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In vitro activities of thiazolidione derivatives combined with daptomycin against clinical Enterococcus faecium strains
BMC Microbiology volume 22, Article number: 16 (2022)
Previous reports have demonstrated two thiazolidione derivatives (H2-60 and H2-81) can robustly inhibit the planktonic growth and biofilm formation of S. epidermidis and S. aureus by targeting the histidine kinase YycG. Whereas the antibacterial and anti-biofilm activity of these two thiazolidione derivatives (H2-60 and H2-81) against Enterococcus faecium remains elusive. Here, the pET28a-YycG recombinant plasmid were in vitro expressed in E. coli competent cell BL21 (DE3) and induced to express YycG’ protein (conding HisKA and HATPase_c domain) by 0.5 mM IPTG and was purified by Ni – NTA agarose and then for the autophosphorylation test. Antimicrobial testing and time-killing assay were also be determined. Anti-biofilm activity of two derivatives with sub-MIC concentration towards positive biofilm producers of clinical E. faecium were detected using polystyrene microtiter plate and CLSM.
The MICs of H2-60 and H2-81 in the clinical isolates of E. faecium were in the range from 3.125 mg/L to 25 mg/L. Moreover, either H2-60 or H2-81 showed the excellent bactericidal activity against E. faecium with monotherapy or its combination with daptomycin by time-killing assay. E. faecium planktonic cells can be decreased by H2-60 or H2-81 for more than 3 × log10 CFU/mL after 24 h treatment when combined with daptomycin. Furthermore, over 90% of E. faecium biofilm formation could markedly be inhibited by H2-60 and H2-81 at 1/4 × MIC value. In addition, the frequency of the eradicated viable cells embedded in mature biofilm were evaluated by the confocal laser microscopy, suggesting that of H2-60 combined with ampicillin or daptomycin was significantly high when compared with single treatment (78.17 and 74.48% vs. 41.59%, respectively, P < 0.01).
These two thiazolidione derivatives (H2-60 and H2-81) could directly impact the kinase phosphoration activity of YycG of E. faecium. H2-60 combined with daptomycin exhibit the excellent antibacterial and anti-biofilm activity against E. faecium by targeting YycG.
Enterococcus spp. is known to be capable of causing nosocomial and life-threatening infections in human. Enterococcus faecium infection can result in a variety of infectious diseases, including intra-abdominal and pelvic regions infections, urinary tract infections, implantable infections, biofilm-related infections, etc. . Pathogens causing hospital acquired infections in the US during 2011–2014 showed an overall contribution of E. faecium of 3.7% . A large proportion (39.9%) of enterococcal bacteremia was caused by E. faecium . Multidrug resistance has been increased globally that is considered public health threat. Several recent studies revealed the emergence of multidrug-resistant bacterial pathogens from different origins including humans, poultry, cattle, and fish that increases the need for new antimicrobial alternatives to the commonly used old antimicrobial agents [4,5,6]. Recently, the increasing reports of multidrug resistant E. faecium strains, including vancomycin-,daptomycin- or linezolid-resistant strains, has attracted the attention of the scientific community [7, 8]. Previous researchers have reported that virulence factors played important roles in the pathogenicity of enterococci . These virulence factors could help E. faecium to break the host immune defense system to accelerate the bacteria to colonize on the infection site and thereby leading to cause E. faecium infection . Virulence factors also have been proved to enhance the biofilm formation of bacteria and cause biofim-related endocarditis and urinary tract infections [11,12,13].
The ideal antimicrobial agent for infection treatments may possess the following characteristics: (1) Highly selectivity for bacteria with clear and conserved target. (2) Low toxicity in vivo. (3) Not easily resistant to bacteria. (4) Potent antimicrobial activity or even broad-spectrum effects.
In addition to focusing on increasing drug resistance, E. faecium can also form biofilms, which could often enhance the difficulty of antimicrobial treatment to suppress the protracted and chronic infections [14,15,16,17]. The biofilm formation limits the diffusion and penetration of bacteria due to the aggregation of extracellular polymeric substances (EPS) matrix. One of the most difficulties for the treatment of biofilm-related infection is to eradicate established biofilms on the surfaces of devices or cavities . Therefore, the development of novel antimicrobial agents against the planktonic growth and biofilm formation of E. faecium would be beneficial for clinicians to improve the prognosis of these infections.
Previous studies have confirmed the decisive role of two-component systems (TCSs) of bacteria in the planktonic growth and biofilm formation of a variety of bacteria [19, 20]. Therefore, TCSs have aroused the increasing attention as potential targets for the development of antibacterial and anti-biofilm drugs. YycFG is one of the TCSs involved in biofilm formation, cell wall metabolism, resistance and regulation of virulence factors in Bacillus subtilis, Staphylococcus aureus, Staphylococcus epidermidis and Streptococcus [21,22,23,24]. The histidine kinase YycG is a transmembrane protein and the kinase ATP-binding domain (HATPase_c domain) can sense external signals and is activated by extracellular signals, which subsequently resulting in the phosphorylation of the histidine site (HisKA domain) of YycG. By targeting YycG, small molecule compounds with antibacterial activity have been effectively developed against the gram-positive bacteria such as B. subtilis, S. aureus [25, 26], S. epidermidis and Streptococcus [8, 27]. Therefore, YycG may be a potential alternative target for the development of antimicrobial agents. Our group previously described the bactericidal and anti-biofilm activities of two YycG inhibitors, H2-60 and H2-81, by targeting the HATPase_c domain of S. epidermidis YycG , S. aureus . But it is still unclear whether the two thiazolidione derivatives (H2-60 and H2-81) are capable to block the planktonic growth and biofilm formation in E. faecium.
