Reham Wasfi
Samira M. Hamed
Mai A. Amer
Lamiaa Ismail Fahmy- Department of Microbiology and Immunology, Faculty of Pharmacy, October University for Modern Sciences and Arts (MSA), Giza, Egypt
Proteus mirabilis is a Gram negative bacterium that is a frequent cause of catheter-associated urinary tract infections (CAUTIs). Its ability to cause such infections is mostly related to the formation of biofilms on catheter surfaces. In order to form biofilms, P. mirabilis expresses a number of virulence factors. Such factors may include adhesion proteins, quorum sensing molecules, lipopolysaccharides, efflux pumps, and urease enzyme. A unique feature of P. mirabilis biofilms that build up on catheter surfaces is their crystalline nature owing to their ureolytic biomineralization. This leads to catheter encrustation and blockage and, in most cases, is accompanied by urine retention and ascending UTIs. Bacteria embedded in crystalline biofilms become highly resistant to conventional antimicrobials as well as the immune system. Being refractory to antimicrobial treatment, alternative approaches for eradicating P. mirabilis biofilms have been sought by many studies. The current review focuses on the mechanism by which P. mirabilis biofilms are formed, and a state of the art update on preventing biofilm formation and reduction of mature biofilms. These treatment approaches include natural, and synthetic compounds targeting virulence factors and quorum sensing, beside other strategies that include carrier-mediated diffusion of antimicrobials into biofilm matrix. Bacteriophage therapy has also shown successful results in vitro for combating P. mirabilis biofilms either merely through their lytic effect or by acting as facilitators for antimicrobials diffusion.
Introduction
The genus Proteus encompasses rod-shaped Gram-negative bacteria that belong to the family Enterobacteriaceae (Penner, 2005). They are widely spread in the environment mainly in water, soil and the gastrointestinal tracts of humans and animals (Drzewiecka, 2016). Of the human gut microbiota, Proteus species comprise <0.05% in healthy subjects (Yatsunenko et al., 2012). Among all Proteus species, Proteus mirabilis is the most frequent cause of human infections (Jacobsen and Shirtliff, 2011). It is an opportunistic pathogen that is implicated in various human diseases of the respiratory tract, gastrointestinal tract, eye, ear, and skin among others (O'hara et al., 2000).
P. mirabilis is also a common cause of complicated urinary tract infections (UTIs) in patients with anatomical or functional problems (Jamil et al., 2020). This is particularly problematic in patients undergoing long-term indwelling urinary catheterization who may develop catheter-associated urinary tract infections (CAUTIs). Such infections are complicated by the unique ability of P. mirabilis to form crystalline biofilms eventually leading to encrusted and blocked catheters (Jones et al., 2007). Patients may then suffer from urine retention and reflux that are accompanied by painful distension of the bladder and pyelonephritis. Fatal complications may then be imminent such as septicemia and endotoxic shock (Chen et al., 2012). Moreover, it may cause trauma to the urethra and bladder mucosa upon removal of the catheter (Vaidyanathan et al., 2010). More nursing visits and emergency referrals may also be demanded for replacement of blocked catheters. In addition, crystalline biofilms have been linked to the persistence of P. mirabilis in the urinary tract through protection from antibiotics and the host immune response (Jacobsen et al., 2008).
Intestinal colonization by P. mirabilis provides a reservoir for intermittent colonization of the periurethral region. During insertion, urinary catheters are contaminated by the organism that is subsequently transmitted to the urinary bladder (Mathur et al., 2005). Adhesion to catheter surface or bladder epithelium induces exopolysaccharides production and biofilm formation (Nicolle, 2014).
Biofilms are well-organized structures of single- or multi-species microbial communities in which microbial cells are irreversibly attached to a substratum and to each other. Within biofilms, cells are embedded in a self-produced matrix of extracellular polymeric substances including: polysaccharides, proteins, lipids, and extracellular DNA (Flemming and Wingender, 2010). Formation of biofilms is a multistage process that starts by reversible bacterial adhesion to biotic or abiotic surfaces followed by an irreversible attachment, formation of microcolonies and finally development of a mature biofilm. The surface of the mature biofilm then starts to shed free bacteria to disseminate into other favorable environmental conditions (O'toole et al., 2000).
Biofilm formation is employed by some microbial species for surviving harsh environmental conditions and enhancing resistance to antibiotics as well as the host immune system. Antimicrobial resistance of biofilm-associated microorganisms has been found to be 10–1,000 times higher than their planktonic counterparts (Hoiby et al., 2010). The reasons behind this dramatic increase in resistance may be related to the biofilm matrix that hinders the penetration of antimicrobial agents through biofilm layers and the physiological attributes of microbial cells within biofilms especially persister cells (Tseng et al., 2013).
Biofilm Formation
Among the huge arsenal of virulence factors employed by P. mirabilis to cause Catheter Associated Urinary Tract Infections (CAUTIs), some virulence factors have been linked to their ability to form biofilms, such as swarming motility, fimbriae, urease production, capsule polysaccharide, and efflux pumps. The role of various virulence factors in P. mirabilis biofilm formation is illustrated in Figure 1.
Figure 1. The role of various virulence factors in the formation of crystalline biofilms by P. mirabilis on catheter surfaces.
