| 传染性法氏囊病病毒抗体间接ELISA检测方法的建立 |
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| 引用本文： | 王晓丽,钱晶,马孙婷,王晶宇,夏兴霞,诸玉梅,郑素雅,王永山,欧阳伟.传染性法氏囊病病毒抗体间接ELISA检测方法的建立[J].中国兽医科学,2020(2):159-167. |
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| 作者姓名： | 王晓丽 钱晶 马孙婷 王晶宇 夏兴霞 诸玉梅 郑素雅 王永山 欧阳伟 |
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| 作者单位： | 江苏省农业科学院兽医研究所农业部兽用生物制品工程技术重点实验室;江苏大学食品与生物工程学院;江苏省动物重要疫病与人兽共患病防控协同创新中心 |
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| 基金项目： | 国家重点研发计划项目（2017YFD0500706,2016YFD0500800,2018YFD0500100）;国家自然科学基金项目（31772723,31572504）;江苏省自然科学基金项目（BK20180299）;江苏省农业科技自主创新资金项目（CX(16)1052) |
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| 摘 要： | 为了建立传染性法氏囊病病毒(IBDV)抗体间接ELISA检测方法,本研究首先将VP2基因分3段(部分序列重叠),分别为VP2(1~600)、VP2(376~975)和VP2(751~1350),并根据大肠杆菌对密码子的偏爱性进行优化,将优化的3个VP2基因片段分别克隆于原核表达载体pET28a(+)中,转化E.coli Rosetta(DE3)感受态细胞,经IPTG诱导后,进行SDS-PAGE和Western-blot,结果3个重组VP2蛋白均获得了表达。用纯化的3个重组VP2蛋白rVP2(1~600)、rVP2(376~975)和rVP2(751~1350)分别作为包被抗原,建立了IBDV抗体间接ELISA(rVP2-ELISA)。用rVP2-ELISA、IDEXX-ELISA(IBDV)及中和试验对96份临床血清样本进行检测,结果显示,3个重组VP2蛋白建立的IBDV抗体间接ELISA检测方法、IDEXX-ELISA(IBDV)与中和试验比较,相对敏感性分别为97.1%、61.8%、58.8%和100%;相对特异性分别为85.5%、82.3%、83.9%和25.8%;符合率分别为89.6%、75.0%、75.0%和52.08%。本研究为研制IBDV抗体间接ELISA检测试剂盒(以重组VP2蛋白作为包被抗原)奠定了基础。
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| 关 键 词： | 传染性法氏囊病病毒 抗体 间接ELISA |
Development of a ELISA using E.coli-expressed truncated VP2 for specific and sensitive detection of antibodies against infectious bursal disease virus |
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| WANG Xiao-li,QIAN Jing,MA Sun-ting,WANG Jing-yu,XIA Xing-xia,ZHU Yu-mei,ZHENG Su-ya,WANG Yong-shan,OUYANG Wei.Development of a ELISA using E.coli-expressed truncated VP2 for specific and sensitive detection of antibodies against infectious bursal disease virus[J].Veterinary Science in China,2020(2):159-167. |
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| Authors: | WANG Xiao-li QIAN Jing MA Sun-ting WANG Jing-yu XIA Xing-xia ZHU Yu-mei ZHENG Su-ya WANG Yong-shan OUYANG Wei |
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| Institution: | (Institute of Veterinary Medicine,Jiangsu Academy of A gricultural Sciences/Key Laboratory of V eterinary Biological Engineering and Technology,Ministry of Agriculture,Nanjing 210014,China;School of Food and Biological Engineering,Jiangs u Univers ity,Zhenjiang 212013,China;Jiangsu Co-innovaiion Center for Prevention and Control of Important Animcd Infectious Diseases and Zoonoses,Yangzhou 225009,China) |
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| Abstract: | Infectious bursa disease(IBD)is an infectious disease caused by infectious bursa disease virus(IBDV)that mainly affects the bursa of young poultry.The aim of the present study is to velop an enzyme-linked immunosorbent assay(ELISA)for detecting the specific antibodies to IBDV using the VP2 protein of IBDV as coating antigen.Three truncated VP2 gene(designated VP2(3-600),VP2(376-975)and VP2(751-1350)were synthesized and expressed in E.coli Rosetta(DE3).These recombinant VP2 proteins were purified and used in enzyme-linked immunosorbent assay(ELISA)for detecting IBDV antibodies in chicken.A total of 96 serum samples obtained from chickens vaccinated with commercial activated vaccine(B87)and non-vaccinated chickens against IBDV were tested using r VP2(3-600)-ELISA,r VP2(376-975)-ELISA,r VP2(751-1350)-ELISA,IDEXX-ELISA(IBDV)and neutralization assay,respectively.The relative sensitivitiy between r VP2(3-600)-ELISA,r VP2(376-975)-ELISA,r VP2(751-1350)-ELISA,IDEXX-ELISA(IBDV)and neutralization assay were 97.1%,61.8%,58.8%and 100%,respectively.The relative specificity between r VP2(3-600)-ELISA,r VP2(376-975)-ELISA,r VP2(751-1350)-ELISA,IDEXX-ELISA(IBDV)and neutralization assay were 85.5%,82.3%,83.9%and 25.8%,respectively.The agreement ratio between r VP2(3-600)-ELISA,r VP2(376-975)-ELISA,r VP2(751-1350)-ELISA,IDEXX-ELISA(IBDV)and neutralization assay were 89.6%,75.0%,75.0%and 52.08%respectively.The sensitivity of the r VP2(3-600)-ELISA,r VP2(376-975)-ELISA and r VP2(751-1350)-ELISA were lower than that of the commercial IDEXX-ELISA(IBDV),but the specificity and agreement ratio were better than that of the commercial IDEXX-ELISA(IBDV).In conclusion,the results demonstrate the potential applicability of the r VP2(3-600)-ELISA,r VP2(376-975)-ELISA and r VP2(751-1350)-ELISA for the determination of antibodies to IBDV in chickens. |
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| Keywords: | infectious bursal disease virus antibody indirect ELISA |
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