The aim of this study was to investigate the phosphorylation inhibitory activities of the thiazolidione derivatives (H2-60 and H2-81) to the YycG protein with kinase ATP-binding site (HATPase_c domain). The antibacterial and anti-biofilm activities of these two derivatives against E. faecium have been evaluated. More important, the potential application prospects of the combination therapy of H2-60 and H2-81 with the common antibiotics on biofilm formation of E. faecium were also assessed.
The inhibitory effect of two thiazolidione derivatives on the kinase activity of the recombinant E. faecium YycG’
In order to verify the impact of two thiazolidione derivatives on the kinase activity of the recombinant YycG’ proteins of E. faeciumin in vitro, Kinase-Glo® Luminescent Kinase (Promega) was adopted to detect the correlation between relative light unit (RLU) and ATP content in the reaction system. Our data indicated the close correlation between the ATP concentration and the RLU (R2 = 0.9671, Fig. 1A). Moreover, the kinase activity of the recombinant protein YycG’ were also verified in vitro, suggesting the optimized amount of ATP (shown in Fig. 1B) and 3 μg YycG’ protein were suitable for the addition with the various concentration gradients of ATP (1.56–50 μM) for the further detection of the kinase activity. RLU value decreased significantly in comparison to the control group without the addition of YycG’ protein in addition of ATP concentration between 3.13–6.25 μM (Fig. 1B). RLU value was also significantly decreased with the increasing concentrations of YycG’ proteins (Fig. 1C). Based on the above results, the effect of two thiazolidione derivatives on the kinase activity of YycG were detected with the concentration of 4 μM ATP and 3 μg recombinant protein, suggesting the concentration-dependent inhibition of the activity of YycG’ protein kinase by H2-60 and H2-81 respectively. The IC50 values (the concentration of compound inhibiting 50% of YycG’ kinase activity) of H2-60 and H2-81 respectively were 25.4 and 26.2 μM respectively (Table 1).
Antibacterial activity of two thiazolidione derivatives (H2-60 and H2-81) against E. faecium
The MIC values of H2-60 and H2-81 determined by broth microdilution method against 102 non-repetitive clinical E. faecium strains were ranging from 3.13 μM to 25 μM. Moreover, the MIC50/MIC90 values of these clinical E. faecium strains were 6.25/6.25 μM for H2-60 and 6.25/12.5 μM for H2-81 respectively (Table 2). The MIC and the MBC value for E. faecium EF16M64 was 3.13 μM and12.5 μM respectively. The MIC and the MBC values of ampicillin, vancomycin, linezolid and daptomycin against E. faecium EF16M64 were listed in Supplementary Table S1. Another clinical antimicrobial agents against 102 E. feacium strains were also determined, showing the MDR phenotypes in Supplementary Table S3, we can see H2-60 and H2-81 also had good activities against multidrug-resistant strains, including vancomycin or linezolid non-susceptible strains. The effect of H2-60 and H2-81 on planktonic bacterial growth at different sub-inhibitory concentrations were evaluated, suggesting the unaffected growth of planktonic bacteria by these two derivatives at the concentration of 1/4 × MIC or below (Table 1 and Fig.2).
Time-killing assay of two thiazolidione derivatives (H2-60 and H2-81) against E. faecium
Time-killing assay were performed with two thiazolidione derivatives (H2-60 and H2-81) alone or combined with ampicillin, vancomycin, linezolid, or daptomycin at concentrations of 4 × MIC respectively. The original amount of viable bacteria cells of all groups were 6.1 log10CFU/mL counts. We observed the bactericidal effect of H2-60 and H2-81 was equivalent to that of ampicillin, vancomycin and linezolid within 24 h, with a reduction of more than 2 orders of magnitudes from baseline of 6.1 to 2.0–3.8 log10CFU/mL. Worthy of our attention, when H2-60 or H2-81 combined with daptomycin, the amount of viable bacteria cells could be decreased from baseline of 6.1 to 3.3–4.0 log10CFU/mL within 11 h, and even to 0.7–0.9 log10CFU/mL within 24 h (Fig. 3).
Anti-biofilm activity of two thiazolidione derivatives (H2-60 and H2-81) against E. faecium
The biofilm formation of 102 E. faecium strains from different sources was assayed using polystyrene microtiter plate. EF16M2 strain (OD570 ≈ 0.207 ± 0.03) was regarded as negative control and OD570 cut-off (ODc) value was calculated to be 0.297. 52.9% (54/102) of the clinical E. faecium strains was shown positively with biofilm formation, 7.8% (8/102) were shown with strong positive biofilm phenotype, 11.8% (12/102) were medium positive biofilm phenotype, and 33.3% (34/102) could form the weak positive biofilm (Table 3).
