Purification of pneumococcal type II topoisomerases and inhibition by gemifloxacin and other quinolones

J Antimicrob Chemother. 2000 Apr:45 Suppl 1:101-6. doi: 10.1093/jac/45.suppl_3.101.

Abstract

Topoisomerase IV and DNA gyrase were purified from a ciprofloxacin-sensitive Streptococcus pneumoniae strain and from two clinical isolates of S. pneumoniae with high-level resistance to ciprofloxacin by means of a gene cloning method in Escherichia coli. All the quinolones tested (gemifloxacin, trovafloxacin, levofloxacin, ciprofloxacin and grepafloxacin) were able to inhibit topoisomerase IV at lower concentrations than those required for DNA gyrase, suggesting that topoisomerase IV is the primary target in the three pneumococci, in agreement with recently published enzyme data. Gemifloxacin (SB-265805) was found to be the most active agent against topoisomerase IV but, surprisingly, not against DNA gyrase. These findings indicate that the potent in vitro activity of gemifloxacin against S. pneumoniae, including ciprofloxacin-resistant strains, results from a strong affinity for pneumococcal topoisomerase IV.

MeSH terms

  • Anti-Infective Agents / pharmacology*
  • DNA Topoisomerase IV
  • DNA Topoisomerases, Type II / isolation & purification
  • Enzyme Inhibitors / pharmacology*
  • Fluoroquinolones*
  • Gemifloxacin
  • Naphthyridines / pharmacology*
  • Streptococcus pneumoniae / drug effects*
  • Streptococcus pneumoniae / enzymology
  • Topoisomerase II Inhibitors*

Substances

  • Anti-Infective Agents
  • Enzyme Inhibitors
  • Fluoroquinolones
  • Naphthyridines
  • Topoisomerase II Inhibitors
  • DNA Topoisomerase IV
  • DNA Topoisomerases, Type II
  • Gemifloxacin