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Isolation and mutation trend analysis of influenza A virus subtype H9N2 in Egypt

BACKGROUND: Avian influenza virus H9N2 is a panzootic pathogen that affects poultry causing mild to moderate respiratory distress but has been associated with high morbidity and considerable mortality. Interspecies transmission of H9N2 from avian species to mammalian hosts does occur. The virus poss...

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Autores principales: Abdel-Moneim, Ahmed S, Afifi, Manal A, El-Kady, Magdy F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492205/
https://www.ncbi.nlm.nih.gov/pubmed/22925485
http://dx.doi.org/10.1186/1743-422X-9-173
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author Abdel-Moneim, Ahmed S
Afifi, Manal A
El-Kady, Magdy F
author_facet Abdel-Moneim, Ahmed S
Afifi, Manal A
El-Kady, Magdy F
author_sort Abdel-Moneim, Ahmed S
collection PubMed
description BACKGROUND: Avian influenza virus H9N2 is a panzootic pathogen that affects poultry causing mild to moderate respiratory distress but has been associated with high morbidity and considerable mortality. Interspecies transmission of H9N2 from avian species to mammalian hosts does occur. The virus possesses human virus-like receptor specificity and it can infect humans producing flu-like illness. METHODS: Recently, mild influenza like symptoms were detected in H5N1 vaccinated flocks. Influenza A subtype H9N2 was isolated from the infected flock. The virus evolution was investigated by sequencing the viral genes to screen the possible virus recombination. The viral amino acid sequences from the isolated H9N2 strains were compared to other related sequences from the flu data base that were used to assess the robustness of the mutation trend. Changes in the species-associated amino acid residues or those that enabled virulence to mammals were allocated. RESULTS: Phylogenetic analyses of haemagglutinin and neuraminidase genes showed that the recently isolated Egyptian strain belonged to the H9N2 sub-lineage that prevails in Israel. The six internal segments of the isolated virus were found to be derived from the same sub-lineage with no new evidence of reassortment. The results demonstrated conserved genetic and biological constitution of H9N2 viruses in the Middle East. The recently isolated H9N2 virus from chicken in Egypt possessed amino acids that could enable the virus to replicate in mammals and caused severe disease in domestic chickens. CONCLUSION: The study highlights the importance of continuous monitoring of the mutations evolved in avian influenza viruses and its impact on virulence to avian species in addition to its importance in the emergence of new strains with the capacity to be a pandemic candidate.
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spelling pubmed-34922052012-11-08 Isolation and mutation trend analysis of influenza A virus subtype H9N2 in Egypt Abdel-Moneim, Ahmed S Afifi, Manal A El-Kady, Magdy F Virol J Research BACKGROUND: Avian influenza virus H9N2 is a panzootic pathogen that affects poultry causing mild to moderate respiratory distress but has been associated with high morbidity and considerable mortality. Interspecies transmission of H9N2 from avian species to mammalian hosts does occur. The virus possesses human virus-like receptor specificity and it can infect humans producing flu-like illness. METHODS: Recently, mild influenza like symptoms were detected in H5N1 vaccinated flocks. Influenza A subtype H9N2 was isolated from the infected flock. The virus evolution was investigated by sequencing the viral genes to screen the possible virus recombination. The viral amino acid sequences from the isolated H9N2 strains were compared to other related sequences from the flu data base that were used to assess the robustness of the mutation trend. Changes in the species-associated amino acid residues or those that enabled virulence to mammals were allocated. RESULTS: Phylogenetic analyses of haemagglutinin and neuraminidase genes showed that the recently isolated Egyptian strain belonged to the H9N2 sub-lineage that prevails in Israel. The six internal segments of the isolated virus were found to be derived from the same sub-lineage with no new evidence of reassortment. The results demonstrated conserved genetic and biological constitution of H9N2 viruses in the Middle East. The recently isolated H9N2 virus from chicken in Egypt possessed amino acids that could enable the virus to replicate in mammals and caused severe disease in domestic chickens. CONCLUSION: The study highlights the importance of continuous monitoring of the mutations evolved in avian influenza viruses and its impact on virulence to avian species in addition to its importance in the emergence of new strains with the capacity to be a pandemic candidate. BioMed Central 2012-08-27 /pmc/articles/PMC3492205/ /pubmed/22925485 http://dx.doi.org/10.1186/1743-422X-9-173 Text en Copyright ©2012 Abdel-Moneim et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Abdel-Moneim, Ahmed S
Afifi, Manal A
El-Kady, Magdy F
Isolation and mutation trend analysis of influenza A virus subtype H9N2 in Egypt
title Isolation and mutation trend analysis of influenza A virus subtype H9N2 in Egypt
title_full Isolation and mutation trend analysis of influenza A virus subtype H9N2 in Egypt
title_fullStr Isolation and mutation trend analysis of influenza A virus subtype H9N2 in Egypt
title_full_unstemmed Isolation and mutation trend analysis of influenza A virus subtype H9N2 in Egypt
title_short Isolation and mutation trend analysis of influenza A virus subtype H9N2 in Egypt
title_sort isolation and mutation trend analysis of influenza a virus subtype h9n2 in egypt
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492205/
https://www.ncbi.nlm.nih.gov/pubmed/22925485
http://dx.doi.org/10.1186/1743-422X-9-173
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