Metabarcoding of Hepatitis E Virus Genotype 3 and Norovirus GII from Wastewater Samples in England Using Nanopore Sequencing.


Journal

Food and environmental virology
ISSN: 1867-0342
Titre abrégé: Food Environ Virol
Pays: United States
ID NLM: 101483831

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 20 05 2023
accepted: 29 09 2023
medline: 17 11 2023
pubmed: 1 11 2023
entrez: 1 11 2023
Statut: ppublish

Résumé

Norovirus is one of the largest causes of gastroenteritis worldwide, and Hepatitis E virus (HEV) is an emerging pathogen that has become the most dominant cause of acute viral hepatitis in recent years. The presence of norovirus and HEV has been reported within wastewater in many countries previously. Here we used amplicon deep sequencing (metabarcoding) to identify norovirus and HEV strains in wastewater samples from England collected in 2019 and 2020. For HEV, we sequenced a fragment of the RNA-dependent RNA polymerase (RdRp) gene targeting genotype three strains. For norovirus, we sequenced the 5' portion of the major capsid protein gene (VP1) of genogroup II strains. Sequencing of the wastewater samples revealed eight different genotypes of norovirus GII (GII.2, GII.3, GII.4, GII.6, GII.7, GII.9, GII.13 and GII.17). Genotypes GII.3 and GII.4 were the most commonly found. The HEV metabarcoding assay was able to identify HEV genotype 3 strains in some samples with a very low viral concentration determined by RT-qPCR. Analysis showed that most HEV strains found in influent wastewater were typed as G3c and G3e and were likely to have originated from humans or swine. However, the small size of the HEV nested PCR amplicon could cause issues with typing, and so this method is more appropriate for samples with high CTs where methods targeting longer genomic regions are unlikely to be successful. This is the first report of HEV RNA in wastewater in England. This study demonstrates the utility of wastewater sequencing and the need for wider surveillance of norovirus and HEV within host species and environments.

Identifiants

pubmed: 37910379
doi: 10.1007/s12560-023-09569-w
pii: 10.1007/s12560-023-09569-w
pmc: PMC7615314
mid: EMS190417
doi:

Substances chimiques

Wastewater 0
RNA, Viral 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

292-306

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 109356
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 109356/Z/15/Z
Pays : United Kingdom

Informations de copyright

© 2023. Crown.

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Auteurs

Samantha Treagus (S)

Centre for Environment, Fisheries and Aquaculture Science, Weymouth, UK. samantha.treagus2@ukhsa.gov.uk.
Centre for Ecology and Conservation, Faculty of Environment, Science and Economy, University of Exeter, Penryn Campus, Cornwall, UK. samantha.treagus2@ukhsa.gov.uk.
UK Health Security Agency, Manor Farm Road, Porton Down, SP4 0JG, Wiltshire, UK. samantha.treagus2@ukhsa.gov.uk.

James Lowther (J)

Centre for Environment, Fisheries and Aquaculture Science, Weymouth, UK.

Ben Longdon (B)

Centre for Ecology and Conservation, Faculty of Environment, Science and Economy, University of Exeter, Penryn Campus, Cornwall, UK.

William Gaze (W)

Faculty of Health and Life Sciences, University of Exeter Medical School, Penryn Campus, Cornwall, UK.

Craig Baker-Austin (C)

Centre for Environment, Fisheries and Aquaculture Science, Weymouth, UK.

David Ryder (D)

Centre for Environment, Fisheries and Aquaculture Science, Weymouth, UK.

Frederico M Batista (FM)

Centre for Environment, Fisheries and Aquaculture Science, Weymouth, UK.

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