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Driving forces behind the evolution of the Aleutian mink disease parvovirus in the context of intensive farming
Aleutian mink disease virus (AMDV) causes plasmacytosis, an immune complex-associated syndrome that affects wild and farmed mink. The virus can also infect other small mammals (e.g., ferrets, skunks, ermines, and raccoons), but the disease in these hosts has been studied less. In 2007, a mink plasma...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989880/ https://www.ncbi.nlm.nih.gov/pubmed/27774297 http://dx.doi.org/10.1093/ve/vew004 |
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author | Canuti, Marta O’Leary, Kimberly E. Hunter, Bruce D. Spearman, Grant Ojkic, Davor Whitney, Hugh G. Lang, Andrew S. |
author_facet | Canuti, Marta O’Leary, Kimberly E. Hunter, Bruce D. Spearman, Grant Ojkic, Davor Whitney, Hugh G. Lang, Andrew S. |
author_sort | Canuti, Marta |
collection | PubMed |
description | Aleutian mink disease virus (AMDV) causes plasmacytosis, an immune complex-associated syndrome that affects wild and farmed mink. The virus can also infect other small mammals (e.g., ferrets, skunks, ermines, and raccoons), but the disease in these hosts has been studied less. In 2007, a mink plasmacytosis outbreak began on the Island of Newfoundland, and the virus has been endemic in farms since then. In this study, we evaluated the molecular epidemiology of AMDV in farmed and wild animals of Newfoundland since before the beginning of the outbreak and investigated the epidemic in a global context by studying AMDV worldwide, thereby examining its diffusion and phylogeography. Furthermore, AMDV evolution was examined in the context of intensive farming, where host population dynamics strongly influence viral evolution. Partial NS1 sequences and several complete genomes were obtained from Newfoundland viruses and analyzed along with numerous sequences from other locations worldwide that were either obtained as part of this study or from public databases. We observed very high viral diversity within Newfoundland and within single farms, where high rates of co-infection, recombinant viruses and polymorphisms were observed within single infected individuals. Worldwide, we documented a partial geographic distribution of strains, where viruses from different countries co-exist within clades but form country-specific subclades. Finally, we observed the occurrence of recombination and the predominance of negative selection pressure on AMDV proteins. A surprisingly low number of immunoepitopic sites were under diversifying pressure, possibly because AMDV gains no benefit by escaping the immune response as viral entry into target cells is mediated through interactions with antibodies, which therefore contribute to cell infection. In conclusion, the high prevalence of AMDV in farms facilitates the establishment of co-infections that can favor the occurrence of recombination and enhance viral diversity. Viruses are then exchanged between different farms and countries and can be introduced into the wild, with the rapidly evolving viruses producing many parallel lineages. |
format | Online Article Text |
id | pubmed-4989880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49898802016-10-21 Driving forces behind the evolution of the Aleutian mink disease parvovirus in the context of intensive farming Canuti, Marta O’Leary, Kimberly E. Hunter, Bruce D. Spearman, Grant Ojkic, Davor Whitney, Hugh G. Lang, Andrew S. Virus Evol Research Article Aleutian mink disease virus (AMDV) causes plasmacytosis, an immune complex-associated syndrome that affects wild and farmed mink. The virus can also infect other small mammals (e.g., ferrets, skunks, ermines, and raccoons), but the disease in these hosts has been studied less. In 2007, a mink plasmacytosis outbreak began on the Island of Newfoundland, and the virus has been endemic in farms since then. In this study, we evaluated the molecular epidemiology of AMDV in farmed and wild animals of Newfoundland since before the beginning of the outbreak and investigated the epidemic in a global context by studying AMDV worldwide, thereby examining its diffusion and phylogeography. Furthermore, AMDV evolution was examined in the context of intensive farming, where host population dynamics strongly influence viral evolution. Partial NS1 sequences and several complete genomes were obtained from Newfoundland viruses and analyzed along with numerous sequences from other locations worldwide that were either obtained as part of this study or from public databases. We observed very high viral diversity within Newfoundland and within single farms, where high rates of co-infection, recombinant viruses and polymorphisms were observed within single infected individuals. Worldwide, we documented a partial geographic distribution of strains, where viruses from different countries co-exist within clades but form country-specific subclades. Finally, we observed the occurrence of recombination and the predominance of negative selection pressure on AMDV proteins. A surprisingly low number of immunoepitopic sites were under diversifying pressure, possibly because AMDV gains no benefit by escaping the immune response as viral entry into target cells is mediated through interactions with antibodies, which therefore contribute to cell infection. In conclusion, the high prevalence of AMDV in farms facilitates the establishment of co-infections that can favor the occurrence of recombination and enhance viral diversity. Viruses are then exchanged between different farms and countries and can be introduced into the wild, with the rapidly evolving viruses producing many parallel lineages. Oxford University Press 2016-02-27 /pmc/articles/PMC4989880/ /pubmed/27774297 http://dx.doi.org/10.1093/ve/vew004 Text en © The Author 2016. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Canuti, Marta O’Leary, Kimberly E. Hunter, Bruce D. Spearman, Grant Ojkic, Davor Whitney, Hugh G. Lang, Andrew S. Driving forces behind the evolution of the Aleutian mink disease parvovirus in the context of intensive farming |
title | Driving forces behind the evolution of the Aleutian mink disease parvovirus in the context of intensive farming |
title_full | Driving forces behind the evolution of the Aleutian mink disease parvovirus in the context of intensive farming |
title_fullStr | Driving forces behind the evolution of the Aleutian mink disease parvovirus in the context of intensive farming |
title_full_unstemmed | Driving forces behind the evolution of the Aleutian mink disease parvovirus in the context of intensive farming |
title_short | Driving forces behind the evolution of the Aleutian mink disease parvovirus in the context of intensive farming |
title_sort | driving forces behind the evolution of the aleutian mink disease parvovirus in the context of intensive farming |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989880/ https://www.ncbi.nlm.nih.gov/pubmed/27774297 http://dx.doi.org/10.1093/ve/vew004 |
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