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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
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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. |
format | Online Article Text |
id | pubmed-6758615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
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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