Mutation frequencies for resistance to fusidic acid and rifampicin in Staphylococcus aureus

J Antimicrob Chemother. 2001 May;47(5):647-50. doi: 10.1093/jac/47.5.647.

Abstract

Frequencies at which mutants resistant to fusidic acid and/or rifampicin arose in vitro were determined in Staphylococcus aureus strains including methicillin-susceptible S. aureus (MSSA), methicillin-resistant S. aureus (MRSA), vancomycin-intermediate resistant S. aureus (VISA) and hetero-VISA. The concentrations of fusidic acid (30 and 15 mg/L) and rifampicin (16 and 1 mg/L) used for selection were equal to the expected maximum and minimum serum concentrations after an oral regimen of rifampicin 900 mg od, together with fusidic acid 500 mg tds. Resistant mutants arose at a frequency of around 10(-8) for selections with rifampicin, but were undetectable (frequency <10(-11)) for selections with fusidic acid. Mutants were not recovered (frequency <10(-11)) after selections in the presence of both fusidic acid and rifampicin at 30/16 and 15/1 mg/L. Our results suggest that these antibiotics, when used in combination, could have a wider role in the management of staphylococcal infections.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / pharmacology*
  • Drug Resistance, Microbial / genetics
  • Drug Resistance, Multiple / genetics*
  • Fusidic Acid / pharmacology*
  • Gene Frequency
  • Humans
  • Microbial Sensitivity Tests
  • Mutation
  • Rifampin / pharmacology*
  • Staphylococcus aureus / drug effects
  • Staphylococcus aureus / genetics*

Substances

  • Anti-Bacterial Agents
  • Fusidic Acid
  • Rifampin