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Classification of infectious bursal disease virus into genogroups

Infectious bursal disease virus (IBDV) causes infectious bursal disease (IBD), an immunosuppressive disease of poultry. The current classification scheme of IBDV is confusing because it is based on antigenic types (variant and classical) as well as pathotypes. Many of the amino acid changes differen...

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Autores principales: Michel, Linda O., Jackwood, Daral J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5671532/
https://www.ncbi.nlm.nih.gov/pubmed/28825213
http://dx.doi.org/10.1007/s00705-017-3500-4
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author Michel, Linda O.
Jackwood, Daral J.
author_facet Michel, Linda O.
Jackwood, Daral J.
author_sort Michel, Linda O.
collection PubMed
description Infectious bursal disease virus (IBDV) causes infectious bursal disease (IBD), an immunosuppressive disease of poultry. The current classification scheme of IBDV is confusing because it is based on antigenic types (variant and classical) as well as pathotypes. Many of the amino acid changes differentiating these various classifications are found in a hypervariable region of the capsid protein VP2 (hvVP2), the major host protective antigen. Data from this study were used to propose a new classification scheme for IBDV based solely on genogroups identified from phylogenetic analysis of the hvVP2 of strains worldwide. Seven major genogroups were identified, some of which are geographically restricted and others that have global dispersion, such as genogroup 1. Genogroup 2 viruses are predominately distributed in North America, while genogroup 3 viruses are most often identified on other continents. Additionally, we have identified a population of genogroup 3 vvIBDV isolates that have an amino acid change from alanine to threonine at position 222 while maintaining other residues conserved in this genogroup (I242, I256 and I294). A222T is an important mutation because amino acid 222 is located in the first of four surface loops of hvVP2. A similar shift from proline to threonine at 222 is believed to play a role in the significant antigenic change of the genogroup 2 IBDV strains, suggesting that antigenic drift may be occurring in genogroup 3, possibly in response to antigenic pressure from vaccination. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00705-017-3500-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-56715322017-11-17 Classification of infectious bursal disease virus into genogroups Michel, Linda O. Jackwood, Daral J. Arch Virol Original Article Infectious bursal disease virus (IBDV) causes infectious bursal disease (IBD), an immunosuppressive disease of poultry. The current classification scheme of IBDV is confusing because it is based on antigenic types (variant and classical) as well as pathotypes. Many of the amino acid changes differentiating these various classifications are found in a hypervariable region of the capsid protein VP2 (hvVP2), the major host protective antigen. Data from this study were used to propose a new classification scheme for IBDV based solely on genogroups identified from phylogenetic analysis of the hvVP2 of strains worldwide. Seven major genogroups were identified, some of which are geographically restricted and others that have global dispersion, such as genogroup 1. Genogroup 2 viruses are predominately distributed in North America, while genogroup 3 viruses are most often identified on other continents. Additionally, we have identified a population of genogroup 3 vvIBDV isolates that have an amino acid change from alanine to threonine at position 222 while maintaining other residues conserved in this genogroup (I242, I256 and I294). A222T is an important mutation because amino acid 222 is located in the first of four surface loops of hvVP2. A similar shift from proline to threonine at 222 is believed to play a role in the significant antigenic change of the genogroup 2 IBDV strains, suggesting that antigenic drift may be occurring in genogroup 3, possibly in response to antigenic pressure from vaccination. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00705-017-3500-4) contains supplementary material, which is available to authorized users. Springer Vienna 2017-08-19 2017 /pmc/articles/PMC5671532/ /pubmed/28825213 http://dx.doi.org/10.1007/s00705-017-3500-4 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.
spellingShingle Original Article
Michel, Linda O.
Jackwood, Daral J.
Classification of infectious bursal disease virus into genogroups
title Classification of infectious bursal disease virus into genogroups
title_full Classification of infectious bursal disease virus into genogroups
title_fullStr Classification of infectious bursal disease virus into genogroups
title_full_unstemmed Classification of infectious bursal disease virus into genogroups
title_short Classification of infectious bursal disease virus into genogroups
title_sort classification of infectious bursal disease virus into genogroups
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5671532/
https://www.ncbi.nlm.nih.gov/pubmed/28825213
http://dx.doi.org/10.1007/s00705-017-3500-4
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