›› 2015, Vol. 42 ›› Issue (2): 337-341.doi: 10.16431/j.cnki.1671-7236.2015.02.015

• 生物技术 • 上一篇    下一篇

猪圆环病毒2型Cap全基因的克隆与原核表达

李海花1, 覃尧2, 张全红3, 李秀丽1   

  1. 1. 天津市畜牧兽医研究所, 天津 300384;
    2. 中国农业大学动物医学院, 北京 100193;
    3. 国家知识产权局专利局专利审查协作北京中心, 北京 100190
  • 收稿日期:2014-10-27 出版日期:2015-02-20 发布日期:2015-02-13
  • 通讯作者: 李海花 E-mail:lihaihuaok@126.com
  • 作者简介:李海花(1981-),女,河南周口人,博士,助理研究员,主要从事微生物学与免疫学研究
  • 基金资助:
    天津市农业科学院院长基金(13004)

Cloning and Prokaryotic Expression of Capsid Protein Gene from Porcine Circovirus Type 2

LI Hai-hua1, QIN Yao2, ZHANG Quan-hong3, LI Xiu-li1   

  1. 1. Tianjin Institute of Animal Husbandry and Veterinary Science, Tianjin 300384, China;
    2. College of Veterinary Medicine, China Agricultural University, Beijing 100193, China;
    3. Patent Examination Cooperation Center of the Patent Office, SIPO Beijing, Beijing 100190, China
  • Received:2014-10-27 Online:2015-02-20 Published:2015-02-13

摘要: Cap蛋白是猪圆环病毒2型(porcine circovirus type 2,PCV2)的主要结构蛋白,能诱导免疫保护,是临床上利用血清学诊断PCV2的主要依据。本研究根据PCV2 TJ株全基因核苷酸序列(GenBank登录号:KC751546)设计特异性引物,利用PCR从PCV2 TJ株扩增获得Cap全基因,将该基因片段连接到原核表达载体pET-32a(+)中,获得重组质粒pET32a-Cap,经IPTG诱导获得约48 ku的重组融合蛋白,Western blotting分析结果表明其与小鼠抗6×His单克隆抗体和PCV2阳性猪血清均呈阳性反应。本研究成功克隆Cap全基因,构建原核表达载体,并实现Cap融合蛋白的表达,这为PCV2 Cap蛋白的功能研究及诊断方法的建立和亚单位疫苗的研制奠定了基础。

关键词: 猪圆环病毒2型; Cap基因; 克隆; 原核表达

Abstract: Capsid (Cap) protein was the main structural protein of porcine circovirus type 2 (PCV2),and used as a main basis for PCV2 serological diagnosis in the clinical.In this study,the complete gene encoding Cap protein of PCV2 TJ strain was amplified by PCR using the specific primers designed according to the strain sequence (GenBank accession No.:KC751546),and then the amplified products were cloned into pET-32a(+) vector to construct recombinant plasmid pET32a-Cap.The recombinant fusion protein with about 48 ku was expressed by IPTG induction.The result of Western blotting analysis showed that the fusion protein had the positive reaction with anti-6×His tag monoclonal antibody and porcine serum against PCV2.We had successfully cloned Cap gene,constructed the prokaryotic expression vector,and then expressed Cap fusion protein,it provided the support for the establishment of PCV2 detection and development of subunit vaccine,and also made a foundation for the study of the function of PCV2.

Key words: porcine circovirus type 2 (PCV2); Cap gene; clone; prokaryotic expression

中图分类号: