Role of topoisomerase mutations and efflux in fluoroquinolone resistance of Bacteroides fragilis clinical isolates and laboratory mutants

被引:31
作者
Ricci, V
Peterson, ML
Rotschafer, JC
Wexler, H
Piddock, LJV [1 ]
机构
[1] Univ Birmingham, Div Immun & Infect, Antimicrobial Agents Res Grp, Birmingham B15 2TT, W Midlands, England
[2] Univ Minnesota, Minneapolis, MN 55455 USA
[3] Univ Calif Los Angeles, Sch Med, Dept Med, Los Angeles, CA 90024 USA
关键词
D O I
10.1128/AAC.48.4.1344-1346.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Twelve laboratory mutants and 32 ciprofloxacin-resistant isolates of Bacteroides fragilis were examined for the mechanism(s) of fluoroquinolone resistance. Five mutants had mutations in gyrA. One mutant and two clinical isolates contained a mutation in gyrB. Eight mutants and five clinical isolates accumulated significantly less ciprofloxacin than did wild-type isolates; the mutants and clinical isolates were restored to wild-type characteristics when carbonyl cyanide m-chlorophenylhydrazone was used.
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收藏
页码:1344 / 1346
页数:3
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