Nilles M L, Fields K A, Straley S C
Department of Microbiology and Immunology, Chandler Medical Center, University of Kentucky, Lexington 40536-0084, USA.
J Bacteriol. 1998 Jul;180(13):3410-20. doi: 10.1128/JB.180.13.3410-3420.1998.
Yersinia pestis expresses a set of secreted proteins called Yops and the bifunctional LcrV, which has both regulatory and antihost functions. Yops and LcrV expression and the activity of the type III mechanism for their secretion are coordinately regulated by environmental signals such as Ca2+ concentration and eukaryotic cell contact. In vitro, Yops and LcrV are secreted into the culture medium in the absence of Ca2+ as part of the low-Ca2+ response (LCR). The LCR is induced in a tissue culture model by contact with eukaryotic cells that results in Yop translocation into cells and subsequent cytotoxicity. The secretion mechanism is believed to indirectly regulate expression of lcrV and yop operons by controlling the intracellular concentration of a secreted negative regulator. LcrG, a secretion-regulatory protein, is thought to block secretion of Yops and LcrV, possibly at the inner face of the inner membrane. A recent model proposes that when the LCR is induced, the increased expression of LcrV yields an excess of LcrV relative to LcrG, and this is sufficient for LcrV to bind LcrG and unblock secretion. To test this LcrG titration model, LcrG and LcrV were expressed alone or together in a newly constructed lcrG deletion strain, a delta lcrG2 mutant, of Y. pestis that produces low levels of LcrV and constitutively expresses and secretes Yops. Overexpression of LcrG in this mutant background was able to block secretion and depress expression of Yops in the presence of Ca2+ and to dramatically decrease Yop expression and secretion in growth medium lacking Ca2+. Overexpression of both LcrG and LcrV in the delta lcrG2 strain restored wild-type levels of Yop expression and Ca2+ control of Yop secretion. Surprisingly, when HeLa cells were infected with the delta lcrG2 strain, no cytotoxicity was apparent and translocation of Yops was abolished. This correlated with an altered distribution of YopB as measured by accessibility to trypsin. These effects were not due to the absence of LcrG, because they were alleviated by restoration of LcrV expression and secretion alone. LcrV itself was found to enter HeLa cells in a nonpolarized manner. These studies supported the LcrG titration model of LcrV's regulatory effect at the level of Yop secretion and revealed a further role of LcrV in the deployment of YopB, which in turn is essential for the vectorial translocation of Yops into eukaryotic cells.
鼠疫耶尔森菌表达一组被称为Yops的分泌蛋白以及具有调节和抗宿主功能的双功能LcrV。Yops和LcrV的表达以及它们分泌的III型机制的活性受Ca2+浓度和真核细胞接触等环境信号的协同调节。在体外,作为低Ca2+反应(LCR)的一部分,Yops和LcrV在无Ca2+的情况下分泌到培养基中。在组织培养模型中,与真核细胞接触可诱导LCR,导致Yop转运到细胞中并随后产生细胞毒性。分泌机制被认为通过控制一种分泌型负调节因子的细胞内浓度间接调节lcrV和yop操纵子的表达。LcrG是一种分泌调节蛋白,被认为可能在内膜内表面阻断Yops和LcrV的分泌。最近的一个模型提出,当诱导LCR时,LcrV表达增加导致相对于LcrG的LcrV过量,这足以使LcrV结合LcrG并解除分泌阻断。为了验证这个LcrG滴定模型,在新构建的鼠疫耶尔森菌lcrG缺失菌株(delta lcrG2突变体)中单独或共同表达LcrG和LcrV,该菌株产生低水平的LcrV并组成型表达和分泌Yops。在这个突变背景中过表达LcrG能够在有Ca2+存在的情况下阻断Yops的分泌并抑制其表达,并且在缺乏Ca2+的生长培养基中显著降低Yop的表达和分泌。在delta lcrG2菌株中同时过表达LcrG和LcrV可恢复Yop表达的野生型水平以及Ca2+对Yop分泌的控制。令人惊讶的是,当用delta lcrG2菌株感染HeLa细胞时,没有明显的细胞毒性,并且Yops的转运被消除。这与通过胰蛋白酶可及性测量的YopB分布改变相关。这些效应不是由于缺乏LcrG,因为仅恢复LcrV的表达和分泌就可缓解这些效应。发现LcrV自身以非极化方式进入HeLa细胞。这些研究支持了LcrV在Yop分泌水平上的调节作用的LcrG滴定模型,并揭示了LcrV在YopB部署中的进一步作用,而YopB对于Yops向真核细胞的矢量转运至关重要。