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Mutations in the non-structural protein region contribute to intra-genotypic evolution of enterovirus 71
BACKGROUND: Clinical manifestations of enterovirus 71 (EV71) range from herpangina, hand-foot-and-mouth disease (HFMD), to severe neurological complications. Unlike the situation of switching genotypes seen in EV71 outbreaks during 1998–2008 in Taiwan, genotype B5 was responsible for two large outbr...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021180/ https://www.ncbi.nlm.nih.gov/pubmed/24766641 http://dx.doi.org/10.1186/1423-0127-21-33 |
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author | Huang, Sheng-Wen Cheng, Hui-Li Hsieh, Hsin-Yi Chang, Chia-Lun Tsai, Huey-Pin Kuo, Pin-Hwa Wang, Shih-Min Liu, Ching-Chuan Su, Ih-Jen Wang, Jen-Ren |
author_facet | Huang, Sheng-Wen Cheng, Hui-Li Hsieh, Hsin-Yi Chang, Chia-Lun Tsai, Huey-Pin Kuo, Pin-Hwa Wang, Shih-Min Liu, Ching-Chuan Su, Ih-Jen Wang, Jen-Ren |
author_sort | Huang, Sheng-Wen |
collection | PubMed |
description | BACKGROUND: Clinical manifestations of enterovirus 71 (EV71) range from herpangina, hand-foot-and-mouth disease (HFMD), to severe neurological complications. Unlike the situation of switching genotypes seen in EV71 outbreaks during 1998–2008 in Taiwan, genotype B5 was responsible for two large outbreaks in 2008 and 2012, respectively. In China, by contrast, EV71 often persists as a single genotype in the population and causes frequent outbreaks. To investigate genetic changes in viral evolution, complete EV71 genome sequences were used to analyze the intra-genotypic evolution pattern in Taiwan, China, and the Netherlands. RESULTS: Genotype B5 was predominant in Taiwan’s 2008 outbreak and was re-emergent in 2012. EV71 strains from both outbreaks were phylogenetically segregated into two lineages containing fourteen non-synonymous substitutions predominantly in the non-structural protein coding region. In China, genotype C4 was first seen in 1998 and caused the latest large outbreak in 2008. Unlike shifting genotypes in Taiwan, genotype C4 persisted with progressive drift through time. A majority of non-synonymous mutations occurred in residues located in the non-structural coding region, showing annual increases. Interestingly, genotype B1/B2 in the Netherlands showed another stepwise evolution with dramatic EV71 activity increase in 1986. Phylogeny of the VP1 coding region in 1971–1986 exhibited similar lineage turnover with genotype C4 in China; however, phylogeny of the 3D-encoding region indicated separate lineage appearing after 1983, suggesting that the 3D-encoding region of genotype B2 was derived from an unidentified ancestor that contributed to intra-genotypic evolution in the Netherlands. CONCLUSIONS: Unlike VP1 coding sequences long used for phylogenetic study of enteroviruses due to expected host immune escape, our study emphasizes a dominant role of non-synonymous mutations in non-structural protein regions that contribute to (re-)emergent genotypes in continuous stepwise evolution. Dozens of amino acid substitutions, especially in non-structural proteins, were identified via genetic changes driven through intra-genotypic evolution worldwide. These identified substitutions appeared to increase viral fitness in the population, affording valuable insights not only for viral evolution but also for prevention, control, and vaccine against EV71 infection. |
format | Online Article Text |
id | pubmed-4021180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40211802014-05-16 Mutations in the non-structural protein region contribute to intra-genotypic evolution of enterovirus 71 Huang, Sheng-Wen Cheng, Hui-Li Hsieh, Hsin-Yi Chang, Chia-Lun Tsai, Huey-Pin Kuo, Pin-Hwa Wang, Shih-Min Liu, Ching-Chuan Su, Ih-Jen Wang, Jen-Ren J Biomed Sci Research BACKGROUND: Clinical manifestations of enterovirus 71 (EV71) range from herpangina, hand-foot-and-mouth disease (HFMD), to severe neurological complications. Unlike the situation of switching genotypes seen in EV71 outbreaks during 1998–2008 in Taiwan, genotype B5 was responsible for two large outbreaks in 2008 and 2012, respectively. In China, by contrast, EV71 often persists as a single genotype in the population and causes frequent outbreaks. To investigate genetic changes in viral evolution, complete EV71 genome sequences were used to analyze the intra-genotypic evolution pattern in Taiwan, China, and the Netherlands. RESULTS: Genotype B5 was predominant in Taiwan’s 2008 outbreak and was re-emergent in 2012. EV71 strains from both outbreaks were phylogenetically segregated into two lineages containing fourteen non-synonymous substitutions predominantly in the non-structural protein coding region. In China, genotype C4 was first seen in 1998 and caused the latest large outbreak in 2008. Unlike shifting genotypes in Taiwan, genotype C4 persisted with progressive drift through time. A majority of non-synonymous mutations occurred in residues located in the non-structural coding region, showing annual increases. Interestingly, genotype B1/B2 in the Netherlands showed another stepwise evolution with dramatic EV71 activity increase in 1986. Phylogeny of the VP1 coding region in 1971–1986 exhibited similar lineage turnover with genotype C4 in China; however, phylogeny of the 3D-encoding region indicated separate lineage appearing after 1983, suggesting that the 3D-encoding region of genotype B2 was derived from an unidentified ancestor that contributed to intra-genotypic evolution in the Netherlands. CONCLUSIONS: Unlike VP1 coding sequences long used for phylogenetic study of enteroviruses due to expected host immune escape, our study emphasizes a dominant role of non-synonymous mutations in non-structural protein regions that contribute to (re-)emergent genotypes in continuous stepwise evolution. Dozens of amino acid substitutions, especially in non-structural proteins, were identified via genetic changes driven through intra-genotypic evolution worldwide. These identified substitutions appeared to increase viral fitness in the population, affording valuable insights not only for viral evolution but also for prevention, control, and vaccine against EV71 infection. BioMed Central 2014-04-26 /pmc/articles/PMC4021180/ /pubmed/24766641 http://dx.doi.org/10.1186/1423-0127-21-33 Text en Copyright © 2014 Huang 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 credited. 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 Huang, Sheng-Wen Cheng, Hui-Li Hsieh, Hsin-Yi Chang, Chia-Lun Tsai, Huey-Pin Kuo, Pin-Hwa Wang, Shih-Min Liu, Ching-Chuan Su, Ih-Jen Wang, Jen-Ren Mutations in the non-structural protein region contribute to intra-genotypic evolution of enterovirus 71 |
title | Mutations in the non-structural protein region contribute to intra-genotypic evolution of enterovirus 71 |
title_full | Mutations in the non-structural protein region contribute to intra-genotypic evolution of enterovirus 71 |
title_fullStr | Mutations in the non-structural protein region contribute to intra-genotypic evolution of enterovirus 71 |
title_full_unstemmed | Mutations in the non-structural protein region contribute to intra-genotypic evolution of enterovirus 71 |
title_short | Mutations in the non-structural protein region contribute to intra-genotypic evolution of enterovirus 71 |
title_sort | mutations in the non-structural protein region contribute to intra-genotypic evolution of enterovirus 71 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021180/ https://www.ncbi.nlm.nih.gov/pubmed/24766641 http://dx.doi.org/10.1186/1423-0127-21-33 |
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