivity to azoles (Flowers et al., 2012). Overexpression of ERG11 is also noted in the frequently intrinsically azole resistant species C. auris. The C. auris genome contains gain-of-function mutations in TAC1 at comparable regions to azole resistant C. albicans, a transient duplication of a region in chromosome 1 that contains ERG11 (Bhattacharya et al., 2019), and a duplication of the whole of chromosome 5 that contains TAC1 (Carolus et al., 2021).
2.2.3 Conformational Changes to the Target Protein
Conformational changes to the target protein due to point mutations at or adjacent to the binding site also result in reduced antifungal susceptibility. More than 100 SNPs in ERG11 that reduce Candida species sensitivity to azoles have been described (Flowers et al., 2015). Fluconazole-resistant C. auris from multiple continents contain amino acid substitutions in the drug target, Erg11, at known azole-resistant sites (e.g. F126T, Y132F, K143R) that are also present in resistant, but not wild-type C. albicans (Lockhart et al., 2017; Chowdhary et al., 2018; Healey et al., 2018). In contrast to azoles where multiple mechanisms of resistance have been identified, resistance to echinocandins in all Candida species is almost always due to a very limited number of mutations in fks1/2 that encodes the echinocandin target enzyme, β-1,3-glucan synthase (Perlin, 2015). Mutation in either of two highly conserved hot spot regions of Fks1 (F641-P649 and R1361) is most frequently the cause of echinocandin resistance and increases the MIC by up to 100-fold (Garcia-Effron et al., 2009). Mutations in equivalent regions of Fks2 have been described in C. glabrata (Arendrup et al., 2012; Arendrup and Perlin, 2014; Jensen et al., 2014).
2.2.4 Alterations to Target Pathway
Azoles and polyenes both target the major yeast sterol, ergosterol. Alterations to membrane ergosterol content through accumulation of the precursor sterol 14-α-methyl fecosterol can occur both through inhibition of Erg11 or reduction in the intracellular concentration/activity of this enzyme. Both mechanisms result in functional yeast cells that can bypass the activity of azoles and polyenes via altered membrane sterol composition (Haynes et al., 1996; Nolte et al., 1997).
2.2.5 Copy Number Variation
Copy number variation of whole or partial regions of chromosomes, as well as loss of heterozygosity, also confer resistance (Coste et al., 2006; Selmecki et al., 2006; Sasse et al., 2012; Yang et al., 2013; Yang et al., 2019), occurring at least twice as frequently as point mutations (Forche et al., 2011). The left arm of chromosome 5 in C. albicans contains both TAC1 and ERG11. Duplication of this portion of the chromosome provides two extra copies of both genes, conferring azole resistance through increasing the amount of drug target whilst simultaneously reducing intracellular drug accumulation (Selmecki et al., 2006). Diploid fungi can undergo loss of heterozygosity such that they become homozygous for alleles containing point mutations associated with resistance. In serial mucosal Candida isolates from an HIV-infected patient on fluconazole treatment, loss-of-heterozygosity resulted in homozygosity for a region of chromosome 5 containing a mutant erg11 allele, and these genetic changes were associated with persistence of infection for 8 months (White, 1997; Ford et al., 2015).
Additional mechanisms of resistance identified in C. auris are driven by physiological differences in cell wall content, sterol composition, glycerolipids, and sphinoglipids relative to other Candida species (Zamith-Miranda et al., 2019). Moreover, biofilm formation is an important property facilitating the development of resistance through persistence on medical devices such as intravenous catheters, providing a physical barrier to antifungal penetration (Borman et al., 2016; Sherry et al., 2017).
In addition to non-pathogen related factors described above, other fungal adaptive strategies beyond the classical resistance mechanisms may precede and facilitate the emergence of classical resistance. These include subpopulations of cells that are ‘heteroresistant’ or ‘tolerant’ to antifungals. Heteroresistance and tolerance are distinct mechanisms of antifungal drug evasion that are missed by standard clinical MIC testing protocols.
2.2.6 Heteroresistance
Fungi are metabolically and physiologically dynamic which is essential to their adaptation and survival in diverse habitats. There is substantial cell-to-cell variation in gene expression even amongst clonal populations grown at constant environmental conditions. This standing variation, referred to as bet-hedging, is a strategy to increase the likelihood of survival of at least some cells under stress conditions (Levy et al., 2012). Heteroresistance is defined as a subpopulation (<0.1%) within an apparently isogenic, susceptible isolate that has an intrinsically higher MIC compared to the rest of the population. Although heteroresistance has been widely studied in bacteria (Pournaras et al., 2005; Nunes et al., 2006; Morand and Mühlemann, 2007; Hofmann-Thiel et al., 2009), limited attention has been given to its role in fungal resistance with the majority of research undertaken on Cryptococcus species (Sionov et al., 2010; Varma and Kwon-Chung, 2010): a PubMed search using the terms ‘heteroresistance’ and ‘yeast’ yielded 24 hits, of which just 2 were related to Candida (Claudino et al., 2009; Ben-Ami et al., 2016).
Heteroresistance can be identified using population analysis profiling (PAP) assays whereby isolates are cultured on solid media across a range of drug concentrations (El-Halfawy and Valvano, 2015). Heteroresistance is an adaptive response such that when isolates are serially cultured onto drug, each generation will demonstrate an expansion in the non-susceptible subpopulation of colonies which can then further adapt to grow at higher concentrations of drug (Marr et al., 2001). Heteroresistance is not detected by current susceptibility testing methods. The implications of failing to consider or detect this phenomenon may be clinical failure and persistent or relapsed infection (Ben-Ami et al., 2016).
The variation in intrapopulation drug susceptibility and thus the degree of heteroresistance of each isolate is likely a consequence of both genetic and epigenetic mechanisms. To date, the majority of heteroresistance studies having been performed with azoles and, at least in Cryptococcus, primarily occurs via the formation of aneuploidies (Sionov et al., 2010; Stone et al., 2019). The fungistatic nature of azoles halts fungal growth and promotes genome instability and consequently the emergence of heteroresistant colonies (Shor and Perlin, 2015). Ben-Ami et al. identified upregulation of the ABC transporter genes CDR1 and PDH1 in heteroresistant C. glabrata isolates, albeit not to the extent of fully resistant isolates, that was associated with enhanced fluconazole efflux and persistent infection in a murine model (Ben-Ami et al., 2016). Studies in Cryptococcus neoformans demonstrated that fluconazole monotherapy in patients with cryptococcal meningitis drove the expansion of aneuploid heteroresistant subpopulations within just two weeks of fluconazole monotherapy. Disomy of chromosome 1, containing ERG11 and the efflux pump AFR1, was most identified as the most common mechanism of heteroresistance (Stone et al., 2019). Importantly, combination therapy of fluconazole with 5FC was sufficient to suppress this resistance emergence. The relevance of heteroresistance in IC, particularly within the context of treatment with fungicidal echinocandins, is unknown. Future work is needed to determine the relevance of heteroresistance in clinical disease progression and the potential of combination therapy to overcome heteroresistance in IC are both fundamental areas to research.
2.2.7 Tolerance
Tolerance is another pathogen factor not detected by the MIC which affects fungal growth in vitro and may play a role in treatment response and resistance emergence. Tolerance is distinct from resistance and is defined as a subpopulation of cells within a susceptible isolate that grow and emerge slowly at supra-MIC fungistatic drug concentrations (azoles) (Berman and Krysan, 2020) or survive at supra-MIC fungicidal concentrations (echinocandins) (Healey and Perlin, 2018; Garcia-Rubio et al., 2021a; Garcia-Rubio et al., 2021b). Tolerant cells are more able to overcome drug pressures relative to the non-tolerant population through enhanced signalling in stress response pathways such as calcium signalling attenuated by the serine/threonine phosphatase calmodulin, HOG, Hsp90 and Tor (Cowen and Steinbach, 2008; Rosenberg et al., 2018). Pharmacological or genetic inhibition of these pathways reduces tolerance to near baseline levels irrespective of initial tolerance level, suggesting a potential role for adjunctive therapies (Cowen et al., 2006; Cowen et al., 2009; Gong et al., 2017). In addition to enhanced signalling, environmental conditions can also select for more highly tolerant strains through increasing cell wall chitin content or enhanced signalling through pathways such as HOG (Lee et al., 2012; Walker et al., 2013).
Given the slow growth of these cells, tolerance is missed by conventional susceptibility assays which generally read the MIC at 24 hours, however measuring at later timepoints (48-72 hours) can demonstrate the degree of strain tolerance. Microbroth dilutions to determine the supra-MIC growth (SMG) or disc assays to measure the fraction of growth (FoG) within the zone of inhibition are two methods for measuring the tolerance of a strain (reviewed in (Berman and Krysan, 2020)). Tolerance has been reported in multiple Candida species, mostly in the context of fluconazole (Rosenberg et al., 2018; Kim et al., 2019; Delarze et al., 2020), although tolerance to echinocandins has also been observed in C. albicans (Yang et al., 2017), C. glabrata (Nagayoshi et al., 2014) and C. auris (Nagayoshi et al., 2014). The contribution of tolerance to antifungal treatment failure has yet to be determined: a single study demonstrated an association between highly tolerant C. albicans and persistent candidemia following azole treatment (Rosenberg et al., 2018).
There is some overlap between mechanisms of resistance and tolerance. Of note, highly tolerant strains also have lower intracellular azole accumulation (Rosenberg et al., 2018). Like resistance, aneuploidy and loss of heterozygosity have also been identified as mechanisms of tolerance (Selmecki et al., 2009; Healey et al., 2018). The degree of tolerance varies between isolates and is likely due to the intrinsic allele diversity at multiple genetic loci affecting multiple pathways to a differing degree. Tolerance also varies between cells within an isolate, and these are likely due to physiological or metabolic shifts (e.g. cell wall content or iron) that are epigenetically mediated. In the mould Mucor circinelloides, RNA interference-dependent epimutations that silence the gene targets of FK506 and rapamycin have been described as mechanisms of tolerance (Calo et al., 2014; Chang et al., 2019). To date, no work has conclusively identified epimutant mechanisms of resistance in Candida species, yet it would not be surprising if isolates with unidentified mechanisms of resistance or tolerance contain epimutations parallel to those identified in other species. It remains to be established whether tolerance exists as an adaptive mechanism to slow growth in the presence of drug to provide time for the acquisition of resistance mutation(s) (Cowen and Lindquist, 2005).
Tolerance and heteroresistance highlight the intrinsic ability of fungi to adapt to dual stressors of host immune responses and antifungal drugs beyond our classical understanding of resistance. Further understanding of heteroresistance and tolerance mechanisms, and their relevance in clinical settings, is an important research priority within the field of Candida resistance.
3 Novel Therapeutic Options for Candida
Fungi are eukaryotes and share many evolutionarily conserved metabolic pathways with humans, which somewhat restricts available drug targets to pathways essential to fungi only. The recent emergence and increased prevalence of multidrug resistant fungal species has propelled research into novel treatments. Below we give an overview of some of the novel and repurposed compounds with antifungal activity that are at various stages of clinical development, as well as discussing the potential of drug combinations (Figure 3 and Table 2). The list of compounds in this section is comprehensive, but not exhaustive. Compounds were selected for discussion based on either their superior activity against a broad spectrum of resistant Candida, for targeting a novel pathway, or being near to clinical deployment with a focus on orally delivered drugs.
![www.frontiersin.org](https://www.frontiersin.org/files/Articles/759408/fcimb-11-759408-HTML/image_m/fcimb-11-759408-t002.jpg)
Table 2 Novel antifungals: target, mechanism of action, spectrum, advantages and stage of development.
3.1 New Members of Existing Classes
Although resistance has been identified against the azoles and echinocandins, they are attractive agents as they target proteins unique to fungi. Given that off-target effects and drug-drug interactions are commonly encountered clinical limitations, optimising these drug classes to enhance fungal-specific, on-target activity is an appealing option.
3.1.1 Tetrazoles
Off target effects of azoles via their high affinity for haem and non-specific binding to human CYP450 enzymes (Yates et al., 2017) lead to drug-drug interactions with agents metabolised via these enzymes as well as effects on liver, skin and vision (Fischer et al., 2005). A new generation of azole-like compounds, the tetrazoles, were rationally designed to target fungal Cyp51 only. A tetrazole metal binding group replaces the triazole and has greater specificity for the fungal lanosterol 14-α demethylase (Erg11) active site over the human Cyp51 isoenzyme (Warrilow et al., 2014; Warrilow et al., 2016).
3.1.1.1 Mechanism
Like the azoles, tetrazoles reversibly and competitively inhibit Erg11p to deplete fungal membranes of ergosterol and disrupt membrane integrity. VT-1129, VT-1598 (quilsecondazole) and VT-1161 (oteseconazole) (Viamet Pharmaceuticals Inc; now Mycovia Pharmaceuticals) were identified as part of a screen for compounds with reduced affinity for human Cyp enzymes (Hoekstra et al., 2014). VT-1161 is more than 1000 times more selective for the C. albicans Cyp51 enzyme compared to the human isoenzyme (Warrilow et al., 2014).
3.1.1.2 Activity
VT-1129, VT-1161, and VT-1598 have potent activity against a broad range of Candida species, including azole and echinocandin-resistant species, at low MICs (Schell et al., 2017a; Break et al., 2018a).
VT-1161 has a low MIC (0.002 μg/ml) against wild-type, fluconazole-sensitive C. albicans (Warrilow et al., 2014) and appears to retain some activity (MIC VT-1161 2 μg/ml) against resistant fluconazole-resistant isolates (MIC FLC 64 μg/ml) and echinocandin-resistant C. albicans, C. glabrata, C. krusei (Garvey et al., 2015; Schell et al., 2017a). In a collection of 68 well-characterised azole-resistant C. albicans isolates, susceptibility to VT-1161 was affected by CDR1 and MDR1 overexpression and the erg11 substitutions Y132F, Y132F and K143R, and Y132 and F145L. Other isolates in this collection with point mutations at additional known azole resistance sites retained VT-1161 sensitivity (e.g. Y132H, F145L) (Nishimoto et al., 2019). Overexpression of CDR1 and MDR1 reduced susceptibility to VT-1161 in C. albicans and C. glabrata in another study (Monk et al., 2019).
VT-1161 treatment significantly reduced fungal burden in murine models of vulvovaginal candidiasis (VVC) and IC due to fluconazole-susceptible and -resistant Candida. VT-1161 was rapidly absorbed in mouse models and extensively distributed to tissues with rapid penetration to vaginal tissues with a long half-life (>48 hours) (Garvey et al., 2015; Break et al., 2018b).
VT-1598 has the broadest spectrum of activity against fungal species, including fluconazole-resistant C. albicans (Break et al., 2018a) and C. auris (MIC 0.03-8 μg/ml) (Wiederhold et al., 2019), with enhanced efficacy in neutropenic murine models compared to either fluconazole or caspofungin.
VT-1129 was designed to treat Cryptococcus, but also has good in vitro activity against many Candida species, including azole- and echinocandin-resistant C. glabrata and C. krusei (Desai et al., 2016; Schell et al., 2017a). No further data on VT-1129 in Candida species are available, however the drug has received FDA fast track orphan drug status for treatment of cryptococcal meningitis.
3.1.1.3 Stage of Development
A phase II dose and duration-ranging placebo-controlled randomised trial (NCT02267382) evaluated the efficacy and safety of lower (150mg) and higher (300mg) 12 or 24-week dosing regimens of oral VT-1161 for recurrent VVC (rVVC) (NCT02267382, 2014). The proportion of subjects with ≥1 acute VVC episodes was superior at 0-7% across the 4 VT-1161 arms vs 52% in the placebo arm. VT-1161 was well-tolerated with a favourable safety profile and importantly, no evidence of hepatoxicity (Brand et al., 2018). Phase III trials in rVVC (NCT03562156 and NCT03561701, VIOLET, and NCT03840616, ultraVIOLET) are ongoing. A press release on July 29th 2021 reported preliminary findings from the two VIOLET trials in 650 women with efficacy of 90% vs 40% (placebo) against recurrence over 48 weeks and excellent tolerability. VT-1161 has received FDA qualified infectious disease product (QIDP) and fast track designation for treatment of rVVC with full approval expected in the US in early 2022.
VT-1598 is undergoing pre-clinical and phase I evaluation for the treatment of C auris, cryptococcal meningitis and coccidioidomycosis, whilst development of VT-1129 appears to have been halted.
3.1.1.4 Advantages
The major advantage of the tetrazoles is their enhanced specificity for fungal Cyp51 making this group of drugs more tolerable.
3.1.2 Rezafungin (CD101)
Currently licensed echinocandins (caspofungin, micafungin and anidulafungin) are fungicidal agents against Candida species, acting via inhibition of the enzyme β-1,3-glucan synthase, causing destabilisation of the cell wall resulting in osmotic instability and cell death. Due to their half-life, echinocandins are given intravenously once daily (24 hours anidulafungin; 9-11 hours caspofungin; 10-17 hours micafungin) (Kofla and Ruhnke, 2011). In addition, the echinocandins have limited penetration into the gastrointestinal tract, the site of Candida colonisation as well as intra-abdominal infection, which may have implications for the development of spontaneous resistance.
