Cargando…
Evaluation of methods to concentrate and purify ocean virus communities through comparative, replicated metagenomics
Viruses have global impact through mortality, nutrient cycling and horizontal gene transfer, yet their study is limited by complex methodologies with little validation. Here, we use triplicate metagenomes to compare common aquatic viral concentration and purification methods across four combinations...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655615/ https://www.ncbi.nlm.nih.gov/pubmed/22845467 http://dx.doi.org/10.1111/j.1462-2920.2012.02836.x |
_version_ | 1782269906506481664 |
---|---|
author | Hurwitz, Bonnie L Deng, Li Poulos, Bonnie T Sullivan, Matthew B |
author_facet | Hurwitz, Bonnie L Deng, Li Poulos, Bonnie T Sullivan, Matthew B |
author_sort | Hurwitz, Bonnie L |
collection | PubMed |
description | Viruses have global impact through mortality, nutrient cycling and horizontal gene transfer, yet their study is limited by complex methodologies with little validation. Here, we use triplicate metagenomes to compare common aquatic viral concentration and purification methods across four combinations as follows: (i) tangential flow filtration (TFF) and DNase + CsCl, (ii) FeCl(3) precipitation and DNase, (iii) FeCl(3) precipitation and DNase + CsCl and (iv) FeCl(3) precipitation and DNase + sucrose. Taxonomic data (30% of reads) suggested that purification methods were statistically indistinguishable at any taxonomic level while concentration methods were significantly different at family and genus levels. Specifically, TFF-concentrated viral metagenomes had significantly fewer abundant viral types (Podoviridae and Phycodnaviridae) and more variability among Myoviridae than FeCl(3)-precipitated viral metagenomes. More comprehensive analyses using protein clusters (66% of reads) and k-mers (100% of reads) showed 50–53% of these data were common to all four methods, and revealed trace bacterial DNA contamination in TFF-concentrated metagenomes and one of three replicates concentrated using FeCl(3) and purified by DNase alone. Shared k-mer analyses also revealed that polymerases used in amplification impact the resulting metagenomes, with TaKaRa enriching for ‘rare’ reads relative to PfuTurbo. Together these results provide empirical data for making experimental design decisions in culture-independent viral ecology studies. |
format | Online Article Text |
id | pubmed-3655615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-36556152013-05-17 Evaluation of methods to concentrate and purify ocean virus communities through comparative, replicated metagenomics Hurwitz, Bonnie L Deng, Li Poulos, Bonnie T Sullivan, Matthew B Environ Microbiol Research Articles Viruses have global impact through mortality, nutrient cycling and horizontal gene transfer, yet their study is limited by complex methodologies with little validation. Here, we use triplicate metagenomes to compare common aquatic viral concentration and purification methods across four combinations as follows: (i) tangential flow filtration (TFF) and DNase + CsCl, (ii) FeCl(3) precipitation and DNase, (iii) FeCl(3) precipitation and DNase + CsCl and (iv) FeCl(3) precipitation and DNase + sucrose. Taxonomic data (30% of reads) suggested that purification methods were statistically indistinguishable at any taxonomic level while concentration methods were significantly different at family and genus levels. Specifically, TFF-concentrated viral metagenomes had significantly fewer abundant viral types (Podoviridae and Phycodnaviridae) and more variability among Myoviridae than FeCl(3)-precipitated viral metagenomes. More comprehensive analyses using protein clusters (66% of reads) and k-mers (100% of reads) showed 50–53% of these data were common to all four methods, and revealed trace bacterial DNA contamination in TFF-concentrated metagenomes and one of three replicates concentrated using FeCl(3) and purified by DNase alone. Shared k-mer analyses also revealed that polymerases used in amplification impact the resulting metagenomes, with TaKaRa enriching for ‘rare’ reads relative to PfuTurbo. Together these results provide empirical data for making experimental design decisions in culture-independent viral ecology studies. Blackwell Publishing Ltd 2013-05 /pmc/articles/PMC3655615/ /pubmed/22845467 http://dx.doi.org/10.1111/j.1462-2920.2012.02836.x Text en Copyright © 2013 Society for Applied Microbiology and Blackwell Publishing Ltd http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Research Articles Hurwitz, Bonnie L Deng, Li Poulos, Bonnie T Sullivan, Matthew B Evaluation of methods to concentrate and purify ocean virus communities through comparative, replicated metagenomics |
title | Evaluation of methods to concentrate and purify ocean virus communities through comparative, replicated metagenomics |
title_full | Evaluation of methods to concentrate and purify ocean virus communities through comparative, replicated metagenomics |
title_fullStr | Evaluation of methods to concentrate and purify ocean virus communities through comparative, replicated metagenomics |
title_full_unstemmed | Evaluation of methods to concentrate and purify ocean virus communities through comparative, replicated metagenomics |
title_short | Evaluation of methods to concentrate and purify ocean virus communities through comparative, replicated metagenomics |
title_sort | evaluation of methods to concentrate and purify ocean virus communities through comparative, replicated metagenomics |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655615/ https://www.ncbi.nlm.nih.gov/pubmed/22845467 http://dx.doi.org/10.1111/j.1462-2920.2012.02836.x |
work_keys_str_mv | AT hurwitzbonniel evaluationofmethodstoconcentrateandpurifyoceanviruscommunitiesthroughcomparativereplicatedmetagenomics AT dengli evaluationofmethodstoconcentrateandpurifyoceanviruscommunitiesthroughcomparativereplicatedmetagenomics AT poulosbonniet evaluationofmethodstoconcentrateandpurifyoceanviruscommunitiesthroughcomparativereplicatedmetagenomics AT sullivanmatthewb evaluationofmethodstoconcentrateandpurifyoceanviruscommunitiesthroughcomparativereplicatedmetagenomics |