The growth curves demonstrated that H2-60 or H2-81 did not affect the growth of E. faecium EF16M64 planktonic cells at 1/4 × MIC or below (shown in Fig. 2). Eight strains of E. faecium with the range of positive biofilm formation OD570 from 1.27 to 2.814 were selected to evaluate the inhibitory effect of H2-60 and H2-81at sub-MIC concentration (1/4 × MIC), indicating that the significantly reduced biofilm formation when treated with 1/4 × MIC of H2-60 or H2-81 for 24 h respectively (Fig. 4, P < 0.0001, Student’s t test) .
Eradication of mature biofilm of E. faecium by two thiazolidione derivatives (H2-60 and H2-81) using CLSM
The optimal concentration of the inhibitor (1 × MIC) and common antibiotics (8 × MIC) was finally defined by exploring the ablating effect of inhibitors on mature biofilm of E. faecium at different concentration gradients (1/4 ×, 1/2 ×, 1 ×, 2 ×, 4 ×, 8 ×, 16 ×, 32 × MICs). Thus, the 1 × MIC of H2-60 or H2-81 was used to explore their effect on the mature biofilm of E. faecium, and compared with ampicillin or daptomycin (8 × MIC). CLSM were performed for the quantification of the amount of the viable bacteria cells, suggesting the amount of viable biofilm-embedded bacteria cells in the mature biofilm were reduced to 41.6 and 29.0% by H2-60 and H2-81 respectively. Interestingly, 78.17 and 74.48% of viable biofilm-embedded bacteria cells in mature biofilms could be significantly eradicated by H2-60 combined with ampicillin or daptomycin in comparison to H2-60 alone (Fig. 5 and Table 4).
The rapid emergence of multidrug-resistant Enterococcus spp. has limited the available drug options for the treatment of Enterococcus infections in human. Currently, just few antimicrobial agents are very effective for the treatment of biofilm-associated infections such as endocarditis, intravascular catheter-related infections, etc. Therefore, it’s urgent for us to develop the effective compounds for the improvement of the clinical outcome of the biofilm-associated infections caused by Enterococcus spp.
YycFG TCS has been shown to play a key role in planktonic growth and biofilm formation in a variety of Gram-positive bacteria [21,22,23]. Previous reports have indicated the excellent antibacterial and anti-biofilm activities of H2-60 and H2-81against S. epidermidis, S. aureus by targeting the histidine kinase YycG of S. epidermidis with low cytotoxicity [22, 29]. Bioinformatics analysis data showed the high homologous characteristics of the YycG-encoded protein of E. faecium compared with that in S. epidermidis and S. aureus (about 60%, Supplementary Table S2). We hypothesize that two thiazolidione derivatives targeting YycG can also be used for E. faecium infection. In this study, our data showed the low MIC values of H2-60 and H2-81 against clinical E. faecium isolates (both MIC50/MIC90: 6.25/12.5 μM). Time-killing assay further indicated the bactericidal activity of H2-60 and H2-81 equivalent to that with ampicillin, vancomycin, and linezolid. IC50 results supported the binding affinity of H2-60 and H2-81 with the recombinant YycG’ protein of E. faecium, which maybe the same target sites in S. epidermidis of YycG.
The present research also found that H2-60 and H2-81 were also effective against different MDR strains, including vancomycin or linezolid non-susceptible strains. Daptomycin and linezolid were first-line therapeutic option for vancomycin-resistant E. faecium infection and high dose are often recommended , but more evidences have been demonstrated that daptomycin use was not associated with better microbiological cure than linezolid and have high mortality . Meanwhile, Time-killing curve of daptomycin treatment alone also showed no bactericidal activity , which were consistent with our results. Interestingly, time-killing results further indicated both H2-60 and H2-81 combined with daptomycin could had strong bactericidal effect and sustained for over 24 h, suggesting the possible synergetic role of these two thiazolidione derivatives with daptomycin. Daptomycin is a lipopeptide antibiotic used for gram-positive bacterial infection, which can block the peptidoglycan biosynthesis of the bacterial cell wall by disturbing the transport of amino acids of the cell membrane. Multiple reports have demonstrated the involvement of YycG in the degradation of S. aureus cell wall by hydrolyzing peptidoglycan, and nucleotide insertion mutation in the yycG gene participate in the reduced daptomycin susceptibility in S. aureus. Therefore, we speculated that H2-61 and H2-80 can exert a synergistic bactericidal role with daptomycin by interfering with the synthesis of bacterial cell wall, but their possible synergetic mechanism needs to be further elucidated.
