Xiaoli Li
Yongqing Cai
Qinchuan Xia4
Rongxin Qin- 1Department of Pharmacology, College of Pharmacy, Chongqing Medical University, Chongqing, China
- 2Chongqing Key Laboratory of Drug Metabolism, Chongqing, China
- 3Department of Pharmacy, Daping Hospital, Army Medical University, Chongqing, China
- 4Fuan Pharmaceutical Group Chongqing Bosen Pharmaceutical Co., Ltd., Chongqing, China
- 5Department of Pharmacology, College of Pharmacy, Army Medical University (The Third Military Medical University), Chongqing, China
Methicillin-resistant Staphylococcus aureus (MRSA) is a drug-resistant bacterium that can cause a range of infections with high morbidity and mortality, including pneumonia, etc. Therefore, development of new drugs or therapeutic strategies against MRSA is urgently needed. Increasing evidence has shown that combining antibiotics with “antibacterial sensitizers” which itself has no effect on MRSA, is highly effective against MRSA. Many studies showed the development of antibacterial sensitizers from natural plants may be a promising strategy against MRSA because of their low side effects, low toxicity and multi-acting target. In our paper, we first reviewed the resistance mechanisms of MRSA including “Resistance to Beta-Lactams”, “Resistance to Glycopeptide antibiotics”, “Resistance to Macrolides, Aminoglycosides, and Oxazolidinones” etc. Moreover, we summarized the possible targets for antibacterial sensitizers against MRSA. Furthermore, we reviewed the synergy effects of active monomeric compounds from natural plants combined with antibiotics against MRSA and their corresponding mechanisms over the last two decades. This review provides a novel approach to overcome antibiotic resistance in MRSA.
1 Introduction
Staphylococcus aureus is one of the most infectious Gram-positive bacteria affecting people in hospitals and communities (de Oliveira Santos et al., 2022). Owing to its relatively high virulence and plasticity, S. aureus can adapt to various environmental conditions, and is resistant to almost all antimicrobial drugs (Mlynarczyk-Bonikowska et al., 2022).
The emergence of methicillin-resistant Staphylococcus aureus (MRSA) strains makes treatment of infections more complicated. MRSA can cause a series of infections such as bacteraemia, pneumonia, as well as complicated skin and soft-tissue infections, which are difficult to treat resulting in high morbidity and mortality (Liang et al., 2022). Furthermore, treatment failure results in enormous medical costs. Therefore, there is an urgent need to develop new and more effective antibacterial strategies to eradicate MRSA.
At present, there are two main antibacterial strategies. The first is “direct antibacterial strategy”, that is, structural modification of existing antimicrobials to obtain compounds with higher activity and fewer side effects. Using this strategy, oxazolidinones, glycopeptides, quinolones, aminoglycosides, tetracyclines, and ketonolactone analogues have entered the clinic (Theuretzbacher, 2011). Unfortunately, with the promotion of their clinical use, there has been a gradual emergence of resistance owing to the selection pressure of antibiotics or the spread of bacteria. For example, simultaneous resistance to vancomycin, daptomycin, and ceftaroline was recently identified in MRSA (Wüthrich et al., 2019). Therefore, it is risky to develop antimicrobials with new targets and skeletons (Warren, 2011). The second antibacterial strategy is the “indirect antibacterial strategy”, which involves the development of drugs (antibacterial sensitizers) that do not themselves have antibacterial activity but can enhance the activity of existing antimicrobial agents. These drugs act by changing or modifying the phenotype of bacteria, thereby allowing existing antimicrobials to inhibit or kill them (Qin et al., 2013). Because antibacterial sensitizers do not exert direct selection pressure on bacteria, they do not induce the production of drug-resistant strains. Thus, antimicrobial sensitizers can enhance the antibacterial ability of existing antibiotics, restore their viability against drug-resistant strains, and reduce dependency on antibiotics (Tyers and Wright, 2019). The clinical application of antibacterial sensitizers has had a profound impact on the development of antimicrobial agents.
