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Discovery of Viral Myosin Genes With Complex Evolutionary History Within Plankton

Nucleocytoplasmic large DNA viruses (NCLDVs) infect diverse eukaryotes and form a group of viruses with capsids encapsulating large genomes. Recent studies are increasingly revealing a spectacular array of functions encoded in their genomes, including genes for energy metabolisms, nutrient uptake, a...

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Autores principales: Kijima, Soichiro, Delmont, Tom O., Miyazaki, Urara, Gaia, Morgan, Endo, Hisashi, Ogata, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8215601/
https://www.ncbi.nlm.nih.gov/pubmed/34163457
http://dx.doi.org/10.3389/fmicb.2021.683294
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author Kijima, Soichiro
Delmont, Tom O.
Miyazaki, Urara
Gaia, Morgan
Endo, Hisashi
Ogata, Hiroyuki
author_facet Kijima, Soichiro
Delmont, Tom O.
Miyazaki, Urara
Gaia, Morgan
Endo, Hisashi
Ogata, Hiroyuki
author_sort Kijima, Soichiro
collection PubMed
description Nucleocytoplasmic large DNA viruses (NCLDVs) infect diverse eukaryotes and form a group of viruses with capsids encapsulating large genomes. Recent studies are increasingly revealing a spectacular array of functions encoded in their genomes, including genes for energy metabolisms, nutrient uptake, as well as cytoskeleton. Here, we report the discovery of genes homologous to myosins, the major eukaryotic motor proteins previously unrecognized in the virosphere, in environmental genomes of NCLDVs from the surface of the oceans. Phylogenetic analyses indicate that most viral myosins (named “virmyosins”) belong to the Imitervirales order, except for one belonging to the Phycodnaviridae family. On the one hand, the phylogenetic positions of virmyosin-encoding Imitervirales are scattered within the Imitervirales. On the other hand, Imitervirales virmyosin genes form a monophyletic group in the phylogeny of diverse myosin sequences. Furthermore, phylogenetic trends for the virmyosin genes and viruses containing them were incongruent. Based on these results, we argue that multiple transfers of myosin homologs have occurred not only from eukaryotes to viruses but also between viruses, supposedly during co-infections of the same host. Like other viruses that use host motor proteins for their intracellular transport or motility, these viruses may use the virally encoded myosins for the intracellular trafficking of giant viral particles.
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spelling pubmed-82156012021-06-22 Discovery of Viral Myosin Genes With Complex Evolutionary History Within Plankton Kijima, Soichiro Delmont, Tom O. Miyazaki, Urara Gaia, Morgan Endo, Hisashi Ogata, Hiroyuki Front Microbiol Microbiology Nucleocytoplasmic large DNA viruses (NCLDVs) infect diverse eukaryotes and form a group of viruses with capsids encapsulating large genomes. Recent studies are increasingly revealing a spectacular array of functions encoded in their genomes, including genes for energy metabolisms, nutrient uptake, as well as cytoskeleton. Here, we report the discovery of genes homologous to myosins, the major eukaryotic motor proteins previously unrecognized in the virosphere, in environmental genomes of NCLDVs from the surface of the oceans. Phylogenetic analyses indicate that most viral myosins (named “virmyosins”) belong to the Imitervirales order, except for one belonging to the Phycodnaviridae family. On the one hand, the phylogenetic positions of virmyosin-encoding Imitervirales are scattered within the Imitervirales. On the other hand, Imitervirales virmyosin genes form a monophyletic group in the phylogeny of diverse myosin sequences. Furthermore, phylogenetic trends for the virmyosin genes and viruses containing them were incongruent. Based on these results, we argue that multiple transfers of myosin homologs have occurred not only from eukaryotes to viruses but also between viruses, supposedly during co-infections of the same host. Like other viruses that use host motor proteins for their intracellular transport or motility, these viruses may use the virally encoded myosins for the intracellular trafficking of giant viral particles. Frontiers Media S.A. 2021-06-07 /pmc/articles/PMC8215601/ /pubmed/34163457 http://dx.doi.org/10.3389/fmicb.2021.683294 Text en Copyright © 2021 Kijima, Delmont, Miyazaki, Gaia, Endo and Ogata. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Kijima, Soichiro
Delmont, Tom O.
Miyazaki, Urara
Gaia, Morgan
Endo, Hisashi
Ogata, Hiroyuki
Discovery of Viral Myosin Genes With Complex Evolutionary History Within Plankton
title Discovery of Viral Myosin Genes With Complex Evolutionary History Within Plankton
title_full Discovery of Viral Myosin Genes With Complex Evolutionary History Within Plankton
title_fullStr Discovery of Viral Myosin Genes With Complex Evolutionary History Within Plankton
title_full_unstemmed Discovery of Viral Myosin Genes With Complex Evolutionary History Within Plankton
title_short Discovery of Viral Myosin Genes With Complex Evolutionary History Within Plankton
title_sort discovery of viral myosin genes with complex evolutionary history within plankton
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8215601/
https://www.ncbi.nlm.nih.gov/pubmed/34163457
http://dx.doi.org/10.3389/fmicb.2021.683294
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