Efficacy of Linezolid and Fosfomycin in Catheter-Related Biofilm Infection Caused by Methicillin-Resistant<i> Staphylococcus aureus</i>

Chai, Dong; Liu, Xu; Wang, Rui; Bai, Yan; Cai, Yun

doi:https://doi.org/10.1155/2016/6413982

BioMed Research International

On this page

Abstract Introduction Methods Discussion Authors’ Contributions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2016 | Article ID 6413982 | https://doi.org/10.1155/2016/6413982

Efficacy of Linezolid and Fosfomycin in Catheter-Related Biofilm Infection Caused by Methicillin-Resistant Staphylococcus aureus

Dong Chai,¹Xu Liu,²Rui Wang,³Yan Bai,²and Yun Cai³

Academic Editor: Oguz R. Sipahi

Received29 Dec 2015

Revised04 Apr 2016

Accepted10 May 2016

Published05 Jun 2016

Abstract

As long-standing clinical problems, catheter-related infections and other chronic biofilm infections are more difficult to treat due to the high antibiotic resistance of biofilm. Therefore, new treatments are needed for more effective bacteria clearance. In this study, we evaluated the antibacterial activities of several common antibiotics alone and their combinations against biofilm-embedded methicillin-resistant staphylococcus aureus (MRSA) infections, both in vitro and in vivo. In brief, fosfomycin, levofloxacin, and rifampin alone or in combination with linezolid were tested in vitro against planktonic and biofilm-embedded MRSA infection in three MRSA stains. The synergistic effects between linezolid and the other three antibiotics were assessed by fractional inhibitory concentration index (FICI) and time-kill curves, where the combination of linezolid plus fosfomycin showed the best synergistic effect in all strains. For further evaluation in vivo, we applied the combination of linezolid and fosfomycin in a catheter-related biofilm rat model and found that viable bacteria counts in biofilm were significantly reduced after treatment (). In summary, we have shown here that the combination of linezolid and fosfomycin treatment had improved therapeutic effects on biofilm-embedded MRSA infection both in vitro and in vivo, which provided important basis for new clinical therapy development.

1. Introduction

Methicillin-resistant Staphylococcus aureus (MRSA) is a common nosocomial pathogen that causes many catheter-related infections and other chronic biofilm infections [1]. Vancomycin has been considered as the standard treatment for invasive MRSA infection, but the recent evidence is suggesting its poor efficacy, mainly caused by the formation of biofilm [2]. With high tolerance to antibiotics, biofilms can serve as protective niches for MRSA within host, which further increases the minimum inhibitory concentration (MIC) of MRSA. Moreover, the small colony variants within biofilms may also play a role in antibiotic resistance [3].

To solve this problem, a potential way is to reassess the older generations of antibiotics and investigate the novel combinations of existing agents [4]. For example, Corvec et al. [5] found that the combinations of colistin with tigecycline or fosfomycin had significantly improved antibacterial activities against biofilm infection caused by fluoroquinolone-resistant Escherichia coli. In another study, Oliva et al. [6] showed the synergistic effect of fosfomycin plus gentamicin in antibacterial activity against Enterococcus faecalis biofilm.

Linezolid is the first synthetic oxazolidinone antibiotic that blocks protein synthesis by preventing the formation of the initiation complex. It has been approved as an alternative drug for the treatment of staphylococcal skin and soft-tissue infections or pneumonia [7]. Chronic osteomyelitis is a multifaceted bacterial infection requiring surgery in concomitance to antibiotics for treatment. Linezolid has a lot of advantages in treatment of chronic osteomyelitis, such as high bone-serum concentration ratio, having high bioavailability, and being minimally affected by renal dysfunction [8]. Linezolid monotherapy has been reported to have inhibitory effects against biofilm-embedded MRSA [2, 9]. However, the doses used in these studies were relatively high, which might lead to linezolid-associated adverse drug reactions, such as dose-dependent thrombocytopenia [10]. Fosfomycin is a broad-spectrum bactericidal drug against both Gram-positive and Gram-negative bacteria. It has good activity against both extended-spectrum beta-lactamases and carbapenemase-producing Enterobacteriaceae and >90% multidrug resistant P. aeruginosa [11]. For MRSA, fosfomycin also has high activity as 87.9% (4240/4892 isolates) cumulative susceptibility rate [12]. Linezolid combined with fosfomycin, rifampin, and levofloxacin has been used to effectively treat planktonic or biofilm MRSA infections in vitro [2, 9, 13]. Therefore, the in vivo studies need to be conducted to evaluate the potential of linezolid combination regimens in clinical treatments against biofilm-associated MRSA infections. In our study, the effects of fosfomycin, rifampin, and levofloxacin alone or in combination with linezolid on viable bacterial counts in biofilms were evaluated both in vitro and in vivo, which provided thorough information about the antibiofilm effects of linezolid combination regimens.