Plants are a huge treasure trove of antibacterial molecules and sensitizers against MRSA. Plants contain a wide variety of secondary metabolites that can resist external stress and pathogenic attacks. These compounds are classified into terpenoids, alkaloids, flavonoids, polyphenols, coumarins, and fatty acids (Shin et al., 2018). The advent of high-throughput screening methods for the assessment of large amounts of plant extracts containing putative biologically active compounds has encouraged industrial interest in plant research. Numerous studies have reported plant-derived small molecules that increase the sensitivity of MRSA to antibiotics. This could be a new strategy for overcoming MRSA infections.
This study reviewed the pharmacological action and preliminary mechanism of small molecular antibacterial sensitizers from natural products (excluding crude extract from plants) in the last 20 years. The aim of this review was to provide new ideas for the research and development of new antibacterial sensitizers.
2 Synergy and antagonism
Synergy is an important concept in the description of the effects of drug combinations and forms the basis for most antibiotic combinations. Synergy occurs when paired combinations of agents exert inhibitory effects that are more than the sum of their effects alone. Antagonism is the opposite of synergy, occurring when the combined activity of components is less than the sum of their individual activities. Synergy and antagonism are calculated using the fractional inhibitory concentration index (FICI) (Odds, 2003). A value of FICI≤0.5 is required for synergy and FICI ≥4.0 is required for antagonism (Tyers and Wright, 2019).
3 Resistant mechanisms of MRSA
3.1 Resistance to beta-lactams
Resistance to β-lactams is the most important mechanism of MRSA resistance. β-lactams targeted at penicillin-binding proteins (PBPs) which are responsible for peptidoglycan (PG) synthesis. PG is the essential component of the cell wall, providing the strength to resist high internal osmotic pressure and maintain cell shape in S. aureus. The inhibition of bacterial cell-wall biosynthesis by β-lactams will lead to bacterial cell death.
Several mechanisms of resistance are used, including the synthesis of β-lactamase and a new PBP (called PBP2a), and mutations in PBP genes (Mlynarczyk-Bonikowska et al., 2022).
3.1.1 Synthesising the beta-lactamases
MRSA commonly synthesises specific hydrolases called β-lactamases, for resistance to β-lactams. The β-lactam ring can be hydrolysed by β-lactamases, which inactivates the β-lactams (Bush and Bradford, 2020). β-lactamases synthesised by S. aureus were classified as group 2a (Bush and Jacoby, 2010) and class A by Ambler (Tooke et al., 2019). At present, β-lactamase inhibitors have been successfully used in the clinic, including clavulanic acid, sulbactam, tazobactam, avibactam, and vaborbactam (Yahav et al., 2020), and many β-lactamase inhibitors are being investigated in clinical studies (Tooke et al., 2019).
3.1.2 Expressing PBP2a and its Co-Factors
The most important factor mediating the resistance of MRSA to β-lactams is obtaining the mecA gene that can express penicillin-binding protein 2a (PBP2a). PBP2a has a very low affinity for β-lactams, but can compensate for the transpeptidase function of PBP2, which is inhibited by β-lactam antibiotics, to maintain the synthesis of the bacterial cell wall leading to bacterial resistance to almost all β-lactam drugs (Vestergaard et al., 2019). However, in several cases, differences in resistance levels did not correlate with the PBP2a expression levels, suggesting that factors other than PBP2a modulate strain-specific levels of β-lactam resistance (Luo et al., 2020; Zhang et al., 2020). Indeed, genetic screening has identified several auxiliary factors essential for methicillin resistance, which are also critical for PBP2a-mediated resistance to β-lactam antibiotics (Roemer et al., 2013). In general, these factors are divided into three categories: (A) factors related to S. aureus cell wall biogenesis, (B) factors related to S. aureus cell wall teichoic acid synthesis, and (C) other factors. Table 1 lists the factors affecting β-lactam resistance induced by PBP2a.
