Activity of tedizolid (TR-700) against well-characterized methicillin-resistant Staphylococcus aureus strains of diverse epidemiological origins

Antimicrob Agents Chemother. 2013 Jun;57(6):2892-5. doi: 10.1128/AAC.00274-13. Epub 2013 Apr 9.

Abstract

The in vitro activities of tedizolid and 10 antistaphylococcal agents were compared against 111 methicillin-resistant Staphylococcus aureus (MRSA) strains from 14 epidemiologically characterized groups. Tedizolid, tigecycline, and daptomycin were the most potent agents, with tedizolid 4-fold more potent than linezolid. Tedizolid, linezolid, and vancomycin were unaffected by epidemiological types. Tigecycline and daptomycin had reduced potency against ST80-MRSA-IV and ST239-MRSA-III, respectively. Overall, tedizolid was highly potent against all MRSA strain types, including those resistant to other classes of drugs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / pharmacology*
  • Daptomycin / pharmacology
  • Humans
  • Methicillin-Resistant Staphylococcus aureus / drug effects*
  • Microbial Sensitivity Tests / standards*
  • Minocycline / analogs & derivatives
  • Minocycline / pharmacology
  • Organophosphates / pharmacology*
  • Oxazoles / pharmacology*
  • Staphylococcal Infections / epidemiology*
  • Staphylococcal Infections / microbiology
  • Tigecycline

Substances

  • Anti-Bacterial Agents
  • Organophosphates
  • Oxazoles
  • Tigecycline
  • Minocycline
  • Daptomycin
  • tedizolid phosphate