Department of Pediatrics, University of Iowa College of Medicine, Iowa City, IA, USA.
Department of Microbiology, Biomedical Sciences Institute, University of São Paulo, 05508-000 São Paulo, Brazil.
Microbiology (Reading). 2013 Aug;159(Pt 8):1725-1735. doi: 10.1099/mic.0.065532-0. Epub 2013 Jun 12.
Colonization surface antigens (CSs) represent key virulence-associated factors of enterotoxigenic Escherichia coli (ETEC) strains. They are required for gut colonization, the first step of the diarrhoeal disease process induced by these bacteria. One of the most prevalent CSs is CS21, or longus, a type IV pili associated with bacterial self-aggregation, protection against environmental stresses, biofilm formation and adherence to epithelial cell lines. The objectives of this study were to assess the role of CS21 in adherence to primary intestinal epithelial cells and to determine if CS21 contributes to the pathogenesis of ETEC infection in vivo. We evaluated adherence of a CS21-expressing wild-type ETEC strain and an isogenic CS21-mutant strain to pig-derived intestinal cell lines. To determine the role of CS21 in pathogenesis we used the above ETEC strains in a neonatal mice challenge infection model to assess mortality. Quantitative adherence assays confirmed that ETEC adheres to primary intestinal epithelial cells lines in a CS21-dependent manner. In addition, the CS21-mediated ETEC adherence to cells was specific as purified LngA protein, the CS21 major subunit, competed for binding with the CS21-expressing ETEC while specific anti-LngA antibodies blocked adhesion to intestinal cells. Neonatal DBA/2 mice died after intra-stomach administration of CS21-expressing strains while lack of CS21 expression drastically reduced the virulence of the wild-type ETEC strain in this animal model. Collectively these results further support the role of CS21 during ETEC infection and add new evidence on its in vivo relevance in pathogenesis.
定植表面抗原(CSs)是肠产毒性大肠杆菌(ETEC)菌株的关键毒力相关因子。它们是细菌定植肠道所必需的,这是这些细菌引起腹泻疾病过程的第一步。最常见的 CSs 之一是 CS21 或长型,与细菌自聚集、抵抗环境应激、生物膜形成和黏附上皮细胞系相关的 IV 型菌毛。本研究的目的是评估 CS21 在黏附原发性肠上皮细胞中的作用,并确定 CS21 是否有助于 ETEC 感染的发病机制。我们评估了表达 CS21 的野生型 ETEC 菌株和 CS21 突变株对猪源性肠细胞系的黏附作用。为了确定 CS21 在发病机制中的作用,我们使用上述 ETEC 菌株在新生小鼠挑战感染模型中评估死亡率。定量黏附试验证实,ETEC 以 CS21 依赖的方式黏附到原发性肠上皮细胞系。此外,CS21 介导的 ETEC 与细胞的黏附是特异性的,因为纯化的 LngA 蛋白,CS21 的主要亚基,与表达 CS21 的 ETEC 竞争结合,而特异性抗 LngA 抗体阻止了对肠道细胞的黏附。CS21 表达株经胃内给药后,新生 DBA/2 小鼠死亡,而缺乏 CS21 表达则大大降低了该动物模型中野生型 ETEC 菌株的毒力。总之,这些结果进一步支持了 CS21 在 ETEC 感染过程中的作用,并提供了其在发病机制中体内相关性的新证据。