Dytoc M, Soni R, Cockerill F, De Azavedo J, Louie M, Brunton J, Sherman P
Division of Gastroenterology, Hospital for Sick Children, Toronto, Ontario, Canada.
Infect Immun. 1993 Aug;61(8):3382-91. doi: 10.1128/iai.61.8.3382-3391.1993.
Verotoxin-producing Escherichia coli strains of the serotype O157:H7 belong to a class of gastrointestinal pathogens that adhere to epithelial cells in a characteristic pattern known as attaching and effacing. Recent insight into the nature of E. coli O157:H7 adhesion was provided by the cloning and sequencing of the chromosomal eaeA (for E. coli attaching and effacing) gene homolog (G. Beebakhee, M. Louie, J. De Azavedo, and J. Brunton, FEMS Microbiol. Lett. 91:63-68, 1992, and J. Yu and J. B. Kaper, Mol. Microbiol. 6:411-417, 1992) and isolation of a 60-MDa plasmid referred to as pO157 (I. Toth, M. L. Cohen, H. S. Rumschlag, L. W. Riley, E. H. White, J. H. Carr, W. W. Bond, and I. K. Wachsmuth, Infect. Immun. 58:1223-1231, 1990, and S. Tzipori, H. Karch, K. I. Wachsmuth, R. M. Robins-Browne, A. D. O'Brien, H. Lior, M. L. Cohen, J. Smithers, and M. M. Levine, Infect. Immun. 55:3117-3125, 1987) and an approximately 94-kDa outer membrane protein (94-kDa OMP; P. Sherman, F. Cockerill III, R. Soni, and J. Brunton, Infect. Immun. 59:890-899, 1991). In this study, we examined the gene products of both eaeA and pO157 in relation to the 94-kDa OMP and as candidate effectors for O157:H7 attachment-effacement. Peptide sequencing and immunoassay demonstrated that the C. coli O157:H7 eaeA gene product is distinct from the 94-kDa OMP. Using ultrastructural analyses, we found that both parent and pO157 plasmid-cured O157:H7 strains demonstrated attaching and effacing adhesion to host epithelial cells and reacted equally well to rabbit antiserum raised against the 94-kDa OMP. By both transmission electron microscopy and light microscopy, E. coli HB101 transformed separately with the cloned eaeA gene and the pO157 plasmid did not form attaching and effacing lesions on cultured epithelial cells in vitro and rabbit intestinal tissues in vivo. Since additional determinants may mediate the attaching and effacing phenotype, we examined transposon TnphoA mutants constructed from E. coli O157:H7 strain CL8. Two TnphoA mutants were found deficient in bacterial factors that are necessary for O157:H7 attachment-effacement and likely distinct from the eaeA gene product.
血清型为O157:H7的产志贺毒素大肠杆菌菌株属于一类胃肠道病原体,它们以一种称为紧密黏附与抹平的特征模式黏附于上皮细胞。最近,通过对染色体eaeA(大肠杆菌紧密黏附与抹平)基因同源物的克隆和测序(G. Beebakhee、M. Louie、J. De Azavedo和J. Brunton,《FEMS微生物学快报》91:63 - 68,1992年;以及J. Yu和J. B. Kaper,《分子微生物学》6:411 - 417,1992年),以及分离出一个称为pO157的60兆道尔顿质粒(I. Toth、M. L. Cohen、H. S. Rumschlag、L. W. Riley、E. H. White、J. H. Carr、W. W. Bond和I. K. Wachsmuth,《感染与免疫》58:1223 - 1231,1990年;以及S. Tzipori、H. Karch、K. I. Wachsmuth、R. M. Robins - Browne、A. D. O'Brien、H. Lior、M. L. Cohen、J. Smithers和M. M. Levine,《感染与免疫》55:3117 - 3125,1987年)和一种约94千道尔顿的外膜蛋白(94 - kDa OMP;P. Sherman、F. Cockerill III、R. Soni和J. Brunton,《感染与免疫》59:890 - 899,1991年),对大肠杆菌O157:H7黏附的本质有了新的认识。在本研究中,我们研究了eaeA和pO157的基因产物与94 - kDa OMP的关系,并将其作为O157:H7紧密黏附与抹平的候选效应因子。肽测序和免疫测定表明,大肠杆菌O157:H7的eaeA基因产物与94 - kDa OMP不同。通过超微结构分析,我们发现亲本菌株和pO157质粒消除的O157:H7菌株均表现出对宿主上皮细胞的紧密黏附与抹平黏附,并且对针对94 - kDa OMP产生的兔抗血清反应同样良好。通过透射电子显微镜和光学显微镜观察,分别用克隆的eaeA基因和pO157质粒转化的大肠杆菌HB101在体外培养的上皮细胞和体内兔肠道组织中均未形成紧密黏附与抹平损伤。由于可能有其他决定因素介导紧密黏附与抹平表型,我们研究了由大肠杆菌O157:H7菌株CL8构建的转座子TnphoA突变体。发现两个TnphoA突变体缺乏O157:H7紧密黏附与抹平所必需的细菌因子,且可能与eaeA基因产物不同。