P. mirabilis is particularly well known for its distinctive swarming ability. Growth of the organism on solid surfaces triggers the differentiation of the short rod-shaped “swimmer cells” into highly elongated and hyper-flagellated “swarmer cells” that are capable of aligning themselves in multicellular rafts. These rafts of cells can migrate rapidly over solid surfaces in a coordinated manner (Stickler and Hughes, 1999; Harshey, 2003) The swarming motility may, therefore, facilitate the migration of P. mirabilis from the periurethral region along the catheter surface into the urinary bladder initiating CAUTIs (Jones et al., 2005). Loss of the swarming ability due to mutations have been linked to the failure of P. mirabilis to migrate over catheter surfaces (Jones et al., 2004). Moreover, swarmer cells often show higher expression of virulence factors that further enhances their ability to adhere to catheter surfaces and bladder epithelium (Allison et al., 1992; Fraser et al., 2002). However, some studies have found that swarming must be repressed in order for P. mirabilis to remain attached to catheter surfaces and initiate biofilm formation (Liaw et al., 2003; Jones et al., 2005).
The initial stage in the formation of biofilms on catheter surfaces is the attachment of fimbriae (adhesins) to the body fluids-derived protein coat on catheter surfaces (Donlan, 2002) or directly to the catheter material (Downer et al., 2003). At least 17 fimbrial operons were identified in the genome of a P. mirabilis isolate by whole genome sequencing. This is mostly the highest among all sequenced bacterial genomes (Pearson et al., 2008; Scavone et al., 2016) and is clearly reflected by its greatest ability to adhere to catheter surfaces among Gram-negative bacteria (Roberts et al., 1990). The most extensively studied fimbriae are mannose-resistant/Proteus-like (MR/P) fimbriae, mannose-resistant/Klebsiella-like (MR/K) hemagglutinins (Old and Adegbola, 1982), P. mirabilis fimbriae (PMF) (Bahrani et al., 1993), uroepithelial cell adhesins (UCA)/nonagglutinating fimbriae (NAF) (Wray et al., 1986), and ambient-temperature fimbriae (ATF) (Massad et al., 1996).
Expression of MR/K hemagglutinins have been linked to the attachment of P. mirabilis to catheter surfaces to initiate biofilm formation during CAUTIs (Jacobsen et al., 2008). However, whether the MR/K hemagglutination pattern is mediated by a specific type of fimbriae or more than one fimbriae type is still unknown. The exact nature of the gene(s) related to the MR/K hemagglutination pattern is also yet to be identified (Schaffer and Pearson, 2015). Both MR/P fimbriae and PMF have been found to play an important role in the selective adherence of P. mirabilis to the bladder epithelium (Sareneva et al., 1990; Rozalski et al., 1997). In a study by Jansen et al. (2004), MR/P fimbriae have been found to be neither necessary nor sufficient to initiate biofilm formation. The same study has yet concluded that their constitutive expression enhanced biofilm formation. The crucial role of MR/P in biofilm formation by P. mirabilis was evidenced by the smaller biofilms formed by MR/P mutants as compared to the wild type strains (Scavone et al., 2016). In contrast, the same study has reported enhanced biofilm formation in isogenic mutants unable to express PMF. UCAs, also named nonagglutinating fimbriae (NAF) (Tolson et al., 1995), were found to be structurally homologous to intestinal colonization fimbriae of E. coli (Cook et al., 1995). Therefore, it has been suggested that they facilitate the intestinal colonization by P. mirabilis thus forming a reservoir of organisms that can potentially cause CAUTIs (Coker et al., 2000). More recently, Wurpel et al. (2016) identified a new UCA-like fimbriae (UCL) in uropathogenic E. coli (UPEC). The authors demonstrated their ability to promote biofilm formation on abiotic surfaces and their involvement in the attachment of UPEC to uroepithelial cells. Meanwhile, the ability to form biofilms was found to be lower in UCA mutant P. mirabilis grown in artificial urine compared to wild type strains (Scavone et al., 2016). Despite their initial report that ATF have no role in P. mirabilis UTIs (Zunino et al., 2000), Scavone et al. (2016) have later demonstrated their role in adhesion and biofilm formation on abiotic surfaces. This could rather be linked to their possible role in the survival of P. mirabilis in the environment as suggested by their optimal expression temperature (23°C) (Rocha et al., 2007).
A characteristic feature of P. mirabilis is its unique ability to form unusual crystalline biofilms that usually lead to encrustation and obstruction of catheters thus making CAUTIs more complicated. Two virulence factors known to be role players in the formation of P. mirabilis crystalline biofilms are urease enzyme and capsule polysaccharides (CPSs) (Jacobsen and Shirtliff, 2011). Virtually all clinical strains of P. mirabilis produce an exceptionally potent urease enzyme. The enzyme catalyzes the hydrolysis of urea in urine into ammonia elevating the local urinary pH (Rozalski et al., 1997). This is usually coupled with local supersaturation and precipitation of minerals normally found in urine forming struvite crystals (ammonium magnesium phosphate) and hydroxyapatite crystals (calcium phosphate) (Bichler et al., 2002). Such crystals become incorporated into the developing biofilm, a process called ureolytic biomineralization (Jacobsen and Shirtliff, 2011). In addition to its major role in crystalline biofilm formation, the strongly alkaline ammonia produced by the urease enzyme is directly toxic to mammalian cells and may cause tissue damage (Burne and Chen, 2000).
Besides the ureolytic activity of P. mirabilis, their CPSs have been found to accelerate mineral crystals growth (Jacobsen and Shirtliff, 2011). Owing to the acidic nature of bacterial CPSs, they have a great affinity for binding metal cations in urine via electrostatic interaction. Nevertheless, bacterial species, as E. coli, with high affinity for Mg2+, were found to inhibit struvite crystal formation at neutral pH. This is possibly due to the strong chelation of Mg2+ ions that become no longer available for crystal growth. In contrast, CPSs of P. mirabilis have lower affinity for Mg2+ ions. The ions are thus weakly bound to the organism. Hence, they become concentrated, yet readily released for struvite crystal formation (Dumanski et al., 1994).