(A) Factors related to S. aureus cell wall biogenesis
TABLE 1. PBP2a relevant factors that can induce beta-lactam resistance.
As we mentioned before, PG, the target of β-lactams, maintain cell shape in S. aureus. The PG monomer is synthesised within the cytoplasm via a multistep process (Figure 1). First, UDP-GlcNAc is converted to UDP-MurNAc through the activities of MurA and MurB. PG ligases (MurC-F) then sequentially synthesise a pentapeptide (L-Ala-D-Glu-L-Lys-D-Ala-D-Ala), forming UDP-MurNAc-pentapeptide, the soluble PG precursor (van Heijenoort, 2001). Then, UDP-MurNAc-pentapeptide is linked to a lipid carrier by the membrane protein MraY, forming lipid I. Finally, MurG utilises the UDP-GlcNAc substrate to build the final PG precursor, lipid II (van Heijenoort, 2001; van Heijenoort, 2007). The S. aureus lipid II is further modified by a family of peptidyltransferases (FemX, FemA, and FemB) which completes a pentaglycine bridge peptide extending from the pentapeptide L-Lys residue, ultimately allowing for the efficient cross-linking of PG in the cell wall (Rohrer and Berger-Bächi, 2003). FemA installs the second and third glycines, forming Gly3-Lipid II, and FemB installs the fourth and fifth glycines, forming Gly5-Lipid II (Severin et al., 2005). Gly5-Lipid II is then flipped to the extracellular surface of the membrane, where it is polymerised and cross-linked catalysed by PBPs, including PBP2a in the case of MRSA. Because bacterial cell wall PGs are not found in mammalian cells, these inhibitors show highly selective toxicity to target cells.
FIGURE 1. The biosynthesis of S. aureus cell wall.
In the process of S. aureus cell wall biogenesis, the peptidyl transferase family (FemX, FemA, FemB) and the Mur family (MurA, MurB, and MurC-F) are two important targets of antibacterial sensitizers.
(B) Factors related to S. aureus Wall Teichoic Acid synthesis
Wall teichoic acid (WTA) is a glycophosphate-rich cell-wall polymer common to Gram-positive bacteria (Swoboda et al., 2010). WTA polymers are sequentially synthesised on the central undecaprenyl phosphate carrier lipid C55-P by a series of Tar enzymes in the cytoplasm and then exported to the cell surface by a two-component ABC transporter system and cross-linked to PG by the LCP protein family (Pasquina et al., 2013). S. aureus WTA is not required for cell survival, but cells lacking WTA cannot complete cell division efficiently, lack fitness, reduce virulence, and become sensitive to β-lactams because PBP2a relies on glycosylated WTA to act as a scaffold/platform (Weidenmaier et al., 2004; Brown et al., 2012; Sewell and Brown, 2014). Thus, inhibitors of WTA synthesis act synergistically with beta-lactams not only by misdirecting PBP4, but also by destabilising PBP2a (Sewell and Brown, 2014).
(C) Other factors.
The cell wall is an important barrier that protects bacteria, such as S. aureus, from the external environment. Factors involved in cell wall synthesis and maintenance are also important for the resistance of S. aureus to antimicrobial agents (Scheffers and Pinho, 2005). Therefore, the cell wall could be a target of antibacterial sensitizers.
