A novel monoclonal antibody efficiently blocks the infection of duck adenovirus 3 by targeting Fiber-2

被引:3
作者
Lin, Yun [1 ,2 ,3 ]
Zhang, Wenyuan [1 ,2 ,3 ]
Xie, Jing [1 ,2 ,3 ]
Xie, Quan [1 ,2 ,3 ]
Li, Tuofan [1 ,2 ,3 ]
Wan, Zhimin [1 ,2 ,3 ]
Shao, Hongxia [1 ,2 ,3 ]
Qin, Aijian [1 ,2 ,3 ]
Ye, Jianqiang [1 ,2 ,3 ]
机构
[1] Yangzhou Univ, Coll Vet Med, Key Lab Jiangsu Prevent Vet Med, Key Lab Avian Prevent Med,Minist Educ, 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 & Agriprod Safety, Minist Educ China, Yangzhou 225009, Jiangsu, Peoples R China
关键词
Duck adenovirus 3; Fiber-2; protein; Monoclonal antibody; Neutralizing activity; Epitope mapping;
D O I
10.1016/j.vetmic.2022.109635
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Duck adenovirus 3 (DAdV-3), identified as the causative agent of a disease characterized by swelling and hemorrhage of liver and kidney, has caused substantial economic losses to duck industry in China. However, the neutralizing epitopes and the infection mechanism of DAdV-3 have not been extensively elucidated. In this study, a novel monoclonal antibody (mAb) targeting Fiber-2 protein of DAdV-3 was generated and designated as mAb 3E7. Indirect immunofluorescence assay showed that mAb 3E7 specifically reacted with the Fiber-2 in LMH cells transfected with pcDNA3.1-Fiber-2 or infected with DAdV-3. Moreover, mAb 3E7 could immunoprecipitate the Fiber-2 and efficiently inhibit the infection of DAdV-3 in vitro. Further epitope mapping revealed mAb 3E7 recognized the epitope 108LALGDGLE115 in Fiber-2, which was highly conserved among DAdV-3 strains. These findings not only identified a novel neutralizing epitope in Fiber-2, but also paved the way for further elucidating the vital roles of Fiber-2 in the infection and pathogenesis of DAdV-3.
引用
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页数:6
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