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Valine/isoleucine variants drive selective pressure in the VP1 sequence of EV-A71 enteroviruses

BACKGROUND: In 2011–2012, Northern Vietnam experienced its first large scale hand foot and mouth disease (HFMD) epidemic. In 2011, a major HFMD epidemic was also reported in South Vietnam with fatal cases. This 2011–2012 outbreak was the first one to occur in North Vietnam providing grounds to study...

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Autores principales: Duy, Nghia Ngu, Huong, Le Thi Thanh, Ravel, Patrice, Huong, Le Thi Song, Dwivedi, Ankit, Sessions, October Michael, Hou, Yan’An, Chua, Robert, Kister, Guilhem, Afelt, Aneta, Moulia, Catherine, Gubler, Duane J., Thiem, Vu Dinh, Thanh, Nguyen Thi Hien, Devaux, Christian, Duong, Tran Nhu, Hien, Nguyen Tran, Cornillot, Emmanuel, Gavotte, Laurent, Frutos, Roger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5422960/
https://www.ncbi.nlm.nih.gov/pubmed/28482808
http://dx.doi.org/10.1186/s12879-017-2427-4
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author Duy, Nghia Ngu
Huong, Le Thi Thanh
Ravel, Patrice
Huong, Le Thi Song
Dwivedi, Ankit
Sessions, October Michael
Hou, Yan’An
Chua, Robert
Kister, Guilhem
Afelt, Aneta
Moulia, Catherine
Gubler, Duane J.
Thiem, Vu Dinh
Thanh, Nguyen Thi Hien
Devaux, Christian
Duong, Tran Nhu
Hien, Nguyen Tran
Cornillot, Emmanuel
Gavotte, Laurent
Frutos, Roger
author_facet Duy, Nghia Ngu
Huong, Le Thi Thanh
Ravel, Patrice
Huong, Le Thi Song
Dwivedi, Ankit
Sessions, October Michael
Hou, Yan’An
Chua, Robert
Kister, Guilhem
Afelt, Aneta
Moulia, Catherine
Gubler, Duane J.
Thiem, Vu Dinh
Thanh, Nguyen Thi Hien
Devaux, Christian
Duong, Tran Nhu
Hien, Nguyen Tran
Cornillot, Emmanuel
Gavotte, Laurent
Frutos, Roger
author_sort Duy, Nghia Ngu
collection PubMed
description BACKGROUND: In 2011–2012, Northern Vietnam experienced its first large scale hand foot and mouth disease (HFMD) epidemic. In 2011, a major HFMD epidemic was also reported in South Vietnam with fatal cases. This 2011–2012 outbreak was the first one to occur in North Vietnam providing grounds to study the etiology, origin and dynamic of the disease. We report here the analysis of the VP1 gene of strains isolated throughout North Vietnam during the 2011–2012 outbreak and before. METHODS: The VP1 gene of 106 EV-A71 isolates from North Vietnam and 2 from Central Vietnam were sequenced. Sequence alignments were analyzed at the nucleic acid and protein level. Gene polymorphism was also analyzed. A Factorial Correspondence Analysis was performed to correlate amino acid mutations with clinical parameters. RESULTS: The sequences were distributed into four phylogenetic clusters. Three clusters corresponded to the subgenogroup C4 and the last one corresponded to the subgenogroup C5. Each cluster displayed different polymorphism characteristics. Proteins were highly conserved but three sites bearing only Isoleucine (I) or Valine (V) were characterized. The isoleucine/valine variability matched the clusters. Spatiotemporal analysis of the I/V variants showed that all variants which emerged in 2011 and then in 2012 were not the same but were all present in the region prior to the 2011–2012 outbreak. Some correlation was found between certain I/V variants and ethnicity and severity. CONCLUSIONS: The 2011–2012 outbreak was not caused by an exogenous strain coming from South Vietnam or elsewhere but by strains already present and circulating at low level in North Vietnam. However, what triggered the outbreak remains unclear. A selective pressure is applied on I/V variants which matches the genetic clusters. I/V variants were shown on other viruses to correlate with pathogenicity. This should be investigated in EV-A71. I/V variants are an easy and efficient way to survey and identify circulating EV-A71 strains. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-017-2427-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-54229602017-05-12 Valine/isoleucine variants drive selective pressure in the VP1 sequence of EV-A71 enteroviruses Duy, Nghia Ngu Huong, Le Thi Thanh Ravel, Patrice Huong, Le Thi Song Dwivedi, Ankit Sessions, October Michael Hou, Yan’An Chua, Robert Kister, Guilhem Afelt, Aneta Moulia, Catherine Gubler, Duane J. Thiem, Vu Dinh Thanh, Nguyen Thi Hien Devaux, Christian Duong, Tran Nhu Hien, Nguyen Tran Cornillot, Emmanuel Gavotte, Laurent Frutos, Roger BMC Infect Dis Research Article BACKGROUND: In 2011–2012, Northern Vietnam experienced its first large scale hand foot and mouth disease (HFMD) epidemic. In 2011, a major HFMD epidemic was also reported in South Vietnam with fatal cases. This 2011–2012 outbreak was the first one to occur in North Vietnam providing grounds to study the etiology, origin and dynamic of the disease. We report here the analysis of the VP1 gene of strains isolated throughout North Vietnam during the 2011–2012 outbreak and before. METHODS: The VP1 gene of 106 EV-A71 isolates from North Vietnam and 2 from Central Vietnam were sequenced. Sequence alignments were analyzed at the nucleic acid and protein level. Gene polymorphism was also analyzed. A Factorial Correspondence Analysis was performed to correlate amino acid mutations with clinical parameters. RESULTS: The sequences were distributed into four phylogenetic clusters. Three clusters corresponded to the subgenogroup C4 and the last one corresponded to the subgenogroup C5. Each cluster displayed different polymorphism characteristics. Proteins were highly conserved but three sites bearing only Isoleucine (I) or Valine (V) were characterized. The isoleucine/valine variability matched the clusters. Spatiotemporal analysis of the I/V variants showed that all variants which emerged in 2011 and then in 2012 were not the same but were all present in the region prior to the 2011–2012 outbreak. Some correlation was found between certain I/V variants and ethnicity and severity. CONCLUSIONS: The 2011–2012 outbreak was not caused by an exogenous strain coming from South Vietnam or elsewhere but by strains already present and circulating at low level in North Vietnam. However, what triggered the outbreak remains unclear. A selective pressure is applied on I/V variants which matches the genetic clusters. I/V variants were shown on other viruses to correlate with pathogenicity. This should be investigated in EV-A71. I/V variants are an easy and efficient way to survey and identify circulating EV-A71 strains. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-017-2427-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-05-08 /pmc/articles/PMC5422960/ /pubmed/28482808 http://dx.doi.org/10.1186/s12879-017-2427-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Duy, Nghia Ngu
Huong, Le Thi Thanh
Ravel, Patrice
Huong, Le Thi Song
Dwivedi, Ankit
Sessions, October Michael
Hou, Yan’An
Chua, Robert
Kister, Guilhem
Afelt, Aneta
Moulia, Catherine
Gubler, Duane J.
Thiem, Vu Dinh
Thanh, Nguyen Thi Hien
Devaux, Christian
Duong, Tran Nhu
Hien, Nguyen Tran
Cornillot, Emmanuel
Gavotte, Laurent
Frutos, Roger
Valine/isoleucine variants drive selective pressure in the VP1 sequence of EV-A71 enteroviruses
title Valine/isoleucine variants drive selective pressure in the VP1 sequence of EV-A71 enteroviruses
title_full Valine/isoleucine variants drive selective pressure in the VP1 sequence of EV-A71 enteroviruses
title_fullStr Valine/isoleucine variants drive selective pressure in the VP1 sequence of EV-A71 enteroviruses
title_full_unstemmed Valine/isoleucine variants drive selective pressure in the VP1 sequence of EV-A71 enteroviruses
title_short Valine/isoleucine variants drive selective pressure in the VP1 sequence of EV-A71 enteroviruses
title_sort valine/isoleucine variants drive selective pressure in the vp1 sequence of ev-a71 enteroviruses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5422960/
https://www.ncbi.nlm.nih.gov/pubmed/28482808
http://dx.doi.org/10.1186/s12879-017-2427-4
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