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Analysis of Amino Acid Variation in the P2 Domain of the GII-4 Norovirus VP1 Protein Reveals Putative Variant-Specific Epitopes

BACKGROUND: Human noroviruses are a highly diverse group of viruses classified into three of the five currently recognised Norovirus genogroups, and contain numerous genotypes or genetic clusters. Noroviruses are the major aetiological agent of endemic gastroenteritis in all age groups, as well as t...

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Autores principales: Allen, David J., Gray, Jim J., Gallimore, Chris I., Xerry, Jacqueline, Iturriza-Gómara, Miren
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194622/
https://www.ncbi.nlm.nih.gov/pubmed/18213393
http://dx.doi.org/10.1371/journal.pone.0001485
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author Allen, David J.
Gray, Jim J.
Gallimore, Chris I.
Xerry, Jacqueline
Iturriza-Gómara, Miren
author_facet Allen, David J.
Gray, Jim J.
Gallimore, Chris I.
Xerry, Jacqueline
Iturriza-Gómara, Miren
author_sort Allen, David J.
collection PubMed
description BACKGROUND: Human noroviruses are a highly diverse group of viruses classified into three of the five currently recognised Norovirus genogroups, and contain numerous genotypes or genetic clusters. Noroviruses are the major aetiological agent of endemic gastroenteritis in all age groups, as well as the cause of periodic epidemic gastroenteritis. The noroviruses most commonly associated with outbreaks of gastroenteritis are genogroup II genotype 4 (GII-4) strains. The relationship between genotypes of noroviruses with their phenotypes and antigenic profile remains poorly understood through an inability to culture these viruses and the lack of a suitable animal model. METHODOLOGY/PRINCIPAL FINDINGS: Here we describe a study of the diversity of amino acid sequences of the highly variable P2 region in the major capsid protein, VP1, of the GII-4 human noroviruses strains using sequence analysis and homology modelling techniques. CONCLUSIONS/SIGNIFICANCE: Our data identifies two sites in this region, which show significant amino acid substitutions associated with the appearance of variant strains responsible for epidemics with major public health impact. Homology modelling studies revealed the exposed nature of these sites on the capsid surface, providing supportive structural data that these two sites are likely to be associated with putative variant-specific epitopes. Furthermore, the patterns in the evolution of these viruses at these sites suggests that noroviruses follow a neutral network pattern of evolution.
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spelling pubmed-21946222008-01-23 Analysis of Amino Acid Variation in the P2 Domain of the GII-4 Norovirus VP1 Protein Reveals Putative Variant-Specific Epitopes Allen, David J. Gray, Jim J. Gallimore, Chris I. Xerry, Jacqueline Iturriza-Gómara, Miren PLoS One Research Article BACKGROUND: Human noroviruses are a highly diverse group of viruses classified into three of the five currently recognised Norovirus genogroups, and contain numerous genotypes or genetic clusters. Noroviruses are the major aetiological agent of endemic gastroenteritis in all age groups, as well as the cause of periodic epidemic gastroenteritis. The noroviruses most commonly associated with outbreaks of gastroenteritis are genogroup II genotype 4 (GII-4) strains. The relationship between genotypes of noroviruses with their phenotypes and antigenic profile remains poorly understood through an inability to culture these viruses and the lack of a suitable animal model. METHODOLOGY/PRINCIPAL FINDINGS: Here we describe a study of the diversity of amino acid sequences of the highly variable P2 region in the major capsid protein, VP1, of the GII-4 human noroviruses strains using sequence analysis and homology modelling techniques. CONCLUSIONS/SIGNIFICANCE: Our data identifies two sites in this region, which show significant amino acid substitutions associated with the appearance of variant strains responsible for epidemics with major public health impact. Homology modelling studies revealed the exposed nature of these sites on the capsid surface, providing supportive structural data that these two sites are likely to be associated with putative variant-specific epitopes. Furthermore, the patterns in the evolution of these viruses at these sites suggests that noroviruses follow a neutral network pattern of evolution. Public Library of Science 2008-01-23 /pmc/articles/PMC2194622/ /pubmed/18213393 http://dx.doi.org/10.1371/journal.pone.0001485 Text en Allen 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
Allen, David J.
Gray, Jim J.
Gallimore, Chris I.
Xerry, Jacqueline
Iturriza-Gómara, Miren
Analysis of Amino Acid Variation in the P2 Domain of the GII-4 Norovirus VP1 Protein Reveals Putative Variant-Specific Epitopes
title Analysis of Amino Acid Variation in the P2 Domain of the GII-4 Norovirus VP1 Protein Reveals Putative Variant-Specific Epitopes
title_full Analysis of Amino Acid Variation in the P2 Domain of the GII-4 Norovirus VP1 Protein Reveals Putative Variant-Specific Epitopes
title_fullStr Analysis of Amino Acid Variation in the P2 Domain of the GII-4 Norovirus VP1 Protein Reveals Putative Variant-Specific Epitopes
title_full_unstemmed Analysis of Amino Acid Variation in the P2 Domain of the GII-4 Norovirus VP1 Protein Reveals Putative Variant-Specific Epitopes
title_short Analysis of Amino Acid Variation in the P2 Domain of the GII-4 Norovirus VP1 Protein Reveals Putative Variant-Specific Epitopes
title_sort analysis of amino acid variation in the p2 domain of the gii-4 norovirus vp1 protein reveals putative variant-specific epitopes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194622/
https://www.ncbi.nlm.nih.gov/pubmed/18213393
http://dx.doi.org/10.1371/journal.pone.0001485
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