畜牧兽医学报 ›› 2009, Vol. 40 ›› Issue (12): 1788-1793.doi:

• 预防兽医 • 上一篇    下一篇

基于重组猪囊虫18 ku抗原的间接ELISA方法的建立

吴国华1,郑亚东1,贾万忠1,张少华1,景志忠1,骆学农1,刘石泉2,才学鹏1*
  

  1. 1.中国农业科学院兰州兽医研究所 家畜疫病病原生物学国家重点实验室 甘肃省动物寄生虫病重点实验室,农业部兽医公共卫生重点开放实验室,兰州 730046;2.江西农业大学 动物科学技术学院, 南昌 330045
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2009-12-24 发布日期:2009-12-24
  • 通讯作者: 才学鹏

Development of an Indirect ELISA for Detecting Antibodies against Cysticercus cellulosae Based on Its Recombinant 18 ku Protein Expressed in E. coli

WU Guohua 1, ZHENG Yadong 1, JIA Wanzhong 1, ZHANG Shaohua 1, JING Zhizhong 1, LUO Xuenong 1,LIU Shiquan 2, CAI Xuepeng 1*
  

  1. 1. Key Laboratory of Veterinary Parasitology of Gansu Province, State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou 730046,China; 2. College of Animal Science and Technology,Jiangxi Agricultural University,Nanchang 330045,China
  • Received:1900-01-01 Revised:1900-01-01 Online:2009-12-24 Published:2009-12-24
  • Contact: CAI Xuepeng

摘要: 利用反转录聚合酶链式反应(RTPCR)从猪囊尾蚴中克隆到18 ku蛋白基因,将扩增产物与pGEMT Easy载体连接后测序分析。将目的基因亚克隆至表达载体,构建重组质粒pGEXCE18,经转化大肠杆菌BL21(DE3)后诱导表达,用SDSPAGE和Westernblot分析表达产物。表达的目的蛋白纯化后作抗原建立检测猪囊虫抗体的重组蛋白间接ELISA方法。结果表明,18 ku 蛋白基因在大肠杆菌中成功表达,表达产物约为35 ku的融合蛋白,并能被猪囊虫感染血清识别。经薄层扫描分析,表达量占菌体蛋白总量的28%。与商品化ELISA试剂盒平行检测178份阳性血清样品,二者的符合率为 98.83%,说明建立的重组蛋白ELISA方法可用于猪囊虫病的诊断。

Abstract: A 18kDacoding gene of Taenia solium metacestodes was amplified by RTPCR and subcloned into pGEMT vector for sequencing. A recombinant plasmid pGEXCE18 was constructed and transformed into E. coli BL21 for in vitro expression. SDSPAGE and Westernblot were employed for analyzing the recombinant protein, which was used for development of an indirect ELISA for detection of anticysticercosis antibodies. The results showed that the interest protein was 35 kDa in size, accounting for 28% of total bacteria proteins, and could be recognized by positive sera against cysticercosis. Using the constructed indirect ELISA and a commercialized ELISA kit, paralleled analysis of 178 serum samples indicated that the concordant rate was 9883% and the ELISA showed good performance in specificity and sensitivity, supporting its application for cysticercosis diagnosis.