Edqvist Petra J, Olsson Jan, Lavander Moa, Sundberg Lena, Forsberg Ake, Wolf-Watz Hans, Lloyd Scott A
Department of Molecular Biology, Umeå University, S-90187 Umeå, Sweden.
J Bacteriol. 2003 Apr;185(7):2259-66. doi: 10.1128/JB.185.7.2259-2266.2003.
Pathogenic Yersinia species use a type III secretion system to inhibit phagocytosis by eukaryotic cells. At 37 degrees C, the secretion system is assembled, forming a needle-like structure on the bacterial cell surface. Upon eukaryotic cell contact, six effector proteins, called Yops, are translocated into the eukaryotic cell cytosol. Here, we show that a yscP mutant exports an increased amount of the needle component YscF to the bacterial cell surface but is unable to efficiently secrete effector Yops. Mutations in the cytoplasmic domain of the inner membrane protein YscU suppress the yscP phenotype by reducing the level of YscF secretion and increasing the level of Yop secretion. These results suggest that YscP and YscU coordinately regulate the substrate specificity of the Yersinia type III secretion system. Furthermore, we show that YscP and YscU act upstream of the cell contact sensor YopN as well as the inner gatekeeper LcrG in the pathway of substrate export regulation. These results further strengthen the strong evolutionary link between flagellar biosynthesis and type III synthesis.
致病性耶尔森氏菌属利用III型分泌系统来抑制真核细胞的吞噬作用。在37摄氏度时,分泌系统组装完成,在细菌细胞表面形成针状结构。与真核细胞接触后,六种效应蛋白(称为Yops)被转运到真核细胞胞质溶胶中。在此,我们表明,yscP突变体将增加量的针状组件YscF输出到细菌细胞表面,但无法有效分泌效应蛋白Yops。内膜蛋白YscU胞质结构域中的突变通过降低YscF分泌水平和增加Yop分泌水平来抑制yscP表型。这些结果表明,YscP和YscU协同调节耶尔森氏菌III型分泌系统的底物特异性。此外,我们表明,YscP和YscU在底物输出调节途径中作用于细胞接触传感器YopN以及内部守门蛋白LcrG的上游。这些结果进一步加强了鞭毛生物合成与III型合成之间强大的进化联系。