Efflux systems were recently found to play a major role in P. mirabilis crystalline biofilms whose formation was reduced by disruption of the bcr gene (Holling et al., 2014). This gene encodes an MFS efflux pump known as bicyclomycin resistance protein. In E. coli, this efflux pump is involved in resistance to sulphonamide and bicyclomycin (Bentley et al., 1993) in addition to exporting short peptides (Hayashi et al., 2010). Being a component of the polymeric matrix produced by biofilms (Flemming and Wingender, 2010), peptide efflux may contribute to biofilm formation (Alav et al., 2018). Peptides may also be part of the quorum sensing (QS) system of P. mirabilis hence, their efflux may affect signaling during biofilm formation (Alav et al., 2018).
Despite the existence of some phenotypes that require intercellular coordination such as swarming, monospecies and multispecies biofilm formation, a fully defined QS system including an autoinducer signal producer and its corresponding receptor has not yet been identified in P. mirabilis (Schaffer and Pearson, 2015). Further research is hence required to fill this gap of knowledge. Unlike Serratia marcescenes where swarming motility is regulated by a homolog of the acylated homoserine lactone (AHL) based LuxI/LuxR QS system (Sakuraoka et al., 2019), homologs of this system were not identified in the genome of P. mirabilis (Armbruster and Mobley, 2012). However, exposure of P. mirabilis to N-butanoyl homoserine lactone (BHL) was found to significantly influence biofilm formation by P. mirabilis O18 (Stankowska et al., 2012). Another QS system widely distributed in Gram negative and Gram positive bacteria is the LuxS/LuxP or LsR system. P. mirabilis was found to possess the LuxS gene which produces the LuxS-dependent QS molecule (AI2) during swarming. However, the null mutation of this gene did not affect swarming motility or virulence (Schneider et al., 2002). On the other hand, neither LuxP nor Lsr homologs were identified in the genome of P. mirabilis (Pearson et al., 2008). Absence of homologs for known AI2 binding sites might indicate the possibility of utilizing this system in interspecies signaling (Pereira et al., 2013). A homolog of LuxQ, a hybrid sensor kinase, in the LuxS/LuxP QS system in Vibrio harveyi was also found to be encoded by RsbA gene in P. mirabilis. This gene was found to have a role in swarming and to be sensitive to bacterial density (Belas et al., 1998).
Therapeutic Strategies
Antimicrobial Agents
As for other biofilm-forming bacteria, biofilm formation by P. mirabilis is accompanied by greater resistance to antimicrobial agents. This was demonstrated by some studies (Aiassa et al., 2006). Hence, many attempts have been made for potentiating antimicrobial agents' activity against P. mirabilis biofilms. One attempt was to administer the antimicrobial agent in a cyclic dosing regimen in which the treatment course is interrupted by a holding time that allows persister cells to lose their tolerance to the antimicrobial agent (Lewis, 2001, 2005). This had been proposed to eliminate biofilms and their persister cells. However, for successful clearance of biofilms using this regimen, the holding time should strictly correlate to the time required for persister cells to regain their antimicrobial susceptibility (Lewis, 2001). This is complicated by the lack of a full understanding of the exact mechanisms by which tolerance is achieved (Azeredo and Sutherland, 2008). On the other hand, two consecutive applications of antimicrobials to P. mirabilis biofilm were found to reduce persister cells by one log only (Abokhalil et al., 2020). In the same study, combining ciprofloxacin with silver nitrate completely eradicated persister cells in planktonic populations of P. mirabilis. This could be attributed to the production of reactive oxygen species and increased permeability of bacterial cells both in active and dormant states under the effect of silver nitrate (Morones-Ramirez et al., 2013).
Studies were also conducted to test the effect of minimum inhibitory concentration (MIC) and sub-MIC levels of antibiotics on inhibiting the adherence of microbial cells to plastic surfaces and consequently inhibiting biofilm formation. Their effect on preformed biofilms was also widely studied. A study by Wasfi et al. (2012) tested the effect of sub-MIC levels of four antibiotics on microbial adherence and biofilm formation by strong biofilm forming clinical strains of P. mirabilis. The tested antibiotics included: ciprofloxacin, ceftriaxone, nitrofurantoin, and gentamicin. Of them, ciprofloxacin showed the highest activity. Up to 93% reduction in biofilm formation was achieved using a concentration of ciprofloxacin corresponding to 1/2MIC. By testing the effect of lower concentrations on the same strains, the inhibitory effect of ciprofloxacin on biofilm formation was dramatically reduced.
On the other hand Kwiecinska-Pirog et al. (2013a) tested the effect of sub-MIC levels of ciprofloxacin and ceftazidime on preformed biofilms. The antibiotics were used at concentrations corresponding to 1/8- 1/4-, 1/2-MIC levels and at the MIC level for each. The effect of the tested antibiotics on biofilms was estimated by a colorimetric assay based on cellular physiology in biofilms using 2,3,5-triphenyl-tetrazolium chloride (TTC). Treatment of preformed biofilm by ciprofloxacin at MIC value showed significant reduction in microbial viability. In contrast, lower concentrations (1/8 MIC) of ciprofloxacin were found to increase TTC color intensity reflecting increased viability compared to the control. However, the validity of using TTC for assessing P. mirabilis biofilms is questionable. Only few studies used this method for P. mirabilis (Kwiecinska-Pirog et al., 2013b, 2014) and none of the published studies optimized this method for this organism. In contrast, this method was optimized for biofilm assays of Pseudomonas aeruginosa (Sabaeifard et al., 2014) and Campylobacter jejuni (Brown et al., 2013) by adjusting the incubation time of biofilms with TTC to 5 and 24 h, respectively. It is noteworthy here, that only 2 h incubation time was applied by Kwiecinska-Piróg and his coworkers.
