Cargando…

The Double-Stranded DNA Virosphere as a Modular Hierarchical Network of Gene Sharing

Virus genomes are prone to extensive gene loss, gain, and exchange and share no universal genes. Therefore, in a broad-scale study of virus evolution, gene and genome network analyses can complement traditional phylogenetics. We performed an exhaustive comparative analysis of the genomes of double-s...

Descripción completa

Detalles Bibliográficos
Autores principales: Iranzo, Jaime, Krupovic, Mart, Koonin, Eugene V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981718/
https://www.ncbi.nlm.nih.gov/pubmed/27486193
http://dx.doi.org/10.1128/mBio.00978-16
_version_ 1782447649206566912
author Iranzo, Jaime
Krupovic, Mart
Koonin, Eugene V.
author_facet Iranzo, Jaime
Krupovic, Mart
Koonin, Eugene V.
author_sort Iranzo, Jaime
collection PubMed
description Virus genomes are prone to extensive gene loss, gain, and exchange and share no universal genes. Therefore, in a broad-scale study of virus evolution, gene and genome network analyses can complement traditional phylogenetics. We performed an exhaustive comparative analysis of the genomes of double-stranded DNA (dsDNA) viruses by using the bipartite network approach and found a robust hierarchical modularity in the dsDNA virosphere. Bipartite networks consist of two classes of nodes, with nodes in one class, in this case genomes, being connected via nodes of the second class, in this case genes. Such a network can be partitioned into modules that combine nodes from both classes. The bipartite network of dsDNA viruses includes 19 modules that form 5 major and 3 minor supermodules. Of these modules, 11 include tailed bacteriophages, reflecting the diversity of this largest group of viruses. The module analysis quantitatively validates and refines previously proposed nontrivial evolutionary relationships. An expansive supermodule combines the large and giant viruses of the putative order “Megavirales” with diverse moderate-sized viruses and related mobile elements. All viruses in this supermodule share a distinct morphogenetic tool kit with a double jelly roll major capsid protein. Herpesviruses and tailed bacteriophages comprise another supermodule, held together by a distinct set of morphogenetic proteins centered on the HK97-like major capsid protein. Together, these two supermodules cover the great majority of currently known dsDNA viruses. We formally identify a set of 14 viral hallmark genes that comprise the hubs of the network and account for most of the intermodule connections.
format Online
Article
Text
id pubmed-4981718
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-49817182016-08-17 The Double-Stranded DNA Virosphere as a Modular Hierarchical Network of Gene Sharing Iranzo, Jaime Krupovic, Mart Koonin, Eugene V. mBio Research Article Virus genomes are prone to extensive gene loss, gain, and exchange and share no universal genes. Therefore, in a broad-scale study of virus evolution, gene and genome network analyses can complement traditional phylogenetics. We performed an exhaustive comparative analysis of the genomes of double-stranded DNA (dsDNA) viruses by using the bipartite network approach and found a robust hierarchical modularity in the dsDNA virosphere. Bipartite networks consist of two classes of nodes, with nodes in one class, in this case genomes, being connected via nodes of the second class, in this case genes. Such a network can be partitioned into modules that combine nodes from both classes. The bipartite network of dsDNA viruses includes 19 modules that form 5 major and 3 minor supermodules. Of these modules, 11 include tailed bacteriophages, reflecting the diversity of this largest group of viruses. The module analysis quantitatively validates and refines previously proposed nontrivial evolutionary relationships. An expansive supermodule combines the large and giant viruses of the putative order “Megavirales” with diverse moderate-sized viruses and related mobile elements. All viruses in this supermodule share a distinct morphogenetic tool kit with a double jelly roll major capsid protein. Herpesviruses and tailed bacteriophages comprise another supermodule, held together by a distinct set of morphogenetic proteins centered on the HK97-like major capsid protein. Together, these two supermodules cover the great majority of currently known dsDNA viruses. We formally identify a set of 14 viral hallmark genes that comprise the hubs of the network and account for most of the intermodule connections. American Society for Microbiology 2016-08-02 /pmc/articles/PMC4981718/ /pubmed/27486193 http://dx.doi.org/10.1128/mBio.00978-16 Text en Copyright © 2016 Iranzo et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Iranzo, Jaime
Krupovic, Mart
Koonin, Eugene V.
The Double-Stranded DNA Virosphere as a Modular Hierarchical Network of Gene Sharing
title The Double-Stranded DNA Virosphere as a Modular Hierarchical Network of Gene Sharing
title_full The Double-Stranded DNA Virosphere as a Modular Hierarchical Network of Gene Sharing
title_fullStr The Double-Stranded DNA Virosphere as a Modular Hierarchical Network of Gene Sharing
title_full_unstemmed The Double-Stranded DNA Virosphere as a Modular Hierarchical Network of Gene Sharing
title_short The Double-Stranded DNA Virosphere as a Modular Hierarchical Network of Gene Sharing
title_sort double-stranded dna virosphere as a modular hierarchical network of gene sharing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981718/
https://www.ncbi.nlm.nih.gov/pubmed/27486193
http://dx.doi.org/10.1128/mBio.00978-16
work_keys_str_mv AT iranzojaime thedoublestrandeddnavirosphereasamodularhierarchicalnetworkofgenesharing
AT krupovicmart thedoublestrandeddnavirosphereasamodularhierarchicalnetworkofgenesharing
AT koonineugenev thedoublestrandeddnavirosphereasamodularhierarchicalnetworkofgenesharing
AT iranzojaime doublestrandeddnavirosphereasamodularhierarchicalnetworkofgenesharing
AT krupovicmart doublestrandeddnavirosphereasamodularhierarchicalnetworkofgenesharing
AT koonineugenev doublestrandeddnavirosphereasamodularhierarchicalnetworkofgenesharing