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鸭甲肝病毒GX株全基因组序列测定及VP1蛋白生物信息学分析
引用本文:黄云秀,李传峰,孟春春,陈宗艳,李露,宋凯杰,刘光清,韦天超. 鸭甲肝病毒GX株全基因组序列测定及VP1蛋白生物信息学分析[J]. 中国畜牧兽医, 2015, 42(5): 1039-1047. DOI: 10.16431/j.cnki.1671-7236.2015.05.001
作者姓名:黄云秀  李传峰  孟春春  陈宗艳  李露  宋凯杰  刘光清  韦天超
作者单位:1. 广西大学动物科学技术学院, 南宁 530005;2. 中国农业科学院上海兽医研究所, 上海 200241;3. 西北农林科技大学动物医学院, 杨凌 712100
基金项目:国家自然科学基金项目(31270194、31101848、31300141);"863"计划(2011AA10A200);广西大学科研基金资助项目(XB2100113)
摘    要:为探讨鸭甲肝病毒(DHAV)GX株基因分型特点及主要衣壳蛋白(VP1)的生物学特性,本试验对其进行全基因组序列测定,并应用分子生物学软件将DHAV GX株与DHAV 3个血清型参考毒株进行序列比对分析。结果显示,其基因组全长7 800 bp,由5'和3'非编码区(UTR)和一个大开放阅读框(ORF)组成。其中,5'UTR和3'UTR的长度分别为652和369 bp;ORF长度为6 756 bp,编码2 251个氨基酸长的多聚蛋白,其编码产物至少有12个(VP0/VP3/VP1/2A1/2A2/2A3/2B/2C/3A/3B/3C/3D);在分类地位上DHAV GX株属于DHAV-3,其与DHAV-3参考株核苷酸、氨基酸同源性最高;与DHAV-3 FS株亲缘关系最近,在同一较小分支上。DHAV GX株结构蛋白VP1以第195—201、211—221位氨基酸区段为B细胞优势表位的可能性较大。提示,VP1基因可作为研制DHAV基因工程疫苗的优势候选基因。

关 键 词:鸭甲肝病毒  全基因组  序列分析  VP1蛋白  B细胞抗原表位  
收稿时间:2014-11-21

Determination of the Complete Genome of DHAV GX Strain and Bioinformatics Analysis of VP1 Protein
HUANG Yun-xiu,LI Chuan-feng,MENG Chun-chun,CHEN Zong-yan,LI Lu,SONG Kai-jie,LIU Guang-qing,WEI Tian-chao. Determination of the Complete Genome of DHAV GX Strain and Bioinformatics Analysis of VP1 Protein[J]. China Animal Husbandry & Veterinary Medicine, 2015, 42(5): 1039-1047. DOI: 10.16431/j.cnki.1671-7236.2015.05.001
Authors:HUANG Yun-xiu  LI Chuan-feng  MENG Chun-chun  CHEN Zong-yan  LI Lu  SONG Kai-jie  LIU Guang-qing  WEI Tian-chao
Affiliation:1. College of Animal Science and Technology, Guangxi University, Nanning 530005, China;2. Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai 200241, China;3. College of Veterinary Medicine, Northwest A&F University, Yangling 712100, China
Abstract:In order to investigate the genotypic characteristics and biological characteristics of major capsid protein (VP1) of duck hepatitis A virus (DHAV) GX strain, the whole genome of GX strain was sequenced and compared with 3 serotypes reference strains of DHAV by the molecular biology software.The results showed that the full-length genome of DHAV GX strain was 7 800 bp, including 5'UTR (652 bp), 3'UTR (369 bp) and ORF (6 756 bp) encoding 2 251 aa and its coding products were 12 (VP0/VP3/VP1/2A1/2A2/2A3/2B/2C/3A/3B/3C/3D) at least.Sequence analysis showed that DHAV GX strain could be ranked DHAV 3 style.This strain shared the highest homology with DHAV-3 reference strains; Furthermore, GX strain and DHAV-3 FS strain were in the same cluster, might come from the same ancestor.Amino acid segments locating in 195 to 201 and 211 to 221 aa could be larvaceous dominant B-cell linear epitopes.It suggested that VP1 gene could be used as a candidate gene for the development of genetic engineering vaccine of DHAV.
Keywords:duck hepatitis A virus  complete genome  sequence analysis  VP1 protein  B cell epitope  
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