The profound inhibitory effect of sub MIC concentrations of ciprofloxacin on P. mirabilis biofilms in comparison to other classes of antimicrobial agents could be attributed to urease inhibition (Abdullah et al., 2016) and reduction of flagellar formation (Horii et al., 2003). An added advantage to ciprofloxacin use in the treatment of infections associated by P. mirabilis biofilms was reported by Irwin et al. (2013). They found that both bacteriostatic and bactericidal effects of ciprofloxacin on P. mirabilis biofilm forming cells were enhanced by increasing pH from 5 to 9. This was reflected by a 10-fold reduction in the minimum biofilm eradication concentration (MBEC). The enhanced activity at high pH levels makes ciprofloxacin a good candidate for use in treatment of P. mirabilis CAUTIs in which urease enzyme is the main player. Irwin et al. (2013) justified their findings by the acquisition of a negative net charge by ciprofloxacin molecules at high pH that enables them to readily diffuse through the biofilm matrix. However, at lower pH the antibiotic molecules acquire a positive net charge and become strongly attracted to the negatively charged exopolymeric biofilm matrix. This hinders the penetration of the antibiotic through the biofilm matrix. In contrast to the previously mentioned results, another study in artificial urine revealed that the penetration of ciprofloxacin into P. mirabilis biofilms was reduced at high pH due to biomineralization. This was evident among urease producing strains compared to urease non-producers by LIVE/DEAD stain (Li et al., 2016).
Several strategies have been employed for controlling biofilm formation in catheters using antimicrobial agents, among them are adsorbing antimicrobial agents on catheter surfaces and using modified coating material thus inhibiting bacterial adherence. Only silver and antibiotic coated catheters have been tested clinically (Singha et al., 2016). Filling catheter balloons with water containing soluble antimicrobials was found to allow adhesion of the antimicrobial agent to the catheter surface thus preventing subsequent adhesion of microorganisms (Stickler et al., 2003; Williams and Stickler, 2008). An example of this strategy is using a mandelic/lactic acid mixture in silicone catheters which gave debatable results (Robertson and Norton, 1990; Stickler and Hewett, 1991). The second strategy is using modified catheter coating with antimicrobial effect to prevent P. mirabilis colonization. Silver coatings and nitrofurazone-coated silicone catheters have shown significant prevention of catheter-associated bacteriuria during the short term catheterization of hospitalized patients (Stensballe et al., 2007; Schumm and Lam, 2008; Johnson et al., 2012). However, crystalline biofilms could still be formed on hydrogel/silver coated Foley catheters, particularly when the antimicrobial coating fails to diffuse out of the catheter material into the catheter lumen (Morgan et al., 2009). On the other hand, incorporating ciprofloxacin in biodegradable waterborne polyurethane was found to enhance the inhibitory effect of ciprofloxacin on biofilm formation by P. mirabilis in artificial urine medium in vitro (Xu et al., 2019).
Phytochemicals
Historically, plants have been considered as a rich source of a wide range of bioactive compounds, known as phytochemicals (Ahmed and Urooj, 2009). Among their diverse applications, phytochemicals have particularly gained much interest for their antibiofilm activity. This activity was attributed to their ability to inhibit virulence factors including: microbial adherence to surfaces, quorum sensing, urease activity and exopolysaccharide matrix production (Table 1). Few studies reported the development of resistance to antivirulence compounds (Beceiro et al., 2013).
Table 1. Overview of phytochemicals assessed for Proteus mirabilis biofilm control.
Being the first step in biofilm formation, inhibiting adherence to surfaces was found to reduce the overall capacity of microorganisms to form biofilms. Numerous studies have shown a correlation between the consumption of cranberries (Vaccinum macrocarpon) and the prevention of UTIs (Nowack and Schmitt, 2008; Tempera et al., 2010). The underlying mechanism has not yet been definitively established. Though, it has been proposed that cranberries interfere with bacterial adhesion to uroepithelial cells leading to failure of bacterial cells to colonize the urinary tract (Nicolosi et al., 2014). Such effect was correlated to two components of cranberries including fructose, that blocks type 1 fimbriae (sensitive to mannose), and the proanthocyanidins (PACs), that inhibit the mannose-resistant P-fimbriae (Ermel et al., 2012). In a study by O'may et al. (2016), cranberry treatment of P. mirabilis reduced adhesion to HT1376 cell line by up to 75%. Motility and urease activity were also reduced in response to the same treatment. On the other hand, cranberry treatment in the mentioned study enhanced biofilm formation by P. mirabilis on plastic surfaces. Such effect was attributed to a transient reduction in bacterial motility. This was also clinically evident by higher rate of P. mirabilis-induced catheter encrustation in urine from individuals that had consumed cranberry juice than those who consumed an equivalent amount of water (Morris et al., 1997; Morris and Stickler, 2001).
Another phytochemical compound that showed inhibitory effect on P. mirabilis biofilms is the extract of Ibicella lutea, a native plant in South America. The antibiofilm activity of Ibicella lutea was coupled to its ability to inhibit the swarming differentiation of P. mirabilis (Sosa and Zunino, 2009). As mentioned before, swarming motility is employed by the organism to move across solid surfaces until it reaches the site of colonization. This is followed by inhibition of flagellar movement and the formation of biofilms (Guttenplan and Kearns, 2013).