In S. aureus, lipoteichoic acid (LTA) is essential for growth and cell division (Gründling and Schneewind, 2007). Depletion of the synthase gene ltaS of LTA strongly resensitises MRSA to β-lactams in vitro (Therien et al., 2012). In addition, cell wall two-component signal transduction systems (TCSs) sense cell surface damage and trigger protective stress responses (Jordan et al., 2008). The sentinel S. aureus cell wall TCS is encoded by vraSR (Kuroda et al., 2003). Deletion of vraSR restored the efficacy of oxacillin in animal infection models against the community-acquired MRSA strain USA300 (Jo et al., 2011). FtsZ, a tubulin-like protein that forms the Z ring involved in cell division at the very beginning of cell wall synthesis, has also attracted much attention (Ferrer-González et al., 2021). PBP2a requires a chaperone, the peptidyl-prolyl cis-trans isomerase PrsA, to fold correctly (Jousselin et al., 2015). In S. aureus, staphyloxanthin is an unphosphorylated membrane saccharolipid that lends bacterial colonies a golden yellow colour (Liu et al., 2008). Inhibition of staphyloxanthin synthesis resulted in reduced PBP2a oligomerisation in the membrane and rendered MRSA cells susceptible to β-lactam antibiotics in a mouse infection model (Hennessy et al., 2016). Therefore, they may also be targets of antibacterial sensitizers.
3.1.3 Mutation-dependent modification of PBP proteins
The criterion for methicillin resistance in S. aureus is an oxacillin MIC >2 mg/L according to the European Committee on Antimicrobial Susceptibility Testing (EUCAST) and oxacillin MIC ≥4 mg/L according to the Clinical and Laboratory Standards Institute (CLSI). The cefoxitin resistance criterion was also used for S. aureus and is defined by MIC >4 mg/L according to EUCAST and MIC ≥8 mg/L according to CLSI. Some S. aureus strains without the mecA gene to produce PBP2a are resistant to β-lactams because of mutations in genes encoding PBP2 and PBP4, albeit very rarely (Boonsiri et al., 2020). These strains were described as modified penicillin-binding protein S. aureus (MODSA) or methicillin-resistant lacking mec (MRLM).
3.2 Resistance to glycopeptide antibiotics
To date, glycopeptide antibiotics are the most frequently used drugs for the treatment of MRSA infections. However, there have been reports of reduced susceptibility and resistance to vancomycin globally since 1990 (Unni et al., 2021). The main mechanism of vancomycin resistance in MRSA is the acquisition of the vanA gene from enterococci (Gardete and Tomasz, 2014) changing the antibiotic target.
3.3 Resistance to macrolides, aminoglycosides, and oxazolidinones
The most common mechanism of resistance to macrolides in MRSA is the modification of the target site. Modification is carried out by the enzymes adenylyl-N-methyl transferase Erm (erythromycin ribosome methylation) and demethylating adenine 2058, which leads to resistance to all macrolides (Miklasińska-Majdanik, 2021). In addition, the expression of efflux pumps belongs to the ATP-binding cassette (ABC) efflux family, and inactivation of enzymes such as macrolide phosphotransferases may also contribute towards resistance to macrolides (Schmitz et al., 2000; Malbruny et al., 2002).
The mechanisms of resistance to aminoglycosides in MRSA include (1) synthesis of transferases (acetyltransferases, phosphotransferases, and nucleotidyl transferases) that modify the aminoglycoside molecule (Chandrakanth et al., 2008); and (2) lack of enzymes responsible for active transport of aminoglycosides into the bacterial cell (Melter and Radojevič, 2010).
Linezolid, an oxazolidinone that is highly active against MRSA, was introduced to treat MRSA after vancomycin-resistant strains were discovered (Quiles-Melero et al., 2013). The main mechanism of resistance to linezolid is mutations in a series of genes, which modifies the target site preventing linezolid action (Mendes et al., 2008; Hill et al., 2010; Liu et al., 2021).
3.4 Resistance to daptomycin
Daptomycin, a cyclic lipopeptide antibiotic, acts on the cytoplasmic membrane of S. aureus, causing loss of potassium ions from the cytoplasm. Resistance to this antibiotic has been attributed to mutations in various genes (dltABCD, mprF, and rpoB) that cause changes in membrane fluidity, cell wall thickness, and membrane charge (Kaatz et al., 2006).