Biofilm matrix is often composed of polysaccharides, extracellular DNA (EDNA), a variety of lipids and proteins et al. It’s difficult to kill the viable bacteria cells that embedded in biofilm from the clinical environment. Currently, limited effective antibiotic can be used for the treatment of biofilm associated infections and the eradication of mature biofilms still remains an urgent clinical problem. This study observed that H2-60 and H2-81 had significant inhibitory effect on the E. faecium biofilm formation and the viable bacteria embedded in the established biofilm detected by CLSM can be eradicated by the H2-60 monotherapy. It is also found for the first time that the combination of H2-60 with daptomycin could enhance the clearance capacity of the viable bacteria embedded in the mature biofilms. This may be that daptomycin disrupted cell membrane stability of E. faecium synergistically with H2-60 targeting YycG to interfere with biofilm formation, which is facilitate to the entry of daptomycin and H2-60 into the established biofilm to kill more viable bacteria.
We also observed the phenomenon that the H2-81 had worse killing effects on adherent cells in the established biofilm than that of H2-60. Which showed the opposite effect as the derivatives agnist S. epidermidi  and S. aureus . This study also indicated that the anti-biofilm activities of ampicillin and daptomycin had been attenuated with H2-81 condition but been enhanced in that of H2-60. Our previous study had found that halogen substituents (F or Cl) on phenyl rings of thiazolidine core structure could improve antibacterial or anti-biofilm activities than its leading compounds . In terms of molecular structure, H2-81 lacked an F element on its phenyl rings, which may change its drug structure-activity and molecular symmetry, thus attenuating the anti-biofilm effect of ampicillin and daptomycin. Another possible reason maybe that ampicillin and itself had a strong bactericidal effect on E. faecium, reducing the counts of bacteria to a very low number in a short time, so that we can not observe the synergistic bactericidal effect. Therefore, the above results suggest that thiazolidione derivatives H2-60 might be used as an adjunct to antimicrobials with potential applications for the treatment of biofilm-associated infections caused by E. faecium, especially when combined with daptomycin.
Two thiazolidione derivatives (H2-60 and H2-81) targeting the HATPase_c domain of S. epidermidis YycG can also bind to the YycG of E. faecium. Time-killing results demonstrated the synergetic bactericidal activity of H2-60 and H2-81 with daptomycin toward the planktonic growth of E. faecium. The combination therapy of H2-60 with daptomycin could enhance the bactericidal activity toward the viable bacteria embedded in the established E. faecium biofilm. Therefore, H2-60 is suitable used as an adjuvant drug to enhance the anti-biofilm activities of other antibiotics. It also suggests that thiazolidione derivatives targeting YycG combined with daptomycin may become a new strategy for the treatment of E. faecium infection and biofilm-related infections.
Bacteria strains and materials
One hundred two non-redundant clinical isolates of E. faecium were obtained from Shenzhen Nanshan People’s Hospital and the 6th Affiliated Hospital of Shenzhen University Health Science Center (Table 3 and Supplementary Table S3). These clinical strains were first identified by the Phoenix 100 automated microbiology system (BD, USA) and then sub-cultured generations were re-identified with matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOFMS, IVD MALDI Biotyper, Germany) . Phoenix 100 automated microbiology system was used for indentification and antimicrobial susceptibility testing of E. faecium by broth microdilution method. By using MALDI-TOFMS technoloty, the unique proteins and peptides of bacteria were arranged according to the molecular weight to form a unique proteome finger map of characteristic pattern peaks for strains identification. The common-used antibiotics, including vancomycin (catalog no. V2002), linezolid (catalog no. PZ0014), ampicillin (catalog no. A9518) and daptomycin (catalog no. SBR 00014), were purchased from Sigma Aldrich (Shanghai, China). Ampicillin was the first choice for E. faecium infection, vancomycin, linezolid, and daptomycin were often used in multidrug resistant strains of E. faecium and other gram-positive bacterial infections. So we choose these four agents to compare their antimicrobial activities to two thiazolidione derivatives. Two YycG inhibitors of the thiazolidione derivatives (H2-60 and H2-81) were synthesized and obtained from WuXiAppTec Co., Ltd. (Shanghai, China). Mueller-Hinton Broth (MHB), CA-Mueller-Hinton Broth (CAMHB), Tryptone Soy Broth (TSB) and Agar were purchased from Oxoid Ltd. (Basingstoke, England). E. faecalis ATCC29212 (biofilm negative) were used as quality control for MIC determination and E. faecium EF16M64 were used as biofilm positive strains.
