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鱼类血浆蛋白与迟缓爱德华氏菌之间相互作用组的鉴定揭示了针对细菌感染的组织特异性策略。

Identification of the interactome between fish plasma proteins and Edwardsiella tarda reveals tissue-specific strategies against bacterial infection.

作者信息

Li Hui, Huang Xiaoyan, Zeng Zaohai, Peng Xuan-Xian, Peng Bo

机构信息

Center for Proteomics and Metabolomics, State Key Laboratory of Bio-Control, MOE Key Lab Aquat Food Safety, School of Life Sciences, Guangdong Province Key Laboratory for Pharmaceutical Functional Genes, Sun Yat-sen University, University City, Guangzhou 510006, People⿿s Republic of China.

Center for Proteomics and Metabolomics, State Key Laboratory of Bio-Control, MOE Key Lab Aquat Food Safety, School of Life Sciences, Guangdong Province Key Laboratory for Pharmaceutical Functional Genes, Sun Yat-sen University, University City, Guangzhou 510006, People⿿s Republic of China.

出版信息

Int J Biochem Cell Biol. 2016 Sep;78:260-267. doi: 10.1016/j.biocel.2016.07.021. Epub 2016 Jul 25.

DOI:10.1016/j.biocel.2016.07.021
PMID:27458055
Abstract

Elucidating the complex pathogen-host interaction is essential for a comprehensive understanding of how these remarkable agents invade their hosts and how the hosts defend against these invaders. During the infection, pathogens interact intensively with host to enable their survival, which can be revealed through their interactome. Edwardsiella tarda is a Gram-negative bacterial pathogen causing huge economic loss in aquaculture and a spectrum of intestinal and extraintestinal diseases in humans. E. tarda is an ideal model for host-pathogen investigation as it infects fish in three distinct steps: entering the host, circulating through the blood and establishing infection. We adopted a previous established proteomic approach that inactivated E. tarda cells and covalent crosslink fish plasma proteins were used to capture plasma proteins and bacterial outer membrane proteins, respectively. By the combinatorial use of proteomic and biochemical approaches, six plasma proteins and seven outer membrane proteins (OMPs) were identified. Interactions among these proteins were validated with protein-array, far-Western blotting and co-immunoprecipitation. At last, seventeen plasma protein-bacteria protein-protein interaction were confirmed to be involved in the interaction network, forming a complex interactome. Compared to our previous results, different host proteins were detected, whereas some of the bacterial proteins were similar, which indicates that hosts adopt tissue-specific strategies to cope with the same pathogen during infection. Thus, our results provide a robust demonstration of both bacterial initiators and host receptors or interacting proteins to further explore infection and anti-infective mechanisms between hosts and microbes.

摘要

阐明复杂的病原体与宿主之间的相互作用,对于全面理解这些病原体如何侵入宿主以及宿主如何抵御这些入侵者至关重要。在感染过程中,病原体与宿主进行密切相互作用以实现自身存活,这可以通过它们的相互作用组来揭示。迟缓爱德华氏菌是一种革兰氏阴性细菌病原体,在水产养殖中造成巨大经济损失,并在人类中引发一系列肠道和肠道外疾病。迟缓爱德华氏菌是宿主 - 病原体研究的理想模型,因为它以三个不同步骤感染鱼类:进入宿主、在血液中循环并建立感染。我们采用了先前建立的蛋白质组学方法,即分别使用灭活的迟缓爱德华氏菌细胞和共价交联鱼血浆蛋白来捕获血浆蛋白和细菌外膜蛋白。通过蛋白质组学和生化方法的联合使用,鉴定出了六种血浆蛋白和七种外膜蛋白(OMPs)。这些蛋白质之间的相互作用通过蛋白质阵列、远缘Western印迹和免疫共沉淀进行了验证。最后,证实十七种血浆蛋白 - 细菌蛋白 - 蛋白相互作用参与了相互作用网络,形成了一个复杂的相互作用组。与我们之前的结果相比,检测到了不同的宿主蛋白,而一些细菌蛋白相似,这表明宿主在感染期间采用组织特异性策略来应对同一病原体。因此,我们的结果有力地证明了细菌起始因子和宿主受体或相互作用蛋白,以进一步探索宿主与微生物之间的感染和抗感染机制。

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