3.5 Resistance to other kind of antibiotics
Expressing efflux pumps is a common resistance mechanism in MRSA against antibiotics such as tigecycline, tetracyclines, and fluoroquinolones. For tigecycline, resistant phenotypes emerged in 2008, and are considered to be caused by mutations in the mepR and mepA genes resulting in the overexpression of efflux pumps (Peterson, 2008). For tetracyclines, there is tet(K), which derives its energy from the proton pump and is classified as major facilitator super family (MFS) (Guay et al., 1993). Finally, for fluoroquinolones, NorA, NorB, NorC, and SdrM, all classified as MFS, are the main reasons for resistance (Xu et al., 2011). Table 2 summarized antibiotic resistant mechanisms in MRSA.
TABLE 2. Summary of antibiotic resistant mechanisms in MRSA.
4 Antibacterial sensitizers
Antibiotic sensitizers are also called “antibiotic adjuvants” or “antibiotic potentiators” (Wright, 2016). They have little or no antibiotic activity, but can enhance the antimicrobial action of a drug when combined with antibiotics. From the perspective of drug discovery, this strategy offers the advantage of overcoming antibiotic resistance.
4.1 Antibacterial sensitizers targeting beta-lactamases and other hydrolytic enzymes
To date, β-lactamase inhibitors have been successfully used in clinical trials, including clavulanic acid, sulbactam, tazobactam, avibactam, and vaborbactam (Yahav et al., 2020). The most commonly reported enzyme inhibitors in plants are β-lactamase inhibitors.
For example, epigallocatechin gallate (EGCG), the major catechin present in Camellia sinensis (L.) Kuntze tea leaves, has been reported to potentiate the activity of β-lactams against MRSA (Abreu et al., 2012). A possible mechanism is the inhibition of β-lactamases in S. aureus (Zhao et al., 2002) and interference with the integrity of the cell wall through direct binding to PG (Zhao et al., 2001). Baicalein, the active constituent of Scutellaria baicalensis, combined with penicillin, showed potent synergistic activity against penicillinase-producing MRSA in vitro (Qian et al., 2015). Alkaloid compounds from Cienfuegosia digitata Cav. Combined with β-lactams showed strong activity against MRSA, probably through the inhibition of β-lactamase (Konaté et al., 2012). Tellimagrandin I, isolated from rose red petals, showed a marked reduction in β-lactams against MRSA. The same effect was observed for rugosin B, which is also a constituent of rose red petals (Shiota et al., 2000). A possible mechanism is the suppression of β-lactamase activity to some extent (Shiota et al., 2004). A combination of ampicillin with 5-O-methylglovanon from Glycosmis showed activity comparable to that of clavulanic acid in combination with ampicillin (Zhou et al., 2011). The mechanism of 5-O-methylglovanon involves the inhibition of β-lactamases (Obiang-Obounou and Jang, 2011). SB-202742 isolated from Spondias mombin showed strong inhibitory activity against β-lactamase and can also sensitise MRSA to β-lactams (Coates et al., 1994). Activity against K. pneumoniae ATCC 700603 was also observed for 2-methoxy chrysophanol from Clutia myricoidesin combination with third-generation cephalosporin antibiotics through the inhibition of extended-spectrum β-lactamases (ESBL), with marked enlargement of inhibition zones (>5 mm) (Elfaky et al., 2020).
Besides β-lactamases, there are other hydrolytic enzymes in MRSA that hydrolyse other types of antibiotics. Aranorosin isolated from Gymnascella aurantiaca inhibited the growth of a MRSA strain in the presence of arbekacin and was confirmed to act by inhibiting a bifunctional aminoglycoside-modifying enzyme (Labby and Garneau-Tsodikova, 2013). Inhibitors of chloramphenicol acetyltransferase have not been reported in the past 20 years Table 3 presents an overview of antibacterial sensitizers that target β-lactamases and other hydrolytic enzymes.
TABLE 3. The compounds from natural products that affect beta-lactamases and other hydrolytic enzymes.