Antimicrobial susceptibility testing and MBC assays
The E. faecium strains were cultured overnight on blood agar plates and these isolates were identified by the Phoenix 100 automated microbiology system (BD, Franklin Lakes, New Jersey, USA). The MIC values of two thiazolidione derivatives (H2-60 and H2-81), vancomycin, linezolid, ampicillin and daptomycin against E. faecium were determined by broth microdilution method according to the standards of Clinical and Laboratory Standards Institute (CLSI) in 2019. The susceptibilities of E. faecalis isolates to another clinical relevant antimicrobials (i.e., teicoplanin, tetracycline, erythromycin, nitrofurantoin, ciprofloxacin, high-level gentamicin and rifampicin) were determined by supporting gram-positive antimicrobial susceptibility test kit of BD automated microbiology system (No. PMIC-92). Briefly to describe the MICs detection of H2-60 and H2-81, two-fold serial dilutions of the compounds at final concentrations from 200 to 0.39 μM were prepared in 96-well microtiter plates (Falcon) containing 100 μL CAMHB medium. The medium was adjusted by sterile saline until the bacterial suspension density was equal to a 0.5 McFarland standard (∼1.0 × 108 CFU/mL) and then diluted to 1:100 into CA-MHB medium. The diluted bacteria were added into 96 well plate (50 μL/well) and mixed and placed in 37 °C incubator and incubated at 220 rpm for 20–24 h. The interpretation of MIC was the lowest concentration without visible cells growth in the well. One hundred microliter of bacteria solution with or above MIC value was coated on a new MHA plate and incubated at 37 °C for 24 h for counting. The MBC value was represented as a 99.99% reduction of the original inoculum or the number of clones on each plate is ≤5. Besides, positive control (without compound) and negative control (without bacterial solution) were also set and E. faecalis ATCC29212 was used as quality control. MIC50/MIC90 was used to represent MIC value distribution of all the clinical strains. All experiments were performed in triplicate.
Cloning, expression and purification of the YycG’ protein
The YycG’ fragment containing the cytoplasmic catalytic and ATP-binding domains (the HisKA and HATPase_c domain, see Fig. 1A) of YycG (377aa to 604aa) in E. faecium was amplified by PCR with the template of genomic DNA of E. faecium DO (Genbank No. NC_017960). The amplified primers were 5′-TTTGGATCCCGTCGTGAATTCGTCTCTAA − 3′ and 5′-TTTCTCGAGTAGGTTCATATGGCAGCGAGAT-3′ respectively. Subsequently, the fragment was digested with BamHI and XhoI (Thermo Fisher Scientific, Massachusetts, USA) and ligated into the corresponding sites of pET28 (a) to obtain pET28 (a)-YycG’. After being transformed into E. coli strain BL21 (DE3), this recombinant plasmid was induced to express YycG′ protein by 0.5 mM isopropyl-1-thio-β-D-galactopyranoside at 22 °C for 12 h. Then, the bacterial cells were disrupted by sonication and centrifuged, the supernatant was purified by Ni–NTA agarose (Qiagen, Los Angeles, CA, USA) using affinity chromatography method. The concentration of recombinant YycG’ protein was determined by the BCA Protein Assay Kit (Thermo Fisher Scientific, Massachusetts, USA), according to the manufacturer’s protocol.
Inhibition assay for phosphorylation activity of the HATPase_c domain of YycG′
In order to verity interaction of two thiazolidione derivatives (H2-60 and H2-81) with the HATPase_c domain of YycG, impact of these two derivatives on the ATPase activity of the YycG′ protein were measured using the Kinase-Glo™ Luminescent Kinase Assay (Promega, Madison, USA). Briefly, 3 μg purified YycG′ protein was pre-incubated with a series of dilutions of the compounds in reaction buffer [40 mM Tris (pH 7.5), 20 mM MgCl2 and 0.1 mg/ml BSA] at room temperature for 30 min, 4 μM ATP was added and incubated for 30 min at room temperature, then Kinase-Glo™ Reagent was added to detect the remaining amount of ATP, and the results were reflected by luminescence intensity value (RLU). Meanwhile, YycG′ protein with no addition of the derivatives was used as the control and ATP only was used as a blank. The rate of inhibition of kinase phosphorylation (Rp) by the derivatives was calculated by the following equation:
IC50 (the concentration resulting in 50% inhibition of YycG′ histidine kinase auto-phosphorylation) was obtained by using GraphPad v7.0 software (San Diego, CA, USA). BSA protein without phosphorylation activity were used as the negative control. All experiments were performed in triplicate.
Growth curves of the planktonic bacteria
After the overnight incubation, liquid cultures of E. faecium EF16M64 were sub-cultured (1:200) in fresh TSB medium and H2-60 and H2-81 were doubling diluted (from 1 × MIC to 1/16 × MIC) by TSB medium. After diluted, totally 300 μL dilution were added to growth curve device (Bioscreen C co., Piscataway, USA) in triplicate. The bacterial solution without the derivatives was used as positive control and the effect of the derivatives on bacterial growth was automatically monitored every hour by measuring the optical density at 600 nm (OD600) continuously for 16 h. The experiments were performed in triplicate.
Time-killing curve of single dose of two derivatives and combination with vancomycin, linezolid, ampicillin, or daptomycin at concentrations of 4 × MIC respectively were assayed with the suspensions of E. faecium EF16M64 (∼1 × 106 CFU/mL). Time-killing experiments were performed at 37 °C with shaking at 220 rpm under aerobic conditions according to previously reported with some modifications . Aliquots (1 mL) were removed at different time points (0, 1, 3, 5, 7, 11, and 24 h), serially diluted with sterile saline, and 100 μL of bacteria were evenly coated on MHA plate and cultured at 37 °C for 24 h, bacterial colonies were counted and determined by plotting log10 colony counts (CFU/mL) against time. Bacteria treated with 0.1% DMSO served as a control. The results were independently presented as the mean ± standard deviations (SD) in triplicate.