The alkaline urinary pH, imparted by the activity of urease enzyme, plays an essential role in the development of crystalline biofilms by P. mirabilis. Accordingly, inhibiting urease production and subsequent pH elevation could be an important target in preventing biofilm formation. A phytochemical compound that targets urease production in P. mirabilis is allicin, extracted from garlic. At sub-MIC levels, it could reduce biomineralized biofilm formation by up to 35%, as reported by Ranjbar-Omid et al. (2015). The authors have also reported complete eradication of established biofilms at higher concentrations of allicin. A unique feature of allicin, among a few other compounds, is its ability to penetrate bacterial cell membrane and inhibit urease enzyme intracellularly (Miron et al., 2000). The clinical use of allicin is, however, hampered by its instability in biological fluids (Rosen et al., 2001). Inhibition of urease production and biofilm formation in P. mirabilis were also evident for N-Acetyl Cysteine (NAC) and dipropyl disulfide, two components in onion oil (Abdel-Baky et al., 2017). In addition to its urease-inhibiting activity, NAC disrupts disulfide bonds in the extracellular polymeric matrix thereby disrupting biofilm architecture (Kregiel et al., 2019).
Despite the lack of clear information about a well-defined QS system in P. mirabilis, anti-quorum sensing effects of some phytochemical compounds have been reported by several studies. Such findings were based on their ability to inhibit violacein production by Chromobacterium violaceum (ATCC 12472) without affecting microbial growth. To the best of our knowledge, none of the published studies investigated AHL production in P. mirabilis by testing the effect of P. mirabilis cultures on the biosensor mutant Chromobacterium violaceum CV026 strain.
In a study by Salini et al. (2015), Hyptis suaveolens, an aromatic perennial herb found in tropical America, was evaluated for potential therapeutic value. The plant extract showed a potent anti-quorum sensing activity, using the QS biosensor Chromobacterium violaceum (ATCC 12472), and could decrease biofilm mass of Proteus sp. in a dose-depended manner. At 200 μg/ml, Hyptis suaveolens extract could effectively dislodge the biofilm of P. mirabilis and P. vulgaris by 42% and 59%, respectively, without affecting microbial growth.
In a study carried by Packiavathy et al. (2014), sub-MIC levels of curcumin, a potent QS inhibitor, were found to reduce polysaccharide production and swarming motility, hence reducing biofilm formation. The compound could also inhibit the formation of microcolonies and disrupt preformed P. mirabilis biofilms.
A phytochemical compound, Pyrrolo [1,2-a] pyrazine-1,4-dione, hexahydro-3-(2-methylpropyl), extracted from endophytic actinomycete Nocardiosis sp., was found to inhibit microbial adherence and biofilm formation. The research group proved the QS inhibitory effect of this compound using the QS biosensor Chromobacterium violaceum (ATCC 12472) (Rajivgandhi et al., 2018).
Capparis spinose is a spice reported to have a number of potentially useful medicinal attributes including antioxidant, antifungal, anti-inflammatory, anti-diabetic, and anti-obesity activities. Issac and coworkers have demonstrated the anti-quorum sensing activity of C. spinose extract. Under the effect of the extract, clear alteration in P. mirabilis biofilm architecture was revealed by confocal laser scanning microscopy (CLSM). This was associated by inhibition of biofilm formation and exopolysaccharide production to 70 and 67%, respectively. One of the bioactive metabolites in C. spinose to which the negative impact on biofilm formation was attributed is vanillic acid (Issac Abraham et al., 2011). The anti-quorum sensing activity of vanillic acid was reported by other studies as well (Choo et al., 2006; Sethupathy et al., 2017).
Euphorbia trigona latex has been used for the treatment of infectious and inflammatory diseases in India as part of their pharmacopeia. Inhibition of swarming motility and virulence factors such as ureases activity in P. mirabilis in the presence of E. trigona latex was reported by Nashikkar et al. (2011). Such effects were attributed to some components of the extract with anti-quorum sensing activity.
Linalool is a monoterpene alcohol found in the essential oils of many floral aromatic and spice plants (Peana et al., 2002). The inhibitory effect of linalool on P. mirabilis virulence factors was the subject of a recent study by Durgadevi et al. (2019). Up to 75% inhibition of crystalline biofilm formation was achieved by linalool at a concentration of 0.4 mg/mL. Transcriptome analysis showed downregulation of the genes flhD, flhB, speA, rsbA, ureR, hpmB, and hpmA. In turn, the mentioned genes affect virulence properties of P. mirabilis such as motility, biofilm formation, urease activity, and hemolysin production.
Apitherapy
One of the natural alternatives to antibiotics for controlling biofilms is apitherapy, a practice in which bee products such as honey, pollen, and propolis are used for prevention or treatment of diseases (Malone and Tsai, 2016).
Honey is a natural compound whose antibiofilm activity was the subject of many studies. The inhibitory effect of several types of honey of different botanical origins on P. mirabilis biofilms was evaluated by Majtan and co-workers. All honey samples were able to significantly inhibit the adherence of P. mirabilis cells to plastic surfaces at sub-MIC value of 10% (w/v). Moreover, partial detachment of preformed biofilms was achieved at a concentration of 50% (w/v) of each. Among the tested types of honey, the most powerful anti-biofilm properties were shown by manuka honey, produced from the nectar of the manuka tree. It could completely eradicate all biofilm-embedded P. mirabilis cells. Methylglyoxal, the major antibacterial component of Manuka honey, is thought to readily diffuse through the established P. mirabilis biofilm matrix and kill bacterial cells (Majtan et al., 2014).
Another proof on the efficacy of Manuka honey in disrupting preformed biofilms of P. mirabilis was presented by Abbas (2014) who also reported the same effect for the Egyptian clover honey. Manuka honey was also acknowledged by another study for its immunostimulant effect and enhancing wound healing (Gannabathula et al., 2012).
