Activity of oxazolidinone TR-700 against linezolid-susceptible and -resistant staphylococci and enterococci

David M. Livermore*, Shazad Mushtaq, Marina Warner, Neil Woodford

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

79 Citations (Scopus)

Abstract

Background: TR-700 is the active moiety of TR-701 (DA-7157), a new oral/intravenous oxazolidinone prodrug. We examined its activity against linezolid-susceptible and -resistant staphylococci and enterococci. Methods: MICs were determined by the CLSI agar dilution method. Results: MICs of TR-700 were tightly clustered around 0.5 mg/L for linezolid-susceptible staphylococci and enterococci compared with 2 mg/L for linezolid. MICs for 52 linezolid-resistant isolates were raised, but only exceeded 4 mg/L for two Enterococcus faecium isolates homozygous for the G2576T 23S rRNA mutation and for one with an unknown mechanism of linezolid resistance. Conclusions: TR-700 is 4- to 16-fold more active than linezolid and overcame most linezolid resistance in vitro.

Original languageEnglish
Pages (from-to)713-715
Number of pages3
JournalJournal of Antimicrobial Chemotherapy
Volume63
Issue number4
DOIs
Publication statusPublished - 2009

Keywords

  • G2576T
  • Gram-positive cocci
  • TR-701

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