Ricci Vito, Peterson Marnie L, Rotschafer John C, Wexler Hannah, Piddock Laura J V
Antimicrobial Agents Research Group, Division of Immunity and Infection, University of Birmingham, Birmingham B15 2TT, United Kingdom.
Antimicrob Agents Chemother. 2004 Apr;48(4):1344-6. doi: 10.1128/AAC.48.4.1344-1346.2004.
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.
对12株实验室突变株和32株脆弱拟杆菌环丙沙星耐药菌株进行了氟喹诺酮耐药机制研究。5株突变株gyrA发生突变。1株突变株和2株临床分离株gyrB发生突变。8株突变株和5株临床分离株积累的环丙沙星明显少于野生型菌株;当使用羰基氰化物间氯苯腙时,这些突变株和临床分离株恢复为野生型特征。