Determination of E. faecium biofilm formation
Biofilm formation assays were performed by using the methods described in our previous study with minor modification . Briefly, overnight cultures of E. faecium EF16M64 were diluted 1:200 with fresh TSBG (TSB plus 0.25% glucose) and inoculated into 96-well polystyrene microtiter plates (200 μL/well, Costar3599, Corning). After incubation at 37 °C for 24 h, the supernatant of the unattached cells was removed and washed with deionized water for three times, adherent biofilms in the plates were fixed with 95% methanol, stained with 1% crystal violet for 20 min and washed, and then dried in air for 2 h. The optical density at 570 nm (OD570) was tested by micro plate spectrophotometer (DTX880, Beckman Coulter, USA). E. faecium strains EF16M64 and EF16M2 were used as the biofilm-positive and -negative controls, respectively. According to the literature , the biofilm formation phenotypes were divided into four categories. The cut-off value of ODc was defined as three standard deviations above the mean OD of the negative control. The classification is as follows: OD570 ≤ ODc, no biofilm formation, ODc<OD570 ≤ 2 × ODc, weak biofilm formation, 2 × ODc<OD570 ≤ 4 × ODc, medium biofilm formation, OD570>4 × ODc, strong biofilm formation.
Anti-biofilm activity of two thiazolidione derivatives with sub-MIC concentration
The inhibitory effect of two derivatives (H2-60 and H2-81) against the biofilms formation of E. faecium for 24 h was observed in TSBG medium using a semi-quantitative assay. An overnight bacteria culture was diluted 1:200 into TSBG. Aliquots of the inhibitors at 1/2 × MIC concentrations were mixed with the same volume of the bacterial cultures in TSBG, added to 96-well polystyrene plates in triplicate, and co-cultured under static conditions for 24 h. After washing with sterile saline, the biofilms were stained with crystal violet and the OD570 was measured. Wells with no derivatives were used as positive control. All the experiments were repeated in triplicate, and the data represent the means ± standard deviations (SD).
Determination of cell viability in mature biofilms by confocal laser scanning microscope
The effect of two thiazolidione derivatives on cell viability in mature biofilms (24 h) was determined using the Live/Dead Bacterial Viability method (Live/Dead BacLight, Molecular Probes, USA) with SYTO 9 and propidium iodide (PI) dyes to stain live and dead cells within mature biofilms . Overnight cultures of E. faecium EF16M64 was grown in cell-culture dishes (Fluorodish, FD35–100) with TSBG medium and incubated at 37 °C for 24 h. Planktonic bacteria were then removed and discarded, and fresh TSBG containing the derivatives monotherapy (at MIC concentrations) or the derivatives combined with a final concentration of 8 × MIC of ampicillin and daptomycin were added and incubated at 37 °C for a further 72 h, exchanging the media every 24 h for fresh media containing appropriate derivatives. After staining, mature biofilms were observed under a confocal laser scanning microscope (CLSM, Leica) with oil-immersion objective. IMARIS 7.0.0 software (Bitplane) was used to edit and analyze the original images. Green and red fluorescence represented the viable and dead cells, respectively. The PI/total percentage, representing the proportion of dead cells within the mature biofilm, was estimated using ImageJ software (Rawak Software Inc., Stuttgart, Germany). This assay was performed in triplicate and similar results were obtained.
Experiments were performed in triplicate and repeated at least three times. Student’s t-test or nonparametric Mann–Whitney U test was utilized for data comparison. Differences in means were considered significant when P < 0.05. All data were analyzed using the statistical software SPSS (version 14.0; SPSS, Chicago, IL, United States).
Availability of data and materials
All data generated or analyzed during this study are included in this published article [and its supplementary information files].
Extracellular polymeric substances
Confocal laser scanning microscope
Sood S, Malhotra M, Das BK, Kapil A. Enterococcal infections & antimicrobial resistance. Indian J Med Res. 2008;128(2):111–21.
Weiner LM, Webb AK, Limbago B, Dudeck MA, Patel J, Kallen AJ, et al. Antimicrobial-resistant pathogens associated with healthcare-associated infections: summary of data reported to the National Healthcare Safety Network at the Centers for Disease Control and Prevention, 2011-2014. Infect Control Hosp Epidemiol. 2016;37(11):1288–301.
Coombs GW, Daley DA, Thin LY, Pang S, Pearson JC, Robinson JO, et al. Australian group on antimicrobial resistance Australian enterococcal sepsis outcome programme annual report, 2014. Commun Dis Intell Q Rep. 2016;40(2):E236–43.
Abolghait SK, Fathi AG, Youssef FM, Algammal AM. Methicillin-resistant Staphylococcus aureus (MRSA) isolated from chicken meat and giblets often produces staphylococcal enterotoxin B (SEB) in non-refrigerated raw chicken livers. Int J Food Microbiol. 2020;328:108669.
