Department of Microbiology, University of Illinois at Urbana-Champaign, Urbana, IL 61821, USA.
Department of Biological Sciences, University of Alabama, Tuscaloosa, AL 35487, USA.
Cell Host Microbe. 2022 Apr 13;30(4):570-582.e7. doi: 10.1016/j.chom.2022.03.001.
The perpetual arms race between bacteria and their viruses (phages) has given rise to diverse immune systems, including restriction-modification and CRISPR-Cas, which sense and degrade phage-derived nucleic acids. These complex systems rely upon production and maintenance of multiple components to achieve antiphage defense. However, the prevalence and effectiveness of minimal, single-component systems that cleave DNA remain unknown. Here, we describe a unique mode of nucleic acid immunity mediated by a single enzyme with nuclease and helicase activities, herein referred to as Nhi (nuclease-helicase immunity). This enzyme provides robust protection against diverse staphylococcal phages and prevents phage DNA accumulation in cells stripped of all other known defenses. Our observations support a model in which Nhi targets and degrades phage-specific replication intermediates. Importantly, Nhi homologs are distributed in diverse bacteria and exhibit functional conservation, highlighting the versatility of such compact weapons as major players in antiphage defense.
细菌与其病毒(噬菌体)之间的永久军备竞赛产生了多种免疫系统,包括限制修饰和 CRISPR-Cas,它们可以感知和降解噬菌体衍生的核酸。这些复杂的系统依赖于多种成分的产生和维持来实现抗噬菌体防御。然而,切割 DNA 的最小、单一成分系统的普遍性和有效性尚不清楚。在这里,我们描述了一种由具有核酸酶和解旋酶活性的单一酶介导的独特核酸免疫模式,本文称之为 Nhi(核酸酶-解旋酶免疫)。这种酶为抵御各种葡萄球菌噬菌体提供了强大的保护,并防止了在去除所有其他已知防御机制的细胞中噬菌体 DNA 的积累。我们的观察结果支持这样一种模型,即 Nhi 靶向并降解噬菌体特异性复制中间体。重要的是,Nhi 同源物分布在多种细菌中,并表现出功能上的保守性,这凸显了这种紧凑武器的多功能性,使其成为抗噬菌体防御的主要参与者。