Cambronne E D, Cheng L W, Schneewind O
Department of Microbiology and Immunology, UCLA School of Medicine, Los Angeles, California 90095, USA.
Mol Microbiol. 2000 Jul;37(2):263-73. doi: 10.1046/j.1365-2958.2000.01974.x.
Pathogenic Yersinia species employ type III machines to secrete YopBDR into the extracellular milieu. After attaching to host cells, yersiniae transform the type III machinery into an injection device and target YopEHMNOPT into eukaryotic cells. Yersinia pseudotuberculosis LcrQ is a transcriptional regulator that prevents the expression of yop genes. We report that LcrQ is injected into eukaryotic cells. YscM1, the transciptional regulator of Yersinia enterocolitica, is also injected into eukaryotic cells, whereas the related YscM2 protein remains associated with bacterial cells. Type III targeting of YscM1 requires binding to the SycH chaperone. Chaperone binding as well as depletion of YscM1 and YscM2 from the cytoplasm of Y. enterocolitica causes an increase in yop expression, whereas a block in regulator export reduces expression. We propose a model whereby the chaperone-mediated injection of LcrQ/YscM1 functions as a regulatory switch for bacteria that are attached to host cells, triggering the expression of Yops that travel the type III targeting pathway.
致病性耶尔森氏菌属利用III型分泌系统将YopBDR分泌到细胞外环境中。附着于宿主细胞后,耶尔森氏菌将III型分泌系统转变为注射装置,并将YopEHMNOPT注入真核细胞。假结核耶尔森氏菌的LcrQ是一种转录调节因子,可阻止yop基因的表达。我们报道LcrQ会被注入真核细胞。小肠结肠炎耶尔森氏菌的转录调节因子YscM1也会被注入真核细胞,而相关的YscM2蛋白则仍与细菌细胞相关联。YscM1的III型靶向作用需要与SycH分子伴侣结合。分子伴侣结合以及从小肠结肠炎耶尔森氏菌细胞质中去除YscM1和YscM2会导致yop表达增加,而调节因子输出受阻则会降低表达。我们提出了一个模型,即分子伴侣介导的LcrQ/YscM1注射作为附着于宿主细胞的细菌的调节开关,触发通过III型靶向途径运输的Yops的表达。