Mechanism of action of sparfloxacin against and mechanism of resistance in gram-negative and gram-positive bacteria

Antimicrob Agents Chemother. 1991 Nov;35(11):2423-7. doi: 10.1128/AAC.35.11.2423.

Abstract

The inhibition of DNA synthesis by sparfloxacin; accumulation of sparfloxacin into members of the family Enterobacteriaceae, Pseudomonas aeruginosa, and staphylococci; induction of recA in Escherichia coli; and the optimum bactericidal concentration (OBC) were measured, and killing kinetics at the OBC were estimated. The OBC and maximum recA-inducing concentration in E. coli were both 1 microgram of sparfloxacin per ml. Accumulation was rapid; two- to threefold more sparfloxacin than ciprofloxacin accumulated in staphylococci and more sparfloxacin accumulated in staphylococci than in gram-negative bacteria. Laboratory mutants with decreased susceptibilities to quinolones alone or multiply resistant were selected from the Enterobacteriaceae and Staphylococcus aureus by using sparfloxacin.

MeSH terms

  • Anti-Bacterial Agents / pharmacology
  • Ciprofloxacin / pharmacology
  • DNA Probes
  • DNA, Bacterial / biosynthesis
  • Drug Resistance, Microbial / physiology
  • Enterobacteriaceae / drug effects
  • Fluoroquinolones*
  • Gram-Negative Bacteria / drug effects*
  • Gram-Negative Bacteria / genetics
  • Gram-Negative Bacteria / metabolism
  • Gram-Positive Bacteria / drug effects*
  • Gram-Positive Bacteria / genetics
  • Gram-Positive Bacteria / metabolism
  • Mutation
  • Phenotype
  • Pseudomonas aeruginosa / drug effects
  • Quinolones / metabolism
  • Quinolones / pharmacology*

Substances

  • Anti-Bacterial Agents
  • DNA Probes
  • DNA, Bacterial
  • Fluoroquinolones
  • Quinolones
  • Ciprofloxacin
  • sparfloxacin