Makharita RR, El-Kholy I, Hetta HF, Abdelaziz MH, Hagagy FI, Ahmed AA, et al. Antibiogram and genetic characterization of Carbapenem-resistant gram-negative pathogens incriminated in healthcare-associated infections. Infect Drug Resist. 2020;13:3991–4002.
Algammal AM, Hashem HR, Alfifi KJ, Hetta HF, Sheraba NS, Ramadan H, et al. atpD gene sequencing, multidrug resistance traits, virulence-determinants, and antimicrobial resistance genes of emerging XDR and MDR-Proteus mirabilis. Sci Rep. 2021;11(1):9476.
Flokas ME, Karageorgos SA, Detsis M, Alevizakos M, Mylonakis E. Vancomycin-resistant enterococci colonisation, risk factors and risk for infection among hospitalised paediatric patients: a systematic review and meta-analysis. Int J Antimicrob Agents. 2017;49(5):565–72.
Gajdacs M, Abrok M, Lazar A, Burian K. Beta-Haemolytic group A, C and G streptococcal infections in southern Hungary: a 10-year population-based retrospective survey (2008-2017) and a review of the literature. Infect Drug Resist. 2020;13:4739–49.
Gao W, Howden BP, Stinear TP. Evolution of virulence in Enterococcus faecium, a hospital-adapted opportunistic pathogen. Curr Opin Microbiol. 2018;41:76–82.
Willems RJ, Homan W, Top J, van Santen-Verheuvel M, Tribe D, Manzioros X, et al. Variant esp gene as a marker of a distinct genetic lineage of vancomycin-resistant Enterococcus faecium spreading in hospitals. Lancet. 2001;357(9259):853–5.
Sillanpaa J, Nallapareddy SR, Singh KV, Prakash VP, Fothergill T, Ton-That H, et al. Characterization of the ebp(fm) pilus-encoding operon of Enterococcus faecium and its role in biofilm formation and virulence in a murine model of urinary tract infection. Virulence. 2010;1(4):236–46.
Shankar N, Lockatell CV, Baghdayan AS, Drachenberg C, Gilmore MS, Johnson DE. Role of Enterococcus faecalis surface protein Esp in the pathogenesis of ascending urinary tract infection. Infect Immun. 2001;69(7):4366–72.
Paganelli FL, Huebner J, Singh KV, Zhang X, van Schaik W, Wobser D, et al. Genome-wide screening identifies phosphotransferase system permease BepA to be involved in enterococcus faecium endocarditis and biofilm formation. J Infect Dis. 2016;214:189–95.
Templer SP, Rohner P, Baumgartner A. Relation of Enterococcus faecalis and Enterococcus faecium isolates from foods and clinical specimens. J Food Prot. 2008;71(10):2100–4.
Van Wamel WJ, Hendrickx AP, Bonten MJ, Top J, Posthuma G, Willems RJ. Growth condition-dependent Esp expression by Enterococcus faecium affects initial adherence and biofilm formation. Infect Immun. 2007;75(2):924–31.
Paganelli FL, van de Kamer T, Brouwer EC, Leavis HL, Woodford N, Bonten MJ, et al. Lipoteichoic acid synthesis inhibition in combination with antibiotics abrogates growth of multidrug-resistant Enterococcus faecium. Int J Antimicrob Agents. 2017;49(3):355–63.
Gajdacs M, Abrok M, Lazar A, Burian K. Increasing relevance of gram-positive cocci in urinary tract infections: a 10-year analysis of their prevalence and resistance trends. Sci Rep. 2020;10(1):17658.
Lewis K. Riddle of biofilm resistance. Antimicrob Agents Chemother. 2001;45(4):999–1007.
Parkinson JS. Signal transduction schemes of bacteria. Cell. 1993;73(5):857–71.
Rowland MA, Deeds EJ. Crosstalk and the evolution of specificity in two-component signaling. Proc Natl Acad Sci U S A. 2014;111(15):5550–5.
Fabret C, Hoch JA. A two-component signal transduction system essential for growth of Bacillus subtilis: implications for anti-infective therapy. J Bacteriol. 1998;180(23):6375–83.
Qin Z, Zhang J, Xu B, Chen L, Wu Y, Yang X, et al. Structure-based discovery of inhibitors of the YycG histidine kinase: new chemical leads to combat Staphylococcus epidermidis infections. BMC Microbiol. 2006;6:96.
Martin PK, Li T, Sun D, Biek DP, Schmid MB. Role in cell permeability of an essential two-component system in Staphylococcus aureus. J Bacteriol. 1999;181(12):3666–73.
Stipp RN, Boisvert H, Smith DJ, Hofling JF, Duncan MJ, Mattos-Graner RO. CovR and VicRK regulate cell surface biogenesis genes required for biofilm formation in Streptococcus mutans. PLoS One. 2013;8(3):e58271.
Watanabe T, Hashimoto Y, Yamamoto K, Hirao K, Ishihama A, Hino M, et al. Isolation and characterization of inhibitors of the essential histidine kinase, YycG in Bacillus subtilis and Staphylococcus aureus. J Antibiot (Tokyo). 2003;56(12):1045–52.
