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噬菌体介导的防御病毒攻击和病毒的反防御。

Prophage-mediated defence against viral attack and viral counter-defence.

机构信息

Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA.

Department of Biology, Baylor University, Waco, Texas 76798, USA.

出版信息

Nat Microbiol. 2017 Jan 9;2:16251. doi: 10.1038/nmicrobiol.2016.251.

Abstract

Temperate phages are common, and prophages are abundant residents of sequenced bacterial genomes. Mycobacteriophages are viruses that infect mycobacterial hosts including Mycobacterium tuberculosis and Mycobacterium smegmatis, encompass substantial genetic diversity and are commonly temperate. Characterization of ten Cluster N temperate mycobacteriophages revealed at least five distinct prophage-expressed viral defence systems that interfere with the infection of lytic and temperate phages that are either closely related (homotypic defence) or unrelated (heterotypic defence) to the prophage. Target specificity is unpredictable, ranging from a single target phage to one-third of those tested. The defence systems include a single-subunit restriction system, a heterotypic exclusion system and a predicted (p)ppGpp synthetase, which blocks lytic phage growth, promotes bacterial survival and enables efficient lysogeny. The predicted (p)ppGpp synthetase coded by the Phrann prophage defends against phage Tweety infection, but Tweety codes for a tetrapeptide repeat protein, gp54, which acts as a highly effective counter-defence system. Prophage-mediated viral defence offers an efficient mechanism for bacterial success in host-virus dynamics, and counter-defence promotes phage co-evolution.

摘要

温和噬菌体很常见,原噬菌体是已测序细菌基因组中丰富的常驻居民。分枝杆菌噬菌体是感染分枝杆菌宿主的病毒,包括结核分枝杆菌和耻垢分枝杆菌,具有丰富的遗传多样性,通常为温和型。对十个聚类 N 温和分枝杆菌噬菌体的特征分析表明,至少存在五个不同的原噬菌体表达的病毒防御系统,这些系统干扰了与原噬菌体密切相关(同型防御)或不相关(异型防御)的裂解和温和噬菌体的感染。靶特异性不可预测,范围从单一靶噬菌体到三分之一已测试的噬菌体。防御系统包括一个单一亚基限制系统、一个异型排除系统和一个预测的(p)ppGpp 合酶,该合酶可阻断裂解噬菌体的生长、促进细菌存活并实现有效的溶原性。由 Phrann 原噬菌体编码的预测的(p)ppGpp 合酶可抵御噬菌体 Tweety 的感染,但 Tweety 编码一个四肽重复蛋白 gp54,该蛋白作为一种高效的对抗防御系统。原噬菌体介导的病毒防御为细菌在宿主-病毒动态中取得成功提供了一种有效的机制,而对抗防御则促进了噬菌体的共同进化。

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