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Prophage-mediated defense against viral attack and viral counter-defense

机译:噬菌体介导的抗病毒攻击和反病毒防御

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摘要

Temperate phages are common and prophages are abundant residents of sequenced bacterial genomes. Mycobacteriophages are viruses infecting mycobacterial hosts including Mycobacterium tuberculosis and Mycobacterium smegmatis, encompass substantial genetic diversity, and are commonly temperate. Characterization of ten Cluster N temperate mycobacteriophages reveals at least five distinct prophage-expressed viral defense systems that interfere with infection of lytic and temperate phages that are either closely-related (homotypic defense) or unrelated (heterotypic defense). Target specificity is unpredictable, ranging from a single target phage to one-third of those tested. The defense 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, that acts as a highly effective counter-defense system. Prophage-mediated viral defense offers an efficient mechanism for bacterial success in host-virus dynamics, and counter-defense promotes phage co-evolution.
机译:温带噬菌体是常见的,而噬菌体是测序细菌基因组的丰富居民。分枝噬菌体是感染包括结核分枝杆菌和耻垢分枝杆菌在内的分枝杆菌宿主的病毒,其包含大量的遗传多样性,并且通常是温带的。十个簇状N温带分枝杆菌噬菌体的特征揭示了至少五个不同的由前噬菌体表达的病毒防御系统,这些系统干扰密切相关(同型防御)或不相关(异型防御)的裂解性和温性噬菌体的感染。目标特异性是不可预测的,范围从单个目标噬菌体到所测试目标的三分之一。防御系统包括单亚基限制系统,异型排斥系统和预测的(p)ppGpp合成酶,该酶可阻止裂解性噬菌体生长,促进细菌存活并实现有效的溶菌性。 Phrann噬菌体编码的预测(p)ppGpp合成酶可抵御噬菌体Tweety感染,但Tweety编码四肽重复蛋白gp54,可作为高效的防御系统。噬菌体介导的病毒防御为细菌在宿主病毒动力学中的成功提供了一种有效的机制,而反防御则促进了噬菌体的共同进化。

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