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蝙蝠TBK1在激活针对RNA病毒的先天免疫中的保守功能:对蝙蝠先天免疫反应的见解

Conserved function of bat TBK1 in activating innate immunity against RNA viruses: insights into the innate immune response in bats.

作者信息

Liu Qiuju, Shao Qi, Xu Caixia, Liu Chao, Li Shuhan, Wang Jie, Liu Xia, Zhang Kehui, Yan Yaxian, Sun Jianhe, Cheng Yuqiang

机构信息

Shanghai Key Laboratory of Veterinary Biotechnology, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai, China.

Key Laboratory of Veterinary Pathobiology and Disease Control, College of Animal Science and Technology, Anhui Agricultural University, Hefei, Anhui, China.

出版信息

Front Immunol. 2025 Jul 28;16:1574866. doi: 10.3389/fimmu.2025.1574866. eCollection 2025.

Abstract

Bats exhibit unique abilities to coexist with viruses asymptomatically, setting them apart among mammals. The innate immune system serves as the primary defense against pathogens. As a crucial central node protein in this system, TANK binding kinase 1(TBK1) can receive signals from multiple pattern recognition receptors (PRRs), and then promote the production of Type I interferon (IFN I) and inflammatory factors. Despite its importance, how TBK1 works in bats remains poorly understood. Here, through bioinformatics analysis, TBK1 was found to exhibit a high sequence conservation across species. Overexpression of bat TBK1 significantly upregulated IFNβ expression, and then inhibited viral replication. Co-expression of bat TBK1 with bat IRF1/3/7 can facilitate the upregulation of IFNβ mediated by bat TBK1, implying the activation signals potentially can be transmitted from bat TBK1 to IRF1/3/7, and then promote IFNβ production. Structurally, protein kinase domain (PKD), ubiquitin-like domain (ULD), and coiled-coil domain 1 (CCD1) are essential domains for bat TBK1 to function normally. In summary, this study elucidated bat TBK1 has a conserved ability to activate bat antiviral innate immunity.

摘要

蝙蝠具有与病毒无症状共存的独特能力,使其在哺乳动物中脱颖而出。先天免疫系统是抵御病原体的主要防线。作为该系统中的关键核心节点蛋白,TANK结合激酶1(TBK1)可以接收来自多种模式识别受体(PRR)的信号,然后促进I型干扰素(IFN I)和炎症因子的产生。尽管其很重要,但TBK1在蝙蝠体内的作用机制仍知之甚少。在此,通过生物信息学分析发现,TBK1在物种间表现出高度的序列保守性。蝙蝠TBK1的过表达显著上调了IFNβ的表达,进而抑制了病毒复制。蝙蝠TBK1与蝙蝠IRF1/3/7共表达可促进蝙蝠TBK1介导的IFNβ上调,这意味着激活信号可能从蝙蝠TBK1传递至IRF1/3/7,进而促进IFNβ的产生。在结构上,蛋白激酶结构域(PKD)、泛素样结构域(ULD)和卷曲螺旋结构域1(CCD1)是蝙蝠TBK1正常发挥功能所必需的结构域。总之,本研究阐明了蝙蝠TBK1具有激活蝙蝠抗病毒先天免疫的保守能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0751/12336183/6e638aea13ca/fimmu-16-1574866-g001.jpg

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