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Transmission of influenza A(H1N1) 2009 pandemic viruses in Australian swine

Please cite this paper as: Deng et al. (2012). Transmission of influenza A(H1N1) 2009 pandemic viruses in Australian swine. Influenza and Other Respiratory Viruses 6(3), e42–e47. Background  Swine have receptors for both human and avian influenza viruses and are a natural host for influenza A viruse...

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Autores principales: Deng, Yi‐Mo, Iannello, Pina, Smith, Ina, Watson, James, Barr, Ian G., Daniels, Peter, Komadina, Naomi, Harrower, Bruce, Wong, Frank Y. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4941678/
https://www.ncbi.nlm.nih.gov/pubmed/22336333
http://dx.doi.org/10.1111/j.1750-2659.2012.00337.x
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author Deng, Yi‐Mo
Iannello, Pina
Smith, Ina
Watson, James
Barr, Ian G.
Daniels, Peter
Komadina, Naomi
Harrower, Bruce
Wong, Frank Y. K.
author_facet Deng, Yi‐Mo
Iannello, Pina
Smith, Ina
Watson, James
Barr, Ian G.
Daniels, Peter
Komadina, Naomi
Harrower, Bruce
Wong, Frank Y. K.
author_sort Deng, Yi‐Mo
collection PubMed
description Please cite this paper as: Deng et al. (2012). Transmission of influenza A(H1N1) 2009 pandemic viruses in Australian swine. Influenza and Other Respiratory Viruses 6(3), e42–e47. Background  Swine have receptors for both human and avian influenza viruses and are a natural host for influenza A viruses. The 2009 influenza A(H1N1) pandemic (H1N1pdm) virus that was derived from avian, human and swine influenza viruses has infected pigs in various countries. Objectives  To investigate the relationship between the H1N1pdm viruses isolated from piggery outbreaks in Australia and human samples associated with one of the outbreaks by phylogenetic analysis, and to determine whether there was any reassortment event occurring during the human‐pig interspecies transmission. Methods  Real‐time RT‐PCR and full genome sequencing were carried out on RNA isolated from nasal swabs and/or virus cultures. Phylogenetic analysis was performed using the Geneious package. Results  The influenza H1N1pdm outbreaks were detected in three pig farms located in three different states in Australia. Further analysis of the Queensland outbreak led to the identification of two distinct virus strains in the pigs. Two staff working in the same piggery were also infected with the same two strains found in the pigs. Full genome sequence analysis on the viruses isolated from pigs and humans did not identify any reassortment of these H1N1pdm viruses with seasonal or avian influenza A viruses. Conclusions  This is the first report of swine infected with influenza in Australia and marked the end of the influenza‐free era for the Australian swine industry. Although no reassortment was detected in these cases, the ability of these viruses to cross between pigs and humans highlights the importance of monitoring swine for novel influenza infections.
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spelling pubmed-49416782016-07-18 Transmission of influenza A(H1N1) 2009 pandemic viruses in Australian swine Deng, Yi‐Mo Iannello, Pina Smith, Ina Watson, James Barr, Ian G. Daniels, Peter Komadina, Naomi Harrower, Bruce Wong, Frank Y. K. Influenza Other Respir Viruses Part 2 (E‐only) Please cite this paper as: Deng et al. (2012). Transmission of influenza A(H1N1) 2009 pandemic viruses in Australian swine. Influenza and Other Respiratory Viruses 6(3), e42–e47. Background  Swine have receptors for both human and avian influenza viruses and are a natural host for influenza A viruses. The 2009 influenza A(H1N1) pandemic (H1N1pdm) virus that was derived from avian, human and swine influenza viruses has infected pigs in various countries. Objectives  To investigate the relationship between the H1N1pdm viruses isolated from piggery outbreaks in Australia and human samples associated with one of the outbreaks by phylogenetic analysis, and to determine whether there was any reassortment event occurring during the human‐pig interspecies transmission. Methods  Real‐time RT‐PCR and full genome sequencing were carried out on RNA isolated from nasal swabs and/or virus cultures. Phylogenetic analysis was performed using the Geneious package. Results  The influenza H1N1pdm outbreaks were detected in three pig farms located in three different states in Australia. Further analysis of the Queensland outbreak led to the identification of two distinct virus strains in the pigs. Two staff working in the same piggery were also infected with the same two strains found in the pigs. Full genome sequence analysis on the viruses isolated from pigs and humans did not identify any reassortment of these H1N1pdm viruses with seasonal or avian influenza A viruses. Conclusions  This is the first report of swine infected with influenza in Australia and marked the end of the influenza‐free era for the Australian swine industry. Although no reassortment was detected in these cases, the ability of these viruses to cross between pigs and humans highlights the importance of monitoring swine for novel influenza infections. Blackwell Publishing Ltd 2012-02-15 2012-05 /pmc/articles/PMC4941678/ /pubmed/22336333 http://dx.doi.org/10.1111/j.1750-2659.2012.00337.x Text en © 2012 Blackwell Publishing Ltd
spellingShingle Part 2 (E‐only)
Deng, Yi‐Mo
Iannello, Pina
Smith, Ina
Watson, James
Barr, Ian G.
Daniels, Peter
Komadina, Naomi
Harrower, Bruce
Wong, Frank Y. K.
Transmission of influenza A(H1N1) 2009 pandemic viruses in Australian swine
title Transmission of influenza A(H1N1) 2009 pandemic viruses in Australian swine
title_full Transmission of influenza A(H1N1) 2009 pandemic viruses in Australian swine
title_fullStr Transmission of influenza A(H1N1) 2009 pandemic viruses in Australian swine
title_full_unstemmed Transmission of influenza A(H1N1) 2009 pandemic viruses in Australian swine
title_short Transmission of influenza A(H1N1) 2009 pandemic viruses in Australian swine
title_sort transmission of influenza a(h1n1) 2009 pandemic viruses in australian swine
topic Part 2 (E‐only)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4941678/
https://www.ncbi.nlm.nih.gov/pubmed/22336333
http://dx.doi.org/10.1111/j.1750-2659.2012.00337.x
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