Another bee-product that is known to be one of the richest sources of active compounds, such as flavonoids and phenolic compounds, is the ethanol extract of propolis (EEP) (Freires et al., 2016). Kwiecinska-Pirog and his coworkers have evaluated the effect of the EEP on the formation of P. mirabilis biofilms as well as its effect on preformed biofilms (Kwiecinska-Pirog et al., 2019). Reduction in biofilm formation was observed at the concertation range of 2.5–100 mg/mL, while higher concentrations (25–100 mg/mL) could successfully reduce preformed biofilms. Meanwhile, biofilm formation by P. mirabilis was enhanced by treatment with a low concentration (1.5 mg/mL) of EEP. This could be attributed to the inhibition of bacterial motility at lower extract concertation that enhances the adherence of cells to surfaces (De Marco et al., 2017).
Repurposed Drugs
Drug repurposing or drug repositioning is the use of approved drugs for treatment of medical conditions other than those for which they have been originally indicated. This offers time and cost savings by skipping some phases of clinical trials required for approval of new drugs (Pushpakom et al., 2019).
Ambroxol is a mucolytic and expectorant agent commonly used in patients with asthma and chronic bronchitis. It has been reported to interfere with biofilm formation as a result of its ability to inhibit adhesion, QS and biofilm matrix production (Lu et al., 2010). In a study by Abbas (2013), ambroxol inhibited biofilm formation and eliminated pre-formed biofilms in a dose-dependent manner. Biofilm inhibition and eradication of preformed biofilm of P. mirabilis reached 80, and 76%, respectively.
Other repurposed drugs with potential antibiofilm activity include fluoxetine and thioridazine which are indicated for treatment of depression and psychosis, respectively. Both were found to significantly reduce the rate of P. mirabilis crystalline biofilm formation on catheter model, and increase the time taken for catheter blockage. A significant reduction in swimming and swarming motilities of P. mirabilis was also evident after treatment with fluoxetine and thioridazine (Nzakizwanayo et al., 2017). Using molecular docking techniques, it was predicted that both drugs strongly interact with the biofilm-associated efflux system Bcr/CflA. This efflux system was previously linked to biofilm formation and motility in P. mirabilis (Holling et al., 2014).
Phage Therapy
Phage therapy (PT) arises as one of the new alternative methods for combating bacteria using a natural predator (bacteriophage) that specifically kills bacteria (Miedzybrodzki et al., 2012). Over the last two decades, more interest in the therapeutic uses of phages has been observed. This was driven by the high prevalence of multidrug-resistant bacteria together with the inadequate discovery of new antibiotics (Skurnik et al., 2007).
Phages may be more advantageous to antibiotics in treatment of bacterial infections for several reasons: (a) Narrow spectrum of activity, thus selectively affecting pathogenic bacteria without affecting normal flora. However, the strain specificity might limit their therapeutic applications and implies the use of cocktails of bacteriophages (Alves et al., 2016; Yazdi et al., 2018). Cocktails are also used to avoid the emergence of phage-resistant strains through alteration of bacterial membrane receptors, (b) The capacity of phage multiplication at the site of infection (Hanlon, 2007; Gorski et al., 2009; Kutter et al., 2010; Harper et al., 2014), (c) Retaining activity against multidrug resistant bacteria as it employs a unique mechanism of action (Sillankorva et al., 2011), (d) low cost (Stafford, 2011), (e) Discovery of new bacteriophages is much easier and less time consuming than that of antibiotics.
Bacteriophages are ubiquitous in the environment. They are also abundant in the digestive tract of humans and animals (Viertel et al., 2014). Several studies have been attempted for the isolation of bacteriophages with the potential of combating P. mirabilis biofilms. Such studies employed enrichment methods in which clinical strains of P. mirabilis were used for the isolation of bacteriophages from sewage samples (Lehman and Donlan, 2015; Nzakizwanayo et al., 2015; Melo et al., 2016) and human feces (Morozova et al., 2016). As revealed by transmission electron microscope (TEM), the bacteriophages with activity against P. mirabilis biofilms, belonged to the order Caudovirales that encompasses tailed bacteriophages. Among which, some belonged to the family Siphoviridae (phages with long, flexible non contractile tail) (Maszewska et al., 2018; Yazdi et al., 2018) and others belonged to the families Podoviridae (phages with short stubby tail) (Kaca et al., 2011; Alves et al., 2016; Melo et al., 2016) and Myoviridae (phages with contractile tail) (Kaca et al., 2011; Melo et al., 2016; Maszewska et al., 2018; Alves et al., 2019). All of them were of the lytic type that replicate inside the host cells eventually causing them to rupture releasing progeny viruses (Skurnik et al., 2007; Gill and Hyman, 2010).
Different mechanisms have been suggested for the antibiofilm activity of phages. Phages can transfer through water channels to reach the biofilm-embeded bacterial cells (Chan and Abedon, 2014). They locally replicate within the cells they have reached to increase in number and spread to nearby cells reducing the total number of cells forming the biofilm. In addition, phages can express or induce the expression of depolymerizing enzymes that degrade the exopolysaccharide and facilitate the spread of phages within biofilms (Latka et al., 2017). Bacteriophages can also infect reactivated persister cells preventing relapse of infections due to this reactivation (Harper et al., 2014).
Several studies, however, showed that phages could more effectively prevent the formation of P. mirabilis biofilm than destroying a preformed one (Carson et al., 2010; Lehman and Donlan, 2015). This was attributed to the poor penetrability of phages within older biofilm layers (Chhibber et al., 2013). Efficient bacteriophage lysis was deficient within biofilms due to the low concentration of actively proliferating cells. This is due to the low metabolic activity within the innermost parts of biofilms (Sillankorva et al., 2004; Cerca et al., 2007). Accordingly, when administered early in the bacterial colonization step, bacteriophages were demonstrated to prevent blockage of Foley catheters due to P. mirabilis biofilms for over 8 days (Nzakizwanayo et al., 2015; Aniejurengho, 2016). On the other hand, established or late stage biofilm related infections were more resistant to eradication by bacteriophages (Aniejurengho, 2016).
