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隐匿生存:噬菌体逃避细菌免疫防御中的海绵状蛋白

Sequestering survival: sponge-like proteins in phage evasion of bacterial immune defenses.

作者信息

Wang Lan, Zheng Ruoqi, Zhang Leiliang

机构信息

Department of Clinical Laboratory Medicine, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, Shandong, China.

Department of Pathogen Biology, School of Clinical and Basic Medical Sciences, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, Shandong, China.

出版信息

Front Immunol. 2025 Apr 17;16:1545308. doi: 10.3389/fimmu.2025.1545308. eCollection 2025.

DOI:10.3389/fimmu.2025.1545308
PMID:40313938
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12043709/
Abstract

By executing abortive infection, bacterial immune defense systems recognize phage components and initiate the production of various second messengers that target specific downstream effectors responsible for nucleic acid degradation, membrane destruction, or metabolite depletion. Notably, the sponge-like proteins encoded by phages, such as Tad1, Tad2, and Acb2, can inhibit abortive infection by sequestering, rather than degrading, these bacterial second messengers. This interference disrupts the activation of the effectors involved in the immune response. Most significantly, sponge-like proteins can simultaneously encapsulate diverse signals, effectively preventing the cell suicide mechanisms triggered by different bacterial immune systems, such as the cyclic nucleotide-based antiphage signaling system (CBASS) and Thoeris. The discovery of these sponge-like proteins reveals a remarkable strategy for suppressing innate immunity, ensuring viral replication and propagation. This greatly enhances our understanding of the ongoing arms race between hosts and viruses.

摘要

通过执行流产感染,细菌免疫防御系统识别噬菌体成分并启动各种第二信使的产生,这些第二信使靶向负责核酸降解、膜破坏或代谢物耗竭的特定下游效应物。值得注意的是,噬菌体编码的海绵状蛋白,如Tad1、Tad2和Acb2,可以通过隔离而不是降解这些细菌第二信使来抑制流产感染。这种干扰破坏了免疫反应中效应物的激活。最重要的是,海绵状蛋白可以同时封装多种信号,有效防止由不同细菌免疫系统触发的细胞自杀机制,如基于环核苷酸的抗噬菌体信号系统(CBASS)和Thoeris。这些海绵状蛋白的发现揭示了一种抑制先天免疫的非凡策略,确保病毒复制和传播。这极大地增进了我们对宿主与病毒之间正在进行的军备竞赛的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1bc/12043709/23740886587d/fimmu-16-1545308-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1bc/12043709/23740886587d/fimmu-16-1545308-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1bc/12043709/23740886587d/fimmu-16-1545308-g001.jpg

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本文引用的文献

1
Single phage proteins sequester signals from TIR and cGAS-like enzymes.单一噬菌体蛋白可从 TIR 和 cGAS 样酶中隔离信号。
Nature. 2024 Nov;635(8039):719-727. doi: 10.1038/s41586-024-08122-4. Epub 2024 Oct 30.
2
Phages reconstitute NAD to counter bacterial immunity.噬菌体合成 NAD 以抵抗细菌免疫。
Nature. 2024 Oct;634(8036):1160-1167. doi: 10.1038/s41586-024-07986-w. Epub 2024 Sep 25.
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Animal and bacterial viruses share conserved mechanisms of immune evasion.动物病毒和细菌病毒具有保守的免疫逃避机制。
Cell. 2024 Oct 3;187(20):5530-5539.e8. doi: 10.1016/j.cell.2024.07.057. Epub 2024 Aug 27.
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Asgard archaea defense systems and their roles in the origin of eukaryotic immunity.古菌防御系统及其在真核生物免疫起源中的作用。
Nat Commun. 2024 Jul 31;15(1):6386. doi: 10.1038/s41467-024-50195-2.
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Reversible conjugation of a CBASS nucleotide cyclase regulates bacterial immune response to phage infection.CBASS 核苷酸环化酶的可逆共轭调节细菌对噬菌体感染的免疫反应。
Nat Microbiol. 2024 Jun;9(6):1579-1592. doi: 10.1038/s41564-024-01670-5. Epub 2024 Apr 8.
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Activation of Thoeris antiviral system via SIR2 effector filament assembly.通过 SIR2 效应器丝组装激活 Thoeris 抗病毒系统。
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8
Phage anti-CBASS protein simultaneously sequesters cyclic trinucleotides and dinucleotides.噬菌体抗 CBASS 蛋白可同时螯合环三核苷酸和二核苷酸。
Mol Cell. 2024 Jan 18;84(2):375-385.e7. doi: 10.1016/j.molcel.2023.11.026. Epub 2023 Dec 15.
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Phages overcome bacterial immunity via diverse anti-defence proteins.噬菌体通过多种抗防御蛋白克服细菌免疫。
Nature. 2024 Jan;625(7994):352-359. doi: 10.1038/s41586-023-06869-w. Epub 2023 Nov 22.
10
Bacterial cGAS senses a viral RNA to initiate immunity.细菌 cGAS 感知病毒 RNA 以启动免疫。
Nature. 2023 Nov;623(7989):1001-1008. doi: 10.1038/s41586-023-06743-9. Epub 2023 Nov 15.