In vitro activities of daptomycin, vancomycin, linezolid, and quinupristin-dalfopristin against Staphylococci and Enterococci, including vancomycin- intermediate and -resistant strains

Antimicrob Agents Chemother. 2000 Apr;44(4):1062-6. doi: 10.1128/AAC.44.4.1062-1066.2000.

Abstract

The in vitro activity of daptomycin was compared with those of vancomycin, linezolid, and quinupristin-dalfopristin against a variety (n = 203) of gram-positive bacteria, including methicillin-resistant Staphylococcus aureus and S. epidermidis (MRSA and MRSE, respectively), vancomycin-resistant enterococci (VRE), and vancomycin-intermediate S. aureus (VISA). Overall, daptomycin was more active against all organisms tested, except Enterococcus faecium and VISA, against which its activity was similar to that of quinupristin-dalfopristin. In time-kill studies with MRSA, MRSE, VRE, and VISA, daptomycin demonstrated greater bactericidal activity than all other drugs tested, killing > or =3 log CFU/ml by 8 h. Daptomycin may be a potential alternative drug therapy for multidrug-resistant gram-positive organisms and warrants further investigation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetamides / pharmacology*
  • Anti-Bacterial Agents / pharmacology*
  • Daptomycin / pharmacology*
  • Drug Resistance, Multiple
  • Enterococcus / drug effects*
  • Linezolid
  • Microbial Sensitivity Tests
  • Oxazoles / pharmacology*
  • Oxazolidinones*
  • Staphylococcus / drug effects*
  • Time Factors
  • Vancomycin / pharmacology*
  • Virginiamycin / analogs & derivatives*
  • Virginiamycin / pharmacology

Substances

  • Acetamides
  • Anti-Bacterial Agents
  • Oxazoles
  • Oxazolidinones
  • Virginiamycin
  • quinupristin
  • Vancomycin
  • Linezolid
  • Daptomycin