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Mechanisms and spread of fluoroquinolone resistance in Streptococcus pneumoniae

E Varon1, L Gutmann

  • 1L.R.M.A., Université Paris-VI, France. Emmanuelle-Sophie.Varon@bhdc.jussieu.fr

Research in Microbiology
|August 29, 2000
PubMed

Insights

New fluoroquinolones (FQs) target Streptococcus pneumoniae, but resistance is emerging. Mutations in FQ targets cause cross-resistance, potentially spreading like beta-lactam resistance.

Area of Science:

  • Microbiology
  • Pharmacology
  • Infectious Diseases

Background:

  • Pneumococcal infections pose treatment challenges, especially with beta-lactam-resistant strains.
  • Fluoroquinolones (FQs) offer potential for treating resistant Streptococcus pneumoniae infections.
  • Emergence of FQ resistance threatens the efficacy of these drugs.

Purpose of the Study:

  • To assess the potential of new fluoroquinolones against Streptococcus pneumoniae.
  • To investigate mechanisms of fluoroquinolone resistance in S. pneumoniae.
  • To anticipate the future spread of FQ resistance.

Main Methods:

  • Analysis of clinical isolates of Streptococcus pneumoniae.
  • Investigation of mutations in fluoroquinolone targets (topoisomerase genes).
  • Comparative studies of resistance patterns to older and newer FQs.

Main Results:

  • Fluoroquinolone-resistant clinical isolates of S. pneumoniae have been identified.
  • Mutations in both FQ targets confer cross-resistance to newer agents.
  • Recombination between topoisomerase genes may facilitate resistance spread.

Conclusions:

  • Fluoroquinolone resistance in S. pneumoniae is an evolving concern.
  • Cross-resistance to newer FQs is mediated by target mutations.
  • The spread of FQ resistance may mirror that of beta-lactam resistance.

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