Prevalence of gyrA , gyrB , parC , and parE Mutations in Clinical Isolates of Streptococcus pneumoniae with Decreased Susceptibilities to Different Fluoroquinolones and Originating from Worldwide Surveillance Studies during the 1997-1998 Respiratory Season

Author:

Jones Mark E.1,Sahm Daniel F.2,Martin Nele3,Scheuring Sibylle3,Heisig Peter4,Thornsberry Clyde2,Köhrer Karl3,Schmitz Franz-Josef3

Affiliation:

1. MRL Pharmaceutical Services, Utrecht, The Netherlands1;

2. MRL Pharmaceutical Services, Herndon, Virginia2; and

3. Institute for Medical Microbiology and Virology, Heinrich-Heine University Düsseldorf, Düsseldorf,3 and

4. Institute of Pharmaceutical Microbiology, University of Bonn, Bonn,4 Germany

Abstract

ABSTRACT From 8,419 worldwide clinical isolates of Streptococcus pneumoniae obtained during 1997-1998, 69 isolates with reduced susceptibility or resistance to fluoroquinolones (FQs) were molecularly characterized. For the isolates in this prevalence study, only parC (Ser-79→Tyr) and gyrA (Ser-81→Phe or Tyr) mutations, especially in combination, were found to contribute significantly to resistance. These mutations influenced the FQ MICs to varying degrees, although the rank order of activity remains independent of mutation type, with ciprofloxacin the least active, followed by levofloxacin, gatifloxacin/grepafloxacin/moxifloxacin/sparfloxacin/trovafloxacin, and clinafloxacin/sitafloxacin. Efflux likely plays a crucial role in reduced susceptibility for new hydrophilic FQs.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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