Cargando…

Bioinformatics analysis of rabbit haemorrhagic disease virus genome

BACKGROUND: Rabbit haemorrhagic disease virus (RHDV), as the pathogeny of Rabbit haemorrhagic disease, can cause a highly infectious and often fatal disease only affecting wild and domestic rabbits. Recent researches revealed that it, as one number of the Caliciviridae, has some specialties in its g...

Descripción completa

Detalles Bibliográficos
Autores principales: Tian, Xiao-ting, Li, Bao-yu, Zhang, Liang, Jiao, Wen-qiang, Liu, Ji-xing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377956/
https://www.ncbi.nlm.nih.gov/pubmed/22044910
http://dx.doi.org/10.1186/1743-422X-8-494
_version_ 1782236010280648704
author Tian, Xiao-ting
Li, Bao-yu
Zhang, Liang
Jiao, Wen-qiang
Liu, Ji-xing
author_facet Tian, Xiao-ting
Li, Bao-yu
Zhang, Liang
Jiao, Wen-qiang
Liu, Ji-xing
author_sort Tian, Xiao-ting
collection PubMed
description BACKGROUND: Rabbit haemorrhagic disease virus (RHDV), as the pathogeny of Rabbit haemorrhagic disease, can cause a highly infectious and often fatal disease only affecting wild and domestic rabbits. Recent researches revealed that it, as one number of the Caliciviridae, has some specialties in its genome, its reproduction and so on. RESULTS: In this report, we firstly analyzed its genome and two open reading frameworks (ORFs) from this aspect of codon usage bias. Our researches indicated that mutation pressure rather than natural is the most important determinant in RHDV with high codon bias, and the codon usage bias is nearly contrary between ORF1 and ORF2, which is maybe one of factors regulating the expression of VP60 (encoding by ORF1) and VP10 (encoding by ORF2). Furthermore, negative selective constraints on the RHDV whole genome implied that VP10 played an important role in RHDV lifecycle. CONCLUSIONS: We conjectured that VP10 might be beneficial for the replication, release or both of virus by inducing infected cell apoptosis initiate by RHDV. According to the results of the principal component analysis for ORF2 of RSCU, we firstly separated 30 RHDV into two genotypes, and the ENC values indicated ORF1 and ORF2 were independent among the evolution of RHDV.
format Online
Article
Text
id pubmed-3377956
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-33779562012-06-20 Bioinformatics analysis of rabbit haemorrhagic disease virus genome Tian, Xiao-ting Li, Bao-yu Zhang, Liang Jiao, Wen-qiang Liu, Ji-xing Virol J Research BACKGROUND: Rabbit haemorrhagic disease virus (RHDV), as the pathogeny of Rabbit haemorrhagic disease, can cause a highly infectious and often fatal disease only affecting wild and domestic rabbits. Recent researches revealed that it, as one number of the Caliciviridae, has some specialties in its genome, its reproduction and so on. RESULTS: In this report, we firstly analyzed its genome and two open reading frameworks (ORFs) from this aspect of codon usage bias. Our researches indicated that mutation pressure rather than natural is the most important determinant in RHDV with high codon bias, and the codon usage bias is nearly contrary between ORF1 and ORF2, which is maybe one of factors regulating the expression of VP60 (encoding by ORF1) and VP10 (encoding by ORF2). Furthermore, negative selective constraints on the RHDV whole genome implied that VP10 played an important role in RHDV lifecycle. CONCLUSIONS: We conjectured that VP10 might be beneficial for the replication, release or both of virus by inducing infected cell apoptosis initiate by RHDV. According to the results of the principal component analysis for ORF2 of RSCU, we firstly separated 30 RHDV into two genotypes, and the ENC values indicated ORF1 and ORF2 were independent among the evolution of RHDV. BioMed Central 2011-11-01 /pmc/articles/PMC3377956/ /pubmed/22044910 http://dx.doi.org/10.1186/1743-422X-8-494 Text en Copyright ©2011 Tian 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
Tian, Xiao-ting
Li, Bao-yu
Zhang, Liang
Jiao, Wen-qiang
Liu, Ji-xing
Bioinformatics analysis of rabbit haemorrhagic disease virus genome
title Bioinformatics analysis of rabbit haemorrhagic disease virus genome
title_full Bioinformatics analysis of rabbit haemorrhagic disease virus genome
title_fullStr Bioinformatics analysis of rabbit haemorrhagic disease virus genome
title_full_unstemmed Bioinformatics analysis of rabbit haemorrhagic disease virus genome
title_short Bioinformatics analysis of rabbit haemorrhagic disease virus genome
title_sort bioinformatics analysis of rabbit haemorrhagic disease virus genome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377956/
https://www.ncbi.nlm.nih.gov/pubmed/22044910
http://dx.doi.org/10.1186/1743-422X-8-494
work_keys_str_mv AT tianxiaoting bioinformaticsanalysisofrabbithaemorrhagicdiseasevirusgenome
AT libaoyu bioinformaticsanalysisofrabbithaemorrhagicdiseasevirusgenome
AT zhangliang bioinformaticsanalysisofrabbithaemorrhagicdiseasevirusgenome
AT jiaowenqiang bioinformaticsanalysisofrabbithaemorrhagicdiseasevirusgenome
AT liujixing bioinformaticsanalysisofrabbithaemorrhagicdiseasevirusgenome