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猪流行性腹泻病毒N蛋白阻断ELISA抗体检测方法的建立及初步应用
引用本文:万颖,周改静,麻园,石正旺,肖书奇,罗俊聪,宋锐,曹丽艳,杨波,王丽娟,田宏,郑海学.猪流行性腹泻病毒N蛋白阻断ELISA抗体检测方法的建立及初步应用[J].畜牧兽医学报,2022,53(4):1173-1181.
作者姓名:万颖  周改静  麻园  石正旺  肖书奇  罗俊聪  宋锐  曹丽艳  杨波  王丽娟  田宏  郑海学
作者单位: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 国家口蹄疫参考实验室, 兰州 730046;2. 西北农林科技大学动物医学院, 杨凌 712100
基金项目:中国农业科学院科技创新工程(CAAS-ASTIP-2020-LYRI)
摘    要:旨在建立一种猪流行性腹泻病毒(PEDV)N蛋白阻断ELISA抗体检测方法.本研究将纯化的N蛋白作为包被抗原,通过棋盘滴定法优化ELISA反应条件,建立了检测PEDV抗体的阻断ELISA方法,并对其进行特异性、敏感性和重复性试验.对140份临床血清样品进行检测,并将检测结果与市售IDvet PEDV间接ELISA抗体检测...

关 键 词:猪流行性腹泻病毒  N蛋白  抗体检测  阻断ELISA
收稿时间:2021-08-13

Development and Application of N-protein Blocking ELISA for Detecting Porcine Epidemic Diarrhea Virus Antibodies
WAN Ying,ZHOU Gaijing,MA Yuan,SHI Zhengwang,XIAO Shuqi,LUO Juncong,SONG Rui,CAO Liyan,YANG bo,WANG Lijuan,TIAN Hong,ZHENG Haixue.Development and Application of N-protein Blocking ELISA for Detecting Porcine Epidemic Diarrhea Virus Antibodies[J].Acta Veterinaria et Zootechnica Sinica,2022,53(4):1173-1181.
Authors:WAN Ying  ZHOU Gaijing  MA Yuan  SHI Zhengwang  XIAO Shuqi  LUO Juncong  SONG Rui  CAO Liyan  YANG bo  WANG Lijuan  TIAN Hong  ZHENG Haixue
Institution:1. National Foot-and-Mouth Disease Reference Laboratory, State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute of Chinese Academy of Agriculture Sciences, Lanzhou 730046, China;2. College of Veterinary Medicine, Northwest A&F University, Yangling 712100, China
Abstract:The purpose of this study is to establish a blocking ELISA antibodies detection method for porcine epidemic diarrhea virus (PEDV). The purified N protein was used as the coating antigen, and the ELISA reaction conditions were optimized by the chess rboard titration. A blocking ELISA method for detecting PEDV antibodies was established, and its specificity, sensitivity and repeatability tests were carried out. One hundred and forty clinical serum samples were tested, and the results were compared with commercially IDvet PEDV indirect ELISA antibodies detection kit. The results showed that the best antigen coating concentration was 625 ng·mL-1, and the best dilution ratio of serum was 1:1; The best dilution of the HRP-conjugated antibody working solution was 1:5 000; There was no cross-reaction with healthy pig serum and the positive sera of common pig disease pathogens, such as classical swine fever virus (CSFV), porcine reproductive and respiratory syndrome virus (PRRSV), porcine circovirus type 2 (PCV2), and transmissible gastroenteritis virus (TGEV). The sensitivity of PEDV positive serum was 1:16, which was equivalent to that of IDvet ELISA kit (titer 1∶32). The coefficient of variation of within-run and between-run repeatability test is less than 10%, so it showed that the blocking ELISA established in this study had good repeatability and stability; the kappa value of detected 140 clinical porcine serum using this method was 0.87 when compared with IDvet ELISA. The above results indicated that the established blocking ELISA method for detecting PEDV antibodies in this study could be applied to the prevention and control of PEDV, epidemiological investigation and the monitoring of antibody levels after vaccine immunization.
Keywords:porcine epidemic diarrhea variant virus  N protein  antibodies detection  blocking ELISA  
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