Metavirome Sequencing to Evaluate Norovirus Diversity in Sewage and Related Bioaccumulated Oysters.

metagenomic sequencing metavirome norovirus oysters sewage

Journal

Frontiers in microbiology
ISSN: 1664-302X
Titre abrégé: Front Microbiol
Pays: Switzerland
ID NLM: 101548977

Informations de publication

Date de publication:
2019
Historique:
received: 24 07 2019
accepted: 03 10 2019
entrez: 5 11 2019
pubmed: 5 11 2019
medline: 5 11 2019
Statut: epublish

Résumé

Metagenomic sequencing is a promising method to determine the virus diversity in environmental samples such as sewage or shellfish. However, to identify the short RNA genomes of human enteric viruses among the large diversity of nucleic acids present in such complex matrices, method optimization is still needed. This work presents methodological developments focused on norovirus, a small ssRNA non-enveloped virus known as the major cause of human gastroenteritis worldwide and frequently present in human excreta and sewage. Different elution protocols were applied and Illumina MiSeq technology were used to study norovirus diversity. A double approach, agnostic deep sequencing and a capture-based approach (VirCapSeq-VERT) was used to identify norovirus in environmental samples. Family-specific viral contigs were classified and sorted by SLIM and final norovirus contigs were genotyped using the online Norovirus genotyping tool v2.0. From sewage samples, 14 norovirus genogroup I sequences were identified of which six were complete genomes. For norovirus genogroup II, nine sequences were identified and three of them comprised more than half of the genome. In oyster samples bioaccumulated with these sewage samples, only the use of an enrichment step during library preparation allowed successful identification of nine different sequences of norovirus genogroup I and four for genogroup II (>500 bp). This study demonstrates the importance of method development to increase virus recovery, and the interest of a capture-based approach to be able to identify viruses present at low concentrations.

Identifiants

pubmed: 31681246
doi: 10.3389/fmicb.2019.02394
pmc: PMC6811496
doi:

Types de publication

Journal Article

Langues

eng

Pagination

2394

Informations de copyright

Copyright © 2019 Strubbia, Schaeffer, Oude Munnink, Besnard, Phan, Nieuwenhuijse, de Graaf, Schapendonk, Wacrenier, Cotten, Koopmans and Le Guyader.

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Auteurs

Sofia Strubbia (S)

Laboratoire de Microbiologie, LSEM-SG2M-RBE, Ifremer, Nantes, France.

Julien Schaeffer (J)

Laboratoire de Microbiologie, LSEM-SG2M-RBE, Ifremer, Nantes, France.

Bas B Oude Munnink (BB)

Department of Viroscience, Erasmus University Medical Center, Rotterdam, Netherlands.

Alban Besnard (A)

Laboratoire de Microbiologie, LSEM-SG2M-RBE, Ifremer, Nantes, France.

My V T Phan (MVT)

Department of Viroscience, Erasmus University Medical Center, Rotterdam, Netherlands.

David F Nieuwenhuijse (DF)

Department of Viroscience, Erasmus University Medical Center, Rotterdam, Netherlands.

Miranda de Graaf (M)

Department of Viroscience, Erasmus University Medical Center, Rotterdam, Netherlands.

Claudia M E Schapendonk (CME)

Department of Viroscience, Erasmus University Medical Center, Rotterdam, Netherlands.

Candice Wacrenier (C)

Laboratoire de Microbiologie, LSEM-SG2M-RBE, Ifremer, Nantes, France.

Matthew Cotten (M)

Department of Viroscience, Erasmus University Medical Center, Rotterdam, Netherlands.

Marion P G Koopmans (MPG)

Department of Viroscience, Erasmus University Medical Center, Rotterdam, Netherlands.

Françoise S Le Guyader (FS)

Laboratoire de Microbiologie, LSEM-SG2M-RBE, Ifremer, Nantes, France.

Classifications MeSH