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Susceptibility of swine to H5 and H7 low pathogenic avian influenza viruses

BACKGROUND: The ability of pigs to become infected with low pathogenic avian influenza (LPAI) viruses and then generate mammalian adaptable influenza A viruses is difficult to determine. Yet, it is an important link to understanding any relationship between LPAI virus ecology and possible epidemics...

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Autores principales: Balzli, Charles, Lager, Kelly, Vincent, Amy, Gauger, Phillip, Brockmeier, Susan, Miller, Laura, Richt, Juergen A, Ma, Wenjun, Suarez, David, Swayne, David E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910171/
https://www.ncbi.nlm.nih.gov/pubmed/26946338
http://dx.doi.org/10.1111/irv.12386
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author Balzli, Charles
Lager, Kelly
Vincent, Amy
Gauger, Phillip
Brockmeier, Susan
Miller, Laura
Richt, Juergen A
Ma, Wenjun
Suarez, David
Swayne, David E
author_facet Balzli, Charles
Lager, Kelly
Vincent, Amy
Gauger, Phillip
Brockmeier, Susan
Miller, Laura
Richt, Juergen A
Ma, Wenjun
Suarez, David
Swayne, David E
author_sort Balzli, Charles
collection PubMed
description BACKGROUND: The ability of pigs to become infected with low pathogenic avian influenza (LPAI) viruses and then generate mammalian adaptable influenza A viruses is difficult to determine. Yet, it is an important link to understanding any relationship between LPAI virus ecology and possible epidemics among swine and/or humans. OBJECTIVES: Assess susceptibility of pigs to LPAI viruses found within the United States and their direct contact transmission potential. METHODS: Pigs were inoculated with one of ten H5 or H7 LPAI viruses selected from seven different bird species to test infectivity, virulence, pathogenesis, and potential to transmit virus to contact pigs through histological, RRT‐PCR and seroconversion data. RESULTS: Although pigs were susceptible to infection with each of the LPAI viruses, no clinical disease was recognized in any pig. During the acute phase of the infection, minor pulmonary lesions were found in some pigs and one or more pigs in each group were RRT‐PCR‐positive in the lower respiratory tract, but no virus was detected in upper respiratory tract (negative nasal swabs). Except for one group, one or more pigs in each LPAI group developed antibody. No LPAI viruses transmitted to contact pigs. CONCLUSIONS: LPAI strains from various bird populations within the United States are capable of infecting pigs. Although adaptability and transmission of individual strains seem unlikely, the subclinical nature of the infections demonstrates the need to improve sampling and testing methods to more accurately measure incidence of LPAI virus infection in pigs, and their potential role in human‐zoonotic LPAI virus dynamics.
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spelling pubmed-49101712016-07-01 Susceptibility of swine to H5 and H7 low pathogenic avian influenza viruses Balzli, Charles Lager, Kelly Vincent, Amy Gauger, Phillip Brockmeier, Susan Miller, Laura Richt, Juergen A Ma, Wenjun Suarez, David Swayne, David E Influenza Other Respir Viruses Original Articles BACKGROUND: The ability of pigs to become infected with low pathogenic avian influenza (LPAI) viruses and then generate mammalian adaptable influenza A viruses is difficult to determine. Yet, it is an important link to understanding any relationship between LPAI virus ecology and possible epidemics among swine and/or humans. OBJECTIVES: Assess susceptibility of pigs to LPAI viruses found within the United States and their direct contact transmission potential. METHODS: Pigs were inoculated with one of ten H5 or H7 LPAI viruses selected from seven different bird species to test infectivity, virulence, pathogenesis, and potential to transmit virus to contact pigs through histological, RRT‐PCR and seroconversion data. RESULTS: Although pigs were susceptible to infection with each of the LPAI viruses, no clinical disease was recognized in any pig. During the acute phase of the infection, minor pulmonary lesions were found in some pigs and one or more pigs in each group were RRT‐PCR‐positive in the lower respiratory tract, but no virus was detected in upper respiratory tract (negative nasal swabs). Except for one group, one or more pigs in each LPAI group developed antibody. No LPAI viruses transmitted to contact pigs. CONCLUSIONS: LPAI strains from various bird populations within the United States are capable of infecting pigs. Although adaptability and transmission of individual strains seem unlikely, the subclinical nature of the infections demonstrates the need to improve sampling and testing methods to more accurately measure incidence of LPAI virus infection in pigs, and their potential role in human‐zoonotic LPAI virus dynamics. John Wiley and Sons Inc. 2016-04-05 2016-07 /pmc/articles/PMC4910171/ /pubmed/26946338 http://dx.doi.org/10.1111/irv.12386 Text en © 2016 The Authors. Influenza and Other Respiratory Viruses Published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Balzli, Charles
Lager, Kelly
Vincent, Amy
Gauger, Phillip
Brockmeier, Susan
Miller, Laura
Richt, Juergen A
Ma, Wenjun
Suarez, David
Swayne, David E
Susceptibility of swine to H5 and H7 low pathogenic avian influenza viruses
title Susceptibility of swine to H5 and H7 low pathogenic avian influenza viruses
title_full Susceptibility of swine to H5 and H7 low pathogenic avian influenza viruses
title_fullStr Susceptibility of swine to H5 and H7 low pathogenic avian influenza viruses
title_full_unstemmed Susceptibility of swine to H5 and H7 low pathogenic avian influenza viruses
title_short Susceptibility of swine to H5 and H7 low pathogenic avian influenza viruses
title_sort susceptibility of swine to h5 and h7 low pathogenic avian influenza viruses
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910171/
https://www.ncbi.nlm.nih.gov/pubmed/26946338
http://dx.doi.org/10.1111/irv.12386
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