3.1.2.1 Mechanism
Rezafungin (Cidara Therapeutics) is a novel β-1,3-glucan synthase inhibitor that is a structural analogue of anidulafungin, but with a much longer half-life, facilitating less frequent dosing.
3.1.2.2 Activity
Rezafungin has similar activity compared to other echinocandins with potent in vivo pharmacodynamic activity against clinically relevant Candida species and greater activity against multidrug resistant strains of C. auris than either caspofungin or micafungin (Pfaller et al., 2016; Pfaller et al., 2017b; Arendrup et al., 2018; Lepak et al., 2018b; Lepak et al., 2018a). Rezafungin retains activity at high doses against echinocandin resistant (fks mutants) Candida species (Berkow and Lockhart, 2018). Rezafungin, but not micafungin, accumulated within intra-abdominal Candida abscesses in a mouse model at a level above the mutant prevention concentration of the infecting strain, which may have implications for resistance (Zhao et al., 2017).
3.1.2.3 Stage of Development
Phase I dose-escalation trials in healthy adults demonstrated that rezafungin was well tolerated and safe with a long half-life and high plasma exposures (Sandison et al., 2017). In a phase II randomised trial (STRIVE) comparing two rezafungin weekly dosing regimens to caspofungin (with fluconazole stepdown) for IC, rezafungin was well tolerated, showed rapid Candida clearance (19.5h) from blood cultures and comparable overall 14-day cure rates (rezafungin 400mg weekly 60.5%, 400mg/200mg weekly 76.1%, caspofungin 70mg/50mg daily 67.2%) (Thompson et al., 2020).
An ongoing phase III trial (RESTORE NCT03667690) in IC is comparing 14-day global cure and 30-day all-cause mortality between weekly rezafungin and daily caspofungin with fluconazole stepdown. Fungal-free survival with rezafungin as prophylaxis against Candida, Aspergillus, and Pneumocytis infection, compared to oral fluconazole or posaconazole, is currently being evaluated in a phase III trial (ResPECT, NCT04368559) in blood or bone marrow transplantation recipients (Cushion et al., 2016; Ong et al., 2016; Cidara Therapeutics, 2020).
The FDA has granted rezafungin QIDP, fast track and orphan drug status for the treatment of candidemia and invasive candidiasis. The long-term effect of the drug’s PK and its relationship to resistance emergence has yet to be investigated.
3.1.2.4 Advantages
The major advantage of rezafungin over other echinocandins are its superior pharmacokinetics. Rezafungin has increased stability and solubility with more extensive tissue distribution, with higher plasma exposure and greater gut penetration than other echinocandins, with minimal urinary excretion (Sandison et al., 2017; Zhao et al., 2017). Rezafungin has a longer half-life than any echinocandin (80 hours following a single dose, and 150 hours after three doses) allowing for reduced dosing frequency to as low as once weekly (Sandison et al., 2017), facilitating its use in prophylaxis. A higher loading dose of rezafungin improves efficacy through enhanced killing when fungal burden is greatest and reduces the occurrence of spontaneous fks mutations compared to either caspofungin or anidulafungin (Locke et al., 2016; Sandison et al., 2017; Lakota et al., 2018). However, cross-resistance has been noted between rezafungin and the other echinocandins (Arendrup et al., 2019).
3.1.3 Encochleated Amphotericin B (MAT2203)
Amphotericin B deoxycholate was the first antifungal licensed in 1959.The drug remains widely used due to its broad spectrum, fungicidal activity with minimal resistance, however its use is compromised by a lack of specificity to fungal sterols resulting in substantial renal toxicity and anaemia (UTZ, 1964; Maddux and Barriere, 1980). Intravenous lipid formulations of amphotericin B have partly but not entirely mitigated these toxicities (Hamill, 2013), and both drugs require intravenous administration. MAT2203 (Matinas BioPharma) is a novel delivery system for AmB deoxycholate consisting of a spiral cochleate lipid bilayer which is orally bioavailable due to its stability in acidic pH (Cuddihy et al., 2019).
3.1.3.1 Mechanism
Like other formulations of amphotericin B, MAT2203 sequesters sterols from fungal membranes. The cochleate is absorbed from the GI tract. Once calcium levels within the cochleate drop sufficiently, the spiral unwinds and releases the drug directly onto fungal cells on contact thereby increasing drug delivery directly onto fungal cells and reducing mammalian cell toxicities (Santangelo et al., 2000). The precise interaction between the cochleate and the fungal cell is not yet fully understood.
3.1.3.2 Activity
The MIC of MAT2203 in C. albicans is equivalent to the deoxycholate formulation (0.5 μg/ml) (Zarif et al., 2000). MAT2203 is extensively distributed with good tissue penetration in murine models, where the liver was shown to act as a reservoir for slow release of the drug (Segarra et al., 2002). Mice with systemic candidiasis treated with the encochleated formulation (0.5-20 mg/kg/day) had improved day 16 survival (100%) and reduction in kidney and lung fungal burden relative to intraperitoneal AmB deoxycholeate (70% survival) or liposomal AmB (90% survival) (Santangelo et al., 2000; Hamill, 2013; Shende et al., 2019). No accumulation was observed in healthy mice highlighting the improved fungal specificity of the cochleate formulation.
3.1.3.3 Stage of Development
MAT2203 was well tolerated in healthy volunteers in a single ascending dose phase I study, with mild gastrointestinal adverse events noted (Aigner and Lass-Flörl, 2020). A randomised phase II study (NCT02971007) in women with moderate to severe VVC refractory or intolerant to current therapy yielded disappointing results with MAT2203 (200 mg or 400 mg daily for 5 days) performing poorly compared to a single dose of fluconazole (150 mg): clinical cure at day 12 was significantly lower at 52% and 54.5% compared to 75% for fluconazole. Preliminary data from a small phase II trial (n=16 women) with refractory mucocutaneous candidiasis using higher (400-800mg/d) MAT2203 doses for longer durations (>6 months) suggests all patients eventually achieved a greater than 50% improvement in clinical signs and symptoms and the drug was well tolerated for prolonged periods.
MAT2203 was granted FDA QIDP and fast track status for the treatment of candidiasis in 2015 (BioPharma, 2014).
3.1.3.4 Advantages
Oral administration of the cochleate and its improved tolerability profile hold promise, though comparable efficacy to standard of care oral treatments for mucosal candidiasis has yet to be demonstrated. Molecular umbrella technology is a promising method for the development of further formulations of amphotericin B.
3.2 Same Target, New Class
3.2.1 Ibrexafungerp (SCY-078)
3.2.1.1 Mechanism
Ibrexafungerp (Scynexis) also targets β-1,3-glucan synthase, but is structurally distinct from the echinocandins and represents the inaugural member of a novel class of antifungals, the triterpenoids (Gintjee et al., 2020), which bind at an independent site on the enzyme (Schell et al., 2017b; Wring et al., 2017).
3.2.1.2 Activity
Ibrexafungerp has broad spectrum, fungicidal activity against Candida species with MIC <2 μg/ml for C. albicans, C. glabrata, C tropicalis, and C. parapsilosis, but no activity against C. krusei and C. lusitaniae (Pfaller et al., 2013). Whilst ibrexafungerp retains activity against some echinocandin-resistant Candida strains (fks1/2 mutants), including C. glabrata (Jiménez-Ortigosa et al., 2017; Nunnally et al., 2019) and C. auris (Berkow et al., 2017; Larkin et al., 2017; Pfaller et al., 2017a; Schell et al., 2017b), presumably due to differential binding on the enzyme, deletion of F625 in fks1 or F659 in fks2 were associated with a 40- and 121-fold increase in MIC for ibrexafungerp in C. glabrata, respectively. Furthermore, W715L or A1390D substitutions, positioned outside of the hotspot region in fks2, increase the MIC to ibrexafungerp by 29 and 20-fold, respectively (Jiménez-Ortigosa et al., 2017).
In murine studies, oral and IV formulations of ibrexafungerp showed extensive distribution and tissue penetration, though not into the CNS (Wring et al., 2017). Ibrexafungerp accumulates at sites with a low pH, with extensive accumulation in vaginal tissue and a necrotic liver abscess in murine models (Larkin et al., 2019; Lee et al., 2020). Neutropenic murine systemic candidiasis models have demonstrated efficacy of ibrexafungerp against C. albicans, C. glabrata and C. parapsilosis, including against an echinocandin-resistant strain of C. glabrata (Lepak et al., 2015; Wring et al., 2017; Wiederhold et al., 2018).
3.2.1.3 Stage of Development
Oral ibrexafungerp was well tolerated in phase I studies even at high doses (up to 1600 mg), with an extensive volume of distribution and good tissue penetration and improved biofilm penetration compared to azoles (Wring et al., 2018; Spec et al., 2019; Azie et al., 2020). A phase II randomised trial (NCT02679456) in rVVC demonstrated superiority of ibrexafungerp relative to fluconazole, with 4-month cure rates of 88% and 65%, respectively, and lower recurrence rates of 4% vs 15% (Helou and Angulo, 2017). A phase II dose-ranging acute VVC study (NCT03253094) investigated range of ibrexafungerp dosing regimens compared to single 150 mg dose fluconazole (NCT03253094, 2017), leading onto two recently completed phase III trials of ibrexafungerp 300 mg twice daily for 1 day for the treatment of acute VVC. Ibrexafungerp demonstrated clinical cure rates of 50-63% by day 8-14 against 29-44% with placebo, however gastrointestinal adverse events did occur more commonly in the ibrexafungerp group (VANISH 303 NCT03734991; VANISH 306 NCT03987620). The FDA approved the drug for treatment of VVC in June 2021, marketed as Brexafemme.
A PK study of ibrexafungerp 500 mg or 750 mg as stepdown therapy following IV echinocandin showed that the higher dose would achieve the target PK exposure, was well tolerated and achieved comparable responses to fluconazole (Spec et al., 2019). Two ongoing phase III trials are evaluating ibrexafungerp fungal diseases (including mucocutaneous and invasive candidiasis) refractory to or intolerant of standard antifungal treatment (FURI, NCT03059992, target n=200) and in treating invasive C. auris infection (CARES, NCT03363841). Ibrexafungerp has been given QIDP status by the FDA for invasive candidiasis.
3.2.1.4 Advantages
Advantages of ibrexafungerp over the echinocandins include oral administration, penetration into intraabdominal abscesses and retained activity against some echinocandin resistant isolates.
3.3 Novel Mechanism of Action
In the context of emerging resistance, the development of antifungals with a novel mechanism of action against a fungal-specific pathway and/or potentiating the activity of the current antifungals is a priority for the research community and the pharmaceutical industry. Finding novel targets that are unique to fungi has been a challenge given that up to 80% of hits turn out to be false positives (Pouliot and Jeanmart, 2016) alongside limited incentives for pharmaceutical investment in antifungal drug development due to the comparatively lower number of patients with invasive fungal infection compared to bacterial infection. In recent years, several novel agents in the pipeline targeting unique pathways give grounds for hope.
3.3.1 Fosmanogepix
3.3.1.1 Mechanism
Fosmanogepix (APX001 and E1211, Amplyx Pharmaceuticals) is the inaugural member of the N-phosphonooxymethylene prodrugs that is efficiently converted to manogepix (APX001A and E1210), an inhibitor of fungal glycosylphosphatidylinositol (GPI) proteins. Manogepix was identified in a screen for compounds that interfere with the correct localisation of cell wall GPI-anchored mannoproteins (Tsukahara et al., 2003). Manogepix is highly specific for fungal, but not human Gwt1, an enzyme that catalyses the acetylation of inositol, an essential step in the early stages of GPI anchor biosynthesis (Miyazaki et al., 2011; Watanabe et al., 2012). Gwt1 is essential for trafficking and anchoring mannoproteins to the cell wall and outer cell membrane to maintain cell wall integrity, adhesion, pathogenicity, and evasion of the host immune system. Inhibition of Gwt1 prevents cell wall reinforcement thereby reducing hyphal formation, virulence, germ tube formation, and biofilm formation, in addition to inducing morphological changes to the cell size and shape resulting in exposure of β-1,3-glucan to host immune cells and ER stress (Watanabe et al., 2012).
3.3.1.2 Activity
Fosmanogepix is highly active against many Candida species: MIC90 C. albicans (0.008-0.06 μg/ml), C. glabrata (0.06-0.12 μg/ml), C. auris (0.03 μg/ml) (Hata et al., 2011; Miyazaki et al., 2011; Pfaller et al., 2011a; Watanabe et al., 2012; Hager et al., 2018; Zhao M. et al., 2018), though lacks activity against C. krusei (MIC90 ≥ 0.5 μg.ml) (Miyazaki et al., 2011). No cross-resistance has been reported between the echinocandins, amphotericin B and fosmanogepix for multiple Candida species (Miyazaki et al., 2011; Pfaller et al., 2011a; Wiederhold et al., 2015b; Zhao, Y et al., 2018), with most studies reporting no cross-resistance to fluconazole-resistant erg11 mutants (Miyazaki et al., 2011; Pfaller et al., 2011a). There does however appear to be a correlation with fluconazole MICs, with a 2-8-fold increase in MIC to fosmanogepix reported in a subset of fluconazole-resistant Candida isolates (Arendrup et al., 2018; Arendrup and Jørgensen, 2020). A recent study of the mechanism of reduced susceptibility to both fosmanogepix and fluconazole identified increased efflux through Cdr11 and Snq2 as a result of a gain-of-function mutation in the transcription factor zcf29 in C. albicans and a mitochondrial DNA deletion activating MDR1 expression in C. parapsilosis (Liston et al., 2020). Despite MIC increases, the MIC of these isolates remained low. Further studies are needed to determine the clinical relevance of these findings and to explore the link with azole cross-resistance via efflux.
In vitro serial passage showed an 8-fold rise in MIC in C. albicans (18 passages) and C. parapilosis (3 passages), with no increase in MIC for C. glabrata, C. auris and C. tropicalis (Kapoor et al., 2020). GWT sequencing of isolates with reduced susceptibility demonstrated a single valine to alanine point mutation in gwt (V163A C. glabrata; V162A C. albicans) which appears to be essential for manogepix binding in all Gwt orthologs. Neither mutation affected susceptibility to echinocandins or azoles. A further study identified enhanced efflux as the mechanism of fosmanogepix resistance in C. parapsilosis and C. albicans that have a 4-8 fold increase in MIC that were not associated with mutations in the GWT gene (Liston et al., 2020).
Fosmanogepix is effective at reducing fungal burden and improving survival in immunosuppressed murine models using wild type, azole- and echinocandin-resistant Candida, including C. auris (Hata et al., 2011; Miyazaki et al., 2011; Wiederhold et al., 2015b; Hager et al., 2018; Zhao et al., 2018). Rodent and primate studies have demonstrated good oral bioavailability and safety and extensive tissue penetration (liver, lungs, spleen, brain, kidney, eye) (Hata et al., 2011; Mansbach et al., 2017). In addition, fosmanogepix has demonstrated synergy with the azoles and echinocandins in animal models (Hata et al., 2011).
3.3.1.3 Stage of Clinical Development
Fosmanogepix has undergone four phase I trials (NCT03333005; NCT04166669; NCT02956499; NCT02957929) using intravenous and oral administration, showing a low propensity for drug-drug interactions, good tolerability and no serious adverse effects reported in healthy volunteers (Hodges et al., 2017a; Hodges et al., 2017b), with findings in acute myeloid leukaemia patients not yet reported.
In an open label phase II trial (NCT03604705), with a minimum of 3 days’ IV therapy followed by oral stepdown, in non-neutropenic patients (n=20) with suspected or confirmed candidemia, 16/20 patients achieved 14-day treatment success (composite of alive, two negative blood cultures and no rescue antifungal treatment). In a phase II trial in C. auris candidemia or IC (NCT04148287, APEX), 9 participants received IV fosmanogepix on days 1-3 followed by oral fosmanogepix for up to 42 days. However, this trial was terminated early due to COVID19. Fosmanogepix has been granted FDA fast track approval for 7 separate indications including invasive candidiasis.
3.3.1.4 Advantages
Fosmanogepix exploits a novel mechanism of action that has limited potential for cross-resistance. It is broad spectrum, effective in animal and early-stage clinical trials, is orally bioavailable and well tolerated, and shows promise for use in infections due to multidrug resistant species such as C. auris.
3.3.2 ATI-2307
3.3.2.1 Mechanism
ATI-2307 (Appili Therapeutics), formerly T-2307 (developed by Toyama Chemical Co), is an arylamidine similar to pentamidine. Its precise mechanism of action remains elusive, however it is selectively taken up into fungal cells via the spermidine transport system (Nishikawa et al., 2010) and initiates the collapse of mitochondrial membrane potential, ultimately inhibiting respiration and energy production resulting in fungicidal activity in C. albicans and C. krusei, but fungistatic activity in C. glabrata and C. parapsilosis (Nishikawa et al., 2010; Shibata et al., 2012; Yamashita et al., 2019).
