Abstract

Numerous metagenomic studies have uncovered a remarkable diversity of circular replication-associated protein (Rep)-encoding single-stranded (CRESS) DNA viruses, the majority of which are uncultured and unclassified. Unlike capsid proteins, the Reps show significant similarity across different groups of CRESS DNA viruses and have conserved domain organization with the N-terminal nuclease and the C-terminal helicase domain. Consequently, Rep is widely used as a marker for identification, classification and assessment of the diversity of CRESS DNA viruses. However, it has been shown that in certain viruses the Rep nuclease and helicase domains display incongruent evolutionary histories. Here, we systematically evaluated the co-evolutionary patterns of the two Rep domains across classified and unclassified CRESS DNA viruses. Our analysis indicates that the Reps encoded by members of the families Bacilladnaviridae, Circoviridae, Geminiviridae, Genomoviridae, Nanoviridae and Smacoviridae display largely congruent evolutionary patterns in the two domains. By contrast, among the unclassified CRESS DNA viruses, 71% appear to have chimeric Reps. Such massive chimerism suggests that unclassified CRESS DNA viruses represent a dynamic population in which exchange of gene fragments encoding the nuclease and helicase domains is extremely common. Furthermore, purging of the chimeric sequences uncovered six monophyletic Rep groups that may represent new families of CRESS DNA viruses.

Highlights

  • The role of genetic recombination in virus evolution cannot be overestimated

  • Our analysis revealed six groups of unclassified circular replication-associated protein (Rep)-encoding single-stranded (CRESS) DNA virus groups in which most of the members displayed congruent evolutionary patterns for the nuclease and helicase domains

  • Various studies have recently shown that CRESS DNA viruses are a major, highly diverse component of the global virome and, in certain environments, represent the dominant virus group [9,13,41,42,43,44,45,46,47,48,49,50,51,52]

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Summary

Introduction

The role of genetic recombination in virus evolution cannot be overestimated. It is a dominant force in shaping viral genomes and associated phenotypes, including adaptation, host switching and virus emergence [1,2,3]. The rate of recombination varies across virus taxa [4], a considerable body of evidence indicates that it has affected viruses with different genome types and has resulted in gene exchange between unrelated viruses, and between viruses and non-viral mobile genetic elements as well as cellular organisms [5]. The very origin of viruses might be a result of an assortment of genes with different evolutionary histories.

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