Bactericidal activities of daptomycin, quinupristin-dalfopristin, and linezolid against vancomycin-resistant Staphylococcus aureus in an in vitro pharmacodynamic model with simulated endocardial vegetations

Antimicrob Agents Chemother. 2003 Dec;47(12):3960-3. doi: 10.1128/AAC.47.12.3960-3963.2003.

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

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetamides / pharmacology*
  • Anti-Bacterial Agents / pharmacology*
  • Anti-Infective Agents / pharmacology*
  • Colony Count, Microbial
  • Culture Media
  • Daptomycin / pharmacology*
  • Drug Therapy, Combination / pharmacology*
  • Endocardium / microbiology*
  • Linezolid
  • Microbial Sensitivity Tests
  • Oxazolidinones / pharmacology*
  • Staphylococcal Infections / microbiology*
  • Staphylococcus aureus / drug effects*
  • Vancomycin Resistance*
  • Virginiamycin / pharmacology*

Substances

  • Acetamides
  • Anti-Bacterial Agents
  • Anti-Infective Agents
  • Culture Media
  • Oxazolidinones
  • Virginiamycin
  • quinupristin-dalfopristin
  • Linezolid
  • Daptomycin