Nucleoid-associated proteins sense phage-induced genome damage to elicit abortive infection
li, z.; Yuan, S.; Ma, J.; Shu, X.; Duque-Pedraza, J. J.; Terenin, I.; Yu, Z.; Cheng, F.; Wang, J.; Pino, A. G.; Atkinson, G.; Yang, H.; Gu, J.; Hauryliuk, V.; Zhang, S.; Liu, B.; Li, M.
Show abstract
Bacteria have evolved diverse immune strategies to detect and neutralize bacteriophage infection. Here, we describe an unprecedented paradigm in which a chromosome-architecting nucleoid-associated protein (NAP) is repurposed as a viral infection sensor. When phage attack leads to genome degradation, the NAP sensor is released from the nucleoid to the cytoplasm, where it binds and activates diverse immune effectors. One such effector is a nucleotide-modifying toxin normally existing as an inactive homotetramer. NAP binding converts it into a catalytically active heterotrimer that halts both transcription and translation. Phylogenetic analyses unveiled the high modularity, polyphyletic origin, and wide distribution of NAP-mediated defenses. Collectively, we define a distinct class of defense systems in which bacteria sense phage-induced genome damage through NAP relocation, highlighting an unexpected but essential role for these proteins as sentinels of genome integrity.
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