3.3.2.2 Activity
ATI-2307 is active against a broad spectrum of Candida species including azole and echinocandin-resistant species and C. auris (Mitsuyama et al., 2008; Yamada et al., 2010; Wiederhold et al., 2015a; Wiederhold et al., 2016; Wiederhold et al., 2020) with lower in vitro MICs (0.0005-0.125 μg/ml) compared to azoles, micafungin, and amphotericin B (Mitsuyama et al., 2008). ATI-2307 exerted a more potent effect at equivalent doses of amphotericin B or micafungin in immunocompetent murine models of systemic wild type C. albicans and echinocandin resistant infections (Mitsuyama et al., 2008). ATI-2307 also reduced kidney fungal burden and improved survival in mice infected with C. auris (Wiederhold et al., 2020), as well as neutropenic mice infected with C. glabrata harbouring the Fks2 substitution R1379S (Wiederhold et al., 2016). ATI-2307 had minimal effect on mitochondrial morphology and potential of rat liver cells (Nishikawa et al., 2010; Yamada et al., 2010; Nishikawa et al., 2016).
3.3.2.3 Stage of Development
One report states that ATI-2307 has completed a phase I study in the USA with no adverse effects noted (Nishikawa et al., 2017), however these data are not currently publicly available.
3.3.2.4 Advantages
Although this compound remains in the early stages of clinical development, ATI-2307 shows promise as a fungal-selective compound (Nishikawa et al., 2010; Nishikawa et al., 2016) and in vitro and in vivo data highlight its potential in treating a range of Candida species including more resistant isolates.
3.3.3 Hydrazycins (BHBM, D0, D13)
Sphingolipid biosynthesis is essential for eukaryotic metabolism as well as fungal pathogenicity (Noble et al., 2010; Oura and Kajiwara, 2010) thus represents an attractive new antifungal target given the structural disparity between fungal and mammalian sphingolipids (Mor et al., 2015; Rollin-Pinheiro et al., 2016). Glucosylceramide is critical for fungal progression through the cell cycle and growth at neutral and alkaline pH (Saito et al., 2006), characteristic of human blood and cerebrospinal fluid. Antibodies that inhibit glucosylceramide have demonstrated extensive antifungal effects both in vitro and in vivo but lack specificity for the fungal sphingolipid (Rodrigues et al., 2007).
3.3.3.1 Mechanism
The hydrazycins, (E)-N′-(3-bromo-6-hydroxybenzylidene)-2-methylbenzohydrazide (BHBM) and benzohydrazide (D0) were identified in a screen for compounds that specifically inhibit the biosynthesis of fungal glucosylceramide. The hydrazycins inhibit the vesicular trafficking of ceramide, a precursor lipid of glucosylceramide, thereby halting glucosylceramide and sphingolipid biosynthesis and disrupting cell division (Mor et al., 2015).
3.3.3.2 Activity
BHBM has variable activity against Candida species with moderate activity against C. krusei and C. glabrata, (MIC 2-32 μg/ml), but poor activity against C. albicans and C parapsilosis (MIC>32 μg/ml) (Mor et al., 2015). A derivative of BHBM, D13, was selected from a screen for enhanced specificity to the fungal target activity and activity, with an MIC of 1 μg/ml in C. albicans and C. krusei (Lazzarini et al., 2018). Synergy of D13 with fluconazole was reported for one of two C. krusei strains (FICI 0.31), and with caspofungin for both isolates, but neither combination was synergistic for fluconazole-sensitive or -resistant C. albicans (Lazzarini et al., 2018).
Two murine systemic candidiasis model studies evaluated the in vivo activity of the hydrazycins. One reported a 75% and 62.5% 21-day survival in the D0 and BHBM arms, respectively (Mor et al., 2015); the other a much lower 20% day 21 survival with either D13 or BHBM against 0% with fluconazole (Lazzarini et al., 2018).
3.3.3.3 Stage of Development
The hydrazycins remain in pre-clinical development. Sphingolipid metabolism is being explored separately for use in fungal vaccines.
3.3.3.4 Advantages
BHBM, D0, and D13 are fungal-specific with a novel sphingolipid target. Although current hydrazycins do not show sufficient spectrum against clinically relevant Candida species, the BHBM derivative, D13, represents an improvement and all congeners have all been reported to re-sensitise some azole-resistant species to azoles. Screens for additional daughter compounds of BHBM may identify novel hydrazycins with superior antifungal activity.
3.3.4 Trehalose Inhibitors
Trehalose is a two glucose non-reducing sugar cleaved to generate glucose for glycolysis. The trehalose pathway is of interest due to its fungal specificity and role in fungal growth and virulence, with trehalose critical for fungal survival at high temperatures, acting as an antioxidant under oxidative stress and protecting against other host-induced stressors through interactions with proteins and phospholipids that reinforce the cell wall and prevent degradation of cell membrane and intracellular proteins (Iturriaga et al., 2009).
Although relatively few trehalose-inhibiting compounds have been identified to date, genetic deletion of either of the primary synthesising enzymes in this pathway (Tps1 (trehalose-6-phosphate synthase) and Tps2 (trehalose-6-phosphate phosphatase)) have been identified as essential for C. albicans infectivity in mammalian studies, preventing hyphal development and macrophage survival (Zaragoza et al., 1998; Van Dijck et al., 2002; Zaragoza et al., 2002; Martínez-Esparza et al., 2007). Tps2 inhibition results in the accumulation of its substrate trehalose-6-phosphate, which is likely toxic to the fungus at very high concentrations (Perfect et al., 2017). Uniquely for phosphatases, inhibition of Tps2 was not associated with any off target activity to other phosphatases (Perfect et al., 2017). Drug discovery of Tps1 and Tps2 inhibitors is underway via two major strategies. Purified Tps1 and Tps2 enzymes are being used to identify inhibitors in a high throughput Transcreener UDP fluorescence polarisation assay (Perfect et al., 2017). Several compounds were identified with activity against Cryptococcus, however murine studies were unfavourable: screens for novel trehalose inhibitors against Candida species are underway. The crystal structures for both Tps1 and Tps2 were recently solved (Miaoa et al., 2016) and are now guiding structure-activity compound design.
Further characterisation in Candida infections and the development of trehalose pathway inhibitors pose an interesting new class of antifungal compounds with potential as treatments of tolerance.
3.3.5 Turbinmicin
Turbinmicin is a promising new antifungal that was recently discovered in a high-throughput screen of bacteria isolated from the microbiome of the sea squirt. Turbinmicin belongs to the group of highly oxidised type II polyketides and is produced by Micromonospora species. Genetic knockdown and haploinsufficiency screens in S. cerevisiae, along with the disruption of ER-Golgi vesicular transport to the plasma membrane identified the essential vesicle transport protein Sec14 as the most likely target (Zhang et al., 2020). Many Candida rely on the vesicular delivery of extracellular matrix components to form extensive biofilms for drug resistance. Turbinmicin is, therefore, particularly promising as an anti-biofilm drug through interference with the assembly of the extracellular matrix: a rat central venous catheter C. albicans biofilm model demonstrated an almost complete elimination of biofilm in turbinmicin treated rats relative to buffer treated controls (Zhao et al., 2021).
Turbinmicin demonstrated broad spectrum, fungicidal activity in vitro, including against pan-resistant C. auris, MDR C. glabrata and triazole-resistant Aspergillus fumigatus, with MICs of 0.5 μg/ml or less (Zhang et al., 2020). Furthermore, a combination of fluconazole and turbinmicin was more efficacious at eliminating biofilm than either drug alone, possibly due to turbinmicin disrupting the extracellular matrix sufficiently to render cells more vulnerable to the azole (Zhao et al., 2021). In vitro safety studies in human red blood cells identified that turbinmicin did not trigger haemolysis even at concentrations 1000 times the MIC. Turbinmicin treatment resulted in a 3.6 log reduction of fungi relative to control vehicle in a disseminated candidiasis mouse model of pan-resistant C. auris, with good tolerability across a range of doses up to 256 mg/kg/d (Zhang et al., 2020).
Turbinmicin would represent the inaugural antifungal to target Sec14, although this protein has similarity to the hsSec14 so further analysis for potential cross-reactivity would be prudent. Further preclinical development will entail studies in additional mammalian species and safety monitoring over longer treatment courses.
3.4 Repurposed
Given the significant resources required for development and clinical validation of novel compounds, a favoured approach is to search for antifungal activity in previously approved non-antifungal therapeutics, which can then potentially be modified to reduce undesirable off-target effects. Large scale, high-throughput screens have identified some promising therapeutic avenues, however in vitro efficacy has not always translated into clinical efficacy.
3.4.1 AR-12
AR-12 (Arno Therapeutics) is a celecoxib derivative that was initially developed as an anticancer protein kinase inhibitor, but also has fungicidal activity at low doses against a range of Candida isolates, including C. albicans biofilms (Baxter et al., 2011; Koselny et al., 2016b).
3.4.1.1 Mechanism
Whilst the anticancer properties of AR-12 are attributed to its kinase inhibition, its antifungal activity is via two distinct routes. Firstly, by the specific inhibition of the fungal acetyl CoA (Acs2p) which has a multitude of effects due to the vast range of processes that acetyl CoA is involved with (e.g. carbon metabolism, histone acetylation, ribosome function and autophagy) (Koselny et al., 2016b). Inhibition of Acs2p ultimately induces cell lysis. Secondly, AR-12 also enhances the host antifungal immune response through down-regulation of host chaperone proteins such as Grp89 and Hsp90, although the precise details have not yet been determined (Koselny et al., 2016b).
3.4.1.2 Activity
AR-12 is fungicidal against Candida species (MIC C. albicans, C. glabrata, C. parapsilosis, C. tropicalis, C. krusei 2-4 μg/ml) and retains activity against strains with intermediate or resistant fluconazole MICs (MIC > 128 μg/ml) due to gain-of-function mutations affecting efflux pump activity (Koselny et al., 2016a). In addition, deletion of neither TAC1 nor MRR1 affected susceptibility of isolates to AR-12. Combination of AR-12 with fluconazole re-sensitised some fluconazole-resistant C. albicans and C. glabrata strains. AR-12 remained active against echinocandin-resistant strains containing FKS mutations and synergised with caspofungin in caspofungin-resistant strains of C. glabrata (Koselny et al., 2016a).
3.4.1.3 Stage of Development
Early phase I studies (NCT00978523) for the anticancer activity of AR-12 identified good serum concentrations with limited adverse effects, however development was halted in 2017 when Arno Therapeutics declared bankruptcy (Koselny et al., 2016b).
3.4.1.4 Advantages
AR-12 has a broad antifungal spectrum in yeasts and moulds and has been shown to be well tolerated in Phase I human clinical trials at doses relevant for antifungal activity. Commonly occurring mechanisms of azole and echinocandin resistance do not appear to affect susceptibility to AR-12. Combinations with existing antifungals may show potential in tackling drug-resistant candidiasis.
3.5 Combination/Adjunctive Therapies
Combination therapy using drugs with distinct targets, including drugs without direct antifungal activity, holds appeal in terms of potentially faster fungal clearance and reduction of resistance emergence, prolonging the longevity of the current antifungal arsenal. This needs to be evaluated carefully and balanced against additional cost and potentially additive toxicities.
3.5.1 Flucytosine (5FC)
5FC is an old antifungal with good oral bioavailability, excellent tissue penetration and fungicidal activity against Candida species (Pfaller et al., 2012), with a target distinct from the widely used cell wall and membrane-acting agents. Secondary resistance develops if used as monotherapy, hence the agent is always used in combination, with currently a niche role, given with amphotericin B in Candida meningitis or endocarditis (Perfect et al., 2010). 5FC has not been widely used to treat candidaemia/IC due to concern regarding its toxicity, namely bone marrow suppression due to its metabolite 5-fluorouracil (5FU). These side effects were more pronounced at the historically higher dosage of 150 (or even 200) mg/kg/day (Francis and Walsh, 1992). More recently however, in the treatment of cryptococcal meningitis, a lower dose of 100 mg/kg/day (25mg/kg four times a day) given for 14 days was well tolerated and enhanced fungal clearance when used in combination with either fluconazole or amphotericin B (Van Der Horst et al., 1997; Day et al., 2013; Molloy et al., 2018).
PK/PD studies have demonstrated that the activity of 5FC (as opposed to toxicity) is concentration-independent, and time-dependent (Hope et al., 2006; Brouwer et al., 2007; Lepak and Andes, 2015). Given the lower MICs for Candida species (MIC90 ~1 μg/mL for C. albicans, as opposed to 8-16 μg/mL for Cryptococcus), lower doses of 25-50mg/kg/day may be sufficient to achieve maximal fungicidal activity against most Candida species. A recent extensive in vitro screen for combinations of licensed antifungals against a large C. auris isolate collection identified synergy when 5FC was combined with echinocandins or amphotericin B, with combinations of anidulafungin or micafungin with 1mg/L 5FC effectively inhibiting echinocandin-resistant C. auris isolates (O’Brien et al., 2020).
The drug is also limited by its four times daily dosing requirement, however a slow-release formulation has been developed in conjunction with DNDi (Drugs for Neglected Diseases initiative) and is entering phase I trials. Combinations of 5FC with azoles and echinocandins as well as the novel anti-Candida agents warrant clinical exploration, particularly in the treatment of IC due to drug resistant Candida species.
3.5.2 Calcineurin and Hsp90 Inhibitors
The serine/threonine phosphatase calcineurin is a conserved regulator of calcium homeostasis in eukaryotes and activates many target genes with a variety of cellular functions, including fungal growth, morphological transition, cell wall integrity and host survival (Sanglard et al., 2003; Reedy et al., 2010; Juvvadi et al., 2014; Juvvadi et al., 2017). Calcineurin is essential for fungal adaptation to multiple environments, including survival to antifungal drugs, with resistance in many strains linked to the calcium-calcineurin pathway (Brand et al., 2007; Zhang et al., 2012). Furthermore, inhibitors of calcineurin (e.g. FK506 and cyclosporin) synergistically enhance the antifungal properties of fluconazole, rendering fungicidal activity against C. albicans (Marchetti et al., 2000a; Cruz and Goldstein, 2002; Onyewu et al., 2003). Deletion of either of the catalytic or regulatory subunits of calcineurin in C. albicans enhances susceptibility to multiple stressors, including disruptors of the cell membrane (e.g. azoles) or cell wall (e.g. echinocandins), serum and alkaline pH, and is associated with hypovirulence in murine models of disseminated candidiasis (Cruz and Goldstein, 2002; Bader et al., 2003; Sanglard et al., 2003; Bader et al., 2006), though not in vaginal candidiasis (Bader et al., 2006). Therefore, inhibition of calcineurin signalling to disrupt fungal virulence represents an attractive adjunctive therapy option.
3.5.2.1 Mechanism
External stressors induce an influx of calcium ions into the fungal cytoplasm, which bind to the calcium-binding protein calmodulin. Calcineurin binds to the calcium-calmodulin complex inducing a conformational change in the phosphatase that removes the autoinhibitory domain, thus activating calcineurin. Calcineurin transmits calcium signals via the dephosphorylation and subsequent nuclear translocation of the transcription factor Crz1 which in turn activates the transcription of calcineurin-dependent genes involved in cellular signalling, growth, vesicular trafficking, and cell wall integrity (Karababa et al., 2006).
FK506 and cyclosporin bind to immunophilins forming a potent calcineurin inhibitor complex thereby preventing the activation of its phosphatase activity and subsequent activation of Crz1 (Liu et al., 1991; Thewes, 2014).
3.5.2.2 Activity
Calcineurin inhibitors abrogate tolerance in Candida and enhance the antifungal activity of current antifungals: Combination of a calcineurin inhibitor with fluconazole renders fungicidal activity in many Candida species with varying levels of tolerance (Marchetti et al., 2000a; Marchetti et al., 2000b; Cruz and Goldstein, 2002; Onyewu et al., 2003). In vitro screens against C. albicans, C. glabrata, and C. krusei using drugs for non-mycological conditions with antifungals identified cyclosporin A and FK506 (tacrolimus) as synergistic with both azole and non-azole inhibitors of ergosterol biosynthesis (e.g. terbinafine). However, cyclosporin A and FK506 are potent immunosuppressants typically prescribed following solid organ transplantation and could thus enhance host susceptibility to Candida infection. FK506 analogues that lack immunosuppressive activity yet retain synergy with antifungals have demonstrated promising in vitro and in vivo results (Lee et al., 2018; Jung and Yoon, 2020).
Calcineurin activity can also be inhibited through depletion of the molecular chaperone heat shock protein 90 (Hsp90). Hsp90 is implicated in the emergence of resistance to fluconazole and echinocandins in C. albicans and C. glabrata and potentiates its activity through binding to the catalytic subunit of calcineurin (Cowen and Lindquist, 2005; Cowen et al., 2006). Hsp90 inhibitors (e.g. geldanamycin and efungumab) induce the degradation of the downstream protein calcineurin and also synergise with azoles and echinocandins in vitro (Singh et al., 2009; Singh-Babak et al., 2012). Moreover, Hsp90 represents a favourable target as it interacts with approximately 10% of the proteome, therefore inhibition could disrupt multiple essential pathways (McClellan et al., 2007). Efungumab (previously Mycograb) is a monoclonal antibody targeting Hsp90 developed by NeuTec Pharma and subsequently acquired by Novartis. Mycograb combined with a lipid formulation of AmB was reported as resulting in faster fungal clearance, improved d10 response rates and reduced mortality in a phase III trial in IC compared to AmB alone (Pachl et al., 2006). However, the study methodology was questioned (Herbrecht et al., 2006) and the European Medicines Agency has subsequently twice refused marketing authorisation for Mycograb, citing product safety and quality issues. Hsp90 inhibitors are currently in development as anti-cancer drugs, however these are precluded from human use due to host toxicities, but recent identification of specific inhibitors of the C. albicans Hsp90 nucleotide binding domain offer a path towards fungal selectivity (Whitesell et al., 2019).
