Cookson S T, Nataro J P
Department of Medicine, University of Maryland School of Medicine, Baltimore, USA.
Microb Pathog. 1996 Dec;21(6):421-34. doi: 10.1006/mpat.1996.0073.
Diffusely adherent Escherichia coli (DAEC) are diarrheagenic E. coli whose pathogenetic mechanisms are largely unknown. DAEC have been shown to induce an unusual phenotype upon adherence to HEp-2 cells in culture characterized by the induction of long thin membrane processes extending from the cell surface. In addition, DAEC have been shown to be protected from the bactericidal effects of gentamicin when incubated with HEp-2 cells. In our studies, we found that three DAEC strains induced formation of eukaryotic cell processes and were protected from gentamicin killing after a 3 h incubation. Preincubation of HEp-2 cells with colchicine or cytochalasin D prior to infection with DAEC strain C1845 resulted in decreased projection formation, suggesting that the effect was dependent upon microfilament and microtubule rearrangement. When the standard gentamicin protection assay was extended for an additional 3 h incubation in the presence of gentamicin, a greater number of DAEC survived gentamicin treatment, more eukaryotic projections were seen in association with the bacteria and the bacteria were actually observed to be "embedded' within these projections. Projection formation was not observed when the bacteria were separated from the cells by a permeable membrane or when the inoculum was inactivated by ultraviolet irradiation. Transposon TnphoA mutants of C1845 were screened for decreased gentamicin protection. All three mutants which were deficient in gentamicin protection demonstrated less projection formation. Insertion mutations affecting gentamicin protection were localized to both the chromosome (two) and a plasmid (one). Eukaryotic projections are a novel interaction of DAEC with epithelial cells, may play a role of the survival of the bacteria against host defenses and may contribute to DAEC pathogenesis. The effect is dependent upon epithelial cell contact and requires multiple bacterial genes.
弥漫性黏附大肠杆菌(DAEC)是致泻性大肠杆菌,其致病机制大多未知。已表明DAEC在培养中黏附于HEp-2细胞后会诱导出一种不寻常的表型,其特征是诱导从细胞表面延伸出长而细的膜突起。此外,已表明DAEC与HEp-2细胞一起孵育时可免受庆大霉素的杀菌作用。在我们的研究中,我们发现三株DAEC菌株在孵育3小时后诱导真核细胞突起形成,并免受庆大霉素杀伤。在用DAEC菌株C1845感染之前,用秋水仙碱或细胞松弛素D对HEp-2细胞进行预孵育会导致突起形成减少,这表明该效应取决于微丝和微管重排。当在庆大霉素存在下将标准庆大霉素保护试验延长额外3小时孵育时,更多的DAEC在庆大霉素处理后存活,在细菌周围可见更多的真核突起,并且实际上观察到细菌“嵌入”在这些突起中。当通过可渗透膜将细菌与细胞分离或接种物经紫外线照射灭活时,未观察到突起形成。筛选C1845的转座子TnphoA突变体以寻找庆大霉素保护作用降低的突变体。所有三个庆大霉素保护作用缺陷的突变体均表现出较少的突起形成。影响庆大霉素保护作用的插入突变定位于染色体(两个)和一个质粒(一个)上。真核突起是DAEC与上皮细胞的一种新型相互作用,可能在细菌抵抗宿主防御的存活中起作用,并可能有助于DAEC的发病机制。该效应取决于上皮细胞接触,并且需要多个细菌基因。