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What happened after the initial global spread of pandemic human influenza virus A (H1N1)? A population genetics approach
Viral population evolution dynamics of influenza A is crucial for surveillance and control. In this paper we analyzed viral genetic features during the recent pandemic caused by the new influenza human virus A H1N1, using a conventional population genetics approach based on 4689 hemagglutinin (HA) a...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936310/ https://www.ncbi.nlm.nih.gov/pubmed/20727188 http://dx.doi.org/10.1186/1743-422X-7-196 |
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author | Martinez-Hernandez, Fernando Jimenez-Gonzalez, Diego Emiliano Martinez-Flores, Arony Villalobos-Castillejos, Guiehdani Vaughan, Gilberto Kawa-Karasik, Simon Flisser, Ana Maravilla, Pablo Romero-Valdovinos, Mirza |
author_facet | Martinez-Hernandez, Fernando Jimenez-Gonzalez, Diego Emiliano Martinez-Flores, Arony Villalobos-Castillejos, Guiehdani Vaughan, Gilberto Kawa-Karasik, Simon Flisser, Ana Maravilla, Pablo Romero-Valdovinos, Mirza |
author_sort | Martinez-Hernandez, Fernando |
collection | PubMed |
description | Viral population evolution dynamics of influenza A is crucial for surveillance and control. In this paper we analyzed viral genetic features during the recent pandemic caused by the new influenza human virus A H1N1, using a conventional population genetics approach based on 4689 hemagglutinin (HA) and neuraminidase (NA) sequences available in GenBank submitted between March and December of 2009. This analysis showed several relevant aspects: a) a scarce initial genetic variability within the viral isolates from some countries that increased along 2009 when influenza was dispersed around the world; b) a worldwide virus polarized behavior identified when comparing paired countries, low differentiation and high gene flow were found in some pairs and high differentiation and moderate or scarce gene flow in others, independently of their geographical closeness, c) lack of positive selection in HA and NA due to increase of the population size of virus variants, d) HA and NA variants spread in a few months all over the world being identified in the same countries in different months along 2009, and e) containment of viral variants in Mexico at the beginning of the outbreak, probably due to the control measures applied by the government. |
format | Text |
id | pubmed-2936310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29363102010-09-10 What happened after the initial global spread of pandemic human influenza virus A (H1N1)? A population genetics approach Martinez-Hernandez, Fernando Jimenez-Gonzalez, Diego Emiliano Martinez-Flores, Arony Villalobos-Castillejos, Guiehdani Vaughan, Gilberto Kawa-Karasik, Simon Flisser, Ana Maravilla, Pablo Romero-Valdovinos, Mirza Virol J Short Report Viral population evolution dynamics of influenza A is crucial for surveillance and control. In this paper we analyzed viral genetic features during the recent pandemic caused by the new influenza human virus A H1N1, using a conventional population genetics approach based on 4689 hemagglutinin (HA) and neuraminidase (NA) sequences available in GenBank submitted between March and December of 2009. This analysis showed several relevant aspects: a) a scarce initial genetic variability within the viral isolates from some countries that increased along 2009 when influenza was dispersed around the world; b) a worldwide virus polarized behavior identified when comparing paired countries, low differentiation and high gene flow were found in some pairs and high differentiation and moderate or scarce gene flow in others, independently of their geographical closeness, c) lack of positive selection in HA and NA due to increase of the population size of virus variants, d) HA and NA variants spread in a few months all over the world being identified in the same countries in different months along 2009, and e) containment of viral variants in Mexico at the beginning of the outbreak, probably due to the control measures applied by the government. BioMed Central 2010-08-20 /pmc/articles/PMC2936310/ /pubmed/20727188 http://dx.doi.org/10.1186/1743-422X-7-196 Text en Copyright ©2010 Martinez-Hernandez 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 | Short Report Martinez-Hernandez, Fernando Jimenez-Gonzalez, Diego Emiliano Martinez-Flores, Arony Villalobos-Castillejos, Guiehdani Vaughan, Gilberto Kawa-Karasik, Simon Flisser, Ana Maravilla, Pablo Romero-Valdovinos, Mirza What happened after the initial global spread of pandemic human influenza virus A (H1N1)? A population genetics approach |
title | What happened after the initial global spread of pandemic human influenza virus A (H1N1)? A population genetics approach |
title_full | What happened after the initial global spread of pandemic human influenza virus A (H1N1)? A population genetics approach |
title_fullStr | What happened after the initial global spread of pandemic human influenza virus A (H1N1)? A population genetics approach |
title_full_unstemmed | What happened after the initial global spread of pandemic human influenza virus A (H1N1)? A population genetics approach |
title_short | What happened after the initial global spread of pandemic human influenza virus A (H1N1)? A population genetics approach |
title_sort | what happened after the initial global spread of pandemic human influenza virus a (h1n1)? a population genetics approach |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936310/ https://www.ncbi.nlm.nih.gov/pubmed/20727188 http://dx.doi.org/10.1186/1743-422X-7-196 |
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