4.2 Antibacterial sensitizers targeting PBP2a and its Co-Factors
4.2.1 Antibacterial sensitizers targeting PBP2a
MRSA contains an SCCmec box encoding PBP2a by horizontal transfer which has a low affinity to most beta-lactam antibiotics (Peacock and Paterson, 2015). Acquiring the PBP2a protein is the most important mechanism underlying MRSA resistance to β-lactams. Numerous studies have indicated that small molecules from herbal medicines combined with β-lactams have a synergistic effect, and their target is PBP2a.
For example, the synergistic effect of oxacillin and morin, a natural pentahydroxy flavonol, against MRSA occurs by reducing the production of PBP2a, encoded by the mecA gene (Mun et al., 2015). The ursolic/oleanolic acids extracted from the leaves of Shea butter trees exhibited synergistic effects in combination with ampicillin/oxacillin against MRSA. The mechanism of reversion of the MRSA phenotype involves the ability to separate PBP2a from the cleavage site of the spacer, which interferes with the synthesis of PGs (Catteau et al., 2017). Another report showed that ampicillin/sulbactam combined with EGCG from tea catechins reversed ampicillin/sulbactam resistance against MRSA in a dose-dependent manner through the direct binding of PGs (Hu et al., 2001). This is consistent with a previous report that oxacillin and EGCG elicit synergistic effects against MRSA by reducing the production of PBP2a or its gene expression (Shiota et al., 1999). The synergistic antimicrobial effect of oxacillin and corilagin/tellimagrandin I demonstrated that corilagin and tellimagrandin I play an important role in inhibiting the activity of PBP2a rather than its production of PBP2a (Shiota et al., 2004). Baicalein, a flavone isolated from this herb, showed asynergistic effect in combination with benzylpenicillin against MRSA in a dose-dependent manner. The mechanism of action of baicalein is related to the inhibition of PBP2a or damage to PG (Liu et al., 2000). 2,3,3-Trimethyl-octane and benzoic acid from the methanolic bark extract of Toxicodendron vernicifluum have been reported to metabolise novel bacterial topoisomerase inhibitors (NBTI) and PBP2a, resulting in excellent antibacterial activity (Saravanakumar et al., 2019). Table 4 presents an overview of antibacterial sensitizers that inhibit PBP2a. (Table 4).
TABLE 4. The compounds from natural products that inhibit PBP2a.
4.2.2 Antibacterial sensitizers targeting factors involved in S. aureus cell wall biogenesis
Several small-molecule inhibitors have been discovered in the field of Mur enzymes in the last decade. However, these inhibitors are mostly derived from chemical synthesis and there are very few small molecules that are derived from natural products (Hrast et al., 2014).
4.2.3 Antibacterial sensitizers targeting factors involved in S. aureus wall teichoic acid synthesis
Numerous studies have reported various molecules targeting Tar enzymes, such as tunicamycin and ticlopidine as tarO inhibitors (Campbell et al., 2011; Farha et al., 2013) as well as targosey and clomiphene as tarG inhibitors (Swoboda et al., 2009; Farha et al., 2015). However, Tar enzyme inhibitors from natural plants have not been reported in the last 20 years.
4.2.4 Antibacterial sensitizers targeting other factors
Compound 1771 and Congo red are the only two inhibitors of ltaS (Richter et al., 2013; Vickery et al., 2018). Novel FtsZ inhibitors, 1-methylquinolinium iodide derivative and quinuclidine 1, have been reported to possess strong and synergistic antibacterial activity against MRSA when combined with β-lactams (Chan et al., 2015; Fang et al., 2018).
