Environment and Sustainability Institute, Biosciences, University of Exeter, Penryn TR10 9FE, UK.
Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool L69 7ZB, UK; Department of Genetics, University of Cambridge, Downing Place, Cambridge CB2 3EH, UK.
Cell Host Microbe. 2024 Aug 14;32(8):1412-1426.e11. doi: 10.1016/j.chom.2024.07.005. Epub 2024 Aug 1.
The constant arms race between bacteria and their parasites has resulted in a large diversity of bacterial defenses, with many bacteria carrying multiple systems. Here, we report the discovery of a phylogenetically widespread defense system, coined methylation-associated defense system (MADS), which is distributed across gram-positive and gram-negative bacteria. MADS interacts with a CRISPR-Cas system in its native host to provide robust and durable resistance against phages. While phages can acquire epigenetic-mediated resistance against MADS, co-existence of MADS and a CRISPR-Cas system limits escape emergence. MADS comprises eight genes with predicted nuclease, ATPase, kinase, and methyltransferase domains, most of which are essential for either self/non-self discrimination, DNA restriction, or both. The complex genetic architecture of MADS and MADS-like systems, relative to other prokaryotic defenses, points toward highly elaborate mechanisms of sensing infections, defense activation, and/or interference.
细菌与其寄生虫之间的持续军备竞赛导致了大量多样化的细菌防御机制,许多细菌携带多种系统。在这里,我们报告了一种广泛存在于进化上的防御系统的发现,称之为甲基化相关防御系统(MADS),它分布在革兰氏阳性和革兰氏阴性细菌中。MADS 与天然宿主中的 CRISPR-Cas 系统相互作用,为噬菌体提供强大而持久的抗性。虽然噬菌体可以获得针对 MADS 的表观遗传介导的抗性,但 MADS 和 CRISPR-Cas 系统的共存限制了逃逸的出现。MADS 由八个具有预测核酸酶、ATP 酶、激酶和甲基转移酶结构域的基因组成,其中大多数基因对于自我/非自我识别、DNA 限制或两者都必不可少。MADS 及其类似系统的复杂遗传结构与其他原核防御系统相比,表明存在高度复杂的感染感应、防御激活和/或干扰机制。