CBASS、Pycsar、Thoeris 和 CRISPR 反虹吸防御中的核苷酸免疫信号转导。

IF 8.5 1区 生物学 Q1 MICROBIOLOGY Annual review of microbiology Pub Date : 2024-11-01 Epub Date: 2024-11-07 DOI:10.1146/annurev-micro-041222-024843
Samuel J Hobbs, Philip J Kranzusch
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引用次数: 0

摘要

细菌编码了一系列不同的系统来抵御噬菌体感染。许多流行的抗噬菌体防御系统的一个共同主题是利用专门的核苷酸信号作为第二信使激活下游效应蛋白并抑制病毒传播。在这篇文章中,我们回顾了四大抗虹吸虫防御系统家族中控制核苷酸免疫信号转导的分子机制:CBASS、Pycsar、Thoeris 和 III 型 CRISPR 免疫。通过分析连接噬菌体检测、核苷酸信号合成和下游效应器功能的各个步骤,我们发现了信号传递的共同核心原理,并揭示了用于增强免疫防御的系统特异性策略。我们比较了最近发现的噬菌体用于规避核苷酸免疫信号的机制,并强调了形成宿主-病毒相互作用的趋同策略。最后,我们解释了细菌抗噬菌体防御与真核生物抗病毒免疫之间的进化联系如何定义了所有生命王国基于核苷酸的免疫的基本规则。
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Nucleotide Immune Signaling in CBASS, Pycsar, Thoeris, and CRISPR Antiphage Defense.

Bacteria encode an arsenal of diverse systems that defend against phage infection. A common theme uniting many prevalent antiphage defense systems is the use of specialized nucleotide signals that function as second messengers to activate downstream effector proteins and inhibit viral propagation. In this article, we review the molecular mechanisms controlling nucleotide immune signaling in four major families of antiphage defense systems: CBASS, Pycsar, Thoeris, and type III CRISPR immunity. Analyses of the individual steps connecting phage detection, nucleotide signal synthesis, and downstream effector function reveal shared core principles of signaling and uncover system-specific strategies used to augment immune defense. We compare recently discovered mechanisms used by phages to evade nucleotide immune signaling and highlight convergent strategies that shape host-virus interactions. Finally, we explain how the evolutionary connection between bacterial antiphage defense and eukaryotic antiviral immunity defines fundamental rules that govern nucleotide-based immunity across all kingdoms of life.

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来源期刊
Annual review of microbiology
Annual review of microbiology 生物-微生物学
CiteScore
18.10
自引率
0.00%
发文量
37
期刊介绍: Annual Review of Microbiology is a Medical and Microbiology Journal and published by Annual Reviews Inc. The Annual Review of Microbiology, in publication since 1947, covers significant developments in the field of microbiology, encompassing bacteria, archaea, viruses, and unicellular eukaryotes. The current volume of this journal has been converted from gated to open access through Annual Reviews' Subscribe to Open program, with all articles published under a CC BY license. The Impact Factor of Annual Review of Microbiology is 10.242 (2024) Impact factor. The Annual Review of Microbiology Journal is Indexed with Pubmed, Scopus, UGC (University Grants Commission).
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