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Giant virus diversity and host interactions through global metagenomics

Our current knowledge about nucleocytoplasmic large DNA viruses (NCLDVs) is largely derived from viral isolates that are co-cultivated with protists and algae. Here we reconstructed 2,074 NCLDV genomes from sampling sites across the globe by building on the rapidly increasing amount of publicly avai...

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Autores principales: Schulz, Frederik, Roux, Simon, Paez-Espino, David, Jungbluth, Sean, Walsh, David A., Denef, Vincent J., McMahon, Katherine D., Konstantinidis, Konstantinos T., Eloe-Fadrosh, Emiley A., Kyrpides, Nikos C., Woyke, Tanja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7162819/
https://www.ncbi.nlm.nih.gov/pubmed/31968354
http://dx.doi.org/10.1038/s41586-020-1957-x
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author Schulz, Frederik
Roux, Simon
Paez-Espino, David
Jungbluth, Sean
Walsh, David A.
Denef, Vincent J.
McMahon, Katherine D.
Konstantinidis, Konstantinos T.
Eloe-Fadrosh, Emiley A.
Kyrpides, Nikos C.
Woyke, Tanja
author_facet Schulz, Frederik
Roux, Simon
Paez-Espino, David
Jungbluth, Sean
Walsh, David A.
Denef, Vincent J.
McMahon, Katherine D.
Konstantinidis, Konstantinos T.
Eloe-Fadrosh, Emiley A.
Kyrpides, Nikos C.
Woyke, Tanja
author_sort Schulz, Frederik
collection PubMed
description Our current knowledge about nucleocytoplasmic large DNA viruses (NCLDVs) is largely derived from viral isolates that are co-cultivated with protists and algae. Here we reconstructed 2,074 NCLDV genomes from sampling sites across the globe by building on the rapidly increasing amount of publicly available metagenome data. This led to an 11-fold increase in phylogenetic diversity and a parallel 10-fold expansion in functional diversity. Analysis of 58,023 major capsid proteins from large and giant viruses using metagenomic data revealed the global distribution patterns and cosmopolitan nature of these viruses. The discovered viral genomes encoded a wide range of proteins with putative roles in photosynthesis and diverse substrate transport processes, indicating that host reprogramming is probably a common strategy in the NCLDVs. Furthermore, inferences of horizontal gene transfer connected viral lineages to diverse eukaryotic hosts. We anticipate that the global diversity of NCLDVs that we describe here will establish giant viruses—which are associated with most major eukaryotic lineages—as important players in ecosystems across Earth’s biomes.
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spelling pubmed-71628192020-04-27 Giant virus diversity and host interactions through global metagenomics Schulz, Frederik Roux, Simon Paez-Espino, David Jungbluth, Sean Walsh, David A. Denef, Vincent J. McMahon, Katherine D. Konstantinidis, Konstantinos T. Eloe-Fadrosh, Emiley A. Kyrpides, Nikos C. Woyke, Tanja Nature Article Our current knowledge about nucleocytoplasmic large DNA viruses (NCLDVs) is largely derived from viral isolates that are co-cultivated with protists and algae. Here we reconstructed 2,074 NCLDV genomes from sampling sites across the globe by building on the rapidly increasing amount of publicly available metagenome data. This led to an 11-fold increase in phylogenetic diversity and a parallel 10-fold expansion in functional diversity. Analysis of 58,023 major capsid proteins from large and giant viruses using metagenomic data revealed the global distribution patterns and cosmopolitan nature of these viruses. The discovered viral genomes encoded a wide range of proteins with putative roles in photosynthesis and diverse substrate transport processes, indicating that host reprogramming is probably a common strategy in the NCLDVs. Furthermore, inferences of horizontal gene transfer connected viral lineages to diverse eukaryotic hosts. We anticipate that the global diversity of NCLDVs that we describe here will establish giant viruses—which are associated with most major eukaryotic lineages—as important players in ecosystems across Earth’s biomes. Nature Publishing Group UK 2020-01-22 2020 /pmc/articles/PMC7162819/ /pubmed/31968354 http://dx.doi.org/10.1038/s41586-020-1957-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Schulz, Frederik
Roux, Simon
Paez-Espino, David
Jungbluth, Sean
Walsh, David A.
Denef, Vincent J.
McMahon, Katherine D.
Konstantinidis, Konstantinos T.
Eloe-Fadrosh, Emiley A.
Kyrpides, Nikos C.
Woyke, Tanja
Giant virus diversity and host interactions through global metagenomics
title Giant virus diversity and host interactions through global metagenomics
title_full Giant virus diversity and host interactions through global metagenomics
title_fullStr Giant virus diversity and host interactions through global metagenomics
title_full_unstemmed Giant virus diversity and host interactions through global metagenomics
title_short Giant virus diversity and host interactions through global metagenomics
title_sort giant virus diversity and host interactions through global metagenomics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7162819/
https://www.ncbi.nlm.nih.gov/pubmed/31968354
http://dx.doi.org/10.1038/s41586-020-1957-x
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