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首页> 外文期刊>The Journal of biological chemistry >LcrV, a Substrate for Yersinia enterocolitica Type III Secretion, Is Required for Toxin Targeting into the Cytosol of HeLa Cells*
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LcrV, a Substrate for Yersinia enterocolitica Type III Secretion, Is Required for Toxin Targeting into the Cytosol of HeLa Cells*

机译:LcrV,一种小肠结肠炎耶尔森氏菌III型分泌的底物,是毒素靶向进入HeLa细胞的细胞溶胶所必需的*

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Pathogenic Yersinia species employ type III machines to transport virulence factors across the bacterial envelope. Some substrates for the type III machinery are secreted into the extracellular medium, whereas others are targeted into the cytosol of host cells. We found that during infection of tissue culture cells, yersiniae secrete small amounts of LcrV into the extracellular medium. Knockout mutations of lcrV abolish Yersiniatargeting and reduce expression of the lcrGVHyopBD operon. In contrast, a block in LcrV secretion does not affect targeting, but results in premature expression and secretion of Yop proteins into the extracellular medium. LcrV-mediated activation of the type III pathway is thought to occur by sequestration of the regulatory factor LcrG, presumably via the formation of LcrV·LcrG complexes. These results suggest that intrabacterial LcrV regulates the expression and targeting of Yop proteins during Yersinia infection, whereas secreted LcrV is required to ensure specificity of Yop injection into eukaryotic cells.
机译:致病性耶尔森氏菌物种采用III型机器在整个细菌包膜中运输毒力因子。 III型机器的某些底物被分泌到细胞外培养基中,而其他底物被靶向到宿主细胞的细胞质中。我们发现,在组织培养细胞感染期间,耶尔森氏菌向细胞外培养基中分泌少量LcrV。 lcrV的敲除突变消除了针对耶尔森氏菌的攻击,并降低了lcrGVHyopBD操纵子的表达。相反,LcrV分泌的阻滞不影响靶向,但会导致Yop蛋白过早表达和分泌到细胞外培养基中。 LcrV介导的III型途径的激活被认为是通过螯合调节因子LcrG而发生的,大概是通过形成LcrV·LcrG复合物。这些结果表明,细菌内LcrV调节耶尔森氏菌感染期间Yop蛋白的表达和靶向,而分泌的LcrV是确保Yop注入真核细胞的特异性所必需的。

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