Host cell death due to enteropathogenic Escherichia coli has features of apoptosis

被引:94
作者
Crane, JK
Majumdar, S
Pickhardt, DF
机构
[1] SUNY Buffalo, Ctr Microbial Pathogenesis, Buffalo, NY 14260 USA
[2] SUNY Buffalo, Div Infect Dis, Buffalo, NY 14260 USA
关键词
D O I
10.1128/IAI.67.5.2575-2584.1999
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Enteropathogenic Escherichia coli (EPEC) is a cause of prolonged watery diarrhea in children in developing countries. The ability of EPEC to kill host cells was investigated in vitro in assays using two human cultured cell lines, HeLa (cervical) and T84 (colonic), EPEC killed epithelial cells as assessed by permeability to the vital dyes trypan blue and propidium iodide, In addition, EPEC triggered changes in the host cell, suggesting apoptosis as the mode of death; such changes included early expression of phosphatidylserine on the host cell surface and internucleosomal cleavage of host cell DNA, Genistein, an inhibitor of tyrosine kinases, and wortmannin, an inhibitor of host phosphatidylinositol 3-kinase, markedly increased EPEC-induced cell death and enhanced the features of apoptosis, EPEC-induced cell death was contact dependent and required adherence of live bacteria to the host cell. A quantitative assay for EPEC-induced cell death was developed by using the propidium iodide uptake method adapted to a fluorescence plate reader. With EPEC, the rate and extent of host cell death were less that what has been reported for Salmonella, Shigella, and Yersinia, three other genera of enteric bacteria known to cause apoptosis, However, rapid apoptosis of the host cell may not favor the pathogenic strategy of EPEC, a mucosa-adhering, noninvasive pathogen.
引用
收藏
页码:2575 / 2584
页数:10
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