Ueda Ohmi, Wexler Hannah M, Hirai Kaname, Shibata Yukinaga, Yoshimura Fuminobu, Fujimura Setsuo
Department of Oral Microbiology, Matsumoto Dental University, 1780 Gobara Hirooka Shiojiri, Nagano 399-0781, Japan.
Antimicrob Agents Chemother. 2005 Jul;49(7):2807-15. doi: 10.1128/AAC.49.7.2807-2815.2005.
Sixteen homologs of multidrug resistance efflux pump operons of the resistance-nodulation-cell division (RND) family were found in the Bacteroides fragilis genome sequence by homology searches. Disruption mutants were made to the mexB homologs of the four genes most similar to Pseudomonas aeruginosa mexB. Reverse transcription-PCR was conducted and indicated that the genes were transcribed in a polycistronic fashion and that the promoter was upstream of bmeA (the mexA homolog). One of these disruption mutants (in bmeB, the mexB homolog) was more susceptible than the parental strain to certain cephems, polypeptide antibiotics, fusidic acid, novobiocin, and puromycin. The gene for this homolog and the adjacent upstream gene, bmeA, were cloned in a hypersensitive Escherichia coli host. The resultant transformants carrying B. fragilis bmeAB were more resistant to certain agents; these agents also had lower MICs for the B. fragilis bmeB disruption mutants than for the parental strain. The putative efflux pump operon is composed of bmeA, bmeB, and bmeC (a putative outer membrane channel protein homologous with OprM). Addition of the efflux pump inhibitors, carbonyl cyanide m-chlorophenylhydrazone (a proton conductor that eliminates the energy source) and Phe-Arg beta-naphthylamide (MC-207,110) (the first specific inhibitor described for RND pumps in P. aeruginosa), resulted in lowered MICs in the parental strain but not in the bmeB disruption mutant, indicating that the bmeB pump is affected by these inhibitors. This is the first description of RND type pumps in the genus Bacteroides.
通过同源性搜索,在脆弱拟杆菌基因组序列中发现了16个耐药-固氮-细胞分裂(RND)家族多药耐药外排泵操纵子的同源物。对与铜绿假单胞菌mexB最相似的四个基因的mexB同源物构建了破坏突变体。进行了逆转录PCR,结果表明这些基因以多顺反子方式转录,且启动子位于bmeA(mexA同源物)的上游。其中一个破坏突变体(bmeB,mexB同源物)对某些头孢菌素、多肽抗生素、夫西地酸、新生霉素和嘌呤霉素比亲本菌株更敏感。该同源物基因和相邻的上游基因bmeA被克隆到一个超敏大肠杆菌宿主中。携带脆弱拟杆菌bmeAB的所得转化子对某些药物更具抗性;这些药物对脆弱拟杆菌bmeB破坏突变体的最低抑菌浓度也低于亲本菌株。推测的外排泵操纵子由bmeA、bmeB和bmeC(一种与OprM同源的推测的外膜通道蛋白)组成。添加外排泵抑制剂羰基氰化物间氯苯腙(一种消除能量来源的质子导体)和苯丙氨酸-精氨酸β-萘酰胺(MC-207,110)(铜绿假单胞菌中描述的第一个针对RND泵的特异性抑制剂),导致亲本菌株的最低抑菌浓度降低,但bmeB破坏突变体中未降低,表明bmeB泵受这些抑制剂影响。这是首次在拟杆菌属中描述RND型泵。