Jerse A E, Yu J, Tall B D, Kaper J B
Department of Medicine, University of Maryland School of Medicine, Baltimore 21201.
Proc Natl Acad Sci U S A. 1990 Oct;87(20):7839-43. doi: 10.1073/pnas.87.20.7839.
The ability of enteropathogenic Escherichia coli (EPEC) to form attaching and effacing intestinal lesions is a major characteristic of EPEC pathogenesis. Using TnphoA mutagenesis we have identified a chromosomal gene (eae, for E. coli attaching and effacing) that is necessary for this activity. A DNA probe derived from this gene hybridizes to 100% of E. coli of EPEC serogroups that demonstrate attaching and effacing activity on tissue culture cells as well as other pathogenic E. coli that produce attaching and effacing intestinal lesions, such as RDEC-1 (an EPEC of weanling rabbits) and enterohemorrhagic E. coli. The predicted amino acid sequence derived from the nucleotide sequence of eae shows significant homology to that of the invasin of Yersinia pseudotuberculosis.
肠道致病性大肠杆菌(EPEC)形成紧密黏附并损伤肠道的能力是EPEC致病机制的主要特征。利用TnphoA诱变技术,我们鉴定出一个染色体基因(eae,即大肠杆菌紧密黏附并损伤基因),该基因对于这种活性是必需的。源自该基因的DNA探针可与100%具有EPEC血清型的大肠杆菌杂交,这些大肠杆菌在组织培养细胞上表现出紧密黏附并损伤的活性,以及其他产生紧密黏附并损伤肠道病变的致病性大肠杆菌,如RDEC-1(断奶兔的一种EPEC)和肠出血性大肠杆菌。从eae核苷酸序列推导的预测氨基酸序列与假结核耶尔森菌侵袭素的氨基酸序列具有显著同源性。