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| 多头带绦虫Tm7基因的表达及间接ELISA检测方法的建立 | |
| 引用本文： | 安晓雪,杨光友,王颖旺,牟静,阳爱国,古小彬,杨应东,韦雷飞,文建国,王淑贤,边尧.多头带绦虫Tm7基因的表达及间接ELISA检测方法的建立[J].畜牧兽医学报,2011,42(9). |
| 作者姓名： | 安晓雪 杨光友 王颖旺 牟静 阳爱国 古小彬 杨应东 韦雷飞 文建国 王淑贤 边尧 |
| 作者单位： | 1. 四川农业大学动物医学院,雅安,625014 2. 四川省动物疫病预防控制中心,成都,610041 3. 四川省攀枝花市农林科学研究院畜牧水产所,攀枝花,617061 4. 四川省雅安市雨城区畜牧局,雅安,625000 |
| 基金项目： | 教育部“长江学者和创新团队发展计划”创新团队项目(IRTO848) |
| 摘 要： | 以多头带绦虫Tm7重组蛋白为抗原,建立动物多头蚴病早期诊断方法.本研究从羊脑多头蚴原头节提取总RNA,采用RT-PCR技术首次扩增出Tm7基因的全序列,该基因的开放阅读框为207 bp,编码68个氨基酸.将此基因克隆到pET-32a(+)载体,构建重组表达质粒pET-32a-Tm7,经转化大肠杆菌BL21(DE3)后IPTG诱导表达,用SDS-PAGE和Western blot检测表达产物.以纯化后的表达蛋白作为抗原,建立检测羊脑多头蚴病抗体的重组蛋白间接ELISA方法.研究结果表明,Tm7基因在大肠杆菌中成功表达,表达产物为约27 ku的融合表达蛋白,该蛋白能识别羊脑多头蚴病阳性血清.建立的间接ELISA方法,检测敏感性可达93.3％,特异性达94.1％,研究结果表明Tm7重组蛋白可作为脑多头蚴病的诊断抗原. |
| 关 键 词： | 脑多头蚴 重组抗原 Tm7 间接ELISA |
Prokaryotic Expression of Tm7 Gene of Taenia multiceps and Establishment of Indirect ELISA Using the Expressed Protein |
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| AN Xiao-xue,YANG Guang-you,WANG Ying-wang,MU Jing,YANG Ai-guo,GU Xiao-bin,YANG Ying-dong,WEI Lei-fei,WEN Jian-guo,WANG Shu-xian,BIAN Yao.Prokaryotic Expression of Tm7 Gene of Taenia multiceps and Establishment of Indirect ELISA Using the Expressed Protein[J].Acta Veterinaria et Zootechnica Sinica,2011,42(9). | |
| Authors: | AN Xiao-xue YANG Guang-you WANG Ying-wang MU Jing YANG Ai-guo GU Xiao-bin YANG Ying-dong WEI Lei-fei WEN Jian-guo WANG Shu-xian BIAN Yao |
| Institution: | AN Xiao-xue1,YANG Guang-you1,WANG Ying-wang1,MU Jing1,YANG Ai-guo3,GU Xiao-bin1,YANG Ying-dong2,WEI Lei-fei2,WEN Jian-guo2,WANG Shu-xian1,BIAN Yao4(1.Collegeof Veterinary Medicine,SichuanAgricultural University,Ya'an625014,China,2.PanzhihuaAnimal Science and Technology Institute,Panzhihua617061,3.Preventiveand Control Center for Animal Disease of Sichuan Province,Chengdu610041,4.Yucheng District Animal Husbandry Bureau of Sichuan Province,Ya'an 625000,China) |
| Abstract: | In order to establish diagnostic method of coenuriasis,total RNA was extracted from protoscoleces of cyst which were recovered from the brain of sheep.The complete sequence of Tm7 was amplified and sequenced.The open reading frame of Tm7 was then amplified,its ORF consisting of 207 bp and encoding 68 amino acids.A recombinant plasmid pET-32a-Tm7 was constructed and transformed into E.coli BL 21 for in vitro expression.SDS-PAGE and Western blot were employed for analyzing the recombinant protein.The purified... |
| Keywords: | Cerebral coenurosis recombinant protein Tm7 indirect ELISA |
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