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产肠毒素大肠杆菌tia侵袭位点的分子特征分析

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

作者信息

Fleckenstein J M, Kopecko D J, Warren R L, Elsinghorst E A

机构信息

Department of Medicine, Walter Reed Army Medical Center, Washington, D.C. 20307-5001, USA.

出版信息

Infect Immun. 1996 Jun;64(6):2256-65. doi: 10.1128/iai.64.6.2256-2265.1996.

Abstract

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.

摘要

产肠毒素大肠杆菌(ETEC)与其他腹泻病原体一样,具有侵入源自人回肠或结肠的上皮细胞系的能力,尽管侵入在ETEC发病机制中的作用仍不明确。先前已从经典ETEC菌株H10407的黏粒文库中分离出两个不同的基因座(tia和tib),它们可使非侵入性大肠杆菌黏附并侵入肠道上皮细胞系。在此,我们报告tia基因座的分子特征。对携带tia阳性黏粒和重组质粒亚克隆的大肠杆菌DH5α细胞组分进行十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳分析,结果显示该基因座指导产生一种25 kDa的蛋白质(Tia蛋白),该蛋白定位于外膜。tia基因座被亚克隆至最大2 kb,并经噬菌体Mud诱变。该蛋白质的合成与亚克隆和Mud转座子突变体黏附并侵入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。所有导致侵入阴性表型的转座子插入均定位于此开放阅读框。该开放阅读框被扩增并定向克隆到pHG165的lac启动子之后。此构建体指导DHα表达一种25 kDa的蛋白质,并黏附并侵入上皮细胞。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基因在指导上皮黏附和侵入中的作用。这些tia缺失菌株无侵入性,且缺乏黏附人回盲部细胞的能力。tia基因与耶尔森菌ail基因座的同源性有限,与从猪ETEC菌株克隆的hra1凝集素基因具有显著同源性。此外,tia探针可与地理上不同的ETEC菌株以及一些肠致病性大肠杆菌、肠聚集性大肠杆菌和宋内志贺菌菌株杂交。

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