Diversity of Bathyarchaeia viruses in metagenomes and virus-encoded CRISPR system components

Author:

Duan Changhai1234,Liu Yang23,Liu Ying5,Liu Lirui23,Cai Mingwei23,Zhang Rui23,Zeng Qinglu4,Koonin Eugene V6,Krupovic Mart5,Li Meng123

Affiliation:

1. SZU-HKUST Joint PhD Program in Marine Environmental Science, Shenzhen University , 518060 Shenzhen, China

2. Archaeal Biology Center, Institute for Advanced Study, Shenzhen University , 518060 Shenzhen, China

3. Shenzhen Key Laboratory of Marine Microbiome Engineering, Institute for Advanced Study, Shenzhen University , 518060 Shenzhen, China

4. Department of Ocean Science, The Hong Kong University of Science and Technology, Clear Water Bay , Hong Kong, China

5. Institut Pasteur, Université Paris Cité, Archaeal Virology Unit , 75015 Paris, France

6. National Center for Biotechnology Information, National Library of Medicine , Bethesda, MD 20894, United States

Abstract

Abstract Bathyarchaeia represent a class of archaea common and abundant in sedimentary ecosystems. Here we report 56 metagenome-assembled genomes of Bathyarchaeia viruses identified in metagenomes from different environments. Gene sharing network and phylogenomic analyses led to the proposal of four virus families, including viruses of the realms Duplodnaviria and Adnaviria, and archaea-specific spindle-shaped viruses. Genomic analyses uncovered diverse CRISPR elements in these viruses. Viruses of the proposed family “Fuxiviridae” harbor an atypical type IV-B CRISPR-Cas system and a Cas4 protein that might interfere with host immunity. Viruses of the family “Chiyouviridae” encode a Cas2-like endonuclease and two mini-CRISPR arrays, one with a repeat identical to that in the host CRISPR array, potentially allowing the virus to recruit the host CRISPR adaptation machinery to acquire spacers that could contribute to competition with other mobile genetic elements or to inhibit host defenses. These findings present an outline of the Bathyarchaeia virome and offer a glimpse into their counter-defense mechanisms.

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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