As for the use of bacteriophages for treatment of P. mirabilis crystalline biofilms, several factors in the urinary tract have been found to influence phage's adsorption to host cells. Such factors include the chemical environment and pH (Jonczyk et al., 2011). Cofactor cations such as CaCl2 and MgCl2, in urine, have been found to increase the infectivity of phages as a result of higher concentration of phages on bacterial cell surface and alteration in the receptors. As a result, phages access to receptors or phage nucleic acid translocation is accelerated (Jamal et al., 2015; Yazdi et al., 2018). On the other hand, the crystals formed in urine during biofilm formation were found to inhibit adsorption of phages to their target cells.
Contradictory results about the effect of pH on the activity of bacteriophages were reported by previous studies. Some of them demonstrated the inactivation of phages at extreme pH values (pH 2 and 11) and reduction of phage titer value at pH 8 by about 30%. Accordingly, the authors suggested that the effectiveness of phages may be impaired by alkaline conditions in urine during P. mirabilis infection. Higher in vivo doses of phages may then be required for biofilm eradication (Maszewska et al., 2018; Yazdi et al., 2018). On the other hand, bacteriophages isolated by Yazdi et al. (2018) showed high stability to a wide range of pH (3–11). A finding that was considered advantageous for treatment of P. mirabilis biofilm with fluctuation in pH. While the outer part of the biofilm is alkaline in nature, low pH is observed within the biofilm matrix due to accumulation of acidic metabolites. The stability of phages over a wide pH range then allows retention of activity during translocation through different parts of the biofilm, thus making phages good candidates for treatment of UTIs caused by P. mirabilis biofilms.
Two phage-based strategies were proposed by Donlan (2009) for combatting bacterial biofilm formation on catheter surfaces. The first strategy based on preventing bacterial adhesion and biofilm formation by coating the catheter surface with phages. The second one employed lytic bacteriophages as well as phage depolymerases for biofilm eradication.
So far, up to 90% reduction in biofilm formation was achieved in phage-coated in vitro catheter models in several studies (Carson et al., 2010; Nzakizwanayo et al., 2015; Melo et al., 2016; Thompson, 2018). A potential drawback of this strategy is the unknown and uncontrolled orientation of the phages. However, this strategy was found to eradicate early biofilm colonization and delay catheter blockage (Nzakizwanayo et al., 2015). Inconsistent findings were reported by another study carried out by Thompson (2018) who showed more adherence of bacterial cells to catheter sections pre-treated by phage, an effect that was strain dependent (Aniejurengho, 2016). A possible explanation to his finding is the formation of conditioning film of lysed bacterial cells which mask the effect of phages and provide a sticky surface for adhesion (Fernandez et al., 2017).
A more successful approach utilizing bacteriophages for fighting biofilms is the use of phage-antibiotic combinations (Yazdi et al., 2018). Failure of this approach in biofilm treatment is unlikely, as bacterial cells which show resistance to one agent will be susceptible to the other (Chhibber et al., 2013). Furthermore, while passing through biofilm layers, bacteriophages will facilitate the diffusion of the antibiotic through biofilm layers (Verma et al., 2009; Harper, 2013; Harper et al., 2014).
Nanoparticles
Nanoscale materials (1–1000 nm) are widely used nowadays owing to their high capacity for tissue targeting (Savolainen et al., 2010). Reducing the size to nanoscale can modify the properties of materials in terms of their chemical, mechanical, electrical, structural, morphological and optical properties (Buzea et al., 2007).
Cationic dendrimeric peptides constitute a novel class of molecules with antimicrobial potential. The positive charge on the surface of such peptides is proposed to interact with negatively charged molecules on the surface of bacterial cells such as phosphate groups of Gram-negative lipopolysaccharides (Jenssen et al., 2006; Weidenmaier and Peschel, 2008). In addition, their hyperbranched nature offers chemically reactive groups to which other molecules can be attached imparting therapeutic properties (Shi et al., 2007). As antibiofilm agents, dendrimers possess several promising characteristics. Owing to their small particle size, they can readily penetrate the EPS matrix exerting some bacteriostatic activity. Dendrimers have been also found to inhibit the formation of the EPS matrix by inducing nucleic acid mutations (Limoli et al., 2014). They are also capable of inhibiting protein synthesis (Mardirossian et al., 2014). Another possible mechanism by which the cationic dendrimeric peptides may act is their detergent-like effect. They interact with the anionic components of bacterial membranes and biofilm matrix leading to loss of membrane potential. Aniejurengho (2016) has demonstrated the ability of dendrons to reduce preformed P. mirabilis biofilms by up to 83.5%. Thus, they provide a clinically beneficial alternative to antibiotics for eradication of preformed biofilms that is achievable only by unattainable in vivo concentrations (Hengzhuang et al., 2011; Belfield et al., 2015; Wu et al., 2015).
Selenium (Se) is a micronutrient metalloid. It is a structural part of several enzymes such as glutathione peroxidases, iodothyronine deiodinases, and thioredoxin reductase, which are involved in antioxidant defense, detoxification and metabolism, respectively (Messarah et al., 2012; Zhai et al., 2017). The effect of biologically synthesized (biogenic) Selenium nanoparticles (SeNPs) on P. mirabilis biofilms was studied by Shakibaie et al. (2015). Interestingly, it inhibited biofilm formation to 53.4%. Based on in vitro and in vivo data, biogenic SeNPs have lower toxicity than that of selenite or selenate (Shakibaie et al., 2010). As a result, biogenic SeNPs or antimicrobials loaded on the surface of SeNPs might be good candidates for use as novel antibiofilm agents.
