Detection and genomic characterization of hepatitis E virus genotype 3 from pigs in Ghana, Africa.

Foodborne diseases Infectious disease reservoirs Livestock One health Viral hepatitis Zoonoses

Journal

One health outlook
ISSN: 2524-4655
Titre abrégé: One Health Outlook
Pays: England
ID NLM: 101769253

Informations de publication

Date de publication:
2020
Historique:
received: 10 01 2020
accepted: 05 05 2020
entrez: 8 4 2021
pubmed: 9 4 2021
medline: 9 4 2021
Statut: epublish

Résumé

Hepatitis E virus (HEV) is a major cause of human hepatitis worldwide. Zoonotic genotypes of the virus have been found in diverse animal species with pigs playing a major role. Putative risk of zoonotic infection from livestock particularly swine in Sub-Saharan Africa including Ghana is poorly understood due to scarcity of available data, especially HEV sequence information. Serum samples were collected from cattle, sheep, goats and pigs from Kumasi in the Ashanti region of Ghana. Samples were subjected to nested RT-PCR screening and quantification of HEV RNA-positive samples using real-time RT-PCR and the World Health Organization International Standard for HEV. Testing of all pig samples for antibodies was done by ELISA. Sanger sequencing and genotyping was performed and one representative complete genome was generated to facilitate genome-wide comparison to other available African HEV sequences by phylogenetic analysis. A total of 420 samples were available from cattle ( HEV genotype 3 is highly endemic in pigs in Ghana and likely poses a zoonotic risk to people exposed to pigs. HEV genotype 3 in Ghana shares a common origin with other virus strains from Sub-Saharan Africa.

Sections du résumé

BACKGROUND BACKGROUND
Hepatitis E virus (HEV) is a major cause of human hepatitis worldwide. Zoonotic genotypes of the virus have been found in diverse animal species with pigs playing a major role. Putative risk of zoonotic infection from livestock particularly swine in Sub-Saharan Africa including Ghana is poorly understood due to scarcity of available data, especially HEV sequence information.
METHODS METHODS
Serum samples were collected from cattle, sheep, goats and pigs from Kumasi in the Ashanti region of Ghana. Samples were subjected to nested RT-PCR screening and quantification of HEV RNA-positive samples using real-time RT-PCR and the World Health Organization International Standard for HEV. Testing of all pig samples for antibodies was done by ELISA. Sanger sequencing and genotyping was performed and one representative complete genome was generated to facilitate genome-wide comparison to other available African HEV sequences by phylogenetic analysis.
RESULTS RESULTS
A total of 420 samples were available from cattle (
CONCLUSION CONCLUSIONS
HEV genotype 3 is highly endemic in pigs in Ghana and likely poses a zoonotic risk to people exposed to pigs. HEV genotype 3 in Ghana shares a common origin with other virus strains from Sub-Saharan Africa.

Identifiants

pubmed: 33829131
doi: 10.1186/s42522-020-00018-3
pii: 18
pmc: PMC7993477
doi:

Types de publication

Journal Article

Langues

eng

Pagination

10

Informations de copyright

© The Author(s) 2020.

Déclaration de conflit d'intérêts

Competing interestsThe authors declare that they have no competing interests.

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Auteurs

Philip El-Duah (P)

Charité-Universitätsmedizin Berlin, Humboldt-Universität zu Berlin, Berlin Institute of Health, Institute of Virology, Berlin, Germany.
Kumasi Centre for Collaborative Research in Tropical Medicine, Kumasi, Ghana.

Dickson Dei (D)

Ghana Veterinary Service, Kumasi, Ghana.
School of Veterinary Medicine, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

Tabea Binger (T)

Kumasi Centre for Collaborative Research in Tropical Medicine, Kumasi, Ghana.

Augustina Sylverken (A)

Kumasi Centre for Collaborative Research in Tropical Medicine, Kumasi, Ghana.
Department of Theoretical and Applied Biology, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

Robert Wollny (R)

Institute of Virology, University of Bonn Medical Centre, Bonn, Germany.

William Tasiame (W)

Charité-Universitätsmedizin Berlin, Humboldt-Universität zu Berlin, Berlin Institute of Health, Institute of Virology, Berlin, Germany.
School of Veterinary Medicine, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

Samuel Oppong (S)

Department of Wildlife and Range Management, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

Yaw Adu-Sarkodie (Y)

Department of Clinical Microbiology, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

Benjamin Emikpe (B)

School of Veterinary Medicine, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

Raphael Folitse (R)

School of Veterinary Medicine, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

Jan Felix Drexler (JF)

Charité-Universitätsmedizin Berlin, Humboldt-Universität zu Berlin, Berlin Institute of Health, Institute of Virology, Berlin, Germany.

Richard Phillips (R)

Kumasi Centre for Collaborative Research in Tropical Medicine, Kumasi, Ghana.

Christian Drosten (C)

Charité-Universitätsmedizin Berlin, Humboldt-Universität zu Berlin, Berlin Institute of Health, Institute of Virology, Berlin, Germany.
German Centre for Infection Research, Berlin, Germany.

Victor Max Corman (VM)

Charité-Universitätsmedizin Berlin, Humboldt-Universität zu Berlin, Berlin Institute of Health, Institute of Virology, Berlin, Germany.
German Centre for Infection Research, Berlin, Germany.

Classifications MeSH