3.5.2.3 Advantages
Calcineurin and Hsp90 are promising targets due to their central role in many fungal growth and invasion pathways, priming host cells to antifungal drugs and antifungal immunity. Combinations of azoles with inhibitors or these pathways renders azoles fungicidal and may limit the development of resistance. Calcineurin and Hsp90 are both structurally highly conserved throughout fungal species offering an opportunity for development of a broad-spectrum, non-immunosuppressive derivative of currently licensed inhibitors.
3.5.3 MGCD290
Histone deacetylases (HDACs) deacetylate lysine residues on histones and cellular proteins, thereby controlling transcription, cell proliferation and cell motility. Again, this class of drugs are cytotoxic and are in use as anti-cancer agents (Eckschlager et al., 2017).
3.5.3.1 Mechanism
HDAC inhibitors (trichostatin A, apicidin and sodium butyrate) induce apoptosis and cell cycle arrest (Grozinger and Schreiber, 2002). MGCD290 (MethylGene, Mirati Therapeutics) inhibits the fungal histone deacetylase 2 (Hos2) with an additional target through inhibition of the deacetylation of fungal Hsp90, involved in fungal stress adaptation (Robbins et al., 2012) and may have a role in addressing fungal tolerance. Like, MGCD290, Trichostatin A reduced tolerance and inhibited upregulation of C. albicans ERG11 and CDR when co-administered with fluconazole, itraconazole and terbinafine (inhibitors of sterol synthesis), but had little effect on a fluconazole-resistant isolate (Smith and Edlind, 2002).
3.5.3.2 Activity
MGCD290 only has modest antifungal activity against Candida species as monotherapy (MIC 0.5–16 μg/ml for C. albicans, C. glabrata, C. krusei), however synergises with azoles and echinocandins at low doses in susceptible as well as azole- and some echinocandin- resistant Candida species (Pfaller et al., 2009; Pfaller et al., 2015). MGCD290 in combination with fluconazole increased survival and significantly reduced fungal burden in the kidney in murine and rat models of systemic candidiasis relative to fluconazole alone (Besterman et al., 2015).
3.5.3.3 Stage of Development
Four phase I trials in healthy volunteers of oral MGCD290 alone or in combination with fluconazole for 14 days demonstrated a good safety profile and favourable PK (Besterman, 2012). Despite compelling in vitro data, MGCD290’s promising antifungal activity failed to translate: a phase II trial of MGCD20 in combination with fluconazole for VVC showed no significant benefit of the combination over fluconazole alone (NCT01497223).
3.5.3.4 Advantages
MGCD290 is an oral agent with a novel target demonstrating potential in vitro through its impact on tolerance, but whose clinical potential has not been realised. Inhibition of Hsp90 through preventing its deacetylation is potentially more attractive given the immunosuppressive consequences of direct Hsp90 pharmacological inhibition.
3.5.4 Colistin
Colistin (polymyxin B) is a positively charged lipopeptide that is bactericidal through binding of membrane lipids and used in treatment of highly resistant gram-negative bacteria but is associated with significant nephrotoxcicity. Although colistin itself has minimal antifungal activity in Candida species (Zhai et al., 2010), it is fungicidal when combined with low doses of fluconazole, an effect that is particularly pronounced in highly azole tolerant strains (Bibi et al., 2021). Colistin enhances the ergosterol-depleting activity of fluconazole through binding to membrane lipids (PS, PI, PE), which was particularly pronounced in ergosterol-depleted cells following fluconazole treatment or genetic knockout of erg11 erg3 erg24. The combination was superior to fluconazole monotherapy in the Galleria mellonella model infected with highly tolerant C. albicans. Colistin also synergises with echinocandins in echinocandin-sensitive, but not -resistant C. albicans (Zeidler et al., 2013) and with caspofungin, but not micafungin in C. auris (Bidaud et al., 2020). It is currently unclear whether colistin has synergy with polyenes or with fluconazole in non-albicans Candida species.
4 Conclusion
With the increasing use of antifungal agents in prophylaxis, empiric, or targeted treatment of invasive candidiasis in an ever-expanding range of susceptible hosts, Candida species have evolved a myriad of resistance mechanisms to established antifungals. For example, poor response to the fungistatic azoles, where either heteroresistance and tolerance may preclude the development of resistance, is most frequently associated with SNPs or aneuploidy-mediated mechanisms that increase the amount of target protein, alter the conformation of the drug binding site, or act to reduce intracellular drug accumulation.
Following slow progress since the early 2000s when the echinocandins were developed, the past decade has witnessed exciting developments and clinical trial progression of novel anti-Candida drugs based on different binding sites on the same target (ibrexafungerp) or completely new targets (fosmanogepix), as well as improved formulations of existing compounds (encochleated amphotericin B, rezafungin, tetrazoles). Other advantages of many novel agents are oral formulations, broad-spectrum anti-Candida activity including effectiveness against drug-resistant Candida species and a lack of cross-resistance with established antifungals. A number of repurposed agents with minimal intrinsic antifungal activity may hold promise as adjunctive therapies providing they can be reconfigured to minimise their off-target effects and toxicities. The old agent flucytosine is an under-utilised partner drug in the treatment of invasive candidiasis, including drug-resistant infections. Additional pathways emerging as promising target pathways have been well reviewed elsewhere (Nguyen et al., 2021).
Future priorities for academia are to better understand the mechanisms of resistance for the novel antifungal drug classes and how these might best be deployed in the clinic to prevent the development of resistance, including optimising PK/PD against resistant species and combination therapy with drugs with distinctive antifungal targets or mechanisms of action.
Author Contributions
SM and TB conceived the Review. SM wrote the first draft, with input from TB. Both authors contributed to the final draft. All authors contributed to the article and approved the submitted version.
Funding
St. George’s Hospital Charity, grant ref = 19-20 001, Emerging Leaders Prize in Antimicrobial resistance from the Medical Research foundation, grant ref = MRF-160-0009-ELP-BICA-C0802.
Conflict of Interest
TB has received Speaking fees from Gilead Sciences and Pfizer and research funding from Gilead Sciences unrelated to the submitted work.
The remaining author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
Aigner, M., Lass-Flörl, C. (2020). Encochleated Amphotericin B: Is the Oral Availability of Amphotericin B Finally Reached? J. Fungi 6 (2), 1–7. doi: 10.3390/jof6020066
Arendrup, M. C., Andersen, J. S., Holten, M. K., Krarup, K. B., Reiter, N., Schierbeck, J., et al. (2019). Diagnostic Performance of T2Candida Among ICU Patients With Risk Factors for Invasive Candidiasis. Open Forum Infect. Dis. 6 (5), 1–9. doi: 10.1093/ofid/ofz136
Arendrup, M. C., Chowdhary, A., Astvad, K. M. T., Meinike Jørgensen, K. (2018). APX001A In Vitro Activity Against Contemporary Blood Isolates and Candida Auris Determined by the EUCAST Reference Method. Antimicrob. Agents Chemother. 62 (10), 1–9. doi: 10.1128/AAC.01225-18
Arendrup, M. C., Cuenca-Estrella, M., Lass-Flörl, C., Hope, W., Arendrup, M. C., Hope, W. W., et al. (2012). EUCAST Technical Note on the EUCAST Definitive Document EDef 7.2: Method for the Determination of Broth Dilution Minimum Inhibitory Concentrations of Antifungal Agents for Yeasts EDef 7.2 (EUCAST-AFST). Clin. Microbiol. Infect. 18 (7), E246–E247.doi: 10.1111/j.1469-0691.2012.03880.x
Arendrup, M. C., Jørgensen, K. M. (2020). Manogepix (APX001A) Displays Potent In Vitro Activity Against Human Pathogenic Yeast, But With an Unexpected Correlation to Fluconazole MICs. Antimicrob. Agents Chemother. 64 (7), 1–9. doi: 10.1128/AAC.00429-20
Arendrup, M. C., Meletiadis, J., Zaragoza, O., Jørgensen, K. M., Marcos-Zambrano, L. J., Kanioura, L., et al. (2018). Multicentre Determination of Rezafungin (CD101) Susceptibility of Candida Species by the EUCAST Method. Clin. Microbiol. Infect. 24 (11), 1200–1204. doi: 10.1016/j.cmi.2018.02.021
Arendrup, M. C., Perlin, D. S. (2014). Echinocandin Resistance: An Emerging Clinical Problem? Curr. Opin. Infect. Dis. 27 (6), 484–492. doi: 10.1097/QCO.0000000000000111
Arendrup, M. C., Perlin, D. S., Jensen, R. H., Howard, S. J., Goodwin, J., Hope, W. (2012). Differential in Vivo Activities of Anidulafungin, Caspofungin, and Micafungin Against Candida Glabrata Isolates With and Without FKS Resistance Mutations. Antimicrob. Agents Chemother. 56 (5), 246–247. doi: 10.1128/AAC.06369-11
Azie, N., Angulo, D., Dehn, B., Sobel, J. D. (2020). Oral Ibrexafungerp: An Investigational Agent for the Treatment of Vulvovaginal Candidiasis. Expert Opin. Invest Drugs 29 (9), 893–900. doi: 10.1080/13543784.2020.1791820
Bader, T., Bodendorfer, B., Schröppel, K., Morschhäuser, J. (2003). Calcineurin Is Essential for Virulence in Candida Albicans. Infect. Immun. 71 (9), 5344–5354. doi: 10.1128/IAI.71.9.5344-5354.2003
Bader, T., Schröppel, K., Bentink, S., Agabian, N., Köhler, G., Morschhäuser, J. (2006). Role of Calcineurin in Stress Resistance, Morphogenesis, and Virulence of a Candida Albicans Wild-Type Strain. Infect. Immun. 74 (7), 4366–4369. doi: 10.1128/IAI.00142-06
Baxter, B. K., Didone, L., Ogu, D., Schor, S., Krysan, D. J. (2011). Identification, In Vitro Activity and Mode of Action of Phosphoinositide-Dependent-1 Kinase Inhibitors as Antifungal Molecules. ACS Chem. Biol. 6, 502–510. NIH Public Access. doi: 10.1021/cb100399x
Ben-Ami, R., Berman, J., Novikov, A., Bash, E., Shachor-Meyouhas, Y., Zakin, S., et al. (2017). Multidrug-Resistant Candida Haemulonii and C. Auris, Tel Aviv, Israel. Emerging Infect. Dis. 23 (2), 195–203. doi: 10.3201/eid2302.161486
Ben-Ami, R., Zimmerman, O., Finn, T., Amit, S., Novikov, A., Wertheimer, N., et al. (2016). Heteroresistance to Fluconazole Is a Continuously Distributed Phenotype Among Candida Glabrata Clinical Strains Associated With In Vivo Persistence. MBio. 7 (4), 1–12. doi: 10.1128/mBio.00655-16
Berkow, E. L., Angulo, D., Lockhart, S. R. (2017). In Vitro Activity of a Novel Glucan Synthase Inhibitor, SCY-078, Against Clinical Isolates of Candida Auris. Antimicrob Agents Chemother 61 (7), 1–2. doi: 10.1128/AAC.00435-17
Berkow, E. L., Lockhart, S. R. (2018). Activity of CD101, a Long-Acting Echinocandin, Against Clinical Isolates of Candida Auris. Diagn. Microbiol. Infect. Dis. 90 (3), 196–197. doi: 10.1016/j.diagmicrobio.2017.10.021
Berman, J., Krysan, D. J. (2020). Drug Resistance and Tolerance in Fungi. Nat. Rev. Microbiol. 18 (6), 319–331. doi: 10.1038/s41579-019-0322-2
Besterman, J. (2012). AD and MAD Studies in Healthy Subjects Demonstrate Safety and Pharmacokinetics of MGCD290, an Oral Fungal Hos2 Inhibitor ± Fluconazole. IDWeek 2012, San Diego, Abstract 1619.
Besterman, J., Nguyen, D. T., Ste-Croix, H. (2015). “MGCD290, an Oral Fungal Hos2 Inhibitor, Enhances the Antifungal Properties of Fluconazole Following Multiple-Or Single-Dose Oral Administration in Pre-And Post-Infection Settings.” in Abstr ICAAC/ICC 2015, San Diego, Abstr M-1711. San Diego: Clinical and Laboratory Standards Institute.
Bhattacharya, S., Holowka, T., Orner, E. P., Fries, B. C. (2019). Gene Duplication Associated With Increased Fluconazole Tolerance in Candida Auris Cells of Advanced Generational Age. Sci. Rep. 9 (1), 1–13. doi: 10.1038/s41598-019-41513-6
Bibi, M., Murphy, S., Benhamou, R. I., Rosenberg, A., Ulman, A., Bicanic, T., et al. (2021). Combining Colistin and Fluconazole Synergistically Increases Fungal Membrane Permeability and Antifungal Cidality. ACS Infect. Dis. 7, 377–389. doi: 10.1021/acsinfecdis.0c00721
Bidaud, A. L., Djenontin, E., Botterel, F., Chowdhary, A., Dannaoui, E. (2020). Colistin Interacts Synergistically With Echinocandins Against Candida Auris. Int. J. Antimicrob Agents 55 (3), 105901. doi: 10.1016/j.ijantimicag.2020.105901
BioPharma, M. (2014) “MAT8800 Discovery Program: Matinas BioPharma Holdings, Inc. (MTNB). Available at: http://www.matinasbiopharma.com/pipeline/mat8800-discovery-program.
Borman, A. M., Szekely, A., Johnson, E. M. (2016). Comparative Pathogenicity of United Kingdom Isolates of the Emerging Pathogen Candida Auris and Other Key Pathogenic Candida Species. MSphere 1 (4), 1–8. doi: 10.1128/mSphere.00189-16
Brand, S. R., Degenhardt, T. P., Person, K., Sobel, J. D., Nyirjesy, P., Schotzinger, R. J., et al. (2018). A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Efficacy and Safety of Orally Administered VT-1161 in the Treatment of Recurrent Vulvovaginal Candidiasis. Am. J. Obstetrics Gynecol. 218 (6), 624.e1–624.e9. doi: 10.1016/j.ajog.2018.03.001
Brand, A., Shanks, S., Duncan, V. M. S., Yang, M., Mackenzie, K., Gow, N. A. R. (2007). Hyphal Orientation of Candida Albicans Is Regulated by a Calcium-Dependent Mechanism. Curr. Biol. 17 (4), 347–352. doi: 10.1016/j.cub.2006.12.043
Break, T. J., Desai, J. V., Healey, K. R., Natarajan, M., Ferre, E. M. N., Henderson, C., et al. (2018a). VT-1598 Inhibits the in Vitro Growth of Mucosal Candida Strains and Protects Against Fluconazole-Susceptible and -Resistant Oral Candidiasis in IL-17 Signalling-Deficient Mice. J. Antimicrob Chemother 73 (8), 2089–2094. doi: 10.1093/jac/dky170
Break, T. J., Desai, J. V., Natarajan, M., Ferre, E. M. N., Henderson, C., Zelazny, A. M., et al. (2018b). VT-1161 Protects Mice Against Oropharyngeal Candidiasis Caused by Fluconazole-Susceptible and -Resistant Candida Albicans. J. Antimicrob. Chemother. 73 (1), 151–155. doi: 10.1093/jac/dkx352
Brouwer, A. E., Van Kan, H. J. M., Johnson, E., Rajanuwong, A., Teparrukkul, P., Wuthiekanun, V., et al. (2007). Oral Versus Intravenous Flucytosine in Patients With Human Immunodeficiency Virus-Associated Cryptococcal Meningitis. Antimicrob. Agents Chemother. 51 (3), 1038–1042. doi: 10.1128/AAC.01188-06
Calo, S., Shertz-Wall, C., Chan Lee, S., Bastidas, R. J., Nicolás, F. E., Granek, J. A., et al. (2014). Antifungal Drug Resistance Evoked via RNAi-Dependent Epimutations. Nature 513(7519), 555–558. doi: 10.1038/nature13575
Calvo, B., Melo, A. S. A., Perozo-Mena, A., Hernandez, M., Francisco, E. C., Hagen, F., et al. (2016). First Report of Candida Auris in America: Clinical and Microbiological Aspects of 18 Episodes of Candidemia. J. Infect. 73 (4), 369–374. doi: 10.1016/j.jinf.2016.07.008
Carolus, H., Pierson, S., Muñoz, J. F., Subotić, A., Cruz, R. B., Cuomo, C. A., et al. (2021). Genome-Wide Analysis of Experimentally Evolved Candida Auris Reveals Multiple Novel Mechanisms of Multidrug Resistance. MBio 12 (2), 1–19. 2020.09.28.317891. doi: 10.1128/mBio.03333-20
Castanheira, M., Messer, S. A., Rhomberg, P. R., Pfaller, M. A. (2016). Antifungal Susceptibility Patterns of a Global Collection of Fungal Isolates: Results of the SENTRY Antifungal Surveillance Program, (2013). Diagn. Microbiol. Infect. Dis. 85 (2), 200–204. doi: 10.1016/j.diagmicrobio.2016.02.009
Chang, Z., Billmyre, R. B., Chan Lee, S., Heitman, J. (2019). Broad Antifungal Resistance Mediated by RNAi-Dependent Epimutation in the Basal Human Fungal Pathogen Mucor Circinelloides” Edited by A. Chowdhary. PloS Genet. 15 (2), e1007957. doi: 10.1371/journal.pgen.1007957
Chowdhary, A., Anil Kumar, V., Sharma, C., Prakash, A., Agarwal, K., Babu, R., et al. (2014). Multidrug-Resistant Endemic Clonal Strain of Candida Auris in India. Eur. J. Clin. Microbiol. Infect. Dis. 33 (6), 919–926. doi: 10.1007/s10096-013-2027-1
Chowdhary, A., Prakash, A., Sharma, C., Kordalewska, M., Kumar, A., Sarma, S., et al. (2018). A Multicentre Study of Antifungal Susceptibility Patterns Among 350 Candida Auris Isolate-17) in India: Role of the ERG11 and FKS1 Genes in Azole and Echinocandin Resistance. J. Antimicrob. Chemother. 73 (4), 891–899. doi: 10.1093/jac/dkx480
Chowdhary, A., Sharma, C., Duggal, S., Agarwal, K., Prakash, A., Kumar Singh, P., et al. (2013). New Clonal Strain of Candida Auris, Delhi, India. Emerging Infect. Dis. 19 (10), 1670–1673. doi: 10.3201/eid1910.130393
Cidara Therapeutics (2020). “Study of Rezafungin Compared to Standard Antimicrobial Regimen for Prevention of Invasive Fungal Diseases in Adults Undergoing Allogeneic Blood and Marrow Transplantation - Full Text View - ClinicalTrials.Gov. Available at: https://clinicaltrials.gov/ct2/show/NCT04368559.
