《中国畜牧兽医》 ›› 2018, Vol. 45 ›› Issue (2): 279-290.doi: 10.16431/j.cnki.1671-7236.2018.02.001

• 生物技术 •    下一篇

表达猪圆环病毒2型衣壳蛋白的重组猪痘病毒的构建及鉴定

钟罗华1, 邓舜洲1, 胡杨1, 徐昌满1, 罗锋2, 张文波1, 陈松昌2   

  1. 1. 江西农业大学动物科学与技术学院, 南昌 330045;
    2. 江西金伊博生物科技有限公司, 南昌 330013
  • 收稿日期:2017-09-15 出版日期:2018-02-20 发布日期:2018-02-10
  • 通讯作者: 邓舜洲 E-mail:shzhdeng@163.com
  • 作者简介:钟罗华(1993-),男,江西赣州人,硕士,研究方向:动物传染病,E-mail:1051327445@qq.com
  • 基金资助:

    国家自然科学基金项目(31460666);江西省科技支撑计划项目(20132BBF60044、20141BBF60039);江西省现代农业产业技术体系建设专项资金(JXARS-03)

Construction and Identification of Recombinant Swinepox Virus Expressing Porcine Circovirus Type 2 Capsid Protein

ZHONG Luohua1, DENG Shunzhou1, HU Yang1, XU Changman1, LUO Feng2, ZHANG Wenbo1, CHEN Songchang2   

  1. 1. College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang 330045, China;
    2. Jiangxi JIN YI BO Biological Technology Co., Ltd., Nanchang 330013, China
  • Received:2017-09-15 Online:2018-02-20 Published:2018-02-10

摘要:

为探索猪痘病毒(swinepox virus,SWPV)作为猪圆环病毒2型(porcine circovirus type 2,PCV2)疫苗载体的可行性,本试验以痘苗病毒启动子P11启动绿色荧光蛋白筛选标记,猪痘病毒TK基因为外源基因的插入位点,P28、P7.5启动子启动PCV2 ORF2基因,以猪痘病毒JX20G株为亲本病毒,采用同源重组技术分别构建了两株表达PCV2衣壳蛋白的重组猪痘病毒rSWPV11-28C和rSWPV11-7.5C。结果显示,重组猪痘病毒rSWPV11-28C和rSWPV11-7.5C均成功表达了PCV2衣壳蛋白,表达的蛋白能与PCV2单克隆抗体6E12发生特异性反应;痘苗病毒启动子P28的启动效果明显优于P7.5,P28适合用于启动目的基因;利用重组猪痘病毒制备的PCV2灭活疫苗免疫小鼠后,rSWPV11-28C疫苗组的PCV2抗体水平与某PCV2商品疫苗相当,该重组病毒的成功构建为PCV2相关疾病及其他疫病在猪群中的防控提供了新的方向。

关键词: 猪圆环病毒2型(PCV2); 衣壳蛋白; 重组猪痘病毒

Abstract:

In order to investigate the feasibility of swinepox virus (SWPV) as porcine circovirus type 2 (PCV2) vaccine carrier, this study utilized promoter P11 of vaccinia virus launching the green protein screening markers, and used SWPV TK gene as the insertion of exogenous gene loci. P28 and P7.5 promoters started PCV2 ORF2 gene to construct two recombinant plasmids of rSWPV11-28C and rSWPV11-7.5C, respectively. SWPV JX20G strain was defined as the parent viruses, homologous recombination technology was used to build two strains (rSWPV11-28C and rSWPV11-7.5C), which expressed the PCV2 recombinant swinepox virus capsid protein. The results showed that the PCV2 capsid protein, which was successfully expressed in recombinant swinepox virus rSWPV11-28C and rSWPV11-7.5C, could react specifically with PCV2 monoclonal antibody 6E12. The PCV2 capsid protein promoted by the vaccinia virus promoter P28 was significantly higher than P7.5, P28 was suitable for starting the target gene. After immunization in mice via recombinant swinepox virus of PCV2 inoculated vaccine, the PCV2 of the rSWPV11-28C vaccine group and commodity vaccine showed equivalent antibody levels. The successful construction of the recombinant virus provided a new direction for the prevention and control of PCV2 related diseases and other diseases in swine.

Key words: porcine circovirus type 2(PCV2); capsid protein; recombinant swinepox virus

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