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...

Descripción completa

Detalles Bibliográficos
Autores principales: Hurwitz, Bonnie L, Deng, Li, Poulos, Bonnie T, Sullivan, Matthew B
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