Claudino, A. L. R., Peixoto Junior, R. F., Melhem, M. S. C., Szeszs, M. W., Lyon, J. P., Chavasco, J. K., et al. (2009). Mutants With Heteroresistance to Amphotericin B And Fluconazole in Candida. Braz. J. Microbiol. 40 (4), 943–951. doi: 10.1590/S1517-83822009000400028
CLSI (2017). M38-A_reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeasts, Vol. 37.
Coste, A., Turner, V., Ischer, F., Morschhäuser, J., Forche, A., Selmecki, A., et al. (2006). A Mutation in Tac1p, a Transcription Factor Regulating CDR1 and CDR2, Is Coupled With Loss of Heterozygosity at Chromosome 5 to Mediate Antifungal Resistance in Candida Albicans. Genetics 172 (4), 2139–2156. doi: 10.1534/genetics.105.054767
Cowen, L. E., Carpenter, A. E., Matangkasombut, O, Fink, G. R., Lindquist, S. (2006). Genetic Architecture of Hsp90-Dependent Drug Resistance. Eukaryotic Cell 5 (12), 2184–2188. doi: 10.1128/EC.00274-06
Cowen, L. E., Lindquist, S. (2005). Hsp90 Potentiates the Rapid Evolution of New Traits: Drug Resistance in Diverse Fungi. Science 309 (5744), 2185–2189. doi: 10.1126/science.1118370
Cowen, L. E., Singh, S. D., Köhler, J. R., Collins, C., Zaas, A. K., Schell, W. A., et al. (2009). Harnessing Hsp90 Function as a Powerful, Broadly Effective Therapeutic Strategy for Fungal Infectious Disease. Proc. Natl. Acad. Sci. U. S. A. 106 (8), 2818–2823. doi: 10.1073/pnas.0813394106
Cowen, L. E., Steinbach, W. J. (2008). Stress, Drugs, and Evolution: The Role of Cellular Signaling in Fungal Drug Resistance. Eukaryotic Cell 7 (5), 747–764. doi: 10.1128/EC.00041-08
Cruz, M. C., Goldstein, A. L. (2002). Calcineurin Is Essential for Survival During Membrane Stress in Candida Albicans. EMBO J. 21 (4), 546–559. doi: 10.1093/emboj/21.4.546
Cuddihy, G., Wasan, E. K., Di, Y., Wasan, K. M. (2019). The Development of Oral Amphotericin B to Treat Systemic Fungal and Parasitic Infections: Has the Myth Been Finally Realized? Pharmaceutics 11 (3), 1–16. doi: 10.3390/pharmaceutics11030099
Cushion, M., Ashbaugh, A., Lynch, K., Linke, M. J., Bartizal, K. (2016). Efficacy of CD101, a Novel Echinocandin, in Prevention of Pneumocystis Pneumonia (PCP): Thwarting the Biphasic Life Cycle of Pneumocystis. Blood 128 (22), 3396–3396. doi: 10.1182/blood.V128.22.3396.3396
Dagi, H. T., Findik, D., Senkeles, C., Arslan, U. (2016). Identification and Antifungal Susceptibility of Candida Species Isolated From Bloodstream Infections in Konya, Turkey. Ann. Clin. Microbiol. Antimicrobials 15 (1), 36. doi: 10.1186/s12941-016-0153-1
Day, J. N., Chau, T. T. H., Wolbers, M., Mai, P. P., Dung, N. T., Nguyen, H., et al. (2013). Combination Antifungal Therapy for Cryptococcal Meningitis. New Engl. J. Med. 368 (14), 1291–1302. doi: 10.1056/NEJMoa1110404
Delarze, E., Brandt, L., Trachsel, E., Patxot, M., Pralong, C., Maranzano, F. (2020). Identification and Characterization of Mediators of Fluconazole Tolerance in Candida Albicans. Front. Microbiol. 11, 2695. doi: 10.3389/fmicb.2020.591140
Desai, J. V., Break, T. J., Natarajan, M., Henderson, C., Zelazny, A. M., Hoekstra, W. J., et al. (2016). VT-1129 and VT-1161 Have in Vitro Activity Against Candida Isolates From Patients With Chronic Mucocutaneous Candidiasis. Open Forum Infect. Dis. 3 (suppl_1). doi: 10.1093/ofid/ofw172.1335
Eckschlager, T., Plch, J., Stiborova, M., Hrabeta, J. (2017). Histone Deacetylase Inhibitors as Anticancer Drugs. Int. J. Mol. Sci. 18 (7), 1–25. doi: 10.3390/ijms18071414
El-Halfawy, O. M., Valvano, M. A. (2015). Antimicrobial Heteroresistance: An Emerging Field in Need of Clarity. Clin. Microbiol. Rev. 28 (1), 191–207. doi: 10.1128/CMR.00058-14
Eyre, D. W., Sheppard, A. E., Madder, H., Moir, I., Moroney, R., Phuong Quan, T., et al. (2018). A Candida Auris Outbreak and Its Control in an Intensive Care Setting. New Engl. J. Med. 379 (14), 1322–1331. doi: 10.1056/NEJMoa1714373
Fischer, M. A., Winkelmayer, W. C., Rubin, R. H., Avorn, J. (2005). The Hepatotoxicity of Antifungal Medications in Bone Marrow Transplant Recipients. Clin. Infect. Dis. 41 (3), 301–307. doi: 10.1086/431586
Flowers, S. A., Barker, K. S., Berkow, E. L., Toner, G., Chadwick, S. G., Gygax, S. E., et al. (2012). Gain-Of-Function Mutations in UPC2 Are a Frequent Cause of ERG11 Upregulation in Azole-Resistant Clinical Isolates of Candida Albicans. Eukaryotic Cell 11 (10), 1289–1299. doi: 10.1128/EC.00215-12
Flowers, S. A., Colón, B., Whaley, S. G., Schuler, M. A., Rogers, P. D. (2015). Contribution of Clinically Derived Mutations in ERG11 to Azole Resistance in Candida Albicans. Antimicrob. Agents Chemother. 59 (1), 450–460. doi: 10.1128/AAC.03470-14
Forche, A., Abbey, D., Pisithkul, T., Weinzierl, M. A., Ringstrom, T., Bruck, D., et al. (2011). Stress Alters Rates and Types of Loss of Heterozygosity in Candida Albicans. MBio. 2 (4), 1–9. doi: 10.1128/mBio.00129-11
Ford, C. B., Funt, J. M., Abbey, D., Issi, L., Guiducci, C., Martinez, D. A., et al. (2015). The Evolution of Drug Resistance in Clinical Isolates of Candida Albicans. ELife 4), 1–27. doi: 10.7554/eLife.00662
Francis, P., Walsh, T. J. (1992). Evolving Role of Flucytosine in Immunocompromised Patients: New Insights Into Safety, Pharmacokinetics, and Anti0066ungal Therapy. Clin. Infect. Dis. 15 (6), 1003–1018. doi: 10.1093/clind/15.6.1003
Garcia-Effron, G., Lee, S., Park, S., Cleary, J. D., Perlin, D. S. (2009). Effect of Candida Glabrata FKS1 and FKS2 Mutations on Echinocandin Sensitivity and Kinetics of 1,3-β-D-Glucan Synthase: Implication for the Existing Susceptibility Breakpoint. Antimicrob. Agents Chemother. 53 (9), 3690–3699. doi: 10.1128/AAC.00443-09
Garcia-Rubio, R., Hernandez, R. Y., Clear, A., Healey, K. R., Shor, E., Perlin, D. S. (2021a). Critical Assessment of Cell Wall Integrity Factors Contributing to In Vivo Echinocandin Tolerance and Resistance in Candida Glabrata. Front. Microbiol. 12, 1797. doi: 10.3389/fmicb.2021.702779
Garcia-Rubio, R., Jimenez-Ortigosa, C., Degregorio, L., Quinteros, C., Shor, E., Perlin, D. S. (2021b). Multifactorial Role of Mitochondria in Echinocandin Tolerance Revealed by Transcriptome Analysis of Drug-Tolerant Cells. MBio. 12 (4), 1–20. doi: 10.1128/mBio.01959-21
Garvey, E. P., Hoekstra, W. J., Schotzinger, R. J., Sobel, J. D., Lilly, E. A., Fidel, P. L. (2015). Efficacy of the Clinical Agent VT-1161 Against Fluconazole-Sensitive and -Resistant Candida Albicans in a Murine Model of Vaginal Candidiasis. Antimicrob. Agents Chemother. 59 (9), 5567–5573. doi: 10.1128/AAC.00185-15
Gintjee, T. J., Donnelley, M. A., Thompson, G. R. (2020). Aspiring Antifungals: Review of Current Antifungal Pipeline Developments. J. Fungi 6 (1), 28. doi: 10.3390/jof6010028
Gong, Y., Li, T., Yu, C., Sun, S. (2017). Candida Albicans Heat Shock Proteins and Hsps-Associated Signaling Pathways as Potential Antifungal Targets. Front. Cell. Infect Microbiol. 7 (DEC), 520. doi: 10.3389/fcimb.2017.00520
Grozinger, C. M., Schreiber, S. L. (2002). Deacetylase Enzymes: Biological Functions and the Use of Small-Molecule Inhibitors. Chem. Biol. 9 (1), 3–16. doi: 10.1016/S1074-5521(02)00092-3
Hager, C. L., Larkin, E. L., Long, L., Zohra Abidi, F., Shaw, K. J., Ghannoum, M. A. (2018). In Vitro and in Vivo Evaluation of the Antifungal Activity of APX001A/APX001 Against Candida Auris. Antimicrob Agents Chemother 62 (3), 1–7. doi: 10.1128/AAC.02319-17
Hamill, R. J. (2013). Amphotericin B Formulations: A Comparative Review of Efficacy and Toxicity. Drugs 73 (9), 919–934. doi: 10.1007/s40265-013-0069-4
Hata, K., Horii, T., Miyazaki, M., Aki Watanabe, N., Okubo, M., Sonoda, J., et al. (2011). Efficacy of Oral E1210, a New Broad-Spectrum Antifungal With a Novel Mechanism of Action, in Murine Models of Candidiasis, Aspergillosis, and Fusariosis. Antimicrob. Agents Chemother. 55 (10), 4543–4551. doi: 10.1128/AAC.00366-11
Haynes, M. P., Lee Gau Chong, P., Buckley, H. R., Pieringer, R. A. (1996). Fluorescence Studies on the Molecular Action of Amphotericin B on Susceptible and Resistant Fungal Cells. Biochemistry 35 (24), 7983–7992. doi: 10.1021/bi952910c
Healey, K. R., Kordalewska, M., Jiménez Ortigosa, C., Singh, A., Berrío, I., Chowdhary, A., et al. (2018). Limited ERG11 Mutations Identified in Isolates of Candida Auris Directly Contribute to Reduced Azole Susceptibility. Antimicrob. Agents Chemother. 62 (10), 1–4. doi: 10.1128/AAC.01427-18
Healey, K. R., Ortigosa, C. J., Shor, E., Perlin, D. S. (2016). Genetic Drivers of Multidrug Resistance in Candida Glabrata. Front. Microbiol. 7 (DEC). doi: 10.3389/fmicb.2016.01995
Healey, K. R., Perlin, D. S. (2018). Fungal Resistance to Echinocandins and the MDR Phenomenon in Candida Glabrata. J. Fungi 4 (3), 1–14. doi: 10.20944/preprints201808.0306.v1
Helou, S., Angulo, D. (2017). A Multicenter, Randomized, Evaluator Blinded, Active-Controlled Study to Evaluate the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in 96 Subjects With Moderate to Severe Vulvovaginal Candidiasis. Am. J. Obstetrics Gynecol 217 (6), 720–721. doi: 10.1016/j.ajog.2017.08.099
Herbrecht, R., Fohrer, C., Nivoix, Y. (2006). Mycograb for the Treatment of Invasive Candidiasis. Clin. Infect. Dis. 43 (8), 1083–1083. doi: 10.1086/507547
Hodges, M. R., Ople, E., Shaw, K. J., Mansbach, R., Van Marle, S. P., Van Hoogdalem, E.-J., et al. (2017b). Phase 1 Study to Assess Safety, Tolerability and Pharmacokinetics of Single and Multiple Oral Doses of APX001 and to Investigate the Effect of Food on APX001 Bioavailability. Open Forum Infect. Dis. 4 (suppl_1), S534–S534. doi: 10.1093/ofid/ofx163.1390
Hodges, M. R., Ople, E., Shaw, K. J., Mansbach, R., Van Marle, S. J., Van Hoogdalem, E.-J., et al. (2017a). First-In-Human Study to Assess Safety, Tolerability and Pharmacokinetics of APX001 Administered by Intravenous Infusion to Healthy Subjects. Open Forum Infect. Dis. 4 (suppl_1), S526–S526. doi: 10.1093/ofid/ofx163.1370
Hoekstra, W. J., Garvey, E. P., Moore, W. R., Rafferty, S. W., Yates, C. M., Schotzinger, R. J. (2014). Design and Optimization of Highly-Selective Fungal CYP51 Inhibitors. Bioorg Med Chem. Lett. 24 (15), 3455–3458. doi: 10.1016/j.bmcl.2014.05.068
Hofmann-Thiel, S., Van Ingen, J., Feldmann, K., Turaev, L., Uzakova, G. T., Murmusaeva, G., et al. (2009). Mechanisms of Heteroresistance to Isoniazid and Rifampin of Mycobacterium Tuberculosis in Tashkent, Uzbekistan. Eur. Respir. J. 33 (2), 368–374. doi: 10.1183/09031936.00089808
Hope, W. W., Warn, P. A., Sharp, A., Howard, S., Kasai, M., Louie, A., et al. (2006). Derivation of an In Vivo Drug Exposure Breakpoint for Flucytosine Against Candida Albicans and Impact of the Mic, Growth Rate, and Resistance Genotype on the Antifungal Effect. Antimicrob. Agents Chemother. 50 (11), 3680–3688. doi: 10.1128/AAC.00369-06
Hutchings, M., Truman, A., Wilkinson, B. (2019). Antibiotics: Past, Present and Future. Curr. Opin. Microbiol. 51, 72–80. doi: 10.1016/j.mib.2019.10.008
Iturriaga, G., Suárez, R., Nova-Franco, B. (2009). Trehalose Metabolism: From Osmoprotection to Signaling. Int. J. Mol. Sci. 10 (9), 3793–3810. doi: 10.3390/ijms10093793
Jensen, R. H., Justesen, U. S., Rewes, A., Perlin, D. S., Cavling Arendrup, M. (2014). Echinocandin Failure Case Due to a Previously Unreported Fks1 Mutation in Candida Krusei. Antimicrob. Agents Chemother. 58 (6), 3550–3552. doi: 10.1128/AAC.02367-14
Jiménez-Ortigosa, C., Perez, W. B., Angulo, D., Borroto-Esoda, K., Perlin, D. S. (2017). De Novo Acquisition of Resistance to SCY-078 in Candida Glabrata Involves FKS Mutations That Both Overlap and Are Distinct From Those Conferring Echinocandin Resistance. Antimicrob. Agents Chemother. 61 (9), 1–6. doi: 10.1128/AAC.00833-17
