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了解抗生素耐药时代的敌人:剖析细菌防御系统的分子基础。

Knowing Our Enemy in the Antimicrobial Resistance Era: Dissecting the Molecular Basis of Bacterial Defense Systems.

机构信息

Department of Crystallography and Structural Biology, Instituto de Química-Física Blas Cabrera, Consejo Superior de Investigaciones Científicas, 28006 Madrid, Spain.

出版信息

Int J Mol Sci. 2024 Apr 30;25(9):4929. doi: 10.3390/ijms25094929.

DOI:10.3390/ijms25094929
PMID:38732145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11084316/
Abstract

Bacteria and their phage adversaries are engaged in an ongoing arms race, resulting in the development of a broad antiphage arsenal and corresponding viral countermeasures. In recent years, the identification and utilization of CRISPR-Cas systems have driven a renewed interest in discovering and characterizing antiphage mechanisms, revealing a richer diversity than initially anticipated. Currently, these defense systems can be categorized based on the bacteria's strategy associated with the infection cycle stage. Thus, bacterial defense systems can degrade the invading genetic material, trigger an abortive infection, or inhibit genome replication. Understanding the molecular mechanisms of processes related to bacterial immunity has significant implications for phage-based therapies and the development of new biotechnological tools. This review aims to comprehensively cover these processes, with a focus on the most recent discoveries.

摘要

细菌及其噬菌体对手正在进行一场持续的军备竞赛,导致了广泛的抗噬菌体武器库和相应的病毒对策的发展。近年来,CRISPR-Cas 系统的鉴定和利用重新激发了人们发现和描述抗噬菌体机制的兴趣,揭示了比最初预期更丰富的多样性。目前,这些防御系统可以根据与感染周期阶段相关的细菌策略进行分类。因此,细菌防御系统可以降解入侵的遗传物质、引发流产感染或抑制基因组复制。了解与细菌免疫相关的过程的分子机制对噬菌体治疗和新生物技术工具的开发具有重要意义。本综述旨在全面涵盖这些过程,并重点介绍最新发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7946/11084316/bb3238d9973a/ijms-25-04929-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7946/11084316/e3c37f3b8eff/ijms-25-04929-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7946/11084316/829849298477/ijms-25-04929-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7946/11084316/bb3238d9973a/ijms-25-04929-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7946/11084316/e3c37f3b8eff/ijms-25-04929-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7946/11084316/829849298477/ijms-25-04929-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7946/11084316/bb3238d9973a/ijms-25-04929-g003.jpg

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引用本文的文献

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Nature. 2024 Jan;625(7994):360-365. doi: 10.1038/s41586-023-06855-2. Epub 2023 Nov 22.
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Defining the expanding mechanisms of phage-mediated activation of bacterial immunity.定义噬菌体介导的细菌免疫激活的扩展机制。
Curr Opin Microbiol. 2023 Aug;74:102325. doi: 10.1016/j.mib.2023.102325. Epub 2023 May 12.
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Bacterial NLR-related proteins protect against phage.细菌 NLR 相关蛋白可抵御噬菌体。
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Defense systems are pervasive across chromosomally integrated mobile genetic elements and are inversely correlated to virulence and antimicrobial resistance.防御系统普遍存在于染色体整合的移动遗传元件中,与毒力和抗微生物药物耐药性呈负相关。
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Discovery of phage determinants that confer sensitivity to bacterial immune systems.噬菌体决定因子的发现赋予了细菌免疫系统对噬菌体的敏感性。
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