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Host genetics determine susceptibility to avian influenza infection and transmission dynamics

Host-genetic control of influenza virus infection has been the object of little attention. In this study we determined that two inbred lines of chicken differing in their genetic background , Lines 0 and C-B12, were respectively relatively resistant and susceptible to infection with the low pathogen...

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Autores principales: Ruiz-Hernandez, Raul, Mwangi, William, Peroval, Marylene, Sadeyen, Jean-Remy, Ascough, Stephanie, Balkissoon, Devanand, Staines, Karen, Boyd, Amy, McCauley, John, Smith, Adrian, Butter, Colin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899695/
https://www.ncbi.nlm.nih.gov/pubmed/27279280
http://dx.doi.org/10.1038/srep26787
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author Ruiz-Hernandez, Raul
Mwangi, William
Peroval, Marylene
Sadeyen, Jean-Remy
Ascough, Stephanie
Balkissoon, Devanand
Staines, Karen
Boyd, Amy
McCauley, John
Smith, Adrian
Butter, Colin
author_facet Ruiz-Hernandez, Raul
Mwangi, William
Peroval, Marylene
Sadeyen, Jean-Remy
Ascough, Stephanie
Balkissoon, Devanand
Staines, Karen
Boyd, Amy
McCauley, John
Smith, Adrian
Butter, Colin
author_sort Ruiz-Hernandez, Raul
collection PubMed
description Host-genetic control of influenza virus infection has been the object of little attention. In this study we determined that two inbred lines of chicken differing in their genetic background , Lines 0 and C-B12, were respectively relatively resistant and susceptible to infection with the low pathogenicity influenza virus A/Turkey/England/647/77 as defined by substantial differences in viral shedding trajectories. Resistant birds, although infected, were unable to transmit virus to contact birds, as ultimately only the presence of a sustained cloacal shedding (and not oropharyngeal shedding) was critical for transmission. Restriction of within-bird transmission of virus occurred in the resistant line, with intra-nares or cloacal infection resulting in only local shedding and failing to transmit fully through the gastro-intestinal-pulmonary tract. Resistance to infection was independent of adaptive immune responses, including the expansion of specific IFNγ secreting cells or production of influenza-specific antibody. Genetic resistance to a novel H9N2 virus was less robust, though significant differences between host genotypes were still clearly evident. The existence of host-genetic determination of the outcome of influenza infection offers tools for the further dissection of this regulation and also for understanding the mechanisms of influenza transmission within and between birds.
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spelling pubmed-48996952016-06-13 Host genetics determine susceptibility to avian influenza infection and transmission dynamics Ruiz-Hernandez, Raul Mwangi, William Peroval, Marylene Sadeyen, Jean-Remy Ascough, Stephanie Balkissoon, Devanand Staines, Karen Boyd, Amy McCauley, John Smith, Adrian Butter, Colin Sci Rep Article Host-genetic control of influenza virus infection has been the object of little attention. In this study we determined that two inbred lines of chicken differing in their genetic background , Lines 0 and C-B12, were respectively relatively resistant and susceptible to infection with the low pathogenicity influenza virus A/Turkey/England/647/77 as defined by substantial differences in viral shedding trajectories. Resistant birds, although infected, were unable to transmit virus to contact birds, as ultimately only the presence of a sustained cloacal shedding (and not oropharyngeal shedding) was critical for transmission. Restriction of within-bird transmission of virus occurred in the resistant line, with intra-nares or cloacal infection resulting in only local shedding and failing to transmit fully through the gastro-intestinal-pulmonary tract. Resistance to infection was independent of adaptive immune responses, including the expansion of specific IFNγ secreting cells or production of influenza-specific antibody. Genetic resistance to a novel H9N2 virus was less robust, though significant differences between host genotypes were still clearly evident. The existence of host-genetic determination of the outcome of influenza infection offers tools for the further dissection of this regulation and also for understanding the mechanisms of influenza transmission within and between birds. Nature Publishing Group 2016-06-09 /pmc/articles/PMC4899695/ /pubmed/27279280 http://dx.doi.org/10.1038/srep26787 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Ruiz-Hernandez, Raul
Mwangi, William
Peroval, Marylene
Sadeyen, Jean-Remy
Ascough, Stephanie
Balkissoon, Devanand
Staines, Karen
Boyd, Amy
McCauley, John
Smith, Adrian
Butter, Colin
Host genetics determine susceptibility to avian influenza infection and transmission dynamics
title Host genetics determine susceptibility to avian influenza infection and transmission dynamics
title_full Host genetics determine susceptibility to avian influenza infection and transmission dynamics
title_fullStr Host genetics determine susceptibility to avian influenza infection and transmission dynamics
title_full_unstemmed Host genetics determine susceptibility to avian influenza infection and transmission dynamics
title_short Host genetics determine susceptibility to avian influenza infection and transmission dynamics
title_sort host genetics determine susceptibility to avian influenza infection and transmission dynamics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899695/
https://www.ncbi.nlm.nih.gov/pubmed/27279280
http://dx.doi.org/10.1038/srep26787
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