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Molecular characterization of the tia invasion locus from enterotoxigenic Escherichia coli.

机译:产肠毒素大肠杆菌的tia侵袭位点的分子表征。

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Enterotoxigenic Escherichia coli (ETEC) shares with other diarrheal pathogens the capacity to invade epithelial cell lines originating from the human ileum or colon, although the role of invasion in ETEC pathogenesis remains undefined. Two distinct loci (tia and tib) that direct noninvasive E. coli to adhere to and invade intestinal epithelial cell lines have previously been isolated from cosmid libraries of the classical ETEC strain H10407. Here, we report the molecular characterization of the tia locus. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis of cellular fractions of E. coli DH5alpha carrying the tia-positive cosmids and recombinant plasmid subclones revealed that this locus directs the production of a 25-kDa protein (the Tia protein) that is localized to the outer membrane. The tia locus was subcloned to a maximum of 2 kb and mutagenized with bacteriophage Mud. Synthesis of this protein was directly correlated with the ability of subclones and Mud transposon mutants to adhere to and invade epithelial cells. Sequencing of the tia locus identified a 756-bp open reading frame. All transposon insertions resulting in an invasion-negative phenotype mapped to this open reading frame. The open reading frame was amplified and directionally cloned behind the lac promoter of pHG165. This construct directed DHalpha to express a 25-kDa protein and to adhere to and invade epithelial cells. The role of the tia gene in directing epithelial adherence and invasion was further assessed by the construction of chromosomal tia deletion derivatives of the parent ETEC strain, H10407. These tia deletion strains were noninvasive and lacked the ability to adhere to human ileocecal cells. The tia gene shares limited homology with the Yersinia ail locus and significant homology with the hra1 agglutinin gene cloned from a porcine ETEC strain. Additionally, tia probes hybridized to geographically diverse ETEC strains, as well as some enteropathogenic E. coli, enteroaggregative E. coli, and Shigella sonnei strains.
机译:肠毒素原性大肠杆菌(ETEC)与其他腹泻病原体共享入侵源自人类回肠或结肠的上皮细胞系的能力,尽管入侵在ETEC发病机理中的作用仍然不确定。先前已从经典ETEC菌株H10407的粘粒文库中分离出两个不同的位点(tia和tib),它们分别引导无创性大肠杆菌粘附并侵入肠道上皮细胞系。在这里,我们报告了tia基因座的分子特征。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析携带tia阳性粘粒和重组质粒亚克隆的大肠杆菌DH5alpha的细胞级分,表明该基因座指导着25kDa蛋白(Tia蛋白)的产生,该蛋白定位于外部膜。将tia基因座亚克隆至最大2 kb,并用噬菌体Mud诱变。该蛋白的合成与亚克隆和Mud转座子突变体粘附和侵袭上皮细胞的能力直接相关。 tia基因座的测序确定了一个756-bp的开放阅读框。所有转座子插入均导致映射到该开放阅读框的侵袭阴性表型。开放阅读框被扩增并定向克隆在pHG165的lac启动子后面。该构建体指导DHalpha表达25 kDa蛋白并粘附并侵袭上皮细胞。通过构建亲本ETEC菌株H10407的染色体tia缺失衍生物进一步评估了tia基因在指导上皮粘附和侵袭中的作用。这些tia缺失菌株是非侵入性的,并且缺乏粘附人回盲细胞的能力。 tia基因与耶尔森氏菌所有基因座具有有限的同源性,与从猪ETEC株克隆的hra1凝集素基因具有显着的同源性。另外,tia探针与地理上不同的ETEC菌株以及一些肠致病性大肠杆菌,肠聚合性大肠杆菌和志贺氏志贺氏菌菌株杂交。

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