Staphylococcus aureus mutants selected by BMS-284756

Antimicrob Agents Chemother. 2001 Nov;45(11):3273-5. doi: 10.1128/AAC.45.11.3273-3275.2001.

Abstract

BMS-284756, a novel des-fluoro(6)-quinolone, was used to select for in vitro mutants of Staphylococcus aureus ISP794. Step mutants were obtained, and the quinolone resistance-determining regions of four target genes, gyrA, gyrB, grlA, and grlB, were sequenced. The data suggest that DNA gyrase is the primary target for BMS-284756 in S. aureus.

MeSH terms

  • Anti-Infective Agents / pharmacology*
  • Ciprofloxacin / pharmacology
  • DNA Gyrase / drug effects
  • DNA Gyrase / genetics
  • DNA, Bacterial / chemistry
  • DNA, Bacterial / genetics
  • Drug Resistance, Microbial
  • Fluoroquinolones*
  • Indoles*
  • Mutation / genetics
  • Quinolones*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Staphylococcus aureus / drug effects*
  • Staphylococcus aureus / metabolism*

Substances

  • Anti-Infective Agents
  • DNA, Bacterial
  • Fluoroquinolones
  • Indoles
  • Quinolones
  • Ciprofloxacin
  • DNA Gyrase
  • garenoxacin