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Analysis of the genomic homologous recombination in Theilovirus based on complete genomes

At present, Theilovirus is considered to comprise four distinct serotypes, including Theiler's murine encephalomyelitis virus, Vilyuisk human encephalomyelitis virus, Thera virus, and Saffold virus. So far, there is no systematical study that investigated the genomic recombination of Theiloviru...

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Autores principales: Sun, Guangming, Zhang, Xiaodan, Yi, Maoli, Shao, Shihe, Zhang, Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3183034/
https://www.ncbi.nlm.nih.gov/pubmed/21923921
http://dx.doi.org/10.1186/1743-422X-8-439
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author Sun, Guangming
Zhang, Xiaodan
Yi, Maoli
Shao, Shihe
Zhang, Wen
author_facet Sun, Guangming
Zhang, Xiaodan
Yi, Maoli
Shao, Shihe
Zhang, Wen
author_sort Sun, Guangming
collection PubMed
description At present, Theilovirus is considered to comprise four distinct serotypes, including Theiler's murine encephalomyelitis virus, Vilyuisk human encephalomyelitis virus, Thera virus, and Saffold virus. So far, there is no systematical study that investigated the genomic recombination of Theilovirus. The present study performed the phylogenetic and recombination analysis of Theilovirus over the complete genomes. Seven potentially significant recombination events were identified. However, according to the strains information and references related to the recombinants and their parental strains, four of the recombination events might happen non-naturally. These results will provide valuable hints for future research on evolution and antigenic variability of Theilovirus.
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spelling pubmed-31830342011-09-30 Analysis of the genomic homologous recombination in Theilovirus based on complete genomes Sun, Guangming Zhang, Xiaodan Yi, Maoli Shao, Shihe Zhang, Wen Virol J Research At present, Theilovirus is considered to comprise four distinct serotypes, including Theiler's murine encephalomyelitis virus, Vilyuisk human encephalomyelitis virus, Thera virus, and Saffold virus. So far, there is no systematical study that investigated the genomic recombination of Theilovirus. The present study performed the phylogenetic and recombination analysis of Theilovirus over the complete genomes. Seven potentially significant recombination events were identified. However, according to the strains information and references related to the recombinants and their parental strains, four of the recombination events might happen non-naturally. These results will provide valuable hints for future research on evolution and antigenic variability of Theilovirus. BioMed Central 2011-09-17 /pmc/articles/PMC3183034/ /pubmed/21923921 http://dx.doi.org/10.1186/1743-422X-8-439 Text en Copyright ©2011 Sun 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 cited.
spellingShingle Research
Sun, Guangming
Zhang, Xiaodan
Yi, Maoli
Shao, Shihe
Zhang, Wen
Analysis of the genomic homologous recombination in Theilovirus based on complete genomes
title Analysis of the genomic homologous recombination in Theilovirus based on complete genomes
title_full Analysis of the genomic homologous recombination in Theilovirus based on complete genomes
title_fullStr Analysis of the genomic homologous recombination in Theilovirus based on complete genomes
title_full_unstemmed Analysis of the genomic homologous recombination in Theilovirus based on complete genomes
title_short Analysis of the genomic homologous recombination in Theilovirus based on complete genomes
title_sort analysis of the genomic homologous recombination in theilovirus based on complete genomes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3183034/
https://www.ncbi.nlm.nih.gov/pubmed/21923921
http://dx.doi.org/10.1186/1743-422X-8-439
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