Department of Microbiology, University of Washington School of Medicine, Seattle, WA 98195, USA.
Department of Pathology, University of Washington School of Medicine, Seattle, WA 98195, USA.
Cell. 2018 Nov 15;175(5):1380-1392.e14. doi: 10.1016/j.cell.2018.09.037. Epub 2018 Oct 18.
ADP-ribosylation of proteins can profoundly impact their function and serves as an effective mechanism by which bacterial toxins impair eukaryotic cell processes. Here, we report the discovery that bacteria also employ ADP-ribosylating toxins against each other during interspecies competition. We demonstrate that one such toxin from Serratia proteamaculans interrupts the division of competing cells by modifying the essential bacterial tubulin-like protein, FtsZ, adjacent to its protomer interface, blocking its capacity to polymerize. The structure of the toxin in complex with its immunity determinant revealed two distinct modes of inhibition: active site occlusion and enzymatic removal of ADP-ribose modifications. We show that each is sufficient to support toxin immunity; however, the latter additionally provides unprecedented broad protection against non-cognate ADP-ribosylating effectors. Our findings reveal how an interbacterial arms race has produced a unique solution for safeguarding the integrity of bacterial cell division machinery against inactivating post-translational modifications.
蛋白质的 ADP-核糖基化可以深刻影响其功能,并且是细菌毒素损害真核细胞过程的有效机制。在这里,我们报告了一个发现,即在种间竞争中,细菌也利用 ADP-核糖基化毒素相互作用。我们证明,来自粘质沙雷氏菌的一种这样的毒素通过修饰与其原体界面相邻的必需细菌微管蛋白样蛋白 FtsZ 来中断竞争细胞的分裂,从而阻止其聚合。毒素与免疫决定簇复合物的结构揭示了两种不同的抑制模式:活性位点封闭和酶促去除 ADP-核糖基修饰。我们表明,每种模式都足以支持毒素免疫;然而,后者还提供了针对非同源 ADP-核糖基化效应物的前所未有的广泛保护。我们的发现揭示了细菌之间的军备竞赛如何产生一种独特的解决方案,以保护细菌细胞分裂机制的完整性,防止使其失活的翻译后修饰。