Microbes in Health and Disease Theme, Newcastle University Biosciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
Division of Evolution, Infection and Genomics, School of Biological Sciences, University of Manchester, Manchester, United Kingdom.
PLoS Genet. 2023 Jun 5;19(6):e1010784. doi: 10.1371/journal.pgen.1010784. eCollection 2023 Jun.
Competitive bacteria-bacteriophage interactions have resulted in the evolution of a plethora of bacterial defense systems preventing phage propagation. In recent years, computational and bioinformatic approaches have underpinned the discovery of numerous novel bacterial defense systems. Anti-phage systems are frequently encoded together in genomic loci termed defense islands. Here we report the identification and characterisation of a novel anti-phage system, that we have termed Shield, which forms part of the Pseudomonas defensive arsenal. The Shield system comprises the core component ShdA, a membrane-bound protein harboring an RmuC domain. Heterologous production of ShdA alone is sufficient to mediate bacterial immunity against several phages. We demonstrate that Shield and ShdA confer population-level immunity and that they can also decrease transformation efficiency. We further show that ShdA homologues can degrade DNA in vitro and, when expressed in a heterologous host, can alter the organisation of the host chromosomal DNA. Use of comparative genomic approaches identified how Shield can be divided into four subtypes, three of which contain additional components that in some cases can negatively affect the activity of ShdA and/or provide additional lines of phage defense. Collectively, our results identify a new player within the Pseudomonas bacterial immunity arsenal that displays a novel mechanism of protection, and reveals a role for RmuC domains in phage defense.
竞争细菌-噬菌体相互作用导致了大量细菌防御系统的进化,以防止噬菌体的繁殖。近年来,计算和生物信息学方法为发现许多新的细菌防御系统提供了支持。抗噬菌体系统通常在称为防御岛的基因组位点中一起编码。在这里,我们报告了一种新型抗噬菌体系统的鉴定和特征,我们将其命名为 Shield,它是假单胞菌防御武器库的一部分。Shield 系统包括核心成分 ShdA,一种具有 RmuC 结构域的膜结合蛋白。单独异源生产 ShdA 足以介导细菌对几种噬菌体的免疫。我们证明了 Shield 和 ShdA 赋予群体水平的免疫力,并且它们还可以降低转化效率。我们进一步表明,ShdA 同源物可以在体外降解 DNA,并且当在异源宿主中表达时,可以改变宿主染色体 DNA 的组织。使用比较基因组学方法确定了 Shield 如何分为四个亚型,其中三个亚型包含额外的成分,在某些情况下,这些成分可能会降低 ShdA 的活性和/或提供额外的噬菌体防御线。总的来说,我们的研究结果确定了假单胞菌细菌免疫武器库中的一个新成员,它显示了一种新的保护机制,并揭示了 RmuC 结构域在噬菌体防御中的作用。