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Adaptation of avian influenza virus to a swine host
The emergence of pathogenic RNA viruses into new hosts can have dramatic consequences for both livestock and public health. Here we characterize the viral genetic changes that were observed in a previous study which experimentally adapted a field isolate of duck influenza virus to swine respiratory...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399929/ https://www.ncbi.nlm.nih.gov/pubmed/28458917 http://dx.doi.org/10.1093/ve/vex007 |
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author | Bourret, Vincent Lyall, Jon Frost, Simon D W Teillaud, Angélique Smith, Catherine A Leclaire, Sarah Fu, JinQi Gandon, Sylvain Guérin, Jean-Luc Tiley, Laurence S |
author_facet | Bourret, Vincent Lyall, Jon Frost, Simon D W Teillaud, Angélique Smith, Catherine A Leclaire, Sarah Fu, JinQi Gandon, Sylvain Guérin, Jean-Luc Tiley, Laurence S |
author_sort | Bourret, Vincent |
collection | PubMed |
description | The emergence of pathogenic RNA viruses into new hosts can have dramatic consequences for both livestock and public health. Here we characterize the viral genetic changes that were observed in a previous study which experimentally adapted a field isolate of duck influenza virus to swine respiratory cells. Both pre-existing and de novo mutations were selected during this adaptation. We compare the in vitro growth dynamics of the adapted virus with those of the original strain as well as all possible reassortants using reverse genetics. This full factorial design showed that viral gene segments are involved in complex epistatic interactions on virus fitness, including negative and sign epistasis. We also identify two point mutations at positions 67 and 113 of the HA2 subunit of the hemagglutinin protein conferring a fast growth phenotype on the naïve avian virus in swine cells. These HA2 mutations enhance the pH dependent, HA-mediated membrane fusion. A global H1 maximum-likelihood phylogenetic analysis, combined with comprehensive ancestry reconstruction and tests for directional selection, confirmed the field relevance of the mutation at position 113 of HA2. Most notably, this mutation was associated with the establishment of the H1 ‘avian-like’ swine influenza lineage, regarded as the most likely to cause the next influenza pandemic in humans. This multidisciplinary approach to study the genetics of viral adaptation provides unique insights on the underlying processes leading to influenza emergence in a new host species, and identifies specific targets for future surveillance and functional studies. |
format | Online Article Text |
id | pubmed-5399929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-53999292017-04-28 Adaptation of avian influenza virus to a swine host Bourret, Vincent Lyall, Jon Frost, Simon D W Teillaud, Angélique Smith, Catherine A Leclaire, Sarah Fu, JinQi Gandon, Sylvain Guérin, Jean-Luc Tiley, Laurence S Virus Evol Research Article The emergence of pathogenic RNA viruses into new hosts can have dramatic consequences for both livestock and public health. Here we characterize the viral genetic changes that were observed in a previous study which experimentally adapted a field isolate of duck influenza virus to swine respiratory cells. Both pre-existing and de novo mutations were selected during this adaptation. We compare the in vitro growth dynamics of the adapted virus with those of the original strain as well as all possible reassortants using reverse genetics. This full factorial design showed that viral gene segments are involved in complex epistatic interactions on virus fitness, including negative and sign epistasis. We also identify two point mutations at positions 67 and 113 of the HA2 subunit of the hemagglutinin protein conferring a fast growth phenotype on the naïve avian virus in swine cells. These HA2 mutations enhance the pH dependent, HA-mediated membrane fusion. A global H1 maximum-likelihood phylogenetic analysis, combined with comprehensive ancestry reconstruction and tests for directional selection, confirmed the field relevance of the mutation at position 113 of HA2. Most notably, this mutation was associated with the establishment of the H1 ‘avian-like’ swine influenza lineage, regarded as the most likely to cause the next influenza pandemic in humans. This multidisciplinary approach to study the genetics of viral adaptation provides unique insights on the underlying processes leading to influenza emergence in a new host species, and identifies specific targets for future surveillance and functional studies. Oxford University Press 2017-03-18 /pmc/articles/PMC5399929/ /pubmed/28458917 http://dx.doi.org/10.1093/ve/vex007 Text en © The Author 2017. Published by Oxford University Press. http://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/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Bourret, Vincent Lyall, Jon Frost, Simon D W Teillaud, Angélique Smith, Catherine A Leclaire, Sarah Fu, JinQi Gandon, Sylvain Guérin, Jean-Luc Tiley, Laurence S Adaptation of avian influenza virus to a swine host |
title | Adaptation of avian influenza virus to a swine host |
title_full | Adaptation of avian influenza virus to a swine host |
title_fullStr | Adaptation of avian influenza virus to a swine host |
title_full_unstemmed | Adaptation of avian influenza virus to a swine host |
title_short | Adaptation of avian influenza virus to a swine host |
title_sort | adaptation of avian influenza virus to a swine host |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399929/ https://www.ncbi.nlm.nih.gov/pubmed/28458917 http://dx.doi.org/10.1093/ve/vex007 |
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