Jung, J. A., Yoon, Y. J. (2020). Development of Non-Immunosuppressive FK506 Derivatives as Antifungal and Neurotrophic Agents. J. Microbiol. Biotechnol. 30 (1), 1–10. doi: 10.4014/jmb.1911.11008
Juvvadi, P. R., Lamoth, F., Steinbach, W. J. (2014). Calcineurin as a Multifunctional Regulator: Unraveling Novel Functions in Fungal Stress Responses, Hyphal Growth, Drug Resistance, and Pathogenesis. Fungal Biol. Rev. 28 (2), 56–69. doi: 10.1016/j.fbr.2014.02.004
Juvvadi, P. R., Lee, S. C., Heitman, J., Steinbach, W. J. (2017). Calcineurin in Fungal Virulence and Drug Resistance: Prospects for Harnessing Targeted Inhibition of Calcineurin for an Antifungal Therapeutic Approach. Virulence 8 (2), 186–197. doi: 10.1080/21505594.2016.1201250
Kapoor, M., Moloney, M., Soltow, Q. A., Pillar, C. M., Shaw, K. J. (2020). Evaluation of Resistance Development to the GWT1 Inhibitor Manogepix (APX001A) in Candida Species. Antimicrob. Agents Chemother. 64 (1), 1–12. doi: 10.1128/AAC.01387-19
Karababa, M., Valentino, E., Pardini, G., Coste, A. T., Bille, J., Sanglard, D. (2006). CRZ1, a Target of the Calcineurin Pathway in Candida Albicans. Mol. Microbiol. 59 (5), 1429–1451. doi: 10.1111/j.1365-2958.2005.05037.x
Kim, S. H., Iyer, K. R., Pardeshi, L., Muñoz, J. F., Robbins, N., Cuomo, C. A., et al. (2019). Genetic Analysis of Candida Auris Implicates Hsp90 in Morphogenesis and Azole Tolerance and Cdr1 in Azole Resistance. MBio. 10 (1), 1–16. doi: 10.1128/mBio.02529-18
Kofla, G., Ruhnke, M. (2011). Pharmacology and Metabolism of Anidulafungin, Caspofungin and Micafungin in the Treatment of Invasive Candidosis - Review of the Literature. Eur. J. Med. Res. 16 (4), 159–166. doi: 10.1186/2047-783X-16-4-159
Koselny, K., Green, J., DiDone, L., Halterman, J. P., Fothergill, A. W., Wiederhold, N. P., et al. (2016a). The Celecoxib Derivative AR-12 Has Broad-Spectrum Antifungal Activity In Vitro and Improves the Activity of Fluconazole in a Murine Model of Cryptococcosis. Antimicrob. Agents Chemother. 60 (12), 7115–7127. doi: 10.1128/AAC.01061-16
Koselny, K., Green, J., Favazzo, L., Glazier, V. E., Didone, L., Ransford, S., et al. (2016b). Antitumor/Antifungal Celecoxib Derivative AR-12 Is a Non-Nucleoside Inhibitor of the ANL-Family Adenylating Enzyme Acetyl CoA Synthetase. ACS Infect. Dis. 2 (4), 268–280. doi: 10.1021/acsinfecdis.5b00134
Lakota, E. A., Ong, V., Flanagan, S., Rubino, C. M. (2018). Population Pharmacokinetic Analyses for Rezafungin (CD101) Efficacy Using Phase 1 Data. Antimicrob Agents Chemother 62 (6), 1–9. doi: 10.1128/AAC.02603-17
Lamoth, F., Kontoyiannis, D. P. (2018). The Candida Auris Alert: Facts and Perspectives. J. Infect. Dis. 217 (4), 516–520. doi: 10.1093/infdis/jix597
Larkin, E., Hager, C., Chandra, J., Mukherjee, P. K., Retuerto, M., Salem, I., et al. (2017). The Emerging Pathogen Candida Auris: Growth Phenotype, Virulence Factors, Activity of Antifungals, and Effect of SCY-078, a Novel Glucan Synthesis Inhibitor, on Growth Morphology and Biofilm Formation. Antimicrob. Agents Chemother. 61 (5), 1–13. doi: 10.1128/AAC.02396-16
Larkin, E. L., Long, L., Isham, N., Borroto-Esoda, K., Barat, S., Angulo, D., et al. (2019). A Novel 1,3-Beta-D-Glucan Inhibitor, IbrexafungeRP (Formerly SCY-078), Shows Potent Activity in the Lower PH Environment of Vulvovaginitis. Antimicrob. Agents Chemother. 63 (5), 1–6. doi: 10.1128/AAC.02611-18
Lazzarini, C., Haranahalli, K., Rieger, R., Krishna Ananthula, H., Desai, P. B., Ashbaugh, A., et al. (2018). Acylhydrazones as Antifungal Agents Targeting the Synthesis of Fungal Sphingolipids. Antimicrob. Agents Chemother. 62 (5), 1–14. doi: 10.1128/AAC.00156-18
Lee, Y., Lee, K. T., Lee, S. J., Yoon Beom, J., Hwangbo, A., Jung, J. A., et al. (2018). In Vitro and In Vivo Assessment of FK506 Analogs as Novel Antifungal Drug Candidates. Antimicrob Agents Chemother 62 (11), 1–17. doi: 10.1128/AAC.01627-18
Lee, K. K., MacCallum, D. M., Jacobsen, M. D., Walker, L. A., Odds, F. C., Gow, N. A. R., et al. (2012). Elevated Cell Wall Chitin in Candida Albicans Confers Echinocandin Resistance In Vivo. Antimicrob. Agents Chemother. 56 (1), 208–217. doi: 10.1128/AAC.00683-11
Lee, A., Prideaux, B., Zimmerman, M., Carter, C., Barat, S., Angulo, D., et al. (2020). Penetration of Ibrexafungerp (Formerly SCY-078) at the Site of Infection in an Intra-Abdominal Candidiasis Mouse Model. Antimicrob. Agents Chemother. 64 (3), 1–11. doi: 10.1128/AAC.02268-19
Lepak, A. J., Andes, D. R. (2015). Antifungal Pharmacokinetics and Pharmacodynamics. Cold Spring Harbor Perspect. Med. 5 (5), 1–23. doi: 10.1101/cshperspect.a019653
Lepak, A. J., Marchillo, K., Andes, D. R. (2015). Pharmacodynamic Target Evaluation of a Novel Oral Glucan Synthase Inhibitor, SCY-078 (MK-3118), Using an in Vivo Murine Invasive Candidiasis Model. Antimicrob Agents Chemother 59 (2), 1265–1272. doi: 10.1128/AAC.04445-14
Lepak, A. J., Zhao, M., Andesa, D. R. (2018a). Pharmacodynamic Evaluation of Rezafungin (CD101) Against Candida Auris in the Neutropenic Mouse Invasive Candidiasis Model. Antimicrob. Agents Chemother. 62 (11), 1–4. doi: 10.1128/AAC.01572-18
Lepak, A. J., Zhao, M., VanScoy, B., Ambrose, P. G., Andes, D. R. (2018b). Pharmacodynamics of a Long-Acting Echinocandin, CD101, in a Neutropenic Invasive-Candidiasis Murine Model Using an Extended-Interval Dosing Design. Antimicrob. Agents Chemother. 62 (2), 1–10. doi: 10.1128/AAC.02154-17
Letscher-Bru, V., Herbrecht, R. (2003). Caspofungin: The First Representative of a New Antifungal Class. J. Antimicrob. Chemother. 51 (3), 513–521. doi: 10.1093/jac/dkg117
Levy, S. F., Ziv, N., Siegal, M. L. (2012). Bet Hedging in Yeast by Heterogeneous, Age-Correlated Expression of a Stress Protectant. PloS Biol. 10 (5), 1001325. doi: 10.1371/journal.pbio.1001325
Liston, S. D., Whitesell, L., Kapoor, M., Shaw, K. J., Cowen, L. E. (2020). Enhanced Efflux Pump Expression in Candida Mutants Results in Decreased Manogepix Susceptibility. Antimicrob. Agents Chemother. 64 (5), 1–7. doi: 10.1128/AAC.00261-20
Liu, J., Farmer, J. D., Lane, W. S., Friedman, J., Weissman, I., Schreiber, S. L. (1991). Calcineurin Is a Common Target of Cyclophilin-Cyclosporin A and FKBP-FK506 Complexes. Cell 66 (4), 807–815. doi: 10.1016/0092-8674(91)90124-H
Liu, T. T., Znaidi, S., Barker, K. S., Xu, L., Homayouni, R., Saidane, S., et al. (2007). Genome-Wide Expression and Location Analyses of the Candida Albicans Tac1p Regulon. Eukaryotic Cell 6 (11), 2122–2138. doi: 10.1128/EC.00327-07
Locke, J. B., Almaguer, A. L., Zuill, D. E., Bartizal, K. (2016). Characterization of In Vitro Resistance Development to the Novel Echinocandin CD101 in Candida Species. Antimicrob. Agents Chemother. 60 (10), 6100–6107. doi: 10.1128/AAC.00620-16
Lockhart, S. R., Etienne, K. A., Vallabhaneni, S., Farooqi, J., Chowdhary, A., Govender, N. P., et al. (2017). Simultaneous Emergence of Multidrug-Resistant Candida Auris on 3 Continents Confirmed by Whole-Genome Sequencing and Epidemiological Analyses. Clin. Infect. Dis. 64 (2), 134–140. doi: 10.1093/cid/ciw691
Maddux, M. S., Barriere, S. L. (1980). A Review of Complications of Amphotericin-B Therapy: Recommendations for Prevention and Management. Drug Intell. Clin. Pharm. 14 (3), 177–181. doi: 10.1177/106002808001400303
Mansbach, R., Shaw, K. J., Hodges, M. R., Coleman, S., Fitzsimmons, M. E. (2017). Absorption, Distribution, and Excretion of 14C-APX001 After Single-Dose Administration to Rats and Monkeys. Open Forum Infect. Dis. 4 (suppl_1), S472–S472. doi: 10.1093/ofid/ofx163.1209
Marchetti, O., Entenza, J. M., Sanglard, D., Bille, J., Glauser, M. P., Moreillon, P. (2000a). Fluconazole Plus Cyclosporine: A Fungicidal Combination Effective Against Experimental Due to Candida Albicans. Antimicrob. Agents Chemother. 44 (11), 2932–2938. doi: 10.1128/AAC.44.11.2932-2938.2000
Marchetti, O., Moreillon, P., Glauser, M. P., Bille, J., Sanglard, D. (2000b). Potent Synergism of the Combination of Fluconazole and Cyclosporine in Candida Albicans. Antimicrob. Agents Chemother. 44 (9), 2373–2381. doi: 10.1128/AAC.44.9.2373-2381.2000
Marr, K. A., Lyons, C. N., Ha, K., Rustad, T. R., White, T. C. (2001). Inducible Azole Resistance Associated With a Heterogeneous Phenotype in Candida Albicans. Antimicrob. Agents Chemother. 45 (1), 52–59. doi: 10.1128/AAC.45.1.52-59.2001
Martínez-Esparza, M., Aguinaga, A., González-Párraga, P., García-Peñarrubia, P., Jouault, T., Argüelles, J. C. (2007). Role of Trehalose in Resistance to Macrophage Killing: Study With a Tps1/Tps1 Trehalose-Deficient Mutant of Candida Albicans. Clin. Microbiol. Infect 13 (4), 384–394. doi: 10.1111/j.1469-0691.2007.01663.x
McClellan, A. J., Xia, Y., Deutschbauer, A. M., Davis, R. W., Gerstein, M., Frydman, J. (2007). Diverse Cellular Functions of the Hsp90 Molecular Chaperone Uncovered Using Systems Approaches. Cell 131 (1), 121–135. doi: 10.1016/j.cell.2007.07.036
Miaoa, Y., Tenorb, J. L., Toffalettib, D. L., Washingtona, E. J., Liuc, J., Shadrickc, W. R., et al. (2016). Structures of Trehalose-6-Phosphate Phosphatase From Pathogenic Fungi Reveal the Mechanisms of Substrate Recognition and Catalysis. Proc. Natl. Acad. Sci. U. S. A. 113 (26), 7148–7153. doi: 10.1073/pnas.1601774113
Miceli, M. H., Kauffman, C. A. (2015). Isavuconazole: A New Broad-Spectrum Triazole Antifungal Agent. Clin. Infect. Dis. 61 (10), 1558–1565. doi: 10.1093/cid/civ571
Mitsuyama, J., Nomura, N., Hashimoto, K., Yamada, E., Nishikawa, H., Kaeriyama, M., et al. (2008). In Vitro and in Vivo Antifungal Activities of T-2307, a Novel Arylamidine. Antimicrob. Agents Chemother. 52 (4), 1318–1324. doi: 10.1128/AAC.01159-07
Miyazaki, M., Horii, T., Hata, K., Aki Watanabe, N., Nakamoto, K., Tanaka, K., et al. (2011). In Vitro Activity of E1210, a Novel Antifungal, Against Clinically Important Yeasts and Molds. Antimicrob. Agents Chemother. 55 (10), 4652–4658. doi: 10.1128/AAC.00291-11
Molloy, S. F., Kanyama, C., Heyderman, R. S., Loyse, A., Kouanfack, C., Chanda, D., et al. (2018). Antifungal Combinations for Treatment of Cryptococcal Meningitis in Africa. New Engl. J. Med. 378 (11), 1004–1017. doi: 10.1056/NEJMoa1710922
Monk, B. C., Keniya, M. V., Sabherwal, M., Wilson, R. K., Graham, D. O., Hassan, H. F., et al. (2019). Azole Resistance Reduces Susceptibility to the Tetrazole Antifungal VT-1161. Antimicrob. Agents Chemother. 63 (1), 1–19. doi: 10.1128/AAC.02114-18
Morand, B., Mühlemann, K. (2007). Heteroresistance to Penicillin in Streptococcus Pneumoniae. Proc. Natl. Acad. Sci. U.S.A. 104 (35), 14098–14103. doi: 10.1073/pnas.0702377104
Mor, V., Rella, A., Farnou, A. M., Singh, A., Munshi, M., Bryan, A., et al. (2015). Identification of a New Class of Antifungals Targeting the Synthesis of Fungal Sphingolipids. MBio 6 (3), 1–2. doi: 10.1128/mBio.00647-15
Nagayoshi, Y., Miyazaki, T., Minematsu, A., Yamauchi, S., Takazono, T., Nakamura, S. (2014). Contribution of the Slt2-Regulated Transcription Factors to Echinocandin Tolerance in Candida Glabrata. FEMS Yeast Res. 14 (7), 1128–1131. doi: 10.1111/1567-1364.12204
NCT02267382 (2014) “A Study to Evaluate Oral VT-1161 in the Treatment of Patients With Recurrent Vaginal Candidiasis (Yeast Infection). Available at: https://www.cochranelibrary.com/central/doi/10.1002/central/CN-01549513/full.
NCT03253094 (2017). “An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis. Available at: https://www.cochranelibrary.com/central/doi/10.1002/central/CN-01495832/full.
