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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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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 |
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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 |
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