A novel monoclonal antibodies-based sandwich ELISA for detection of serotype 4 fowl adenovirus

被引:21
|
作者
Shao, Hongxia [1 ,2 ,3 ]
Wang, Ping [1 ,2 ,3 ]
Wang, Weikang [1 ,2 ,3 ]
Zhang, Jianjun [4 ]
Li, Tuofan [1 ,2 ,3 ]
Liang, Guangchen [1 ,2 ,3 ]
Gao, Wei [1 ,2 ,3 ]
Qin, Aijian [1 ,2 ,3 ]
Ye, Jianqiang [1 ,2 ,3 ]
机构
[1] Yangzhou Univ, Key Lab Jiangsu Prevent Vet Med, Key Lab Avian Prevent Med, Minist Educ,Coll Vet Med, 12 East Wenhui Rd, Yangzhou 225009, Jiangsu, Peoples R China
[2] Jiangsu Coinnovat Ctr Prevent & Control Important, Yangzhou 225009, Jiangsu, Peoples R China
[3] Yangzhou Univ, Joint Int Res Lab Agr & Agri Prod Safety, Minist Educ Peoples Republ China, Yangzhou 225009, Jiangsu, Peoples R China
[4] Sinopharm Yangzhou VAC Biol Engn Co Ltd, Yangzhou, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Serotype 4 fowl adenovirus; monoclonal antibody; sandwich ELISA; RECOMBINANT FIBER-2 PROTEIN; HYDROPERICARDIUM SYNDROME; CHICKENS; HEPATITIS;
D O I
10.1080/03079457.2019.1566595
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
As a major causative agent for hepatitis-hydropericardium syndrome (HPS) in chickens, serotype 4 fowl adenovirus (FAdV-4) has caused huge economic losses in the poultry industry globally. However, there is no commercial diagnostic test for FAdV-4 antigens. To generate a rapid approach for specific detection of FAdV-4, a monoclonal antibodies (mAbs)-based sandwich ELISA was developed. In this ELISA, a purified mAb 4A3 and a HRP-labelled mAb 3C2 specific to the fiber-2 of FAdV-4 were used as the capture antibody and detection antibody respectively. Specificity assay revealed the ELISA only reacted with FAdV-4, not with other avian viruses tested. Sensitivity assay showed the limit of detection of the ELISA was 1000 TCID50/ml and 12.5 ng/ml for the FAdV-4 and the purified GST-Fiber2 protein respectively. Moreover, the ELISA could be efficiently applied in detecting the FAdV-4 in tissue samples from a clinically-diseased chicken flock. All these data demonstrated that the ELISA developed here provides a promising tool for rapid and efficient diagnosis of clinical infection with FAdV-4.
引用
收藏
页码:204 / 208
页数:5
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