Low concentrations of ZnO:MgO NPs have been found to affect the development of P. mirabilis biofilm regarding bacterial number and extracellular matrix. This has been linked to preventing the bacterium from colonizing surfaces and formation of mature biofilms. ZnO:MgO NPs were also found to affect the production of extracellular matrix, an essential component of biofilm that protects bacteria from environmental stress (Iribarnegaray et al., 2019). Reduction in bacterial numbers within biofilms may also be attributed to the antibacterial activity of the NPs. ZnO nanoparticles (ZnO NPs) have shown great antibacterial activity against P. mirabilis (Gunalan et al., 2012). The main mechanisms whereby ZnO NPs may exert their antibacterial activity are alteration of cell membrane integrity (Brayner et al., 2006; Irzh et al., 2010) and generation of reactive oxygen species (Sawai, 2003; Jones et al., 2008). Synergistic activity may also be achieved with MgO NPs (Pradeev Raj et al., 2018) that have also shown great antibacterial activity against both Gram-negative and Gram-positive bacteria (Hayat et al., 2018).
Conclusion
Proteus mirabilis is one of the leading causes of CAUTIs. Such infections are complicated by the unique ability of P. mirabilis to form crystalline biofilms. Compared to their planktonic counterparts, biofilm-embedded cells are considerably recalcitrant to antimicrobial treatment and host immune response. Biofilm formation is a multistage process that starts by the reversible adhesion of bacterial cells to biotic or abiotic surfaces followed by an irreversible attachment, formation of microcolonies and finally development of a mature biofilm. Some virulence factors have been linked to the ability of P. mirabilis to form crystalline biofilms. Such factors include swarming motility, fimbriae, urease production, capsule polysaccharide, and efflux pumps. The inhibitory effect of different antimicrobials on P. mirabilis biofilms was evaluated by many studies. A broad agreement on the efficacy of ciprofloxacin in inhibiting biofilm formation and eradication of preformed biofilms was found. Showing activity at high pH levels was an added advantage. The cyclic administration of antimicrobials also showed promising results for controlling biofilms. However, the efficacy of this approach was tightly linked to better understanding of persister cells and the mechanisms underlying their tolerance to antimicrobials. Some information on the performance of persister cells in planktonic cultures of P. mirabilis were provided by recent studies. However, more studies are required to fill the gap of knowledge on their performance within biofilms as well as the impact of antimicrobial combinations on their viability. Other studies were concerned with the antibiofilm effect of different phytochemicals extracted from herbs used in folk medicine. Many phytochemicals showed promising antivirulence effects including effect on: motility, urease activity, production of polysaccharide and adherence. This raises the demand for conducting more studies on the effect of phytochemical-antimicrobial combinations. Such combinations might decrease the selective pressure on microorganisms upon using antimicrobials alone which leads to the development of antimicrobial resistance. Apitherapy is among the natural alternatives whose antibiofilm activity was demonstrated by some studies. Inhibition of biofilm formation and eradication of preformed biofilms of P. mirabilis were proven for different types of honey as well as the ethanolic extract of propolis. Repurposing of some FDA-approved drugs for controlling P. mirabilis biofilms was also recommended by some studies. Among these drugs are ambroxol, fluoxetine and thioridazine. Apart from their promising application in treatment of bacterial infections, the role of bacteriophages in combating biofilms was also a matter of concern. Different types of bacteriophages showing inhibitory effect on P. mirabilis biofilms were successfully isolated. However, their higher ability to effectively prevent the formation of P. mirabilis biofilm than destroying a preformed one was noted. For treatment and/or prevention of P. mirabilis-mediated CAUTIs, bacteriophages have shown several advantages. Most importantly are their ability to withstand high pH levels and the enhanced activity in presence of urinary cations. Effectiveness of phage-antimicrobials combinations was also evident. Finally, among the emerging fields of study in fighting P. mirabilis biofilms is the nanoparticles. For this purpose, the activity of different compounds with a nanoscale size was evaluated. Among which cationic dendrimeric peptides, biogenic selenium NPs and ZNO:MgO NPs showed promising results.
All therapeutic strategies mentioned in this review should be considered for controlling P. mirabilis biofilms. Unique mechanisms of action are employed by each allowing the use of combined strategies for better results. However, more investigations are required for examining some of these products for their in vivo effect and to ensure tolerability and lack of toxicity.
Author Contributions
RW, SH, MA, and LF took part in drafting, revising, and preparation of the manuscript. The manuscript was finalized and prepared for submission by RW and SH. All authors contributed to the article and approved the submitted version.
Conflict of Interest
The 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.
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Keywords: Proteus mirabilis, crystalline biofilm, CAUTI, antivirulence, quorum sensing, bacteriophage
Citation: Wasfi R, Hamed SM, Amer MA and Fahmy LI (2020) Proteus mirabilis Biofilm: Development and Therapeutic Strategies. Front. Cell. Infect. Microbiol. 10:414. doi: 10.3389/fcimb.2020.00414
Received: 28 March 2020; Accepted: 06 July 2020;
Published: 14 August 2020.
Edited by:
Andres Felipe Opazo-Capurro, University of Concepcion, ChileReviewed by:
Brendan Gilmore, Queen's University Belfast, United KingdomPablo Zunino, Instituto de Investigaciones Biológicas Clemente Estable (IIBCE), Uruguay
Copyright © 2020 Wasfi, Hamed, Amer and Fahmy. 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: Reham Wasfi, rwasfi@msa.eun.eg