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副溶血弧菌保守 GTPase YchF 参与巨噬细胞细胞毒性、铁摄取和小鼠毒力。

A conserved GTPase YchF of Vibrio vulnificus is involved in macrophage cytotoxicity, iron acquisition, and mouse virulence.

机构信息

Department of Biotechnology, College of Pharmacy and Science, Chia Nan University of Pharmacy and Science, Tainan, Taiwan.

出版信息

Int J Med Microbiol. 2011 Aug;301(6):469-74. doi: 10.1016/j.ijmm.2011.02.002. Epub 2011 May 13.

Abstract

Vibrio vulnificus, a highly virulent marine bacterium, causes serious wound infections and fatal septicemia in many areas of the world. To identify V. vulnificus genes required for killing macrophages, we made an insertional mutant library of V. vulnificus and screened it for reduced macrophage cytotoxicity. One mutant defective in macrophage cytotoxicity had an insertion in ychF, a gene encoding a putative GTPase. In addition to reduced cytotoxicity, this mutant had attenuated growth in iron-limited medium and reduced virulence in iron-overloaded mice. The ychF mutation also down-regulated the transcription level of the rtxA1 gene. RtxA1 mutants significantly decreased cytotoxicity to macrophages compared to wild-type bacteria. Overall, these results show that YchF elicits macrophage cytotoxicity through an rtxA1 pathway and is important for mouse virulence.

摘要

创伤弧菌是一种高致病性海洋细菌,在世界许多地区可导致严重的伤口感染和致命性败血症。为了鉴定创伤弧菌中杀伤巨噬细胞所必需的基因,我们构建了创伤弧菌的插入突变体文库,并对其进行了杀伤巨噬细胞活性降低的筛选。一个在 ychF 基因中发生插入突变的缺失株,该基因编码一个假定的 GTPase。除了杀伤活性降低之外,这个突变株在缺铁培养基中的生长能力减弱,在铁超负荷小鼠中的毒力降低。ychF 突变也下调了 rtxA1 基因的转录水平。与野生型细菌相比,rtxA1 突变体杀伤巨噬细胞的活性显著降低。总的来说,这些结果表明 YchF 通过 rtxA1 途径引发巨噬细胞毒性,并且对小鼠毒力很重要。

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