Guiney D G, Hasegawa P, Bouic K, Matthews B
Department of Medicine, University of California, San Diego 92103.
Mol Microbiol. 1989 Nov;3(11):1617-23. doi: 10.1111/j.1365-2958.1989.tb00147.x.
Conjugation systems that transfer antibiotic resistance in the absence of detectable plasmids are common in Bacteroides, but the mechanism of transfer is poorly understood. We found that linked transfer of tetracycline (TcR) and clindamycin (ClR) resistance by Bacteroides fragilis strain 1126 is induced by growth in either Tc or Cl. We cloned the transferable TcR locus as a 13 kb fragment on the shuttle vector pPH6 in Escherichia coli and showed that this region expresses TcR in Bacteroides but not E. coli. The TcR gene was mapped to a 3 kb region and the ClR gene was shown not to be present in the 13 kb insert. Homologous TcR genes are found in B. fragilis V479 and 1792. Using pulsed-field electrophoresis, the transferable TcR gene was shown to be physically associated with high molecular-weight DNA, suggesting that it is located on the chromosome. A new TcR shuttle vector, pPH7 delta 1.1, was constructed to facilitate use of this selective marker in Bacteroides genetics.
在拟杆菌属中,在没有可检测到的质粒情况下传递抗生素抗性的接合系统很常见,但传递机制却知之甚少。我们发现,脆弱拟杆菌菌株1126对四环素(TcR)和克林霉素(ClR)抗性的连锁传递是由在Tc或Cl中生长诱导的。我们将可转移的TcR基因座作为一个13 kb的片段克隆到大肠杆菌的穿梭载体pPH6上,并表明该区域在拟杆菌中表达TcR,而在大肠杆菌中不表达。TcR基因定位于一个3 kb的区域,并且ClR基因在13 kb的插入片段中未被发现。在脆弱拟杆菌V479和1792中发现了同源的TcR基因。使用脉冲场电泳,可转移的TcR基因显示与高分子量DNA物理相关,表明它位于染色体上。构建了一种新的TcR穿梭载体pPH7 delta 1.1,以促进该选择标记在拟杆菌遗传学中的应用。