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Monitoring Antigenic Variations of Enterovirus 71: Implications for Virus Surveillance and Vaccine Development

Enterovirus 71 (EV71) causes life-threatening epidemics in Asia and can be phylogenetically classified into three major genogroups (A∼C) including 11 genotypes (A, B1∼B5, and C1∼C5). Recently, EV71 epidemics occurred cyclically in Taiwan with different genotypes. In recent years, human studies using...

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Autores principales: Chia, Min-Yuan, Chung, Wan-Yu, Chiang, Pai-Shan, Chien, Yeh-Sheng, Ho, Mei-Shang, Lee, Min-Shi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4109910/
https://www.ncbi.nlm.nih.gov/pubmed/25058733
http://dx.doi.org/10.1371/journal.pntd.0003044
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author Chia, Min-Yuan
Chung, Wan-Yu
Chiang, Pai-Shan
Chien, Yeh-Sheng
Ho, Mei-Shang
Lee, Min-Shi
author_facet Chia, Min-Yuan
Chung, Wan-Yu
Chiang, Pai-Shan
Chien, Yeh-Sheng
Ho, Mei-Shang
Lee, Min-Shi
author_sort Chia, Min-Yuan
collection PubMed
description Enterovirus 71 (EV71) causes life-threatening epidemics in Asia and can be phylogenetically classified into three major genogroups (A∼C) including 11 genotypes (A, B1∼B5, and C1∼C5). Recently, EV71 epidemics occurred cyclically in Taiwan with different genotypes. In recent years, human studies using post-infection sera obtained from children have detected antigenic variations among different EV71 strains. Therefore, surveillance of enterovirus 71 should include phylogenetic and antigenic analysis. Due to limitation of sera available from children with EV71 primary infection, suitable animal models should be developed to generate a panel of antisera for monitoring EV71 antigenic variations. Twelve reference strains representing the 11 EV71 genotypes were grown in rhabdomyosarcoma cells. Infectious EV71 particles were purified and collected to immunize rabbits. The rabbit antisera were then employed to measure neutralizing antibody titers against the 12 reference strains and 5 recent strains. Rabbits immunized with genogroup B and C viruses consistently have a lower neutralizing antibody titers against genogroup A (≧8-fold difference) and antigenic variations between genogroup B and C viruses can be detected but did not have a clear pattern, which are consistent with previous human studies. Comparison between human and rabbit neutralizing antibody profiles, the results showed that ≧8-fold difference in rabbit cross-reactive antibody ratios could be used to screen EV71 isolates for identifying potential antigenic variants. In conclusion, a rabbit model was developed to monitor antigenic variations of EV71, which are critical to select vaccine strains and predict epidemics.
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spelling pubmed-41099102014-07-29 Monitoring Antigenic Variations of Enterovirus 71: Implications for Virus Surveillance and Vaccine Development Chia, Min-Yuan Chung, Wan-Yu Chiang, Pai-Shan Chien, Yeh-Sheng Ho, Mei-Shang Lee, Min-Shi PLoS Negl Trop Dis Research Article Enterovirus 71 (EV71) causes life-threatening epidemics in Asia and can be phylogenetically classified into three major genogroups (A∼C) including 11 genotypes (A, B1∼B5, and C1∼C5). Recently, EV71 epidemics occurred cyclically in Taiwan with different genotypes. In recent years, human studies using post-infection sera obtained from children have detected antigenic variations among different EV71 strains. Therefore, surveillance of enterovirus 71 should include phylogenetic and antigenic analysis. Due to limitation of sera available from children with EV71 primary infection, suitable animal models should be developed to generate a panel of antisera for monitoring EV71 antigenic variations. Twelve reference strains representing the 11 EV71 genotypes were grown in rhabdomyosarcoma cells. Infectious EV71 particles were purified and collected to immunize rabbits. The rabbit antisera were then employed to measure neutralizing antibody titers against the 12 reference strains and 5 recent strains. Rabbits immunized with genogroup B and C viruses consistently have a lower neutralizing antibody titers against genogroup A (≧8-fold difference) and antigenic variations between genogroup B and C viruses can be detected but did not have a clear pattern, which are consistent with previous human studies. Comparison between human and rabbit neutralizing antibody profiles, the results showed that ≧8-fold difference in rabbit cross-reactive antibody ratios could be used to screen EV71 isolates for identifying potential antigenic variants. In conclusion, a rabbit model was developed to monitor antigenic variations of EV71, which are critical to select vaccine strains and predict epidemics. Public Library of Science 2014-07-24 /pmc/articles/PMC4109910/ /pubmed/25058733 http://dx.doi.org/10.1371/journal.pntd.0003044 Text en © 2014 Chia et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chia, Min-Yuan
Chung, Wan-Yu
Chiang, Pai-Shan
Chien, Yeh-Sheng
Ho, Mei-Shang
Lee, Min-Shi
Monitoring Antigenic Variations of Enterovirus 71: Implications for Virus Surveillance and Vaccine Development
title Monitoring Antigenic Variations of Enterovirus 71: Implications for Virus Surveillance and Vaccine Development
title_full Monitoring Antigenic Variations of Enterovirus 71: Implications for Virus Surveillance and Vaccine Development
title_fullStr Monitoring Antigenic Variations of Enterovirus 71: Implications for Virus Surveillance and Vaccine Development
title_full_unstemmed Monitoring Antigenic Variations of Enterovirus 71: Implications for Virus Surveillance and Vaccine Development
title_short Monitoring Antigenic Variations of Enterovirus 71: Implications for Virus Surveillance and Vaccine Development
title_sort monitoring antigenic variations of enterovirus 71: implications for virus surveillance and vaccine development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4109910/
https://www.ncbi.nlm.nih.gov/pubmed/25058733
http://dx.doi.org/10.1371/journal.pntd.0003044
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