Abstract
In search of treatment alternatives against vancomycin-resistant S. aureus (VRSA), an in vitro pharmacodynamic model with simulated endocardial vegetations incorporating protein and a high inoculum was used to simulate daptomycin, linezolid, quinupristin-dalfopristin, and vancomycin against the Michigan VRSA strain. Daptomycin and quinupristin-dalfopristin exhibited the greatest bacterial reductions, and all tested agents except vancomycin exhibited bactericidal activity against the VRSA.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Acetamides / pharmacology*
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Anti-Bacterial Agents / pharmacology*
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Anti-Infective Agents / pharmacology*
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Colony Count, Microbial
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Culture Media
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Daptomycin / pharmacology*
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Drug Therapy, Combination / pharmacology*
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Endocardium / microbiology*
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Linezolid
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Microbial Sensitivity Tests
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Oxazolidinones / pharmacology*
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Staphylococcal Infections / microbiology*
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Staphylococcus aureus / drug effects*
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Vancomycin Resistance*
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Virginiamycin / pharmacology*
Substances
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Acetamides
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Anti-Bacterial Agents
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Anti-Infective Agents
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Culture Media
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Oxazolidinones
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Virginiamycin
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quinupristin-dalfopristin
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Linezolid
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Daptomycin