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中国生物工程杂志

CHINA BIOTECHNOLOGY
中国生物工程杂志  2010, Vol. 30 Issue (02): 60-65    
研究报告     
非洲猪瘟病毒VP73基因主要抗原表位区的融合原核表达
李秋霞1,2,滕达2**,童德文1,杨雅麟2,田子罡2,王建华2**
1.西北农林科技大学动物医学院 杨凌 712100
2.中国农业科学院饲料研究所基因工程室农业部饲料生物技术重点开放实验室 北京 100081
Prokaryotic Expression of Major Epitope Domain of African Swine Fever Virus VP73 Gene
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摘要:

人工合成VP73基因全长序列,利用DNAstar软件确定其中抗原性较高的区域,利用Primer Premier5.0设计一对特异性引物,通过PCR扩增得到243bp的非洲猪瘟病毒VP73基因片段(vp73l)。将该片段与表达载体pET-32a连接克隆至大肠杆菌Escherichia coli(E.coli)DH5α菌株,经测序、菌落PCR和酶切鉴定,选取VP73L基因正向插入,读码框正确的阳性克隆。构建重组质粒并转化BL21(DE3),经IPTG诱导,融合蛋白以可溶性形式在E.coli BL2(DE3)高效表达,经His亲和层析柱得以纯化。Western blotting显示,该融合蛋白能与兔抗非洲猪瘟病毒VP73多克隆抗体发生特异性反应。所得结果为进一步研究:分离纯化该重组融合蛋白;确证目标抗原蛋白VP73L免疫原性及其特异性,进而达到建立非洲猪瘟病毒的免疫检测方法奠定了必要的材料与技术基础。

关键词: 非洲猪瘟病毒VP73基因主要抗原表位区表达    
Abstract:

A full-length VP73 gene sequence was synthesized, the its higher antigen area is predicted by using DNAStar software, and one pair of specific primers for this area are designed by using Primer Premier 5.0. Amplified 243bp fragment of the VP73 gene (vp73l) by PCR was digested and cloned into the prokaryotic expression vector pET-32a. The positive clone of inserting VP73L gene with correct reading frame was confirmed by sequencing and colony PCR. After induction by IPTG, the fusion protein was highly expressed in Escherichia coli BL21 (DE3) in soluble form. The recombinant protein was purified with His-Bind affinity chromatography. Western blotting analysis revealed that the recombinant protein could react with rabbit anti-African swine fever virus VP73 polyclonal antibody. Fusion expression of African swine fever virus VP73L is helpful to to prepare ASFVserological diagnostic reagent in next work.

Key words: African swine fever virus    VP73gene    Major epitope domain    Expresion
收稿日期: 2009-09-21 出版日期: 2010-02-26
基金资助:

“十一五”国家科技支撑计划(2006BAD06A14)资助项目

通讯作者: 王建华     E-mail: tengda@mail.caas.net.cn,wangjianhua@mail.caas.net.cn
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引用本文:

李秋霞 腾达 童德文 杨雅麟 田子罡 王建华. 非洲猪瘟病毒VP73基因主要抗原表位区的融合原核表达[J]. 中国生物工程杂志, 2010, 30(02): 60-65.

LI Qiu-Xia, TENG Da, TONG De-Wen, YANG Ya-Lin, TIAN Zi-Gang, WANG Jian-Hua. Prokaryotic Expression of Major Epitope Domain of African Swine Fever Virus VP73 Gene. China Biotechnology, 2010, 30(02): 60-65.

链接本文:

https://manu60.magtech.com.cn/biotech/CN/        https://manu60.magtech.com.cn/biotech/CN/Y2010/V30/I02/60

[1] 蔡宝祥. 家畜传染病学.北京: 中国农业出版社, 2001. Cai B X. Animal Infectious Diseases.Beijing: China Agriculture Press,2001. 
[2] Hess W R. African swine fever:a reassessment. Adv Vet Sci Comp Med,1982, 25: 3969. 
[3] Carmina G,Dufton M M,Joseph M M,et al.Enhanced discrimination of African swine fever virus isolates through nucleotide sequencing of the p54, p72, and pB602L (CVR).Virus Genes,2009,38:8595. 
[4] Tulman E R, Rock D L. Novel virulence and host range genes of African swine fever virus. Curr Opin Microbiol, 2001, 4: 456461. 
[5] Reis A L,Parkhouse R M,Penedos A R,et al.Systematic analysis of longitudinal serological responses of pigs infected experimentally with African swine fever virus.J Gen Virol,2007, 88:24262434. 
[6] Gallardo C ,Reis A L, KalemaZikusoka G,et al.Recombinant antigen targets for serodiagnosis of African swine fever.Clin Vaccine Immunol,2009,6: 130. 
[7] Tulman E R,Delhon G A,Ku B K,et al.African swine fever virus.Curr To PMicrobiol Immunol,2009,328:4387. 
[8] Alcaroz C, Brun A. Cell culture propagation modifies theAfrican swine fever virus replication phenotype in macrophagesand generates virus subpopulations dilfering in protein P54.Virus Research, 1992, 23: 173182. 
[9] Yu M,Morrissy J C,Westbury A H.Strong sequence conservation of African swine fever virus p72 protein provides the molecular basis for its antigenic stability.Arch Virol,1996,141(9):17951802. 
[10] Rodrigues F, Alacaraz C, Eiras A, et al. Characterization and molecular basis of heterogeneity of the African swine fever virus envelope protein p54. J Virol,1994 ,68:72447252. 
[11] Hutchings G H, Ferris N P. Indirect sandwich ELISA for antigen detection of African swine fever virus: Comparison of polyclonal and monoclonal antibodies. Journal of Virological Methods, 2006,131(2): 213217. 
[12] 吴玉章,朱锡华.一种病毒蛋白B细胞表位预测方法的建立.科学通报,1994,39(24):22752279. Wu Y Z, Zhu X H.Chinese Science Bulletin, 1994, 39 (24) :2275  2279. 
[13] CistuéC, Tabarés E. Expression in vivo and in vitro of the major structural protein(VP73) of African swine fever virus. Arch Virol,1992, 123:111124. 
[14] Gomezpuertas P,Oviedo J M,Ramiroibanez F,et al.Neutralizing antibodies to different proteins of African swine fever virus inhibit both virus attachment and internalization.J Virol,1996,70:56895694. 
[15] Zsak L,OniskD V,Afonso C L,et al.Virulent African swine fever virus isolates are neutralized by swine immune serum and by monoclonal antibodies recognizing a 72Ku viral protein.Virology,1993,196:596602. 
[16] 梁秀丽,方丽云,王东方,等. 猪细小病毒HN3 株VP2基因克隆与抗原性分析. 河南农业科学,2007,11:100103. Liang X L,Fang L Y,Wang D F,et al.Journal of Henan Agricultural Sciences,2007, 11:100103. 
[17] 李倩,姚淑霞.非洲猪瘟病毒VP73蛋白的B细胞表位预测.农业科学与技术,2008,9(1):9294. Li Q,Yao S X.Agricultural Science & Technology,2008,9(1):9294.

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