School of Molecular Biosciences, Washington State University, Pullman WA, USA.
Front Cell Infect Microbiol. 2012 Mar 20;2:31. doi: 10.3389/fcimb.2012.00031. eCollection 2012.
Campylobacter jejuni is a leading cause of bacterial gastroenteritis worldwide. Acute C. jejuni-mediated disease (campylobacteriosis) involves C. jejuni invasion of host epithelial cells using adhesins (e.g., CadF and FlpA) and secreted proteins [e.g., the Campylobacter invasion antigens (Cia)]. The genes encoding the Cia proteins are up-regulated upon co-culture of C. jejuni with epithelial cells. One of the Cia proteins, CiaC, is required for maximal invasion of host cells by C. jejuni. Previous work has also revealed that CiaC is, in part, responsible for host cell cytoskeletal rearrangements that result in membrane ruffling. This study was performed to test the hypothesis that CiaC is delivered to the cytosol of host cells. To detect the delivery of CiaC into cultured epithelial cells, we used the adenylate cyclase domain (ACD) of Bordetella pertussis CyaA as a reporter. In this study, we found that export and delivery of the C. jejuni Cia proteins into human INT 407 epithelial cells required a functional flagellar hook complex composed of FlgE, FlgK, and FlgL. Assays performed with bacterial culture supernatants supported the hypothesis that CiaC delivery requires bacteria-host cell contact. We also found that CiaC was delivered to host cells by cell-associated (bound) bacteria, as judged by experiments performed with inhibitors that specifically target the cell signaling pathways utilized by C. jejuni for cell invasion. Interestingly, the C. jejuni flgL mutant, which is incapable of exporting and delivering the Cia proteins, did not induce INT 407 cell membrane ruffles. Complementation of the flgL mutant with plasmid-encoded flgL restored the motility and membrane ruffling. These data support the hypothesis that the C. jejuni Cia proteins, which are exported from the flagellum, are delivered to the cytosol of host cells.
空肠弯曲菌是全世界细菌性肠胃炎的主要病因。急性空肠弯曲菌介导的疾病(弯曲菌病)涉及空肠弯曲菌使用黏附素(例如 CadF 和 FlpA)和分泌蛋白(例如弯曲菌侵袭抗原(Cia))侵袭宿主上皮细胞。当空肠弯曲菌与上皮细胞共培养时,编码 Cia 蛋白的基因上调。Cia 蛋白中的一种,CiaC,是空肠弯曲菌最大程度侵袭宿主细胞所必需的。先前的工作还表明,CiaC 在一定程度上负责导致细胞膜皱襞的宿主细胞细胞骨架重排。本研究旨在检验 CiaC 被递送至宿主细胞细胞质的假说。为了检测 CiaC 递送至培养上皮细胞中的情况,我们使用百日咳博德特氏菌 CyaA 的腺苷酸环化酶结构域(ACD)作为报告。在这项研究中,我们发现空肠弯曲菌 Cia 蛋白的出口和递送至人 INT 407 上皮细胞需要由 FlgE、FlgK 和 FlgL 组成的功能性鞭毛钩复合物。使用细菌培养上清液进行的测定支持了 CiaC 递送至宿主细胞需要细菌-宿主细胞接触的假说。我们还发现,CiaC 通过细胞相关(结合)细菌递送至宿主细胞,这可以通过使用专门针对空肠弯曲菌用于细胞侵袭的细胞信号转导途径的抑制剂进行的实验来判断。有趣的是,无法出口和递送 Cia 蛋白的空肠弯曲菌 flgL 突变体不会诱导 INT 407 细胞膜皱襞。用质粒编码的 flgL 补充 flgL 突变体恢复了运动性和细胞膜皱襞。这些数据支持了这样的假说,即从鞭毛中输出的空肠弯曲菌 Cia 蛋白被递送至宿主细胞的细胞质中。