Molecular epidemiology of peste des petits ruminants virus emergence in critically endangered Mongolian saiga antelope and other wild ungulates.

PPR Global Eradication Programme PPR, saiga antelope PPRV emergence PPRV host range PPRV molecular epidemiology Phylogeography peste des petits ruminants virus wildlife-livestock interface

Journal

Virus evolution
ISSN: 2057-1577
Titre abrégé: Virus Evol
Pays: England
ID NLM: 101664675

Informations de publication

Date de publication:
2021
Historique:
received: 12 05 2021
revised: 18 06 2021
accepted: 24 06 2021
entrez: 10 11 2021
pubmed: 11 11 2021
medline: 11 11 2021
Statut: epublish

Résumé

Peste des petits ruminants virus (PPRV) causes disease in domestic and wild ungulates, is the target of a Global Eradication Programme, and threatens biodiversity. Understanding the epidemiology and evolution of PPRV in wildlife is important but hampered by the paucity of wildlife-origin PPRV genomes. In this study, full PPRV genomes were generated from three Mongolian saiga antelope, one Siberian ibex, and one goitered gazelle from the 2016-2017 PPRV outbreak. Phylogenetic analysis showed that for Mongolian and Chinese PPRV since 2013, the wildlife and livestock-origin genomes were closely related and interspersed. There was strong phylogenetic support for a monophyletic group of PPRV from Mongolian wildlife and livestock, belonging to a clade of lineage IV PPRV from livestock and wildlife from China since 2013. Discrete diffusion analysis found strong support for PPRV spread into Mongolia from China, and phylogeographic analysis indicated Xinjiang Province as the most likely origin, although genomic surveillance for PPRV is poor and lack of sampling from other regions could bias this result. Times of most recent common ancestor (TMRCA) were June 2015 (95 per cent highest posterior density (HPD): August 2014 to March 2016) for all Mongolian PPRV genomes and May 2016 (95 per cent HPD: October 2015 to October 2016) for Mongolian wildlife-origin PPRV. This suggests that PPRV was circulating undetected in Mongolia for at least 6 months before the first reported outbreak in August 2016 and that wildlife were likely infected before livestock vaccination began in October 2016. Finally, genetic variation and positively selected sites were identified that might be related to PPRV emergence in Mongolian wildlife. This study is the first to sequence multiple PPRV genomes from a wildlife outbreak, across several host species. Additional full PPRV genomes and associated metadata from the livestock-wildlife interface are needed to enhance the power of molecular epidemiology, support PPRV eradication, and safeguard the health of the whole ungulate community.

Identifiants

pubmed: 34754511
doi: 10.1093/ve/veab062
pii: veab062
pmc: PMC8570150
doi:

Types de publication

Journal Article

Langues

eng

Pagination

veab062

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press.

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Auteurs

Camilla T O Benfield (CTO)

Department of Pathobiology and Population Sciences, The Royal Veterinary College, Hatfield, AL9 7TA UK.

Sarah Hill (S)

Department of Pathobiology and Population Sciences, The Royal Veterinary College, Hatfield, AL9 7TA UK.

Munkduuren Shatar (M)

Department of Veterinary Services of Dundgobi province, General Authority for Veterinary Services of Mongolia (GAVS), Mandalgobi, Dundgobi Province 4800 Mongolia.

Enkhtuvshin Shiilegdamba (E)

Wildlife Conservation Society, Mongolia Program, Post Office 20A, PO Box 21 Ulaanbaatar 14200, Mongolia.

Batchuluun Damdinjav (B)

State Central Veterinary Laboratory, Ulaanbaatar 17024, Mongolia.

Amanda Fine (A)

Health Program, Wildlife Conservation Society, Bronx, New York 10460, USA.

Brian Willett (B)

MRC-University of Glasgow Centre for Virus Research, Henry Wellcome Building, Garscube Glasgow, G61 1QH UK.

Richard Kock (R)

Department of Pathobiology and Population Sciences, The Royal Veterinary College, Hatfield, AL9 7TA UK.

Arnaud Bataille (A)

CIRAD, UMR ASTRE, F-34398 Montpellier, France.

Classifications MeSH