Prevalence of gyrA, gyrB, parC, and parE mutations in clinical isolates ofStreptococcus pneumoniae with decreased susceptibilities to different fluoroquinolones and originating from worldwide surveillance studies during the1997-1998 respiratory season

Citation
Me. Jones et al., Prevalence of gyrA, gyrB, parC, and parE mutations in clinical isolates ofStreptococcus pneumoniae with decreased susceptibilities to different fluoroquinolones and originating from worldwide surveillance studies during the1997-1998 respiratory season, ANTIM AG CH, 44(2), 2000, pp. 462-466
Citations number
35
Categorie Soggetti
Microbiology
Journal title
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
ISSN journal
00664804 → ACNP
Volume
44
Issue
2
Year of publication
2000
Pages
462 - 466
Database
ISI
SICI code
0066-4804(200002)44:2<462:POGGPA>2.0.ZU;2-A
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 signifi cantly to resistance. These mutations influenced the FQ MICs to varying deg rees, although the rank order of activity remains independent of mutation t ype, with ciprofloxacin the least active, followed by levofloxacin, gatiflo xacin/grepafloxacin/moxifloxacin/sparfloxacin/trovafloxacin, and clinafloxa cin/sitafloxacin. Efflux likely plays a crucial role in reduced susceptibil ity for new hydrophilic FQs.