Abstract
Objectives: Infections of hospitalized patients caused by biofilms formed by Staphylococcus aureus represent a major problem. Using in vitro and in vivo biofilm models, we evaluated the efficacy of the novel oxazolidinone FYL-67, by using linezolid (the only clinically approved oxazolidinone antibiotic) as a control, for inhibiting S. aureus biofilm formation. Methods: Antibiofilm activity was determined using strains of methicillin-susceptible S. aureus and methicillinresistant S. aureus. We studied the mechanism(s) and pharmacodynamics of antibiofilm activity as follows: (i) effects of pre-and post-exposure to FYL-67 or linezolid on biofilm formation; (ii) the effect of FYL-67 on biofilm structure; (iii) the role of FYL-67 in biofilm composition; (iv) effects on cell morphology; and (v) efficacy of FYL-67 and linezolid using an in vivo murine model of catheter infection. Results: FYL-67 effectively inhibited biofilm formation using in vitro and in vivo assays. Conclusions: Our data suggest that oxazolidinone compounds, such as FYL-67, may serve as antibiofilm agents.
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Wu, S., Yang, T., Luo, Y., Li, X., Zhang, X., Tang, J., … Wang, Z. (2014). Efficacy of the novel oxazolidinone compound FYL-67 for preventing biofilm formation by Staphylococcus aureus. Journal of Antimicrobial Chemotherapy, 69(11), 3011–3019. https://doi.org/10.1093/jac/dku240
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