Velikova N, Fulle S, Manso AS, Mechkarska M, Finn P, Conlon JM, et al. Putative histidine kinase inhibitors with antibacterial effect against multi-drug resistant clinical isolates identified by in vitro and in silico screens. Sci Rep. 2016;6:26085.
Li N, Wang F, Niu S, Cao J, Wu K, Li Y, et al. Discovery of novel inhibitors of Streptococcus pneumoniae based on the virtual screening with the homology-modeled structure of histidine kinase (VicK). BMC Microbiol. 2009;9:129.
Liu H, Zhao D, Chang J, Yan L, Zhao F, Wu Y, et al. Efficacy of novel antibacterial compounds targeting histidine kinase YycG protein. Appl Microbiol Biotechnol. 2014;98(13):6003–13.
Liu H, Zhao Y, Zhao D, Gong T, Wu Y, Han H, et al. Antibacterial and anti-biofilm activities of thiazolidione derivatives against clinical staphylococcus strains. Emerg Microbes Infect. 2015;4(1):e1.
Reissier S, Saleh-Mghir A, Guerin F, Massias L, Ghout I, Sinel C, et al. In vivo daptomycin efficacy against experimental vancomycin-resistant Enterococcus faecium endocarditis. J Antimicrob Chemother. 2018;73(4):981–6.
Chuang YC, Wang JT, Lin HY, Chang SC. Daptomycin versus linezolid for treatment of vancomycin-resistant enterococcal bacteremia: systematic review and meta-analysis. BMC Infect Dis. 2014;14:687.
Smith JR, Barber KE, Raut A, Aboutaleb M, Sakoulas G, Rybak MJ. Beta-lactam combinations with daptomycin provide synergy against vancomycin-resistant Enterococcus faecalis and Enterococcus faecium. J Antimicrob Chemother. 2015;70(6):1738–43.
Lay JJ, Holland RD. Rapid identification of bacteria based on spectral patterns using MALDI-TOFMS. Methods Mol Biol. 2000;146:461–87.
Wang Y, Xiong Y, Wang Z, Zheng J, Xu G, Deng Q, et al. Comparison of solithromycin with erythromycin in Enterococcus faecalis and Enterococcus faecium from China: antibacterial activity, clonality, resistance mechanism, and inhibition of biofilm formation. J Antibiot (Tokyo). 2021;74(2):143–51.
Zheng JX, Wu Y, Lin ZW, Pu ZY, Yao WM, Chen Z, et al. Characteristics of and virulence factors associated with biofilm formation in clinical Enterococcus faecalis isolates in China. Front Microbiol. 2017;8:2338.
Lv Z, Zhao D, Chang J, Liu H, Wang X, Zheng J, et al. Anti-bacterial and anti-biofilm evaluation of thiazolopyrimidinone derivatives targeting the histidine kinase YycG protein of staphylococcus epidermidis. Front Microbiol. 2017;8:549.
The authors thank Weiguang Pan and Jie Lian (Department of Laboratory Medicine, Shenzhen Nanshan People’s Hospital and the 6th Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen 518052, China) for helping identify and preserve the bacterial strains.
This work was supported by the following grants: the Sanming Project of Medicine in Shenzhen (No.SMGC201705029); Shenzhen Key Medical Discipline Construction Fund (No. SZXK06162); Natural Science Foundation of Guangdong Province, China (No. 2020A1515011049, 2020A1515111146); Science, Technology and Innovation Commission of Shenzhen Municipality of key funds (JCYJ20180508162403996) and basic research funds (JCYJ20180302144340004, JCYJ20190809151817062, JCYJ20190809110209389, JCYJ20190809102219774).
Ethics approval and consent to participate
All methods were carried out in accordance with relevant guidelines and regulations and were approved by the institutional ethical committee of Shenzhen Nanshan People’s Hospital. All experimental procedures involving human subjects were approved by the institutional ethical committee of Shenzhen Nanshan People’s Hospital. Bacterial strains were collected as part of the routine clinical management of patients, according to the national guidelines in China. Therefore, informed consent was not sought, and informed consent waiver was approved by the institutional ethical committee of Shenzhen Nanshan People’s Hospital.
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Additional file 1
: Table S1. MIC values of YycG inhibitors, ampicillin vancomycin linezolid and daptomycin against E. faecium EF16M64. Table S2. Sequence analysis of Enterococcus faecium DO YycG with other homologues. Table S3. MICs and MDR phenotypes of two thiazolidione derivatives and clinical relevant agents against 102 clinical E faecium strains. Table S4. The RLU values of the kinase activities with different concentration of H2-60 and H2-81.
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Chen, Z., Xiong, Y., Tang, Y. et al. In vitro activities of thiazolidione derivatives combined with daptomycin against clinical Enterococcus faecium strains. BMC Microbiol 22, 16 (2022). https://doi.org/10.1186/s12866-021-02423-8
- Enterococcus faecium
- Biofilm formation