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细菌如何攻破基质并躲避免疫的“子弹”。

How bacteria hack the matrix and dodge the bullets of immunity.

机构信息

Division for Infectious Diseases, Skåne University Hospital, Lund, Sweden.

Clinical Microbiology, Dept of Translational Medicine, Faculty of Medicine, Lund University, Malmö, Sweden.

出版信息

Eur Respir Rev. 2018 Jun 27;27(148). doi: 10.1183/16000617.0018-2018. Print 2018 Jun 30.

Abstract

, and are common Gram-negative pathogens associated with an array of pulmonary diseases. All three species have multiple adhesins in their outer membrane, surface structures that confer the ability to bind to surrounding cells, proteins or tissues. This mini-review focuses on proteins with high affinity for the components of the extracellular matrix such as collagen, laminin, fibronectin and vitronectin. Adhesins are not structurally related and may be lipoproteins, transmembrane porins or large protruding trimeric auto-transporters. They enable bacteria to avoid being cleared together with mucus by attaching to patches of exposed extracellular matrix, or indirectly adhering to epithelial cells using matrix proteins as bridging molecules. As more adhesins are being unravelled, it is apparent that bacterial adhesion is a highly conserved mechanism, and that most adhesins target the same regions on the proteins of the extracellular matrix. The surface exposed adhesins are prime targets for new vaccines and the interactions between proteins are often possible to inhibit with interfering molecules, heparin. In conclusion, this highly interesting research field of microbiology has unravelled host-pathogen interactions with high therapeutic potential.

摘要

、 和 是常见的革兰氏阴性病原体,与多种肺部疾病有关。这三个物种的外膜上都有多种黏附素,这是一种赋予它们与周围细胞、蛋白质或组织结合能力的表面结构。这篇迷你综述重点介绍了与细胞外基质成分(如胶原蛋白、层粘连蛋白、纤维连接蛋白和玻连蛋白)具有高亲和力的蛋白质。黏附素在结构上没有相关性,可能是脂蛋白、跨膜孔蛋白或大型突出的三聚体自转运蛋白。它们使细菌能够通过附着在暴露的细胞外基质斑块上,或者使用基质蛋白作为桥接分子间接附着在上皮细胞上,从而避免与黏液一起被清除。随着越来越多的黏附素被揭示出来,很明显,细菌黏附是一种高度保守的机制,大多数黏附素都针对细胞外基质蛋白的相同区域。暴露在表面的黏附素是新型疫苗的主要目标,并且蛋白质之间的相互作用通常可以用干扰分子肝素来抑制。总之,这个具有高度治疗潜力的微生物学研究领域已经揭示了宿主-病原体的相互作用。

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