Identifying the core genome of the nucleus-forming bacteriophage family and characterization of Erwinia phage RAY

Amy Prichard,Jina Lee,Thomas G. Laughlin, Amber Lee, Kyle P. Thomas,Annika Sy, Tara Spencer,Aileen Asavavimol,Allison Cafferata,Mia Cameron,Nicholas Chiu,Demyan Davydov,Isha Desai,Gabriel Diaz,Melissa Guereca,Kiley Hearst,Leyi Huang,Emily Jacobs,Annika Johnson,Samuel Kahn, Ryan Koch, Adamari Martinez, Meliné Norquist, Tyler Pau, Gino Prasad, Katrina Saam, Milan Sandhu, Angel Jose Sarabia, Siena Schumaker, Aaron Sonin, Ariya Uyeno, Alison Zhao,Kevin Corbett,Kit Pogliano,Justin Meyer,Julianne H. Grose,Elizabeth Villa,Rachel Dutton,Joe Pogliano

biorxiv(2023)

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摘要
We recently discovered that some bacteriophages establish a nucleus-like replication compartment (phage nucleus), but the core genes that define nucleus-based phage replication and their phylogenetic distribution were unknown. By studying phages that encode the major phage nucleus protein chimallin, including previously sequenced yet uncharacterized phages, we discovered that chimallin-encoding phages share a set of 72 highly conserved genes encoded within seven distinct gene blocks. Of these, 21 core genes are unique to this group, and all but one of these unique genes encode proteins of unknown function. We propose that phages with this core genome comprise a novel viral family we term Chimalliviridae. Fluorescence microscopy and cryo-electron tomography studies of Erwinia phage vB\_EamM\_RAY confirm that many of the key steps of nucleus-based replication encoded in the core genome are conserved among diverse chimalliviruses, and reveal that non-core components can confer intriguing variations on this replication mechanism. For instance, unlike previously studied nucleus-forming phages, RAY doesn’t degrade the host genome, and its PhuZ homolog appears to form a five-stranded filament with a lumen. This work expands our understanding of phage nucleus and PhuZ spindle diversity and function, providing a roadmap for identifying key mechanisms underlying nucleus-based phage replication. ### Competing Interest Statement The authors have declared no competing interest.
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