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Antigenic Relatedness of Norovirus GII.4 Variants Determined by Human Challenge Sera

The GII.4 noroviruses (NoVs) are a single genotype that is responsible for over 50% of NoV gastroenteritis epidemics worldwide. However, GII.4 NoVs have been found to undergo antigenic drifts, likely selected by host herd immunity, which raises an issue for vaccine strategies against NoVs. We previo...

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Autores principales: Dai, Ying-Chun, Zhang, Xu-Fu, Xia, Ming, Tan, Ming, Quigley, Christina, Lei, Wen, Fang, Hao, Zhong, Weiming, Lee, Bonita, Pang, Xiaoli, Nie, Jun, Jiang, Xi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4411064/
https://www.ncbi.nlm.nih.gov/pubmed/25915764
http://dx.doi.org/10.1371/journal.pone.0124945
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author Dai, Ying-Chun
Zhang, Xu-Fu
Xia, Ming
Tan, Ming
Quigley, Christina
Lei, Wen
Fang, Hao
Zhong, Weiming
Lee, Bonita
Pang, Xiaoli
Nie, Jun
Jiang, Xi
author_facet Dai, Ying-Chun
Zhang, Xu-Fu
Xia, Ming
Tan, Ming
Quigley, Christina
Lei, Wen
Fang, Hao
Zhong, Weiming
Lee, Bonita
Pang, Xiaoli
Nie, Jun
Jiang, Xi
author_sort Dai, Ying-Chun
collection PubMed
description The GII.4 noroviruses (NoVs) are a single genotype that is responsible for over 50% of NoV gastroenteritis epidemics worldwide. However, GII.4 NoVs have been found to undergo antigenic drifts, likely selected by host herd immunity, which raises an issue for vaccine strategies against NoVs. We previously characterized GII.4 NoV antigenic variations and found significant levels of antigenic relatedness among different GII.4 variants. Further characterization of the genetic and antigenic relatedness of recent GII.4 variants (2008b and 2010 cluster) was performed in this study. The amino acid sequences of the receptor binding interfaces were highly conserved among all GII.4 variants from the past two decades. Using serum samples from patients enrolled in a GII.4 virus challenge study, significant cross-reactivity between major GII.4 variants from 1998 to 2012 was observed using enzyme-linked immunosorbent assays and HBGA receptor blocking assays. The overall abilities of GII.4 NoVs to bind to the A/B/H HBGAs were maintained while their binding affinities to individual ABH antigens varied. These results highlight the importance of human HBGAs in NoV evolution and how conserved antigenic types impact vaccine development against GII.4 variants.
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spelling pubmed-44110642015-05-07 Antigenic Relatedness of Norovirus GII.4 Variants Determined by Human Challenge Sera Dai, Ying-Chun Zhang, Xu-Fu Xia, Ming Tan, Ming Quigley, Christina Lei, Wen Fang, Hao Zhong, Weiming Lee, Bonita Pang, Xiaoli Nie, Jun Jiang, Xi PLoS One Research Article The GII.4 noroviruses (NoVs) are a single genotype that is responsible for over 50% of NoV gastroenteritis epidemics worldwide. However, GII.4 NoVs have been found to undergo antigenic drifts, likely selected by host herd immunity, which raises an issue for vaccine strategies against NoVs. We previously characterized GII.4 NoV antigenic variations and found significant levels of antigenic relatedness among different GII.4 variants. Further characterization of the genetic and antigenic relatedness of recent GII.4 variants (2008b and 2010 cluster) was performed in this study. The amino acid sequences of the receptor binding interfaces were highly conserved among all GII.4 variants from the past two decades. Using serum samples from patients enrolled in a GII.4 virus challenge study, significant cross-reactivity between major GII.4 variants from 1998 to 2012 was observed using enzyme-linked immunosorbent assays and HBGA receptor blocking assays. The overall abilities of GII.4 NoVs to bind to the A/B/H HBGAs were maintained while their binding affinities to individual ABH antigens varied. These results highlight the importance of human HBGAs in NoV evolution and how conserved antigenic types impact vaccine development against GII.4 variants. Public Library of Science 2015-04-27 /pmc/articles/PMC4411064/ /pubmed/25915764 http://dx.doi.org/10.1371/journal.pone.0124945 Text en © 2015 Dai 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
Dai, Ying-Chun
Zhang, Xu-Fu
Xia, Ming
Tan, Ming
Quigley, Christina
Lei, Wen
Fang, Hao
Zhong, Weiming
Lee, Bonita
Pang, Xiaoli
Nie, Jun
Jiang, Xi
Antigenic Relatedness of Norovirus GII.4 Variants Determined by Human Challenge Sera
title Antigenic Relatedness of Norovirus GII.4 Variants Determined by Human Challenge Sera
title_full Antigenic Relatedness of Norovirus GII.4 Variants Determined by Human Challenge Sera
title_fullStr Antigenic Relatedness of Norovirus GII.4 Variants Determined by Human Challenge Sera
title_full_unstemmed Antigenic Relatedness of Norovirus GII.4 Variants Determined by Human Challenge Sera
title_short Antigenic Relatedness of Norovirus GII.4 Variants Determined by Human Challenge Sera
title_sort antigenic relatedness of norovirus gii.4 variants determined by human challenge sera
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4411064/
https://www.ncbi.nlm.nih.gov/pubmed/25915764
http://dx.doi.org/10.1371/journal.pone.0124945
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