Nguyen, S., Truong, J. Q., Bruning, J. B. (2021). Targeting Unconventional Pathways in Pursuit of Novel Antifungals. Front. Mol. Biosci. 7, 479. doi: 10.3389/fmolb.2020.621366
Nishikawa, H., Fukuda, Y., Mitsuyama, J., Tashiro, M., Tanaka, A., Takazono, T., et al. (2017). In Vitro and in Vivo Antifungal Activities of T-2307, a Novel Arylamidine, Against Cryptococcus Gattii: An Emerging Fungal Pathogen. J. Antimicrob. Chemother. 72 (6), 1709–1713. doi: 10.1093/jac/dkx020
Nishikawa, H., Sakagami, T., Yamada, E., Fukuda, Y., Hayakawa, H., Nomura, N., et al. (2016). T-2307, a Novel Arylamidine, Is Transported Into Candida Albicans by a High-Affinity Spermine and Spermidine Carrier Regulated by Agp2. J. Antimicrob Chemother 71 (7), 1845–1855. doi: 10.1093/jac/dkw095
Nishikawa, H., Yamada, E., Shibata, T., Uchihashi, S., Fan, H., Hayakawa, H., et al. (2010). Uptake of T-2307, a Novel Arylamidine, in Candida Albicans. J. Antimicrob. Chemother. 65 (8), 1681–1687. doi: 10.1093/jac/dkq177
Nishimoto, A. T., Wiederhold, N. P., Flowers, S. A., Zhang, Q., Kelly, S. L., Morschhäuser, J., et al. (2019). In Vitro Activities of the Novel Investigational Tetrazoles Vt-1161 and Vt-1598 Compared to the Triazole Antifungals Against Azole-Resistant Strains and Clinical Isolates of Candida Albicans. Antimicrob. Agents Chemother. 63 (6), 1–11. doi: 10.1128/AAC.00341-19
Noble, S. M., French, S., Kohn, L. A., Chen, V., Johnson, A. D. (2010). Systematic Screens of a Candida Albicans Homozygous Deletion Library Decouple Morphogenetic Switching and Pathogenicity. Nat. Genet. 42 (7), 590–598. doi: 10.1038/ng.605
Nolte, F. S., Parkinson, T., Falconer, D. J., Dix, S., Williams, J., Gilmore, C., et al. (1997). Isolation and Characterization of Fluconazole- and Amphotericin B- Resistant Candida Albicans From Blood of Two Patients With Leukemia. Antimicrob Agents Chemother 41 (1), 196–199. doi: 10.1128/AAC.41.1.196
Nunes, A. P. F., Teixeira, L. M., Lopes Pontes Iorio, N., Callegário Reis Bastos, C., de Sousa Fonseca, L., Souto-Padrón, T., et al. (2006). Heterogeneous Resistance to Vancomycin in Staphylococcus Epidermidis, Staphylococcus Haemolyticus and Staphylococcus Warneri Clinical Strains: Characterisation of Glycopeptide Susceptibility Profiles and Cell Wall Thickening. Int. J. Antimicrob. Agents 27 (4), 307–315. doi: 10.1016/j.ijantimicag.2005.11.013
Nunnally, N. S., Etienne, K. A., Angulo, D., Lockhart, S. R., Berkow, E. L. (2019). In Vitro Activity of Ibrexafungerp, a Novel Glucan Synthase Inhibitor Against Candida Glabrata Isolates With FKS Mutations. Antimicrob. Agents Chemother. 63 (11), 1–4. doi: 10.1128/AAC.01692-19
O’Brien, B., Chaturvedi, S., Chaturvedi, V. (2020). In Vitro Evaluation of Antifungal Drug Combinations Against Multidrug-Resistant Candida Auris Isolates From New York Outbreak. Antimicrob Agents Chemother 64 (4), 1–5. doi: 10.1128/AAC.02195-19
Ong, V., Hough, G., Schlosser, M., Bartizal, K., Balkovec, J. M., James, K. D., et al. (2016). Preclinical Evaluation of the Stability, Safety, and Efficacy of CD101, a Novel Echinocandin. Antimicrob. Agents Chemother. 60 (11), 6872–6879. doi: 10.1128/AAC.00701-16
Onyewu, C., Blankenship, J. R., Del Poeta, M., Heitman, J. (2003). Ergosterol Biosynthesis Inhibitors Become Fungicidal When Combined With Calcineurin Inhibitors Against Candida Albicans, Candida Glabrata, and Candida Krusei. Antimicrob. Agents Chemother. 47 (3), 956–964. doi: 10.1128/AAC.47.3.956-964.2003
Oura, T., Kajiwara, S. (2010). Candida Albicans Sphingolipid C9-Methyltransferase Is Involved in Hyphal Elongation. Microbiology 156 (4), 1234–1243. doi: 10.1099/mic.0.033985-0
Pachl, J., Svododa, P., Jacobs, F., Vandewoude, K., van der Hoven, B., Spronk, P., et al. (2006). A Randomized, Blinded, Multicenter Trial of Lipid-Associated Amphotericin B Alone Versus in Combination With an Antibody-Based Inhibitor of Heat Shock Protein 90 in Patients With Invasive Candidiasis. Clin. Infect. Dis. 42 (10), 1404–1413. doi: 10.1086/503428
Pappas, P. G., Kauffman, C. A., Andes, D. R., Clancy, C. J., Marr, K. A., Ostrosky-Zeichner, L. (2015). Clinical Practice Guideline for the Management of Candidiasis: 2016 Update by the Infectious Diseases Society of America. Clin. Infect. Dis. 62 (4), e1–50. doi: 10.1093/cid/civ933
Pappas, P. G., Lionakis, M. S., Arendrup, M. C., Ostrosky-Zeichner, L., Jan Kullberg, B. (2018). Invasive Candidiasis. Nat. Rev. Dis. Primers 4 (1), 1–20. doi: 10.1038/nrdp.2018.26
Pegorie, M., Denning, D. W., Welfare, W. (2017). Estimating the Burden of Invasive and Serious Fungal Disease in the United Kingdom. J. Infect. 74 (1), 60–71. doi: 10.1016/j.jinf.2016.10.005
Perfect, J. R., Dismukes, W. E., Dromer, F., Goldman, D. L., Graybill, J. R., Hamill, R. J. (2010). Clinical Practice Guidelines for the Management of Cryptococcal Disease: 2010 Update by the Infectious Diseases Society of America. Clin. Infect. Dis. 50 (3), 291–322. doi: 10.1086/649858
Perfect, J. R., Ghannoum, M. (2020). Emerging Issues in Antifungal Resistance. Infect. Dis. Clinics North America 34 (4), 921–943. doi: 10.1016/j.idc.2020.05.003
Perfect, J. R., Tenor, J. L., Miao, Y, Brennan, R. G. (2017). Trehalose Pathway as an Antifungal Target. Virulence 8 (2), 143–149. doi: 10.1080/21505594.2016.1195529
Perlin, D. S. (2015). Echinocandin Resistance in Candida. Clin. Infect. Dis. 61 (Suppl 6), S612–S617. doi: 10.1093/cid/civ791
Pfaller, M. A., Diekema, D. J., Turnidge, J. D., Castanheira, M., Jones, R. N. (2019). Twenty Years of the SENTRY Antifungal Surveillance Program: Results for Candida Species From 1997-2016. Open Forum Infect. Dis. 6 (Suppl 1), S79–S94. doi: 10.1093/ofid/ofy358
Pfaller, M. A., Espinel-Ingroff, A., Canton, E., Castanheira, M., Cuenca-Estrella, M., Diekema, D. J., et al. (2012). Wild-Type MIC Distributions and Epidemiological Cutoff Values for Amphotericin B, Flucytosine, and Itraconazole and Candida Spp. As Determined by CLSI Broth Microdilution. J. Clin. Microbiol. 50 (6), 2040–2046. doi: 10.1128/JCM.00248-12
Pfaller, M. A., Hata, K., Jones, R. N., Messer, S. A., Moet, G. J., Castanheira, M. (2011a). In Vitro Activity of a Novel Broad-Spectrum Antifungal, E1210, Tested Against Candida Spp. As Determined by Clsi Broth Microdilution Method. Diagn. Microbiol. Infect. Dis. 71 (2), 167–170. doi: 10.1016/j.diagmicrobio.2011.05.001
Pfaller, M. A., Messer, S. A., Georgopapadakou, N., Martell, L. A., Besterman, J. M., Diekema, D. J. (2009). Activity of MGCD290, a Hos2 Histone Deacetylase Inhibitor, in Combination With Azole Antifungals Against Opportunistic Fungal Pathogens. J. Clin. Microbiol. 47 (12), 3797–3804. doi: 10.1128/JCM.00618-09
Pfaller, M. A., Messer, S. A., Motyl, M. R., Jones, R. N., Castanheira, M. (2013). Activity of MK-3118, a New Oral Glucan Synthase Inhibitor, Tested Against Candida Spp. By Two International Methods (CLSI and EUCAST). J. Antimicrob Chemother 68 (4), 858–863. doi: 10.1093/jac/dks466
Pfaller, M. A., Messer, S. A., Rhomberg, P. R., Borroto-Esoda, K., Castanheira, M. (2017a). Differential Activity of the Oral Glucan Synthase Inhibitor SCY-078 Against Wild-Type and Echinocandin-Resistant Strains of Candida Species. Antimicrob. Agents Chemother. 61 (8), 1–9. doi: 10.1128/AAC.00161-17
Pfaller, M. A., Messer, S. A., Rhomberg, P. R., Castanheira, M. (2017b). CD101, a Long-Acting Echinocandin, and Comparator Antifungal Agents Tested Against a Global Collection of Invasive Fungal Isolates in the SENTRY 2015 Antifungal Surveillance Program. Int. J. Antimicrob. Agents 50 (3), 352–358. doi: 10.1016/j.ijantimicag.2017.03.028
Pfaller, M. A., Messer, S. A., Rhomberg, P. R., Jones, R. N., Castanheira, M. (2016). Activity of a Long-Acting Echinocandin, CD101, Determined Using CLSI and EUCAST Reference Methods, Against Candida and Aspergillus Spp., Including Echinocandin- and Azole-Resistant Isolates. J. Antimicrob. Chemother. 71 (10), 2868–2873. doi: 10.1093/jac/dkw214
Pfaller, M., Moet, G. J., Messer, S. A., Jones, R. N., Castanheira, M. (2011b). Geographic Variations in Species Distribution and Echinocandin and Azole Antifungal Resistance Rates Among Candida Bloodstream Infection Isolates: Report From the SENTRY Antimicrobial Surveillance Program, (2008 to 2009). J. Clin. Microbiol. 49 (1), 396–399. doi: 10.1128/JCM.01398-10
Pfaller, M. A., Rhomberg, P. R., Messer, S. A., Castanheira, M. (2015). In Vitro Activity of a Hos2 Deacetylase Inhibitor, MGCD290, in Combination With Echinocandins Against Echinocandin-Resistant Candida Species. Diagn. Microbiol. Infect. Dis. 81 (4), 259–263. doi: 10.1016/j.diagmicrobio.2014.11.008
Pouliot, M., Jeanmart, S. (2016). Pan Assay Interference Compounds (PAINS) and Other Promiscuous Compounds in Antifungal Research. J. Med Chem. 59 (2), 497–503. doi: 10.1021/acs.jmedchem.5b00361
Pournaras, S., Ikonomidis, A., Markogiannakis, A., Maniatis, A. N., Tsakris, A. (2005). Heteroresistance to Carbapenems in Acinetobacter Baumannii. J. Antimicrob. Chemother. 55 (6), 1055–1056. doi: 10.1093/jac/dki115
Prasad, R., Rawal, M. K., Haseeb Shah, A. (2016). “Candida Efflux ATPases and Antiporters in Clinical Drug Resistance.,” in Advances in Experimental Medicine and Biology, vol. 892. (Cham: Springer New York LLC), 351–376.
Reedy, J. L., Filler, S. G., Heitman, J. (2010). Elucidating the Candida Albicans Calcineurin Signaling Cascade Controlling Stress Response and Virulence. Fungal Genet. Biol. 47 (2), 107–116. doi: 10.1016/j.fgb.2009.09.002
Robbins, N., Leach, M. D., Cowen, L. E. (2012). Lysine Deacetylases Hda1 and Rpd3 Regulate Hsp90 Function Thereby Governing Fungal Drug Resistance. Cell Rep. 2 (4), 878–888. doi: 10.1016/j.celrep.2012.08.035
Rodrigues, M. L., Shi, L., Barreto-Bergter, E., Nimrichter, L., Farias, S. E., Rodrigues, E. G., et al. (2007). Monoclonal Antibody to Fungal Glucosylceramide Protects Mice Against Lethal Cryptococcus Neoformans Infection. Clin. Vaccine Immunol. 14 (10), 1372–1376. doi: 10.1128/CVI.00202-07
Rogers, P. D., Barker, K. S. (2002). Evaluation of Differential Gene Expression in Fluconazole-Susceptible and -Resistant Isolates of Candida Albicans by CDNA Microarray Analysis. Antimicrob. Agents Chemother. 46 (11), 3412–3417. doi: 10.1128/AAC.46.11.3412-3417.2002
Rollin-Pinheiro, R., Singh, A., Barreto-Bergter, E., Del Poeta, M. (2016). Sphingolipids as Targets for Treatment of Fungal Infections. Future Med. Chem. 8 (12), 1469–1484. doi: 10.4155/fmc-2016-0053
Rosenberg, A., Ene, I. V., Bibi, M., Zakin, S., Shtifman Segal, E., Ziv, N., et al. (2018). Antifungal Tolerance Is a Subpopulation Effect Distinct From Resistance and Is Associated With Persistent Candidemia. Nat. Commun. 9 (1), 1–14. doi: 10.1038/s41467-018-04926-x
Ruiz-Gaitán, A., Moret, A. M., Tasias-Pitarch, M., Aleixandre-López, A. I., Martínez-Morel, H., Calabuig, E., et al. (2018). An Outbreak Due to Candida Auris With Prolonged Colonisation and Candidaemia in a Tertiary Care European Hospital. Mycoses 61 (7), 498–505. doi: 10.1111/myc.12781
Saito, K., Takakuwa, N., Ohnishi, M., Oda, Y. (2006). Presence of Glucosylceramide in Yeast and Its Relation to Alkali Tolerance of Yeast. Appl. Microbiol. Biotechnol. 71 (4), 515–521. doi: 10.1007/s00253-005-0187-3
Sandison, T., Ong, V., Lee, J., Thye, D. (2017). Safety and Pharmacokinetics of CD101 IV, a Novel Echinocandin, in Healthy Adults. Antimicrob. Agents Chemother. 61 (2), 1–11. doi: 10.1128/AAC.01627-16
Sanglard, D., Ischer, F., Marchetti, O., Entenza, J., Bille, J. (2003). Calcineurin A of Candida Albicans: Involvement in Antifungal Tolerance, Cell Morphogenesis and Virulence. Mol. Microbiol. 48 (4), 959–976. doi: 10.1046/j.1365-2958.2003.03495.x
Santangelo, R., Paderu, P., Delmas, G., Chen, Z. W., Mannino, R., Zarif, L., et al. (2000). Efficacy of Oral Cochleate-Amphotericin B in a Mouse Model of Systemic Candidiasis. Antimicrob. Agents Chemother. 44 (9), 2356–2360. doi: 10.1128/AAC.44.9.2356-2360.2000
Sasse, C., Dunkel, N., Schäfer, T., Schneider, S., Dierolf, F., Ohlsen, K., et al. (2012). The Stepwise Acquisition of Fluconazole Resistance Mutations Causes a Gradual Loss of Fitness in Candida Albicans. Mol. Microbiol. 86 (3), 539–556. doi: 10.1111/j.1365-2958.2012.08210.x
Schelenz, S., Hagen, F., Rhodes, J. L., Abdolrasouli, A., Chowdhary, A., Hall, A., et al. (2016). First Hospital Outbreak of the Globally Emerging Candida Auris in a European Hospital. Antimicrob. Resist. Infect Control 5 (1), 35. doi: 10.1186/s13756-016-0132-5
Schell, W. A., Jones, A. M., Garvey, E. P., Hoekstra, W. J., Schotzinger, R. J., Alexander, B. D. (2017a). Fungal CYP51 Inhibitors VT-1161 and VT-1129 Exhibit Strong In Vitro Activity Against Candida Glabrata and C. Krusei Isolates Clinically Resistant to Azole and Echinocandin Antifungal Compounds. Antimicrob. Agents Chemother. 61 (3), 1–3. doi: 10.1128/AAC.01817-16
Schell, W. A., Jones, A. M., Borroto-Esoda, K., Alexander, B. D. (2017b). Antifungal Activity of SCY-078 and Standard Antifungal Agents Against 178 Clinical Isolates of Resistant and Susceptible Candida Species. Antimicrob. Agents Chemother. 61 (11), 1–6. doi: 10.1128/AAC.01102-17
Sears, D., Schwartz, B. S. (2017). Candida Auris: An Emerging Multidrug-Resistant Pathogen. Int. J. Infect. Dis. 63, 95–98. doi: 10.1016/j.ijid.2017.08.017
Segarra, I., Movshin, D. A., Zarif, L. (2002). Pharmacokinetics and Tissue Distribution After Intravenous Administration of a Single Dose of Amphotericin B Cochleates, a New Lipid-Based Delivery System. J. Pharm. Sci. 91 (8), 1827–1837. doi: 10.1002/jps.10173
Selmecki, A. M., Dulmage, K., Cowen, L. E., Anderson, J. B., Berman, J. (2009). Acquisition of Aneuploidy Provides Increased Fitness During the Evolution of Antifungal Drug Resistance” Edited by H. D. Madhani. PloS Genet. 5 (10), 1–16. doi: 10.1371/journal.pgen.1000705
Selmecki, A., Forche, A., Berman, J. (2006). Aneuploidy and Isochromosome Formation in Drug-Resistant Candida Albicans, Science Vol. 313.