2. Methods

2.1. Strains and Agents

In the previous study, we found 98.04% synergy of the combination of linezolid and fosfomycin against 102 planktonic MRSA strains by fractional inhibitory concentration index (FICI) in vitro [7]. Therefore, 3 MRSA strains with numbers 154311, 152898, and 159228 were randomly selected from the 102 strains for both in vitro and in vivo studies. The strains were clinically isolated from PLA General Hospital and were identified by the automated VITEK-2 system (bioMérieux, Marcy l’Etoile, France) with a rapid latex agglutination test. Staphylococcus aureus ATCC 25923 was used as the quality control strain.

Fosfomycin, rifampin, and levofloxacin (National Institute for Food and Drug Control, Beijing, China) were used for the in vitro study. Fosfomycin sodium (Northeast Pharm, Shenyang, China) and linezolid (for injection, Pfizer, Madison, USA) were used in the biofilm-infection rat model.

2.2. Fractional Inhibitory Concentration Assay

Synergy of antibiotics was assessed using the checkerboard broth microdilution method assays as described previously [7]. In brief, 96-well plates were set up with increasing concentrations of linezolid in the horizontal wells and fosfomycin, rifampin, and levofloxacin in the vertical wells. Each well was inoculated with 5 × 10⁵ cfu/mL MRSA prepared in broth. Three MRSA strains (154311, 152898, and 159228) were determined in FIC assay. The plates were incubated at 37°C for 24 hours and visually inspected for turbidity to determine the growth. Experiments were performed in triplicate. The interactions between two tested antimicrobials were evaluated by FICI, calculated as follows: FICI = (MIC of drug A in combination/MIC of drug A alone) + (MIC of drug B in combination/MIC of drug B alone). The FICI was interpreted as follows: FICI ≤ 0.5, synergy; 0.5 < FICI ≤ 4.0, indifference; FICI > 4.0, antagonism [7].

2.3. Time-Kill Assay

Time-kill experiments were performed on MRSA 154311 according to the Clinical and Laboratory Standards Institute (CLSI) methodology [14]. Briefly, bacterial suspensions were diluted to 1.5 × 10⁵ cfu/mL in 10 mL of Muller-Hinton Broth (MHB) (BD Difco, Franklin Lakes, USA) for inoculation. The concentrations of fosfomycin were adjusted to 1/16x (4 mg/L), 1/8x (8 mg/L), 1/4x MIC (16 mg/L), and 1/2x MIC (32 mg/L). Each concentration was tested alone or in combination with 1/2x MIC (1 mg/L) linezolid for time-kill curve assays. Bacterial counts were done at 0, 2, 4, 8, 12, and 24 h by spreading 10-fold serial dilutions onto Muller-Hinton agar plates (BD Difco, Franklin Lakes, USA). The experiments described above were repeated three times. Synergy was defined as more than 2 lg 10 cfu/mL decrease between the combination and its most active constituent after 24 h (at least one of the drugs must be present at a concentration that does not affect the growth curve of the tested organism), and the number of viable organisms in the presence of the combination must be ≥2 lg 10 cfu/mL below the starting inoculum [15].

