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嗜铬粒蛋白致病性岛1型III型分泌系统是嗜铬粒蛋白紫色杆菌诱导肝细胞死亡的主要毒力决定因素。

Chromobacterium pathogenicity island 1 type III secretion system is a major virulence determinant for Chromobacterium violaceum-induced cell death in hepatocytes.

作者信息

Miki Tsuyoshi, Iguchi Mirei, Akiba Kinari, Hosono Masato, Sobue Tomoyoshi, Danbara Hirofumi, Okada Nobuhiko

机构信息

Department of Microbiology, School of Pharmacy, Kitasato University, Minato-ku, Tokyo 108-8641, Japan.

出版信息

Mol Microbiol. 2010 Aug;77(4):855-72. doi: 10.1111/j.1365-2958.2010.07248.x. Epub 2010 Jun 10.

DOI:10.1111/j.1365-2958.2010.07248.x
PMID:20545857
Abstract

Chromobacterium violaceum is a Gram-negative bacterium that causes fatal septicaemia in humans and animals. C. violaceum ATCC 12472 possesses genes associated with two distinct type III secretion systems (T3SSs). One of these systems is encoded by Chromobacterium pathogenicity islands 1 and 1a (Cpi-1/-1a), another is encoded by Chromobacterium pathogenicity island 2 (Cpi-2). Here we show that C. violaceum causes fulminant hepatitis in a mouse infection model, and Cpi-1/-1a-encoded T3SS is required for its virulence. In addition, using C. violaceum strains with defined mutations in the genes that encode the Cpi-1/-1a or Cpi-2 locus in combination with cultured mammalian cell lines, we found that C. violaceum is able to induce cytotoxicity in a Cpi-1/-1a-dependent manner. Characterization of Chromobacterium-induced cytotoxicity revealed that cell lysis by C. violaceum infection involves the formation of pore structures on the host cell membrane, as demonstrated by protection by cytotoxicity in the presence of osmoprotectants. Finally, we demonstrated that CipB, a Cpi-1/-1a effector, is implicated in translocator-mediated pore formation and the ability of CipB to form a pore is essential for Chromobacterium-induced cytotoxicity. These results strongly suggest that Cpi-1/-1a-encoded T3SS is a virulence determinant that causes fatal infection by the induction of cell death in hepatocytes.

摘要

紫色色杆菌是一种革兰氏阴性细菌,可导致人类和动物发生致命性败血症。紫色色杆菌ATCC 12472拥有与两种不同的III型分泌系统(T3SS)相关的基因。其中一种系统由紫色色杆菌致病岛1和1a(Cpi-1/-1a)编码,另一种由紫色色杆菌致病岛2(Cpi-2)编码。在此我们表明,紫色色杆菌在小鼠感染模型中可引起暴发性肝炎,并且Cpi-1/-1a编码的T3SS是其毒力所必需的。此外,使用在编码Cpi-1/-1a或Cpi-2位点的基因中具有特定突变的紫色色杆菌菌株,结合培养的哺乳动物细胞系,我们发现紫色色杆菌能够以Cpi-1/-1a依赖的方式诱导细胞毒性。对紫色色杆菌诱导的细胞毒性的表征显示,紫色色杆菌感染引起的细胞裂解涉及宿主细胞膜上孔结构的形成,这在存在渗透保护剂时细胞毒性受到保护的情况下得到了证明。最后,我们证明CipB是一种Cpi-1/-1a效应蛋白,与转运体介导的孔形成有关,并且CipB形成孔的能力对于紫色色杆菌诱导的细胞毒性至关重要。这些结果强烈表明,Cpi-1/-1a编码的T3SS是一种毒力决定因素,通过诱导肝细胞死亡导致致命感染。

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