Taylor D E, Newnham P J, Sherburne C, Lawley T D, Rooker M M
Department of Medical Microbiology and Immunology, University of Alberta, Edmonton, Alberta, T6G 2H7, Canada.
Plasmid. 1999 May;41(3):207-18. doi: 10.1006/plas.1999.1394.
IncHI1 plasmids are one of the few plasmids known to mediate multiple antibiotic resistance in Salmonella typhi. These plasmids are temperature-sensitive for transfer and R27 is the prototype plasmid. DNA sequencing within the Tra2 region of R27, encoding genes involved in mating pair formation, identified trhC encoding the TrhC protein of 90,000 Da, which was visualized using an in vitro transcription/translation system. Expression of the TrhC protein also identified two smaller protein products of approximately 23 and 25 kDa which are predicted to be protease digestion products. The migration of these smaller products changed when the reactions were run at 28 vs 37 degrees C. The TrhC protein contained a putative nucleotide triphosphate-binding protein and exhibited sequence similarities with several other proteins implicated in bacterial conjugation, including TraC (F), TraB (pKM101), VirB4 (Ti), TrbE (RP4). Phylogenetic analysis showed TrhC was most closely related to TraC. Mini-Tn10 insertions in trhC generated transfer defective mutants, and no pili were specified by the trhC mutants. The trhC gene appeared to be a hot spot for transposon insertion as 37.5% mapped into this open reading frame. One trhC mutant, pDT2990, was able to be complemented by a cloned trhC gene giving a transfer frequency of 1 x 10(-3) transconjugants per recipient in an 18-h mating, whereas the wild-type transfer frequency of R27 was 1 x 10(-2) transconjugants per recipient.
IncHI1质粒是已知能介导伤寒沙门氏菌多重耐药性的少数质粒之一。这些质粒的转移对温度敏感,R27是原型质粒。对R27的Tra2区域进行DNA测序,该区域编码参与配对形成的基因,鉴定出编码90,000 Da的TrhC蛋白的trhC基因,该蛋白通过体外转录/翻译系统进行可视化。TrhC蛋白的表达还鉴定出两种较小的蛋白产物,大小约为23和25 kDa,预计是蛋白酶消化产物。当反应在28℃和37℃下进行时,这些较小产物的迁移发生了变化。TrhC蛋白含有一个假定的核苷酸三磷酸结合蛋白,并且与其他几种参与细菌接合的蛋白具有序列相似性,包括TraC(F)、TraB(pKM101)、VirB4(Ti)、TrbE(RP4)。系统发育分析表明TrhC与TraC关系最为密切。trhC中的Mini-Tn10插入产生了转移缺陷型突变体,trhC突变体未产生菌毛。trhC基因似乎是转座子插入的热点,因为37.5%的插入定位到这个开放阅读框中。一个trhC突变体pDT2990能够被克隆的trhC基因互补,在18小时的交配中,每个受体产生1×10⁻³个转接合子的转移频率,而R27的野生型转移频率是每个受体1×10⁻²个转接合子。