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

被引:132
作者
Jones, ME
Sahm, DF
Martin, N
Scheuring, S
Heisig, P
Thornsberry, C
Köhrer, K
Schmitz, FJ
机构
[1] MRL Pharmaceut Serv, NL-3554 XD Utrecht, Netherlands
[2] MRL Pharmaceut Serv, Herndon, VA USA
[3] Univ Dusseldorf, Inst Med Microbiol & Virol, D-4000 Dusseldorf, Germany
[4] Univ Bonn, Inst Pharmaceut Microbiol, D-5300 Bonn, Germany
基金
英国惠康基金;
关键词
D O I
10.1128/AAC.44.2.462-466.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:462 / 466
页数:5
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