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Metagenomic Analysis of Viral Communities in (Hado)Pelagic Sediments

In this study, we analyzed viral metagenomes (viromes) in the sedimentary habitats of three geographically and geologically distinct (hado)pelagic environments in the northwest Pacific; the Izu-Ogasawara Trench (water depth = 9,760 m) (OG), the Challenger Deep in the Mariana Trench (10,325 m) (MA),...

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Autores principales: Yoshida, Mitsuhiro, Takaki, Yoshihiro, Eitoku, Masamitsu, Nunoura, Takuro, Takai, Ken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3584133/
https://www.ncbi.nlm.nih.gov/pubmed/23468952
http://dx.doi.org/10.1371/journal.pone.0057271
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author Yoshida, Mitsuhiro
Takaki, Yoshihiro
Eitoku, Masamitsu
Nunoura, Takuro
Takai, Ken
author_facet Yoshida, Mitsuhiro
Takaki, Yoshihiro
Eitoku, Masamitsu
Nunoura, Takuro
Takai, Ken
author_sort Yoshida, Mitsuhiro
collection PubMed
description In this study, we analyzed viral metagenomes (viromes) in the sedimentary habitats of three geographically and geologically distinct (hado)pelagic environments in the northwest Pacific; the Izu-Ogasawara Trench (water depth = 9,760 m) (OG), the Challenger Deep in the Mariana Trench (10,325 m) (MA), and the forearc basin off the Shimokita Peninsula (1,181 m) (SH). Virus abundance ranged from 10(6) to 10(11) viruses/cm(3) of sediments (down to 30 cm below the seafloor [cmbsf]). We recovered viral DNA assemblages (viromes) from the (hado)pelagic sediment samples and obtained a total of 37,458, 39,882, and 70,882 sequence reads by 454 GS FLX Titanium pyrosequencing from the virome libraries of the OG, MA, and SH (hado)pelagic sediments, respectively. Only 24−30% of the sequence reads from each virome library exhibited significant similarities to the sequences deposited in the public nr protein database (E-value <10(−3) in BLAST). Among the sequences identified as potential viral genes based on the BLAST search, 95−99% of the sequence reads in each library were related to genes from single-stranded DNA (ssDNA) viral families, including Microviridae, Circoviridae, and Geminiviridae. A relatively high abundance of sequences related to the genetic markers (major capsid protein [VP1] and replication protein [Rep]) of two ssDNA viral groups were also detected in these libraries, thereby revealing a high genotypic diversity of their viruses (833 genotypes for VP1 and 2,551 genotypes for Rep). A majority of the viral genes predicted from each library were classified into three ssDNA viral protein categories: Rep, VP1, and minor capsid protein. The deep-sea sedimentary viromes were distinct from the viromes obtained from the oceanic and fresh waters and marine eukaryotes, and thus, deep-sea sediments harbor novel viromes, including previously unidentified ssDNA viruses.
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spelling pubmed-35841332013-03-06 Metagenomic Analysis of Viral Communities in (Hado)Pelagic Sediments Yoshida, Mitsuhiro Takaki, Yoshihiro Eitoku, Masamitsu Nunoura, Takuro Takai, Ken PLoS One Research Article In this study, we analyzed viral metagenomes (viromes) in the sedimentary habitats of three geographically and geologically distinct (hado)pelagic environments in the northwest Pacific; the Izu-Ogasawara Trench (water depth = 9,760 m) (OG), the Challenger Deep in the Mariana Trench (10,325 m) (MA), and the forearc basin off the Shimokita Peninsula (1,181 m) (SH). Virus abundance ranged from 10(6) to 10(11) viruses/cm(3) of sediments (down to 30 cm below the seafloor [cmbsf]). We recovered viral DNA assemblages (viromes) from the (hado)pelagic sediment samples and obtained a total of 37,458, 39,882, and 70,882 sequence reads by 454 GS FLX Titanium pyrosequencing from the virome libraries of the OG, MA, and SH (hado)pelagic sediments, respectively. Only 24−30% of the sequence reads from each virome library exhibited significant similarities to the sequences deposited in the public nr protein database (E-value <10(−3) in BLAST). Among the sequences identified as potential viral genes based on the BLAST search, 95−99% of the sequence reads in each library were related to genes from single-stranded DNA (ssDNA) viral families, including Microviridae, Circoviridae, and Geminiviridae. A relatively high abundance of sequences related to the genetic markers (major capsid protein [VP1] and replication protein [Rep]) of two ssDNA viral groups were also detected in these libraries, thereby revealing a high genotypic diversity of their viruses (833 genotypes for VP1 and 2,551 genotypes for Rep). A majority of the viral genes predicted from each library were classified into three ssDNA viral protein categories: Rep, VP1, and minor capsid protein. The deep-sea sedimentary viromes were distinct from the viromes obtained from the oceanic and fresh waters and marine eukaryotes, and thus, deep-sea sediments harbor novel viromes, including previously unidentified ssDNA viruses. Public Library of Science 2013-02-27 /pmc/articles/PMC3584133/ /pubmed/23468952 http://dx.doi.org/10.1371/journal.pone.0057271 Text en © 2013 Yoshida 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Yoshida, Mitsuhiro
Takaki, Yoshihiro
Eitoku, Masamitsu
Nunoura, Takuro
Takai, Ken
Metagenomic Analysis of Viral Communities in (Hado)Pelagic Sediments
title Metagenomic Analysis of Viral Communities in (Hado)Pelagic Sediments
title_full Metagenomic Analysis of Viral Communities in (Hado)Pelagic Sediments
title_fullStr Metagenomic Analysis of Viral Communities in (Hado)Pelagic Sediments
title_full_unstemmed Metagenomic Analysis of Viral Communities in (Hado)Pelagic Sediments
title_short Metagenomic Analysis of Viral Communities in (Hado)Pelagic Sediments
title_sort metagenomic analysis of viral communities in (hado)pelagic sediments
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3584133/
https://www.ncbi.nlm.nih.gov/pubmed/23468952
http://dx.doi.org/10.1371/journal.pone.0057271
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