Abstract
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.
Original language | English (US) |
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Pages (from-to) | 1344-1346 |
Number of pages | 3 |
Journal | Antimicrobial agents and chemotherapy |
Volume | 48 |
Issue number | 4 |
DOIs | |
State | Published - Apr 2004 |