4.3 Antibacterial sensitizers targeting efflux pumps
Baicalein has previously been shown to significantly reverse ciprofloxacin resistance in MRSA, possibly by inhibiting the NorA efflux pump in vitro (Chan et al., 2011). 5'-Methoxyhydnocarpin (5'-MHC) was previously reported to have no antimicrobial activity but strongly potentiated the action of berberine and other NorA substrates, such as ethidium bromide, against S. aureus (Stermitz et al., 2000a). Piperine, in combination with ciprofloxacin, markedly reduced the MICs of ciprofloxacin against MRSA. The enhanced accumulation and decreased efflux of ethidium bromide in the wild type and mutant (CIPr-1) strains in the presence of piperine suggests its involvement in the inhibition of NorA pumps (Khan et al., 2006). The ethanolic extract of Persea lingue, kaempferol-3-O-alpha-L-(2, 4-bis-E-p-coumaroyl) rhamnoside, when combined with ciprofloxacin, resulted in a synergistic effect with antimicrobial activity against a NorA overexpressor increasing to 8-fold higher than the activity of ciprofloxacin monotherapy. However, a similar trend was not observed against a norA deletion mutant (Holler et al., 2012). Indirubin was isolated from a chloroform extract of W. tinctoria R. Br. leaves, capsaicin from chilli peppers, and carnosol/carnosic acid from Rosmarinus officinalis synergistically potentiated the activity of ciprofloxacin and erythromycin, probably by inhibiting the NorA efflux pump (Oluwatuyi et al., 2004; Ponnusamy et al., 2010; Kalia et al., 2012). Silybin, a flavonolignan component of milk thistle seed extract, has been shown to restore the sensitivity of MRSA 41577 to antibiotics. The possible mechanism was related to the reduction in the expression of the quinolone resistance protein NorA (norA) and quaternary ammonium resistance protein A/B (qacA/B) efflux genes in MRSA through reverse transcription-quantitative polymerase chain reaction analysis (Wang et al., 2018). Many herbal compounds can inhibit the NorA pump in S. aureus to restore bacterial resistance to antibiotics. Table 5 summarises the compounds from plants that inhibit the NorA pump.
TABLE 5. The compounds from natural products that inhibit NorA pump.
Except for NorA, the proton-driven multidrug efflux pump LmrS actively exports structurally distinct antimicrobials. Cumin inhibited the growth of S. aureus and LmrS ethidium transport in a dose-dependent manner (Kakarla et al., 2017). In a previous study, EGCG also enhanced oxytetracycline activity against MRSA, and the MIC of oxytetracycline was reduced 4–12-fold when it was combined with EGCG and the possible mechanism is inhibition of the efflux pump tet(K) (Novy et al., 2013). Baicalein also inhibits tet(K) pumps to potentiate tetracycline antibiotics (Fujita et al., 2005). Diosmetin showed a strong synergistic effect against MRSA strains when combined with antibiotics. The probable mechanism may be the inhibition of efflux pumps (Wang et al., 2014).
4.4 Antibacterial sensitizers targeting the cell membrane and other targets
Gallic acid-grafted chitosans (I), which have the highest gallic acid content, exhibited synergistic effects when combined with β-lactams by damaging the cell membrane (Lee et al., 2014). The natural polyphenolic flavonoid apigenin has been found to enhance the activity of ampicillin and ceftriaxone against MRSA. Apigenin may damage the MRSA cytoplasmic membrane and cause subsequent leakage of intracellular constituents (Akilandeswari and Ruckmani, 2016). In addition, many compounds have synergistic effects when combined with antibiotics and other mechanisms. It has been found that lipoic acid derivatives exhibit excellent activity against multidrug-resistant S. aureus with no cytotoxicity and sensitise fluoroquinolones towards fluoroquinolone-resistant methicillin-resistant S. aureus strains, with DNA gyrase B as the likely molecular target, as determined by molecular dynamics (MD) simulations (Panjla et al., 2019). C-geranylated flavonoids from Paulownia tomentosa fruits have been reported to reverse the antibiotic effects of oxacillin (Navrátilová et al., 2016). It is mechanism was not determined.
