Prophages encode phage-defense systems with cognate self-immunity.
Prophages encode phage-defense systems with cognate self-immunity.
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DOI:
10.1016/j.chom.2021.09.002
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发表时间:
2021-11-10
影响因子:
30.3
通讯作者:
Hinton JCD
中科院分区:
文献类型:
--
作者:
Owen SV;Wenner N;Dulberger CL;Rodwell EV;Bowers-Barnard A;Quinones-Olvera N;Rigden DJ;Rubin EJ;Garner EC;Baym M;Hinton JCD
Temperate phages are pervasive in bacterial genomes, existing as vertically inherited islands termed prophages. Prophages are vulnerable to predation of their host bacterium by exogenous phages. Here, we identify BstA, a family of prophage-encoded phage-defense proteins in diverse Gram-negative bacteria. BstA localizes to sites of exogenous phage DNA replication and mediates abortive infection, suppressing the competing phage epidemic. During lytic replication, the BstA-encoding prophage is not itself inhibited by BstA due to self-immunity conferred by the anti-BstA (aba) element, a short stretch of DNA within the bstA locus. Inhibition of phage replication by distinct BstA proteins from Salmonella, Klebsiella, and Escherichia prophages is generally interchangeable, but each possesses a cognate aba element. The specificity of the aba element ensures that immunity is exclusive to the replicating prophage, preventing exploitation by variant BstA-encoding phages. The BstA protein allows prophages to defend host cells against exogenous phage attack without sacrificing the ability to replicate lytically. BstA is an abortive infection protein found in prophages of Gram-negative bacteria aba, a short DNA sequence within the bstA locus, acts as a self-immunity element aba gives BstA-encoding prophages immunity to BstA-driven abortive infection Variant BstA proteins have distinct and cognate aba elements Prophages can encode abortive infection proteins that give their bacterial hosts population-level phage defense. Owen et al. show that some of these proteins contain internal self-immunity systems so that the prophage is not self-targeted by its own phage-defense protein.
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