Ecology and evolution of phages encoding anti-CRISPR proteins

被引:4
|
作者
Pons, Benoit J. [1 ]
van Houte, Stineke [1 ]
Westra, Edze R. [1 ]
Chevallereau, Anne [2 ]
机构
[1] Univ Exeter, ESI Biosci, Cornwall Campus, Cornwall Campus, Penryn, England
[2] Univ Paris Cite, CNRS, Inserm, UMR8104,U1016,Inst Cochin, F-75014 Paris, France
基金
英国生物技术与生命科学研究理事会; 英国工程与自然科学研究理事会; 欧洲研究理事会;
关键词
Bacteriophage; Bacteria; Phage-bacteria interactions; CRISPR-Cas; Anti-CRISPR proteins; IMMUNE-SYSTEM; BACTERIAL; RESISTANCE; INHIBITION; MECHANISMS; DIVERSITY; ISLANDS; DEFENSE; RNA;
D O I
10.1016/j.jmb.2023.167974
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
CRISPR-Cas are prokaryotic defence systems that provide protection against invasion by mobile genetic elements (MGE), including bacteriophages. MGE can overcome CRISPR-Cas defences by encoding anti-CRISPR (Acr) proteins. These proteins are produced in the early stages of the infection and inhibit the CRISPR-Cas machinery to allow phage replication. While research on Acr has mainly focused on their discovery, structure and mode of action, and their applications in biotechnology, the impact of Acr on the ecology of MGE as well as on the coevolution with their bacterial hosts only begins to be unravelled. In this review, we summarise our current understanding on the distribution of anti-CRISPR genes in MGE, the ecology of phages encoding Acr, and their coevolution with bacterial defence mechanisms. We high-light the need to use more diverse and complex experimental models to better understand the impact of anti-CRISPR in MGE-host interactions.(c) 2023 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecom-mons.org/licenses/by/4.0/).
引用
收藏
页数:12
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