5 Conclusion and perspectives
In this review, we have summarised the mechanisms of resistance in MRSA and investigations regarding antibacterial sensitizers from natural products and their possible mechanisms over the last two decades. The main mechanisms of antibacterial sensitizers were showed in Figure 2. There still were a lot of reports showed that not only isolated pure natural products but also extracts from plants exhibited strong synergy effects with antibiotics. So antibacterial sensitizers and antimicrobial drugs combinations have revealed promising results in the fight against multidrug-resistant bacteria.
FIGURE 2. The mechanisms of antibacterial sensitizers against MRSA.
The rich chemical diversity of plants makes them a renewable and attractive potential source of antimicrobial sensitizers. Numerous studies have demonstrated the therapeutic potential of phytochemical products as antibiotics. However, there are no reports on the clinical applications of natural-product-derived antibacterial sensitizers. The reasons may be as follows: (1) the chemical complexity of plant extracts, often undocumented toxicity, poor water solubility, and lack of standardisation (Cos et al., 2006; Spížek et al., 2010), (2) the uncertainty in the chemical composition of natural plants, (3) the inherent time consumption of working with natural products, and (4) additional limitations such as the costs of collection, extraction, and isolation (Harvey, 2008). Therefore, there is still a long way to go before antimicrobial sensitizers from natural plants can be used in clinical settings.
Because plant-derived antibacterial sensitizers faced so many problems, there are several methods that may be used to solve them. On one hand, we can use some new techniques to discover new antibacterial sensitizers and their mechanisms of action. (1) With the development of genomics, proteomics, and metabolomics, they create a platform for the screening of antibacterial sensitizers and the study of their pharmacological effect and mechanism. (2) Molecular docking and simulation studies can also help researchers to quickly screen the potential candidate drugs based on the resistant targets of MRSA, and understand the possible relationship of antibacterial sensitizers and targets. (3) Bioassay-guiding isolation of active products is crucial to study the synergistic mechanism in-depth. On the other hand, we can use some approaches to improve the sensitizing effect of existing antibacterial sensitizers. (1) Improve the quality standard of active compounds when they were extracted and separated. For example, the picking season and origin of the herb, the process of extraction and the using of solvent, etc., needed to be strictly controlled. (2) Optimizing the combination ratio and proper dosage regimen of the combinations are still important. (3) Furthermore, comparable pharmacokinetic profiles of both drugs can bring more effective synergistic combinations, so future studies could focus on pharmacokinetic behaviours of antibacterial sensitizers and antibiotics.
Author contributions
XL collected documents and wrote the manuscript. YC wrote the manuscript and drew the figure. QX and YL gathered the material. RQ conceived ideas, designed the structure of the manuscript and revised the manuscript. All authors read and approved the submitted version.
Funding
This project was supported by a grant from National Natural Science Foundation of China (81402977), Technology Project of Chongqing Health and Family Planning Commission (2019MSXM010), and Natural Science Foundation of Chongqing (No. cstc2020jcyj-msxmX0223).
Conflict of interest
QX and YL were employed by Fuan Pharmaceutical Group Chongqing Bosen Pharmaceutical Co., Ltd.
The remaining authors declare 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
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Keywords: MRSA, antibacterial sensitizers, natural products, PBP2a, efflux pumps
Citation: Li X, Cai Y, Xia Q, Liao Y and Qin R (2023) Antibacterial sensitizers from natural plants: A powerful weapon against methicillin-resistant Staphylococcus aureus. Front. Pharmacol. 14:1118793. doi: 10.3389/fphar.2023.1118793
Received: 08 December 2022; Accepted: 13 February 2023;
Published: 24 February 2023.
Edited by:
Linda Boniface Oyama, Queen’s University Belfast, United KingdomReviewed by:
Wenchang Yuan, Guangzhou Medical University, ChinaAbbas Yadegar, Shahid Beheshti University of Medical Sciences, Iran
Copyright © 2023 Li, Cai, Xia, Liao and Qin. 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: Rongxin Qin, bWljaGVsXzA0MTVAMTYzLmNvbQ==
†These authors have contributed equally to this work and share first authorship