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宿主来源的脂肪酸激活. 型 VII 分泌。

Host-derived fatty acids activate type VII secretion in .

机构信息

Department of Infectious Disease, Genentech Inc., South San Francisco, CA 94080;

Department of Infectious Disease, Genentech Inc., South San Francisco, CA 94080.

出版信息

Proc Natl Acad Sci U S A. 2017 Oct 17;114(42):11223-11228. doi: 10.1073/pnas.1700627114. Epub 2017 Oct 2.

Abstract

The type VII secretion system (T7SS) of is a multiprotein complex dedicated to the export of several virulence factors during host infection. This virulence pathway plays a key role in promoting bacterial survival and the long-term persistence of staphylococcal abscess communities. The expression of the T7SS is activated by bacterial interaction with host tissues including blood serum, nasal secretions, and pulmonary surfactant. In this work we identify the major stimulatory factors as host-specific -unsaturated fatty acids. Increased T7SS expression requires host fatty acid incorporation into bacterial biosynthetic pathways by the fatty acid kinase (FAK) complex, and FakA is required for virulence. The incorporated -unsaturated fatty acids decrease membrane fluidity, and these altered membrane dynamics are partially responsible for T7SS activation. These data define a molecular mechanism by which cells sense the host environment and implement appropriate virulence pathways.

摘要

是一种 VII 型分泌系统(T7SS),是一种专门用于在宿主感染期间输出几种毒力因子的多蛋白复合物。这种毒力途径在促进葡萄球菌脓肿群落的细菌存活和长期持续方面起着关键作用。T7SS 的表达是由细菌与宿主组织(包括血清、鼻分泌物和肺表面活性剂)相互作用激活的。在这项工作中,我们确定了主要的刺激因素是宿主特异性的不饱和脂肪酸。T7SS 表达的增加需要通过 脂肪酸激酶(FAK)复合物将宿主脂肪酸纳入细菌生物合成途径,并且 FakA 是毒力所必需的。所结合的不饱和脂肪酸降低了 细胞膜的流动性,这些改变的膜动力学部分负责 T7SS 的激活。这些数据定义了一种分子机制,通过该机制,细胞可以感知宿主环境并实施适当的毒力途径。

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