2.4. Synergy Test in Biofilm In Vitro

Synergy test was performed on all MRSA strains. Biofilm was cultivated on disks in 24-well plates. Bacterial suspension was adjusted to 0.5 McFarland (1.5 × 10⁸ cfu/mL). 2 mL of MHB II and 100 μL of bacterial suspension were added to each well containing 3 catheter disks (diameter, 0.5 cm). The plates were then incubated at 37°C for 5 days, and MHB II was renewed daily. The catheter disk with biofilm model used in this study was based on several published articles that focused on antibiofilm effects of some antimicrobial agents [16, 17]. The produced catheter disks were then cut and put into Portex endotracheal tubes (Smiths Medical Ltd, Hythe, UK) using a prototype mold with diameter of 0.5 cm. The endotracheal tube was made of transparent polyvinyl chloride (PVC). The tests were performed in 96-well plates, and each well contained 200 μL linezolid at 1/2x MIC, 1/4x MIC, and 1/8x MIC, together with fosfomycin or levofloxacin at 1/2x MIC, 1/4x MIC, and 1/8x MIC, and rifampin at a fixed concentration of 1 mg/L, according to previous studies [9]. Biofilm disks were randomly selected from the 24-well plates, rinsed with physiological saline to remove planktonic bacteria, and then placed into 96-well plates. Each well contained one disk. After 24 h of treatment at 37°C, these disks were taken out and washed with saline three times to remove planktonic bacteria. The adherent bacteria were collected from disks by using an ultrasonic cleaning bath in 10 min. The bacterial solution was vigorously mixed and plated on agar plates as 10-fold serial dilutions and cultured for 16~24 h. The colony numbers between 30 and 300 per plate were considered as good results, and this standard was also used for the in vivo study in biofilm-infection rat model. Each treatment had six catheters. Bacteria counts were repeated three times.

2.5. Synergy Test in Biofilm-Infection Rat Model

MRSA 154311 biofilm was grown on catheters (length = 3.5 cm, cm). Each catheter was placed into a 5 mL tube containing 3 mL MHB for culture. 100 μL MRSA suspension at 0.5 McFarland which includes 1.5 × 10⁷ bacteria cells was inoculated into each tube (5 × 10⁵ cfu/mL) and cultured for 5 days at 37°C. The catheters were the same as those used in in vitro experiments. Twenty-eight Wistar male rats, weighing 200–250 g, were anesthetized with intraperitoneal injection of 4% chloral hydrate at 0.01 mL/g. Then the catheters with biofilms were rinsed with sterile physiological saline solution and implanted at dorsal midline, as previously described [18]. Rats were randomly divided into four groups with 7 rats in each group: group LIN (linezolid 40 mg/kg/12 h); group FOS (fosfomycin, 300 mg/kg/12 h); group LIN + FOS (linezolid 40 mg/kg/12 h plus fosfomycin 300 mg/kg/12 h); and group control (saline/12 h). The dosage and delivery methods were according to previous studies [19, 20]. After implantation, the antimicrobial agents were immediately injected intraperitoneally. At the end of antimicrobials therapy (7 days after), the implanted catheters in all four groups were taken out to examine the bacterial counts in biofilms. The method for counting bacteria in biofilm was the same as that in the in vitro synergy test. Real-time monitoring of WBCs changes in rats reflected infection conditions. Twenty microliters of blood was drawn from the tail vein of each rat before infection and at days 1, 3, and 5 during therapy. WBCs were examined using an animal blood analytical instrument (Mindray BC-2800Vet, Shenzhen, China). The data are presented as mean ± standard deviation (SD) ().

2.6. Statistical Analysis

All the data were presented as mean ± standard deviation. Differences in lg cfu counts among groups were assessed by one-way analysis of variance (ANOVA). SPSS 12.0 was used for statistical analyses. Differences with were considered significant.

3. Result

3.1. Synergistic Effect of Linezolid and Fosfomycin on Planktonic MRSA In Vitro

The MICs and FICI of the tested antimicrobial agents were summarized in Table 1. For number 154311 strain, both linezolid plus fosfomycin and linezolid plus levofloxacin showed synergistic effect revealed by FICI. The MICs of linezolid and fosfomycin were 2 mg/L and 64 mg/L, respectively, and the FICI 0.375 was obtained with 0.5 mg/L linezolid (1/4x MIC) and 8 mg/L fosfomycin (1/8x MIC). To confirm the synergistic activity between linezolid and fosfomycin, time-kill experiments were performed. As shown in Figure 1, all the combination groups had significantly reduced bacterial counts at 24 h time point compared to either linezolid or fosfomycin alone (). In addition, 1/2x MIC (1 mg/L) of linezolid combined with 1/4x MIC (16 mg/L) or 1/2x MIC (32 mg/L) of fosfomycin exhibited synergistic effect. These results indicated that the linezolid-fosfomycin combination had improved efficiency against planktonic MRSA.

