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猪瘟病毒石门株与兔化弱毒株E0糖蛋白基因的克隆及序列分析
引用本文:王家富,张楚瑜,王宁,傅烈振,黄茜华.猪瘟病毒石门株与兔化弱毒株E0糖蛋白基因的克隆及序列分析[J].微生物学报,2000,40(1):32-37.
作者姓名:王家富  张楚瑜  王宁  傅烈振  黄茜华
作者单位:武汉大学病毒研究所,武汉,430072
基金项目:国家攀登计划B类项目85-41子专题资助课题
摘    要:参考已发表的猪瘟病毒序列,设计并合成了一对引物,应用RTPCR 技术,扩增了猪瘟兔化弱毒(Hog cholera virus lapinized Chinese strain , HCLV) 和石门强毒株的E0 糖蛋白基因,并将其克隆到pGEMT 载体中,测定了其核苷酸序列,并推导了其氨基酸序列。结果表明我国这两株强弱不同毒株E0 糖蛋白核苷酸序列同源性和推导的氨基酸序列同源性分别为95-0 % 和94-3 % ,有13 个氨基酸的差异,HCLV 比石门株多了一个潜在的N糖基化位点。将我国这两株病毒与国外已报导的HCV 毒株E0 基因序列进行了比较,发现石门株与日本的两株毒株ALD 和GPE- 同源性较高,核苷酸序列同源性分别为97-4 % 和96-5 % ,氨基酸同源性分别为97-4 % 和96-0 % ,而与欧洲Brescia 株和Alfort 株同源性较低,核苷酸同源性分别为92-2 % 和86-5 % ,氨基酸同源性为95-2 % 和92-5 % , HCLV 与ALD、GPE- 、Brescia、Alfort 株核苷酸同源性分别为95-6 % 、94-9 % 、91-3 % 、85-5 % …

关 键 词:猪瘟病毒    E0基因    克隆    序列分析
文章编号:0001-6209(2000)01-0032-37

CLONING AND SEQUENCE ANALYSIS OF E0 GENE OF HOG CHOLERA VIRUS LAPINIZED CHINESE STRAIN AND VIRULENT SHIMEN STRAIN
Wang Jiafu,Zhang Chuyu,Wang Ning,Fu Liezhen,Huang Qianhua.CLONING AND SEQUENCE ANALYSIS OF E0 GENE OF HOG CHOLERA VIRUS LAPINIZED CHINESE STRAIN AND VIRULENT SHIMEN STRAIN[J].Acta Microbiologica Sinica,2000,40(1):32-37.
Authors:Wang Jiafu  Zhang Chuyu  Wang Ning  Fu Liezhen  Huang Qianhua
Institution:Wang Jiafu ,Zhang Chuyu ,Wang Ning ,Fu Liezhen ,Huang Qianhua ;(Institute of Virology, Wuhan University, Wuhan 430072)
Abstract:According to the published nucleotide sequences of genome of hog cholera virus, one pair of specific primers were designed and synthesized. From the spleen of rabbits which were infected with HCLV and HCV Shimen strain infected pig blood, the two E0 genes were amplifed by RTPCR. The amplified fragments were cloned into pGEM-T vector and sequenced. Sequence analysis showed nucleotide sequence and deduced amino acid sequence homologies of the E0 gene between HCLV and Shimen strain were 95.0 % and 94.3 %. There was 13 amino acid substitutions between them. One N-glycosylation site was missing from E0 gene of the Shimen strain. The nucleotide sequence homologies of the Shimen strain with the ALD, GPE-, Brescia and Alfort strains were 97.4 %, 96.5 %, 92.2 % and 86.5 %, respectively, the deduced amino acid sequence homologies were 97.4 %, 96.0 %, 95.2 96 and 92.5 %, respectively. The nucleotide sequence homologies of EO gene of the HCLV strain with the ALD, GPE , Brescia and Alfort strains were 95.6 %, 94.9%, 91.3% and 85.5%, respectively, the deduced amino acid sequence homologies were 93.4 %, 92.5 %, 91.6 % and 90.7 %, respectively. EO gene from HCV was shown to be similar to a family of fungal and plant ribonuclease. The catalytically important residues were 28 to 40 and 71 to 89 of HCV EO gene.
Keywords:Hog cholera virus  EO gene  Cloning  Sequence analysis
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