Sharma, C., Kumar, N., Pandey, R., Meis, J. F., Chowdhary, A. (2016). Whole Genome Sequencing of Emerging Multidrug Resistant Candida Auris Isolates in India Demonstrates Low Genetic Variation. New Microbes New Infect. 13, 77–82. doi: 10.1016/j.nmni.2016.07.003
Shende, P., Khair, R., Gaud, R. S. (2019). Nanostructured Cochleates: A Multi-Layered Platform for Cellular Transportation of Therapeutics. Drug Dev. Ind. Pharm. 45 (6), 869–881. doi: 10.1080/03639045.2019.1583757
Sherry, L., Ramage, G., Kean, R., Borman, A., Johnson, E. M., Richardson, M. D., et al. (2017). Biofilm-Forming Capability of Highly Virulent, Multidrug-Resistant Candida Auris. Emerging Infect. Dis. 23 (2), 328–331. doi: 10.3201/eid2302.161320
Shibata, T., Takahashi, T., Yamada, E., Kimura, A., Nishikawa, H., Hayakawa, H., et al. (2012). T-2307 Causes Collapse of Mitochondrial Membrane Potential in Yeast. Antimicrob. Agents Chemother. 56 (11), 5892–5897. doi: 10.1128/AAC.05954-11
Shor, E., Perlin, D. S. (2015). Coping With Stress and the Emergence of Multidrug Resistance in Fungi” Edited by J. Heitman. PloS Pathog. 11 (3), 1–7. doi: 10.1371/journal.ppat.1004668
Singh-Babak, S. D., Babak, T., Diezmann, S., Hill, J. A., Lucy Xie, J., Lien Chen, Y., et al. (2012). Global Analysis of the Evolution and Mechanism of Echinocandin Resistance in Candida Glabrata. PloS Pathog. 8 (5), e1002718. doi: 10.1371/journal.ppat.1002718
Singh, S. D., Robbins, N., Zaas, A. K., Schell, W. A., Perfect, J. R., Cowen, L. E. (2009). Hsp90 Governs Echinocandin Resistance in the Pathogenic Yeast Candida Albicans via Calcineurin” Edited by A. P. Mitchell. PloS Pathog. 5 (7), e1000532. doi: 10.1371/journal.ppat.1000532
Sionov, E., Lee, H., Chang, Y. C., Kwon-Chung, K. J. (2010). Cryptococcus Neoformans Overcomes Stress of Azole Drugs by Formation of Disomy in Specific Multiple Chromosomes. PloS Pathog. 6 (4), 1–13. doi: 10.1371/journal.ppat.1000848
Smith, W. L., Edlind, T. D. (2002). Histone Deacetylase Inhibitors Enhance Candida Albicans Sensitivity to Azoles and Related Antifungals: Correlation With Reduction in CDR and ERG Upregulation. Antimicrob. Agents Chemother. 46 (11), 3532–3539. doi: 10.1128/AAC.46.11.3532-3539.2002
Spec, AJ, Pullman, J., Thompson, G. R., Powderly, W. G., Tobin, E. H., Vazquez, J., et al. (2019). MSG-10: A Phase 2 Study of Oral Ibrexafungerp (SCY-078) Following Initial Echinocandin Therapy in Non-Neutropenic Patients With Invasive Candidiasis. J. Antimicrob. Chemother. 74 (10), 3056–3062. doi: 10.1093/jac/dkz277
Stone, N. R. H., Rhodes, J., Fisher, M. C., Mfinanga, S., Kivuyo, S., Rugemalila, J., et al. (2019). Dynamic Ploidy Changes Drive Fluconazole Resistance in Human Cryptococcal Meningitis. J. Clin. Invest. 129 (3), 999–1014. doi: 10.1172/JCI124516
Thewes, S. (2014). Calcineurin-Crz1 Signaling in Lower Eukaryotes. Eukaryotic Cell 13 (6), 694–705. doi: 10.1128/EC.00038-14
Thompson, G. R., Soriano, A., Skoutelis, A., Vazquez, J. A., Honore, P. M., Horcajada, J. P., et al. (2020). Rezafungin Versus Caspofungin in a Phase 2, Randomized, Double-Blind Study for the Treatment of Candidemia and Invasive Candidiasis: The STRIVE Trial. Clin. Infect. Dis. 1–9. doi: 10.1093/cid/ciaa1380
Toda, M., Williams, S. R., Berkow, E. L., Farley, M. M., Harrison, L. H., Bonner, L., et al. (2019). Population-Based Active Surveillance for Culture-Confirmed Candidemia — Four Sites, United State–2016. MMWR Surveillance Summaries 68 (8), 1–17. doi: 10.15585/mmwr.ss6808a1
Tsukahara, K., Hata, K., Nakamoto, K., Sagane, K., Aki Watanabe, N., Kuromitsu, J., et al. (2003). Medicinal Genetics Approach Towards Identifying the Molecular Target of a Novel Inhibitor of Fungal Cell Wall Assembly. Mol. Microbiol. 48 (4), 1029–1042. doi: 10.1046/j.1365-2958.2003.03481.x
UTZ, J. P. (1964). Amphotericin B Toxicity. Ann. Internal Med. 61 (2), 334. doi: 10.7326/0003-4819-61-2-334
Vallabhaneni, S., Kallen, A., Tsay, S., Chow, N., Welsh, R., Kerins, J., et al. (2017). Investigation of the First Seven Reported Cases of Candida Auris, a Globally Emerging Invasive, Multidrug-Resistant Fungus—United States, May 2013–August 2016. Am. J. Transplant. 17 (1), 296–299. doi: 10.1111/ajt.14121
Van Der Horst, C. M., Saag, M. S., Cloud, G. A., Hamill, R. J., Graybill, J. R., Sobel, J. D., et al. (1997). Treatment of Cryptococcal Meningitis Associated With the Acquired Immunodeficiency Syndrome. New Engl. J. Med. 337 (1), 15–21. doi: 10.1056/NEJM199707033370103
Van Dijck, P., De Rop, L., Szlufcik, K., Van Ael, E., Thevelein, J. M. (2002). Disruption of the Candida Albicans TPS2 Gene Encoding Trehalose-6-Phosphate Phosphatase Decreases Infectivity Without Affecting Hypha Formation. Infect. Immun. 70 (4), 1772–1782. doi: 10.1128/IAI.70.4.1772-1782.2002
Varma, A., Kwon-Chung, K. J. (2010). Heteroresistance of Cryptococcus Gattii to Fluconazole. Antimicrob. Agents Chemother. 54 (6), 2303–2311. doi: 10.1128/AAC.00153-10
Walker, L. A., Gow, N. A. R., Munro, C. A. (2013). Elevated Chitin Content Reduces the Susceptibility of Candida Species to Caspofungin. Antimicrob. Agents Chemother. 57 (1), 146–154. doi: 10.1128/AAC.01486-12
Warrilow, A. G. S., Hull, C. M., Parker, J. E., Garvey, E. P., Hoekstra, W. J., Moore, W. R., et al. (2014). The Clinical Candidate VT-1161 Is a Highly Potent Inhibitor of Candida Albicans CYP51 But Fails to Bind the Human Enzyme. Antimicrob. Agents Chemother. 58 (12), 7121–7127. doi: 10.1128/AAC.03707-14
Warrilow, A. G. S., Parker, J. E., Price, C. L., Nes, W. D., Garvey, E. P., Hoekstra, W. J. (2016). The Investigational Drug VT-1129 Is a Highly Potent Inhibitor of Cryptococcus Species CYP51 But Only Weakly Inhibits the Human Enzyme. Antimicrob. Agents Chemother. 60 (8), 4530–4538. doi: 10.1128/AAC.00349-16
Watanabe, N. A., Miyazaki, M., Horii, T., Sagane, K., Tsukahara, K., Hata, K. (2012). E1210, a New Broad-Spectrum Antifungal, Suppresses Candida Albicans Hyphal Growth Through Inhibition of Glycosylphosphatidylinositol Biosynthesis. Antimicrob. Agents Chemother. 56 (2), 960–971. doi: 10.1128/AAC.00731-11
White, T. C. (1997). Increased MRNA Levels of ERG16, CDR, and MDR1 Correlate, With Increases in Azole Resistance in Candida Albicans Isolates From a Patient Infected With Human Immunodeficiency Virus. Antimicrob. Agents Chemother. 41.
Whitesell, L., Robbins, N., Huang, D. S., McLellan, C. A., Shekhar-Guturja, T., LeBlanc, E. V. (2019). Structural Basis for Species-Selective Targeting of Hsp90 in a Pathogenic Fungus. Nat. Commun. 10 (1), 1–17. doi: 10.1038/s41467-018-08248-w
Wiederhold, N. P., Lockhart, S. R., Najvar, L. K., Berkow, E. L., Jaramillo, R., Olivo, M., et al. (2019). The Fungal Cyp51-Specific Inhibitor VT-1598 Demonstrates In Vitro and In Vivo Activity Against Candida Auris. Antimicrob. Agents Chemother. 63 (3), 1–9. doi: 10.1128/AAC.02233-18
Wiederhold, N. P., Najvar, L. K., Fothergill, A. W., Bocanegra, R., Olivo, M., McCarthy, D. I., et al. (2016). The Novel Arylamidine T-2307 Demonstrates in Vitro and in Vivo Activity Against Echinocandin-Resistant Candida Glabrata. J. Antimicrob. Chemother. 71 (3), 692–695. doi: 10.1093/jac/dkv398
Wiederhold, N. P., Najvar, L. K., Fothergill, A. W., Bocanegra, R., Olivo, M., McCarthy, D. I., et al. (2015a). The Novel Arylamidine T-2307 Maintains in Vitro and in Vivo Activity Against Echinocandin-Resistant Candida Albicans. Antimicrob. Agents Chemother. 59 (2), 1341–1343. doi: 10.1128/AAC.04228-14
Wiederhold, N. P., Najvar, L. K., Fothergill, A. W., McCarthy, D. I., Bocanegra, R., Olivo, M. (2015b). The Investigational Agent E1210 Is Effective in Treatment of Experimental Invasive Candidiasis Caused by Resistant Candida Albicans. Antimicrob. Agents Chemother. 59 (1), 690–692. doi: 10.1128/AAC.03944-14
Wiederhold, N. P., Najvar, L. K., Jaramillo, R., Olivo, M., Patterson, H., Connell, A. (2020). The Novel Arylamidine T-2307 Demonstrates in Vitro and in Vivo Activity Against Candida Auris. Antimicrob. Agents Chemother. 64 (3), 1–5. doi: 10.1128/AAC.02198-19
Wiederhold, N. P., Najvar, L. K., Jaramillo, R., Olivo, M., Pizzini, J., Catano, G., et al. (2018). Oral Glucan Synthase Inhibitor SCY-078 Is Effective in an Experimental Murine Model of Invasive Candidiasis Caused by WT and Echinocandin-Resistant Candida Glabrata. J. Antimicrob. Chemother. 73 (2), 448–451. doi: 10.1093/jac/dkx422
Wring, S., Murphy, G., Atiee, G., Corr, C., Hyman, M., Willett, M., et al. (2018). Lack of Impact by SCY-078, a First-In-Class Oral Fungicidal Glucan Synthase Inhibitor, on the Pharmacokinetics of Rosiglitazone, a Substrate for CYP450 2c8, Supports the Low Risk for Clinically Relevant Metabolic Drug-Drug Interactions. J. Clin. Pharmacol. 58 (10), 1305–1313. doi: 10.1002/jcph.1146
Wring, S. A., Randolph, R., Hee Park, S., Abruzzo, G., Chen, Q., Flattery, A., et al. (2017). Preclinical Pharmacokinetics and Pharmacodynamic Target of SCY-078, a First-In-Class Orally Active Antifungal Glucan Synthesis Inhibitor, in Murine Models of Disseminated Candidiasis. Antimicrob. Agents Chemother. 61 (4). doi: 10.1128/AAC.02068-16
Yamada, E., Nishikawa, H, Nomura, N., Mitsuyama, J. (2010). T-2307 Shows Efficacy in a Murine Model of Candida Glabrata Infection Despite In Vitro Trailing Growth Phenomena. Antimicrob. Agents Chemother. 54 (9), 3630–3634. doi: 10.1128/AAC.00355-10
Yamashita, K., Miyazaki, T., Fukuda, Y., Mitsuyama, J., Saijo, T., Shimamura, S., et al. (2019). The Novel Arylamidine T-2307 Selectively Disrupts Yeast Mitochondrial Function by Inhibiting Respiratory Chain Complexes. Antimicrob. Agents Chemother. 63 (8), 1–10. doi: 10.1128/AAC.00374-19
Yang, F., Kravets, A., Bethlendy, G., Welle, S., Rustchenko, E. (2013). Chromosome 5 Monosomy of Candida Albicans Controls Susceptibility to Various Toxic Agents, Including Major Antifungals. Antimicrob. Agents Chemother. 57 (10), 5026–5036. doi: 10.1128/AAC.00516-13
Yang, F., Teoh, F., Shin Min Tan, A., Cao, Y., Pavelka, N., Berman, J., et al. (2019). Aneuploidy Enables Cross-Adaptation to Unrelated Drugs. Mol. Biol. Evol. 36 (8), 1768–1782. doi: 10.1093/molbev/msz104
Yang, F., Zhang, L., Wakabayashi, H., Myers, J., Jiang, Y., Cao, Y. (2017). Tolerance to Caspofungin in Candida Albicans Is Associated With at Least Three Distinctive Mechanisms That Govern Expression of FKS Genes and Cell Wall Remodeling. Antimicrob. Agents Chemother. 61 (5), 1–13. doi: 10.1128/AAC.00071-17
Yates, C. M., Garvey, E. P., Shaver, S. R., Schotzinger, R. J., Hoekstra, W. J. (2017). Design and Optimization of Highly-Selective, Broad Spectrum Fungal CYP51 Inhibitors. Bioorg Med Chem. Lett. 27 (15), 3243–3248. doi: 10.1016/j.bmcl.2017.06.037
Zamith-Miranda, D., Heyman, H. M., Cleare, L. G., Couvillion, S. P., Clair, G. C., Bredeweg, E. L., et al. (2019). Multi-Omics Signature of Candida Auris , an Emerging and Multidrug-Resistant Pathogen. MSystems 4 (4), 1–14. doi: 10.1128/mSystems.00257-19
Zaoutis, T. E., Argon, J., Chu, J., Berlin, J. A., Walsh, T. J., Feudtner, C. (2005). The Epidemiology and Attributable Outcomes of Candidemia in Adults and Children Hospitalized in the United States: A Propensity Analysis. Clin. Infect. Dis. 41 (9), 1232–1239. doi: 10.1086/496922
Zaragoza, O., Blazquez, M. A., Gancedo, C. (1998). Disruption of the Candida Albicans TPS1 Gene Encoding Trehalose-6- Phosphate Synthase Impairs Formation of Hyphae and Decreases Infectivity. J. Bacteriol 180 (15), 3809–3815. doi: 10.1128/JB.180.15.3809-3815.1998
Zaragoza, O., de Virgilio, C., Pontón, J., Gancedo, C. (2002). Disruption in Candida Albicans of the TPS2 Gene Encoding Trehalose-6-Phosphate Phosphatase Affects Cell Integrity and Decreases Infectivity. Microbiology 148 (5), 1281–1290. doi: 10.1128/IAI.70.4.1772-1782.2002
Zarif, L., Graybill, J. R., Perlin, D., Najvar, L., Bocanegra, R., Mannino, R. J. (2000). Antifungal Activity of Amphotericin B Cochleates Against Candida Albicans Infection in a Mouse Model. Antimicrob. Agents Chemother. 44 (6), 1463–1469. doi: 10.1128/AAC.44.6.1463-1469.2000
Zeidler, U., Bougnoux, M. E., Lupan, A., Helynck, O., Doyen, A., Garcia, Z., et al. (2013). Synergy of the Antibiotic Colistin With Echinocandin Antifungals in Candida Species. J. Antimicrob. Chemother. 68 (6), 1285–1296. doi: 10.1093/jac/dks538
Zhai, B., Zhou, H., Yang, L., Zhang, J., Jung, K., Zen Giam, C. (2010). Polymyxin B, in Combination With Fluconazole, Exerts a Potent Fungicidal Effect. J. Antimicrob. Chemother. 65 (5), 931–938. doi: 10.1093/jac/dkq046
Zhang, J., Silao, F. G. S., Bigol, U. G., Bungay, A. A. C., Nicolas, M. G., Heitman, J., et al. (2012). Calcineurin Is Required for Pseudohyphal Growth, Virulence, and Drug Resistance in Candida Lusitaniae. PloS One 7 (8), 1–14. doi: 10.1371/journal.pone.0044192
Zhang, F., Zhao, M., Braun, D. R., Ericksen, S. S., Piotrowski, J. S., Nelson, J., et al. (2020). A Marine Microbiome Antifungal Targets Urgent-Threat Drug-Resistant Fungi. Science 370 (6519), 974–978. doi: 10.1126/science.abd6919
Zhao, M., Fan, Z., Zarnowski, R., Barns, K., Jones, R., Fossen, J., et al. (2021). Turbinmicin Inhibits Candida Biofilm Growth by Disrupting Fungal Vesicle-Mediated Trafficking. J. Clin. Invest. 131 (5), 1–5. doi: 10.1172/JCI145123
Zhao, Y., Hee Lee, M., Paderu, P., Lee, A., Jimenez-Ortigosa, C., Park, S., et al. (2018). Significantly Improved Pharmacokinetics Enhances in Vivo Efficacy of APX001 Against Echinocandin-And Multidrug-Resistant Candida Isolates in a Mouse Model of Invasive Candidiasis. Antimicrob. Agents Chemother. 62, 1–8. doi: 10.1128/aac.00425-18
Zhao, M., Lepak, A. J., VanScoy, B., Bader, J. C., Marchillo, K., Vanhecker, J., et al. (2018). In Vivo Pharmacokinetics and Pharmacodynamics of APX001 Against Candida Spp. in a Neutropenic Disseminated Candidiasis Mouse Model. Antimicrob. Agents Chemother. 62 (4).
Keywords: Candida, invasive candidiasis, candidaemia, antifungal resistance, antifungal drugs, drug therapy, drug resistance, antimicrobial resistance
Citation: Murphy SE and Bicanic T (2021) Drug Resistance and Novel Therapeutic Approaches in Invasive Candidiasis. Front. Cell. Infect. Microbiol. 11:759408. doi: 10.3389/fcimb.2021.759408
Received: 16 August 2021; Accepted: 08 November 2021;
Published: 14 December 2021.
Edited by:
Jessica C. S. Brown, The University of Utah, United StatesReviewed by:
Erika Shor, Hackensack Meridian Health, United StatesSoo Chan Lee, University of Texas at San Antonio, United States
Copyright © 2021 Murphy and Bicanic. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Tihana Bicanic, tbicanic@sgul.ac.uk