- Prichard, Amy;
- Lee, Jina;
- Laughlin, Thomas G;
- Lee, Amber;
- Thomas, Kyle P;
- Sy, Annika E;
- Spencer, Tara;
- Asavavimol, Aileen;
- Cafferata, Allison;
- Cameron, Mia;
- Chiu, Nicholas;
- Davydov, Demyan;
- Desai, Isha;
- Diaz, Gabriel;
- Guereca, Melissa;
- Hearst, Kiley;
- Huang, Leyi;
- Jacobs, Emily;
- Johnson, Annika;
- Kahn, Samuel;
- Koch, Ryan;
- Martinez, Adamari;
- Norquist, Meliné;
- Pau, Tyler;
- Prasad, Gino;
- Saam, Katrina;
- Sandhu, Milan;
- Sarabia, Angel Jose;
- Schumaker, Siena;
- Sonin, Aaron;
- Uyeno, Ariya;
- Zhao, Alison;
- Corbett, Kevin D;
- Pogliano, Kit;
- Meyer, Justin;
- Grose, Julianne H;
- Villa, Elizabeth;
- Dutton, Rachel;
- Pogliano, Joe
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 still to be determined. Here, we show that phages encoding the major phage nucleus protein chimallin share 72 conserved genes encoded within seven gene blocks. Of these, 21 core genes are unique to nucleus-forming phage, and all but one of these genes encode proteins of unknown function. We propose that these phages comprise a novel viral family we term Chimalliviridae. Fluorescence microscopy and cryoelectron tomography studies of Erwinia phage vB_EamM_RAY confirm that many of the key steps of nucleus-based replication are conserved among diverse chimalliviruses and reveal variations on this replication mechanism. 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.