Neutralization Analysis of a Chicken Single-Chain Variable Fragment Derived from an Immune Antibody Library Against Infectious Bronchitis Virus

被引:5
|
作者
Lin, Yuan [1 ,2 ,3 ]
Li, Benqiang [1 ]
Ye, Jiaxin [1 ]
Wang, Man [1 ]
Wang, Jianhua [3 ]
Zhang, Ying [4 ]
Zhu, Jianguo [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Key Lab Vet Biol, Sch Agr & Biol, Shanghai 200240, Peoples R China
[2] Ningxia Med Univ, Sch Basic Med Sci, Yinchuan, Peoples R China
[3] Northwest Agr & Forestry Univ, Coll Vet Med, Dept Internal Med, Yangling, Peoples R China
[4] ABBIOSCI Inc, Seattle, WA USA
关键词
RECOMBINANT SCFV ANTIBODIES; PHAGE-DISPLAY; MONOCLONAL-ANTIBODIES; SURFACE-ANTIGENS; SPIKE PROTEIN; GENERATION; SELECTION; EPITOPES; BINDING; GENE;
D O I
10.1089/vim.2014.0104
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Avian infectious bronchitis virus (IBV), which is prevalent in many countries causing severe economic loss to the poultry industry, causes infectious bronchitis (IB) in birds. Recombinant single-chain variable fragments (scFvs) have been proven to effectively inhibit many viruses, both in vitro and in vivo, and they could be a potential diagnostic and therapeutic reagent to control IB. In this study, six anti-IBV chicken scFvs, ZL.10, ZL.64, ZL.78, ZL.80, ZL.138, and ZL.256, were obtained by screening random clones from an immune antibody library. An analysis of nucleotide sequences revealed that they represented distinctive genetic sequences and greatly varied in complementarity-determining region three of the heavy chain. Neutralization tests showed that ZL.10, which bound the S1 protein in western blots, inhibited the formation of syncytia in Vero cells 48h post IBV infection and decreased the transcriptional level of nucleoprotein mRNA to 17.2%, while the other five scFvs, including ZL.78 and ZL.256, that bound the N protein did not. In conclusion, the results suggested that specific and neutralizing chicken scFvs against IBV, which can be safe and economical antibody reagents, can be produced in vitro through prokaryotic expression.
引用
收藏
页码:397 / 404
页数:8
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