Mahajan Arvind, Currie Carol G, Mackie Shona, Tree Jai, McAteer Sean, McKendrick Iain, McNeilly Tom N, Roe Andrew, La Ragione Roberto M, Woodward Martin J, Gally David L, Smith David G E
Division of Infection and Immunity, The Roslin Institute, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Penicuik EH25 9EZ, UK.
Cell Microbiol. 2009 Jan;11(1):121-37. doi: 10.1111/j.1462-5822.2008.01244.x. Epub 2008 Oct 30.
Enterohaemorrhagic Escherichia coli O157 : H7 is a bacterial pathogen that can cause haemorrhagic colitis and haemolytic uremic syndrome. In the primary reservoir host, cattle, the terminal rectum is the principal site of E. coli O157 colonization. In this study, bovine terminal rectal primary epithelial cells were used to examine the role of H7 flagella in epithelial adherence. Binding of a fliC(H7) mutant O157 strain to rectal epithelium was significantly reduced as was binding of the flagellated wild-type strain following incubation with H7-specific antibodies. Complementation of fliC(H7) mutant O157 strain with fliC(H7) restored the adherence to wild-type levels; however, complementation with fliC(H6) did not restore it. High-resolution ultrastructural and imunofluorescence studies demonstrated the presence of abundant flagella forming physical contact points with the rectal epithelium. Binding to terminal rectal epithelium was specific to H7 by comparison with other flagellin types tested. In-cell Western assays confirmed temporal expression of flagella during O157 interaction with epithelium, early expression was suppressed during the later stages of microcolony and attaching and effacing lesion formation. H7 flagella are expressed in vivo by individual bacteria in contact with rectal mucosa. Our data demonstrate that the H7 flagellum acts as an adhesin to bovine intestinal epithelium and its involvement in this crucial initiating step for colonization indicates that H7 flagella could be an important target in intervention strategies.
肠出血性大肠杆菌O157 : H7是一种可导致出血性结肠炎和溶血性尿毒综合征的细菌病原体。在主要储存宿主牛中,直肠末端是大肠杆菌O157定植的主要部位。在本研究中,使用牛直肠末端原代上皮细胞来研究H7鞭毛在上皮黏附中的作用。fliC(H7)突变型O157菌株与直肠上皮的结合显著减少,与H7特异性抗体孵育后的鞭毛野生型菌株的结合也显著减少。用fliC(H7)对fliC(H7)突变型O157菌株进行互补可将黏附恢复到野生型水平;然而,用fliC(H6)进行互补则不能恢复。高分辨率超微结构和免疫荧光研究表明,大量鞭毛与直肠上皮形成物理接触点。与其他测试的鞭毛蛋白类型相比,与直肠末端上皮的结合对H7具有特异性。细胞内蛋白质免疫印迹分析证实了在O157与上皮细胞相互作用期间鞭毛的瞬时表达,在微菌落形成以及黏附和损伤形成的后期阶段早期表达受到抑制。H7鞭毛在体内由与直肠黏膜接触的单个细菌表达。我们的数据表明,H7鞭毛作为一种黏附素作用于牛肠道上皮,并且其参与定植这一关键起始步骤表明H7鞭毛可能是干预策略中的一个重要靶点。