Nataro J P, Hicks S, Phillips A D, Vial P A, Sears C L
Department of Pediatrics, University of Maryland School of Medicine, Baltimore 21201, USA.
Infect Immun. 1996 Nov;64(11):4761-8. doi: 10.1128/iai.64.11.4761-4768.1996.
Enteroaggregative Escherichia coli (EAEC) is an important cause of persistent diarrhea in many developing parts of the world, yet the pathogenetic mechanisms of EAEC diarrhea are unknown. Experiments with animal models suggest that EAEC strains damage the intestinal mucosa, and a putative cytotoxin has been described. To characterize the mucosal effects of EAEC, we studied strain 042, which we have shown to cause diarrhea in adult volunteers. Strain 042 was incubated in an in vitro organ culture model with biopsy-derived normal intestinal mucosa from pediatric patients. Strain 042 adhered strongly to samples of jejunal, ileal, and colonic mucosa. In addition, scanning electron microscopic examination of in vitro-infected intestinal biopsies revealed cytotoxic effects marked by exfoliation of mucosal epithelial cells. To develop an in vitro model to study these effects, we incubated 042 with polarized monolayers of the human intestinal epithelial cell lines Caco-2 and T84. Strain 042 adhered strongly to T84 cells but not to Caco-2 cells. T84 cells infected with 042 displayed marked toxic effects, most prominently in areas where bacteria were adhering. The apical membrane of damaged cells exhibited vesiculation and shedding of microvilli. The cytoplasm of affected cells displayed subnuclear vacuolization, and in some cases, nuclei of affected cells became separated from the surrounding cytoplasm. Severely affected cells ruptured, releasing their nuclei. Vacuolated remnant cells were seen throughout the monolayer. Strain 042 was not internalized by T84 cells. We concluded that EAEC strain 042 alters intestinal cell morphology, ultimately leading to cell death. Although the factor(s) required for this effect remains to be elucidated, T84 cells may serve as a valuable model in EAEC pathogenesis studies.
肠集聚性大肠杆菌(EAEC)是世界上许多发展中地区持续性腹泻的重要病因,但EAEC腹泻的发病机制尚不清楚。动物模型实验表明,EAEC菌株会损害肠黏膜,并且已描述了一种假定的细胞毒素。为了表征EAEC对黏膜的影响,我们研究了042菌株,我们已证明该菌株可导致成年志愿者腹泻。将042菌株与来自儿科患者活检获得的正常肠黏膜在体外器官培养模型中孵育。042菌株与空肠、回肠和结肠黏膜样本强烈黏附。此外,对体外感染的肠活检组织进行扫描电子显微镜检查发现了细胞毒性作用,其特征为黏膜上皮细胞脱落。为了建立一个研究这些影响的体外模型,我们将042与人类肠上皮细胞系Caco-2和T84的极化单层细胞一起孵育。042菌株与T84细胞强烈黏附,但不与Caco-2细胞黏附。感染042的T84细胞表现出明显的毒性作用,最明显的是在细菌黏附的区域。受损细胞的顶端膜出现小泡形成和微绒毛脱落。受影响细胞的细胞质显示核下空泡化,在某些情况下,受影响细胞的细胞核与周围细胞质分离。严重受影响的细胞破裂,释放出细胞核。在整个单层细胞中都可以看到空泡化的残余细胞。042菌株未被T84细胞内化。我们得出结论,EAEC 042菌株会改变肠道细胞形态,最终导致细胞死亡。尽管这种作用所需的因素仍有待阐明,但T84细胞可能是EAEC发病机制研究中的一个有价值的模型。