Adaptive loss of tRNA gene expression leads to phage resistance in a marine Synechococcus cyanobacterium.

Autor: Zborowsky S; Faculty of Biology, Technion-Israel Institute of Technology, Haifa, Israel.; Living Systems Institute, University of Exeter, Exeter, UK., Tahan R; Faculty of Biology, Technion-Israel Institute of Technology, Haifa, Israel., Lindell D; Faculty of Biology, Technion-Israel Institute of Technology, Haifa, Israel. dlindell@technion.ac.il.
Jazyk: angličtina
Zdroj: Nature microbiology [Nat Microbiol] 2025 Jan 03. Date of Electronic Publication: 2025 Jan 03.
DOI: 10.1038/s41564-024-01877-6
Abstrakt: Synechococcus is a significant primary producer in the oceans, coexisting with cyanophages, which are important agents of mortality. Bacterial resistance against phage infection is a topic of significant interest, yet little is known for ecologically relevant systems. Here we use exogenous gene expression and gene disruption to investigate mechanisms underlying intracellular resistance of marine Synechococcus WH5701 to the Syn9 cyanophage. The restriction-modification and Gabija defence systems possessed by Synechococcus WH5701 did not contribute to resistance. Instead, resistance was primarily driven by insufficient levels of Leu TAA tRNA, preventing translation of key phage genes in a passive, intracellular mode of resistance. Restoring cellular tRNA expression rendered the cyanobacterium sensitive to infection. We propose an evolutionary scenario whereby changes in cell codon usage, acquisition of tRNAs by the phage and loss of cell and phage tRNA expression resulted in an effective means of resistance, highlighting the dynamic interplay between bacteria and phages in shaping their co-evolutionary trajectories.
Competing Interests: Competing interests: The authors declare no competing interests.
(© 2025. The Author(s).)
Databáze: MEDLINE
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