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An evolutionary divergent pestivirus lacking the N(pro) gene systemically infects a whale species

Pestiviruses typically infect members of the order Artiodactyla, including ruminants and pigs, although putative rat and bat pestiviruses have also been described. In the present study, we identified and characterized an evolutionary divergent pestivirus in the toothed whale species, harbour porpois...

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Autores principales: Jo, Wendy K., van Elk, Cornelis, van de Bildt, Marco, van Run, Peter, Petry, Monique, Jesse, Sonja T., Jung, Klaus, Ludlow, Martin, Kuiken, Thijs, Osterhaus, Albert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6758615/
https://www.ncbi.nlm.nih.gov/pubmed/31526243
http://dx.doi.org/10.1080/22221751.2019.1664940
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author Jo, Wendy K.
van Elk, Cornelis
van de Bildt, Marco
van Run, Peter
Petry, Monique
Jesse, Sonja T.
Jung, Klaus
Ludlow, Martin
Kuiken, Thijs
Osterhaus, Albert
author_facet Jo, Wendy K.
van Elk, Cornelis
van de Bildt, Marco
van Run, Peter
Petry, Monique
Jesse, Sonja T.
Jung, Klaus
Ludlow, Martin
Kuiken, Thijs
Osterhaus, Albert
author_sort Jo, Wendy K.
collection PubMed
description Pestiviruses typically infect members of the order Artiodactyla, including ruminants and pigs, although putative rat and bat pestiviruses have also been described. In the present study, we identified and characterized an evolutionary divergent pestivirus in the toothed whale species, harbour porpoise (Phocoena phocoena). We tentatively named the virus Phocoena pestivirus (PhoPeV). PhoPeV displays a typical pestivirus genome organization except for the unique absence of N(pro), an N-terminal autoprotease that targets the innate host immune response. Evolutionary evidence indicates that PhoPeV emerged following an interspecies transmission event from an ancestral pestivirus that expressed N(pro). We show that 9% (n = 10) of stranded porpoises from the Dutch North Sea coast (n = 112) were positive for PhoPeV and they displayed a systemic infection reminiscent of non-cytopathogenic persistent pestivirus infection. The identification of PhoPeV extends the host range of pestiviruses to cetaceans (dolphins, whales, porpoises), which are considered to have evolved from artiodactyls (even-toed ungulates). Elucidation of the pathophysiology of PhoPeV infection and N(pro) unique absence will add to our understanding of molecular mechanisms governing pestivirus pathogenesis.
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spelling pubmed-67586152019-10-09 An evolutionary divergent pestivirus lacking the N(pro) gene systemically infects a whale species Jo, Wendy K. van Elk, Cornelis van de Bildt, Marco van Run, Peter Petry, Monique Jesse, Sonja T. Jung, Klaus Ludlow, Martin Kuiken, Thijs Osterhaus, Albert Emerg Microbes Infect Original Articles Pestiviruses typically infect members of the order Artiodactyla, including ruminants and pigs, although putative rat and bat pestiviruses have also been described. In the present study, we identified and characterized an evolutionary divergent pestivirus in the toothed whale species, harbour porpoise (Phocoena phocoena). We tentatively named the virus Phocoena pestivirus (PhoPeV). PhoPeV displays a typical pestivirus genome organization except for the unique absence of N(pro), an N-terminal autoprotease that targets the innate host immune response. Evolutionary evidence indicates that PhoPeV emerged following an interspecies transmission event from an ancestral pestivirus that expressed N(pro). We show that 9% (n = 10) of stranded porpoises from the Dutch North Sea coast (n = 112) were positive for PhoPeV and they displayed a systemic infection reminiscent of non-cytopathogenic persistent pestivirus infection. The identification of PhoPeV extends the host range of pestiviruses to cetaceans (dolphins, whales, porpoises), which are considered to have evolved from artiodactyls (even-toed ungulates). Elucidation of the pathophysiology of PhoPeV infection and N(pro) unique absence will add to our understanding of molecular mechanisms governing pestivirus pathogenesis. Taylor & Francis 2019-09-17 /pmc/articles/PMC6758615/ /pubmed/31526243 http://dx.doi.org/10.1080/22221751.2019.1664940 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Jo, Wendy K.
van Elk, Cornelis
van de Bildt, Marco
van Run, Peter
Petry, Monique
Jesse, Sonja T.
Jung, Klaus
Ludlow, Martin
Kuiken, Thijs
Osterhaus, Albert
An evolutionary divergent pestivirus lacking the N(pro) gene systemically infects a whale species
title An evolutionary divergent pestivirus lacking the N(pro) gene systemically infects a whale species
title_full An evolutionary divergent pestivirus lacking the N(pro) gene systemically infects a whale species
title_fullStr An evolutionary divergent pestivirus lacking the N(pro) gene systemically infects a whale species
title_full_unstemmed An evolutionary divergent pestivirus lacking the N(pro) gene systemically infects a whale species
title_short An evolutionary divergent pestivirus lacking the N(pro) gene systemically infects a whale species
title_sort evolutionary divergent pestivirus lacking the n(pro) gene systemically infects a whale species
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6758615/
https://www.ncbi.nlm.nih.gov/pubmed/31526243
http://dx.doi.org/10.1080/22221751.2019.1664940
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