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Different evolutionary trends of swine H1N2 influenza viruses in Italy compared to European viruses

European H1N2 swine influenza viruses (EU H1N2SIVs) arose from multiple reassortment events among human H1N1, human H3N2, and avian influenza viruses. We investigated the evolutionary dynamics of 53 Italian H1N2 strains by comparing them with EU H1N2 SIVs. Hemagglutinin (HA) phylogeny revealed Itali...

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Autores principales: Moreno, Ana, Gabanelli, Elena, Sozzi, Enrica, Lelli, Davide, Chiapponi, Chiara, Ciccozzi, Massimo, Zehender, Gianguglielmo, Cordioli, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4176092/
https://www.ncbi.nlm.nih.gov/pubmed/24289094
http://dx.doi.org/10.1186/1297-9716-44-112
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author Moreno, Ana
Gabanelli, Elena
Sozzi, Enrica
Lelli, Davide
Chiapponi, Chiara
Ciccozzi, Massimo
Zehender, Gianguglielmo
Cordioli, Paolo
author_facet Moreno, Ana
Gabanelli, Elena
Sozzi, Enrica
Lelli, Davide
Chiapponi, Chiara
Ciccozzi, Massimo
Zehender, Gianguglielmo
Cordioli, Paolo
author_sort Moreno, Ana
collection PubMed
description European H1N2 swine influenza viruses (EU H1N2SIVs) arose from multiple reassortment events among human H1N1, human H3N2, and avian influenza viruses. We investigated the evolutionary dynamics of 53 Italian H1N2 strains by comparing them with EU H1N2 SIVs. Hemagglutinin (HA) phylogeny revealed Italian strains fell into four groups: Group A and B (41 strains) had a human H1 similar to EU H1N2SIVs, which probably originated in 1986. However Group B (38 strains) formed a subgroup that had a two-amino acid deletion at positions 146/147 in HA. Group C (11 strains) contained an avian H1 that probably originated in 1996, and Group D (1 strain) had an H1 characteristic of the 2009 pandemic strain. Neuraminidase (NA) phylogeny suggested a series of genomic reassortments had occurred. Group A had an N2 that originated from human H3N2 in the late 1970s. Group B had different human N2 that most likely arose from a reassortment with the more recent human H3N2 virus, which probably occurred in 2000. Group C had an avian-like H1 combined with an N2 gene from one of EU H1N2SIVs, EU H3N2SIVs or Human H3N2. Group D was part of the EU H3N2SIVs clade. Although selection pressure for HA and NA was low, several positively selected sites were identified in both proteins, some of which were antigenic, suggesting selection influenced the evolution of SIV. The data highlight different evolutionary trends between European viruses and currently circulating Italian B strains and show the establishment of reassortant strains involving human viruses in Italian pigs.
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spelling pubmed-41760922014-09-27 Different evolutionary trends of swine H1N2 influenza viruses in Italy compared to European viruses Moreno, Ana Gabanelli, Elena Sozzi, Enrica Lelli, Davide Chiapponi, Chiara Ciccozzi, Massimo Zehender, Gianguglielmo Cordioli, Paolo Vet Res Research European H1N2 swine influenza viruses (EU H1N2SIVs) arose from multiple reassortment events among human H1N1, human H3N2, and avian influenza viruses. We investigated the evolutionary dynamics of 53 Italian H1N2 strains by comparing them with EU H1N2 SIVs. Hemagglutinin (HA) phylogeny revealed Italian strains fell into four groups: Group A and B (41 strains) had a human H1 similar to EU H1N2SIVs, which probably originated in 1986. However Group B (38 strains) formed a subgroup that had a two-amino acid deletion at positions 146/147 in HA. Group C (11 strains) contained an avian H1 that probably originated in 1996, and Group D (1 strain) had an H1 characteristic of the 2009 pandemic strain. Neuraminidase (NA) phylogeny suggested a series of genomic reassortments had occurred. Group A had an N2 that originated from human H3N2 in the late 1970s. Group B had different human N2 that most likely arose from a reassortment with the more recent human H3N2 virus, which probably occurred in 2000. Group C had an avian-like H1 combined with an N2 gene from one of EU H1N2SIVs, EU H3N2SIVs or Human H3N2. Group D was part of the EU H3N2SIVs clade. Although selection pressure for HA and NA was low, several positively selected sites were identified in both proteins, some of which were antigenic, suggesting selection influenced the evolution of SIV. The data highlight different evolutionary trends between European viruses and currently circulating Italian B strains and show the establishment of reassortant strains involving human viruses in Italian pigs. BioMed Central 2013 2013-12-01 /pmc/articles/PMC4176092/ /pubmed/24289094 http://dx.doi.org/10.1186/1297-9716-44-112 Text en Copyright © 2013 Moreno 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
Moreno, Ana
Gabanelli, Elena
Sozzi, Enrica
Lelli, Davide
Chiapponi, Chiara
Ciccozzi, Massimo
Zehender, Gianguglielmo
Cordioli, Paolo
Different evolutionary trends of swine H1N2 influenza viruses in Italy compared to European viruses
title Different evolutionary trends of swine H1N2 influenza viruses in Italy compared to European viruses
title_full Different evolutionary trends of swine H1N2 influenza viruses in Italy compared to European viruses
title_fullStr Different evolutionary trends of swine H1N2 influenza viruses in Italy compared to European viruses
title_full_unstemmed Different evolutionary trends of swine H1N2 influenza viruses in Italy compared to European viruses
title_short Different evolutionary trends of swine H1N2 influenza viruses in Italy compared to European viruses
title_sort different evolutionary trends of swine h1n2 influenza viruses in italy compared to european viruses
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4176092/
https://www.ncbi.nlm.nih.gov/pubmed/24289094
http://dx.doi.org/10.1186/1297-9716-44-112
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