衣壳
生物
先天免疫系统
溶解循环
效应器
病原相关分子模式
长尾病毒科
细胞生物学
免疫系统
噬菌体
病毒学
微生物学
受体
清脆的
免疫
模式识别受体
诱饵
病毒复制
血浆蛋白结合
病毒蛋白
病菌
信号转导
病毒进入
保守序列
感应(电子)
反式激活crRNA
溶原循环
蛋白质结构
补体受体
病毒
遗传学
寄主(生物学)
功能(生物学)
补体系统
作者
Cameron G. Roberts,Chloe B. Fishman,Zhiying Zhang,Dalton V. Banh,Dinshaw J. Patel,Luciano A. Marraffini
标识
DOI:10.1038/s41564-025-02150-0
摘要
Abstract Thoeris systems use proteins with Toll/interleukin-1 receptor domains to protect prokaryotes from phage infection through the synthesis of a cyclic adenosine diphosphate ribose signalling molecule, which activates an effector that depletes the host of the essential metabolite NAD + to limit viral propagation. How infection is recognized during Thoeris immunity is not known. Here we investigate the staphylococcal Thoeris defense system, ThsA–B1–B2, and found that, upon infection, the major capsid proteins of Siphoviridae phages from serogroup B, but not A, form a complex with ThsB1 and ThsB2 to activate Thoeris defense. Thoeris cyclases from Streptococcus also recognize major capsid proteins. Our results suggest that the accumulation of capsid mutations that enable avoidance of Thoeris recognition may be an important evolutionary force behind the structural diversity of prokaryotic viruses. More broadly, given that some mammalian immune pathways contain Toll/interleukin-1 receptor domains that recognize viral structures, our findings highlight a conserved mechanism of innate antiviral immunity.
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