Figure 1

Time-kill curves of linezolid plus fosfomycin in vitro. 154311 MRSA strain was used in this assay. The concentrations of antimicrobial agents in each group were LIN, 1/2x MIC (1 mg/L) linezolid; FOS, 1/16x MIC (4 mg/L), 1/8x MIC (8 mg/L), 1/4x MIC (16 mg/L), and 1/2x MIC (32 mg/L) fosfomycin; LIN + FOS, 1/2x MIC (1 mg/L) linezolid plus 1/16x (4 mg/L), 1/8x (8 mg/L), 1/4x (16 mg/L), and 1/2x MIC (32 mg/L) fosfomycin; control: broth alone. Data are presented as mean ± SD. All experiments were repeated three times.

3.2. Synergistic Effect of Linezolid and Fosfomycin on MRSA Biofilm In Vitro

Table 2 summarized the test results of linezolid in combination with fosfomycin, levofloxacin, and rifampin against three kinds of MRSA biofilms. Linezolid plus levofloxacin or rifampin showed reduced viable bacterial counts in biofilm for two stains. And linezolid at 1/2x MIC plus fosfomycin at 1/2x MIC exhibited significantly reduced viable bacterial counts in biofilm for all stains, with the biggest effect on strain 154311 cultured biofilm. These results also suggested that the synergistic effect of linezolid plus fosfomycin was dose-dependent. Based on these in vitro results, we chose the combination of linezolid plus fosfomycin and further investigated its antibacterial effect against strain 154311 MRSA biofilm in vivo.

3.3. Synergistic Effect of Linezolid and Fosfomycin on MRSA Biofilm In Vivo

At 7 days after infection, the colony counts in biofilms of control, LIN, FOS, and LIN + FOS groups were , , , and lg cfu/mL, respectively. Both linezolid and fosfomycin alone showed decreased colony counts compared to control group (), and LIN + FOS group, with the colony counts reduced by 4.5 lg cfu/mL, showed significant lower colony numbers than any other groups ().

To examine the effects of the drugs on inflammation of the biofilm-infected rats, the values and normal rate of WBCs (defined as the number of rats whose WBCs counts ranged from 2.9 to 15.3 × 10⁹/L divided by the total number of rats in group) were evaluated before infection and at 1, 3, and 5 days after infection. WBC results were as follows: control group: (100%), (100%), (100%), and (33.33%); LIN: (100%), (100%), (100%), and (71.43%); FOS: (100%), (100%), (100%), and (57.14%); LIN + FOS: (100%), (100%), (100%), and (85.71%). WBCs of the four groups were all continuously increasing from day 0 to day 5. At day 5, the WBCs of LIN + FOS group was , lower than the other groups. But no significant difference among groups was observed.

4. Discussion

In this study, the combination of linezolid and fosfomycin displayed the most effective antibacterial effect against MRSA in vitro, compared with other combinations. A synergistic effect of linezolid and fosfomycin has been observed in vitro in previous studies. Pachón-Ibáñez et al. evaluated the efficacy of the combination of fosfomycin and linezolid against Staphylococcus aureus strain using time-kill curve. Compared with the initial bacterial counts, a nearly 3 lg cfu/mL reduction at 24 h time point was observed from the treatment of 1x MIC linezolid plus 1x MIC fosfomycin [21]. Similar results were also seen in our study. More than 3 lg cfu/mL decrease compared to starting inoculum at 24 h point was observed from the treatment of 1/2x MIC (1 mg/L) linezolid plus 1/4x MIC (16 mg/L) or 1/2x MIC (32 mg/L) fosfomycin.

