| Literature DB >> 35817891 |
Nitzan Tal1, Adi Millman1, Avigail Stokar-Avihail1, Taya Fedorenko1, Azita Leavitt1, Sarah Melamed1, Erez Yirmiya1, Carmel Avraham1, Alexander Brandis2, Tevie Mehlman2, Gil Amitai1, Rotem Sorek3.
Abstract
DNA viruses and retroviruses consume large quantities of deoxynucleotides (dNTPs) when replicating. The human antiviral factor SAMHD1 takes advantage of this vulnerability in the viral lifecycle, and inhibits viral replication by degrading dNTPs into their constituent deoxynucleosides and inorganic phosphate. Here, we report that bacteria use a similar strategy to defend against bacteriophage infection. We identify a family of defensive bacterial deoxycytidine triphosphate (dCTP) deaminase proteins that convert dCTP into deoxyuracil nucleotides in response to phage infection. We also identify a family of phage resistance genes that encode deoxyguanosine triphosphatase (dGTPase) enzymes, which degrade dGTP into phosphate-free deoxyguanosine and are distant homologues of human SAMHD1. Our results suggest that bacterial defensive proteins deplete specific deoxynucleotides (either dCTP or dGTP) from the nucleotide pool during phage infection, thus starving the phage of an essential DNA building block and halting its replication. Our study shows that manipulation of the dNTP pool is a potent antiviral strategy shared by both prokaryotes and eukaryotes.Entities:
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Year: 2022 PMID: 35817891 DOI: 10.1038/s41564-022-01158-0
Source DB: PubMed Journal: Nat Microbiol ISSN: 2058-5276 Impact factor: 30.964