Prichard Amy, Lee Jina, Laughlin Thomas G, Lee Amber, Thomas Kyle P, Sy Annika, 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, Pogliano Kit, Meyer Justin, Grose Julianne H, Villa Elizabeth, Dutton Rachel, Pogliano Joe
bioRxiv. 2023 Feb 25:2023.02.24.529968. doi: 10.1101/2023.02.24.529968.
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 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.
我们最近发现,一些噬菌体建立了一个类似细胞核的复制区室(噬菌体细胞核),但定义基于细胞核的噬菌体复制的核心基因及其系统发育分布尚不清楚。通过研究编码主要噬菌体细胞核蛋白奇马林的噬菌体,包括先前测序但未表征的噬菌体,我们发现编码奇马林的噬菌体共享一组72个高度保守的基因,这些基因编码在七个不同的基因块中。其中,21个核心基因是该组所特有的,除了一个之外,所有这些独特基因都编码功能未知的蛋白质。我们提出,具有这种核心基因组的噬菌体构成了一个新的病毒科,我们称之为奇马林病毒科。对噬菌体vB_EamM_RAY的荧光显微镜和冷冻电子断层扫描研究证实,核心基因组中编码的基于细胞核的复制的许多关键步骤在不同的奇马林病毒中是保守的,并揭示非核心成分可以赋予这种复制机制有趣的变化。例如,与先前研究的形成细胞核的噬菌体不同,RAY不会降解宿主基因组,其PhuZ同源物似乎形成了一个有内腔的五链细丝。这项工作扩展了我们对噬菌体细胞核和PhuZ纺锤体多样性及功能的理解,为确定基于细胞核的噬菌体复制的关键机制提供了路线图。