Our study also demonstrates that linezolid plus fosfomycin is an effective combination against MRSA biofilm in vitro. Several mechanisms have been proposed to explain why only a few antibiotics are capable of fighting against biofilms. Fosfomycin has been reported to be involved in some combination therapies that showed increased therapeutic effects. The low molecular weight of fosfomycin could partially explain its facilitated effect in antibacterial activity against biofilm-related organisms [2]. Fosfomycin was reported to destroy or change the outer layer of bacteria and thus inhibit the first step of cell wall synthesis. As a result, linezolid can easily get into the cells and act synergistically with fosfomycin [19]. In addition, fosfomycin alone treatment against strain 154311 biofilms showed a concentration-dependent activity from 1/8x MIC (8 mg/L) to 1/2x MIC (32 mg/L), which may lead to the concentration-dependent manner of linezolid plus fosfomycin treatment in this study.

For in vivo studies, Mihailescu et al. and Baldoni et al. [22, 23] used a guinea pig model to evaluate the effects of fosfomycin and linezolid, alone or in combination with rifampin, against MRSA biofilm infection. Animals with cage implant infections were treated with antimicrobial agents. The efficacy was evaluated by cure rate defined as the number of cage cultures without MRSA growth divided by the total number of cages in the treatment group. Antimicrobial agent alone was unable to eradicate biofilm MRSA from cages. But linezolid plus rifampin achieved 50% to 60% cure rate, and fosfomycin plus rifampin achieved 83% cure rate. We also found consistent results in our study. Only a decrease of about 2 lg cfu/mL in bacterial counts was observed in fosfomycin or linezolid alone groups compared to control group, but a much larger decrease of 4.5 lg cfu/mL was shown in linezolid plus fosfomycin group. However, no catheter cultures without MRSA growth were observed in linezolid plus fosfomycin treatment in our study. This might be due to the difference in biofilm incubation time. In their studies, they percutaneously inoculated MRSA planktonic bacteria into cages after implanting sterile cages in guinea pigs, and antimicrobial treatment was initiated 24 h or 3 days after infection. However, we investigated the antibacterial efficacy on mature biofilms, which were incubated for 5 days before treatment. Mature biofilm was more resistant than those in the initial stage, which may cause the complete clearance of infection in other studies but not ours [24].

White blood cells are a part of the immune system that helps body fight infection. The endotoxins produced by bacteria may elicit immune responses [25], which result in WBC production. In this study, we found that the combined agents had higher normal rates (85.71%) than other groups, although they were not significantly different. This could be due to the better antibacterial effects of combination agents that led to decreased bacterial counts and reduced endotoxins production, which in turn resulted in less WBC and weaker host responses.

As reported previously, high concentrations of antibiotics might be necessary to treat biofilm-related infections. However, high doses of linezolid or fosfomycin can cause some adverse effects, such as thrombocytopenia and peripheral neuropathy [10]. The treatment of linezolid in combination with fosfomycin could decrease the concentration of both. Therefore, it can not only enhance the treatment efficacy but also reduce the risk of adverse effects.

In conclusion, we found linezolid plus fosfomycin combination showed antibiofilm effect against MRSA strains both in vitro and in vivo. These results provided important basis for developing new regimens to treat patients with biofilm-associated MRSA infections, especially for catheter-related infections.

Competing Interests

The authors have no competing interests to declare.

Authors’ Contributions

Dong Chai and Xu Liu contributed equally to this paper.

Acknowledgments

This study was supported by CWS11J107 from Bacterial Biofilm-Related ACEOPD Intervention Study of Military Twelve Five General Program, 81573472 from National Natural Science Foundation, and 2015FC-TSYS-1042 from Clinical Research Support Funding of PLA General Hospital.

