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Long-read viral metagenomics captures abundant and microdiverse viral populations and their niche-defining genomic islands
Marine viruses impact global biogeochemical cycles via their influence on host community structure and function, yet our understanding of viral ecology is constrained by limitations in host culturing and a lack of reference genomes and ‘universal’ gene markers to facilitate community surveys. Short-...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6487183/ https://www.ncbi.nlm.nih.gov/pubmed/31086738 http://dx.doi.org/10.7717/peerj.6800 |
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author | Warwick-Dugdale, Joanna Solonenko, Natalie Moore, Karen Chittick, Lauren Gregory, Ann C. Allen, Michael J. Sullivan, Matthew B. Temperton, Ben |
author_facet | Warwick-Dugdale, Joanna Solonenko, Natalie Moore, Karen Chittick, Lauren Gregory, Ann C. Allen, Michael J. Sullivan, Matthew B. Temperton, Ben |
author_sort | Warwick-Dugdale, Joanna |
collection | PubMed |
description | Marine viruses impact global biogeochemical cycles via their influence on host community structure and function, yet our understanding of viral ecology is constrained by limitations in host culturing and a lack of reference genomes and ‘universal’ gene markers to facilitate community surveys. Short-read viral metagenomic studies have provided clues to viral function and first estimates of global viral gene abundance and distribution, but their assemblies are confounded by populations with high levels of strain evenness and nucleotide diversity (microdiversity), limiting assembly of some of the most abundant viruses on Earth. Such features also challenge assembly across genomic islands containing niche-defining genes that drive ecological speciation. These populations and features may be successfully captured by single-virus genomics and fosmid-based approaches, at least in abundant taxa, but at considerable cost and technical expertise. Here we established a low-cost, low-input, high throughput alternative sequencing and informatics workflow to improve viral metagenomic assemblies using short-read and long-read technology. The ‘VirION’ (Viral, long-read metagenomics via MinION sequencing) approach was first validated using mock communities where it was found to be as relatively quantitative as short-read methods and provided significant improvements in recovery of viral genomes. We then then applied VirION to the first metagenome from a natural viral community from the Western English Channel. In comparison to a short-read only approach, VirION: (i) increased number and completeness of assembled viral genomes; (ii) captured abundant, highly microdiverse virus populations, and (iii) captured more and longer genomic islands. Together, these findings suggest that VirION provides a high throughput and cost-effective alternative to fosmid and single-virus genomic approaches to more comprehensively explore viral communities in nature. |
format | Online Article Text |
id | pubmed-6487183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64871832019-05-13 Long-read viral metagenomics captures abundant and microdiverse viral populations and their niche-defining genomic islands Warwick-Dugdale, Joanna Solonenko, Natalie Moore, Karen Chittick, Lauren Gregory, Ann C. Allen, Michael J. Sullivan, Matthew B. Temperton, Ben PeerJ Bioinformatics Marine viruses impact global biogeochemical cycles via their influence on host community structure and function, yet our understanding of viral ecology is constrained by limitations in host culturing and a lack of reference genomes and ‘universal’ gene markers to facilitate community surveys. Short-read viral metagenomic studies have provided clues to viral function and first estimates of global viral gene abundance and distribution, but their assemblies are confounded by populations with high levels of strain evenness and nucleotide diversity (microdiversity), limiting assembly of some of the most abundant viruses on Earth. Such features also challenge assembly across genomic islands containing niche-defining genes that drive ecological speciation. These populations and features may be successfully captured by single-virus genomics and fosmid-based approaches, at least in abundant taxa, but at considerable cost and technical expertise. Here we established a low-cost, low-input, high throughput alternative sequencing and informatics workflow to improve viral metagenomic assemblies using short-read and long-read technology. The ‘VirION’ (Viral, long-read metagenomics via MinION sequencing) approach was first validated using mock communities where it was found to be as relatively quantitative as short-read methods and provided significant improvements in recovery of viral genomes. We then then applied VirION to the first metagenome from a natural viral community from the Western English Channel. In comparison to a short-read only approach, VirION: (i) increased number and completeness of assembled viral genomes; (ii) captured abundant, highly microdiverse virus populations, and (iii) captured more and longer genomic islands. Together, these findings suggest that VirION provides a high throughput and cost-effective alternative to fosmid and single-virus genomic approaches to more comprehensively explore viral communities in nature. PeerJ Inc. 2019-04-25 /pmc/articles/PMC6487183/ /pubmed/31086738 http://dx.doi.org/10.7717/peerj.6800 Text en ©2019 Warwick-Dugdale et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Bioinformatics Warwick-Dugdale, Joanna Solonenko, Natalie Moore, Karen Chittick, Lauren Gregory, Ann C. Allen, Michael J. Sullivan, Matthew B. Temperton, Ben Long-read viral metagenomics captures abundant and microdiverse viral populations and their niche-defining genomic islands |
title | Long-read viral metagenomics captures abundant and microdiverse viral populations and their niche-defining genomic islands |
title_full | Long-read viral metagenomics captures abundant and microdiverse viral populations and their niche-defining genomic islands |
title_fullStr | Long-read viral metagenomics captures abundant and microdiverse viral populations and their niche-defining genomic islands |
title_full_unstemmed | Long-read viral metagenomics captures abundant and microdiverse viral populations and their niche-defining genomic islands |
title_short | Long-read viral metagenomics captures abundant and microdiverse viral populations and their niche-defining genomic islands |
title_sort | long-read viral metagenomics captures abundant and microdiverse viral populations and their niche-defining genomic islands |
topic | Bioinformatics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6487183/ https://www.ncbi.nlm.nih.gov/pubmed/31086738 http://dx.doi.org/10.7717/peerj.6800 |
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