References

J. O. Cha, J. I. Yoo, J. S. Yoo et al., “Investigation of biofilm formation and its association with the molecular and clinical characteristics of methicillin-resistant Staphylococcus aureus,” Osong Public Health and Research Perspectives, vol. 4, no. 5, pp. 225–232, 2013.
View at: Google Scholar
H.-J. Tang, C.-C. Chen, K.-C. Cheng et al., “In vitro efficacy of fosfomycin-containing regimens against methicillin-resistant Staphylococcus aureus in biofilms,” Journal of Antimicrobial Chemotherapy, vol. 67, no. 4, Article ID dkr535, pp. 944–950, 2012.
View at: Publisher Site | Google Scholar
S. J. Dancer, “The effect of antibiotics on methicillin-resistant Staphylococcus aureus,” Journal of Antimicrobial Chemotherapy, vol. 61, no. 2, pp. 246–253, 2008.
View at: Publisher Site | Google Scholar
N. C. Gordon, K. Png, and D. W. Wareham, “Potent synergy and sustained bactericidal activity of a vancomycin-colistin combination versus multidrug-resistant strains of Acinetobacter baumannii,” Antimicrobial Agents and Chemotherapy, vol. 54, no. 12, pp. 5316–5322, 2010.
View at: Publisher Site | Google Scholar
S. Corvec, U. F. Tafin, B. Betrisey, O. Borens, and A. Trampuz, “Activities of fosfomycin, tigecycline, colistin, and gentamicin against extended-spectrum-β-lactamase-producing Escherichia coli in a foreign-body infection model,” Antimicrobial Agents and Chemotherapy, vol. 57, no. 3, pp. 1421–1427, 2013.
View at: Publisher Site | Google Scholar
A. Oliva, U. Furustrand Tafin, E. M. Maiolo, S. Jeddari, B. Bétrisey, and A. Trampuza, “Activities of fosfomycin and rifampin on planktonic and adherent Enterococcus faecalis strains in an experimental foreign-body infection model,” Antimicrobial Agents and Chemotherapy, vol. 58, no. 3, pp. 1284–1293, 2014.
View at: Publisher Site | Google Scholar
Y. Xu-Hong, M. E. Falagas, W. Dong, D. E. Karageorgopoulos, L. De-Feng, and W. Rui, “In vitro activity of fosfomycin in combination with linezolid against clinical isolates of methicillin-resistant Staphylococcus aureus,” Journal of Antibiotics, vol. 67, no. 5, pp. 369–371, 2014.
View at: Publisher Site | Google Scholar
D. Luca, P. Leonardo, and U. İlker, “Modern antibiotic treatment of chronic long bone infections in adults-theory, evidence and practice,” Mediterranean Journal of Infection Microbes and Antimicrobials, vol. 3, article 9, 2014.
View at: Google Scholar
H.-J. Tang, C.-C. Chen, K.-C. Cheng et al., “In Vitro efficacies and resistance profiles of rifampin-based combination regimens for biofilm-embedded methicillin-resistant Staphylococcus aureus,” Antimicrobial Agents and Chemotherapy, vol. 57, no. 11, pp. 5717–5720, 2013.
View at: Publisher Site | Google Scholar
B. Natsumoto, K. Yokota, F. Omata, and K. Furukawa, “Risk factors for linezolid-associated thrombocytopenia in adult patients,” Infection, vol. 42, no. 6, pp. 1007–1012, 2014.
View at: Publisher Site | Google Scholar
N. Taneja and H. Kaur, “Insights into newer antimicrobial agents against gram-negative bacteria,” Microbiology Insights, vol. 9, pp. 9–19, 2016.
View at: Publisher Site | Google Scholar
M. E. Falagas, N. Roussos, I. D. Gkegkes, P. I. Rafailidis, and D. E. Karageorgopoulos, “Fosfomycin for the treatment of infections caused by Gram-positive cocci with advanced antimicrobial drug resistance: a review of microbiological, animal and clinical studies,” Expert Opinion on Investigational Drugs, vol. 18, no. 7, pp. 921–944, 2009.
View at: Publisher Site | Google Scholar
J. M. Sahuquillo Arce, E. Colombo Gainza, A. Gil Brusola, R. Ortiz Estévez, E. Cantón, and M. Gobernado, “In vitro activity of linezolid in combination with doxycycline, fosfomycin, levofloxacin, rifampicin and vancomycin against methicillin-susceptible Staphylococcus aureus,” Revista Espanola de Quimioterapia, vol. 19, no. 3, pp. 252–257, 2006.
View at: Google Scholar
National Committee for Clinical Laboratory Standards (NCCLS), “Methods for determining bactericidal activity of antimicrobial agents,” Approved Guideline M26-A, National Committee for Clinical Laboratory Standards (NCCLS), Wayne, Pa, USA, 1999.
View at: Google Scholar
O. Soren, K. S. Brinch, D. Patel et al., “Antimicrobial peptide novicidin synergizes with rifampin, ceftriaxone, and ceftazidime against antibiotic-resistant Enterobacteriaceae in vitro,” Antimicrobial Agents and Chemotherapy, vol. 59, no. 10, pp. 6233–6240, 2015.
View at: Publisher Site | Google Scholar
M. A. Jabra-Rizk, T. F. Meiller, C. E. James, and M. E. Shirtliff, “Effect of farnesol on Staphylococcus aureus biofilm formation and antimicrobial susceptibility,” Antimicrobial Agents and Chemotherapy, vol. 50, no. 4, pp. 1463–1469, 2006.
View at: Publisher Site | Google Scholar
S. A. Ochoa, F. López-Montiel, G. Escalona et al., “Pathogenic characteristics of Pseudomonas aeruginosa strains resistant to carbapenems associated with biofilm formation,” Boletin Medico del Hospital Infantil de Mexico, vol. 70, no. 2, pp. 138–150, 2013.
View at: Google Scholar
A. Chauhan, D. Lebeaux, J.-M. Ghigo, and C. Beloin, “Full and broad-spectrum in vivo eradication of catheter-associated biofilms using gentamicin-EDTA antibiotic lock therapy,” Antimicrobial Agents and Chemotherapy, vol. 56, no. 12, pp. 6310–6318, 2012.
View at: Publisher Site | Google Scholar
Y. Cai, Y. Fan, R. Wang, M.-M. An, and B.-B. Liang, “Synergistic effects of aminoglycosides and fosfomycin on Pseudomonas aeruginosa in vitro and biofilm infections in a rat model,” Journal of Antimicrobial Chemotherapy, vol. 64, no. 3, pp. 563–566, 2009.
View at: Publisher Site | Google Scholar
C. Garrigós, O. Murillo, G. Euba et al., “Efficacy of usual and high doses of daptomycin in combination with rifampin versus alternative therapies in experimental foreign-body infection by methicillin-resistant Staphylococcus aureus,” Antimicrobial Agents and Chemotherapy, vol. 54, no. 12, pp. 5251–5256, 2010.
View at: Publisher Site | Google Scholar
M. E. Pachón-Ibáñez, S. Ribes, M. Á. Domínguez et al., “Efficacy of fosfomycin and its combination with linezolid, vancomycin and imipenem in an experimental peritonitis model caused by a Staphylococcus aureus strain with reduced susceptibility to vancomycin,” European Journal of Clinical Microbiology and Infectious Diseases, vol. 30, no. 1, pp. 89–95, 2011.
View at: Publisher Site | Google Scholar
R. Mihailescu, U. F. Tafin, S. Corvec et al., “High activity of fosfomycin and rifampin against methicillin-resistant Staphylococcus aureus biofilm in vitro and in an experimental foreign-body infection model,” Antimicrobial Agents and Chemotherapy, vol. 58, no. 5, pp. 2547–2553, 2014.
View at: Publisher Site | Google Scholar
D. Baldoni, M. Haschke, Z. Rajacic, W. Zimmerli, and A. Trampuz, “Linezolid alone or combined with rifampin against methicillin-resistant Staphylococcus aureus in experimental foreign-body infection,” Antimicrobial Agents and Chemotherapy, vol. 53, no. 3, pp. 1142–1148, 2009.
View at: Publisher Site | Google Scholar
L. L. Bowler, G. G. Zhanel, T. B. Ball, and L. L. Saward, “Mature Pseudomonas aeruginosa biofilms prevail compared to young biofilms in the presence of ceftazidime,” Antimicrobial Agents and Chemotherapy, vol. 56, no. 9, pp. 4976–4979, 2012.
View at: Publisher Site | Google Scholar
C. Vuong, S. Kocianova, J. M. Voyich et al., “A crucial role for exopolysaccharide modification in bacterial biofilm formation, immune evasion, and virulence,” The Journal of Biological Chemistry, vol. 279, no. 52, pp. 54881–54886, 2004.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2016 Dong Chai et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

PDF Download Citation

Download other formats

Order printed copies

Views

2389

Downloads

1152

Citations