重组DNA
病毒学
生物
抗体
口蹄疫病毒
大肠杆菌
病毒
接种疫苗
抗原
免疫学
基因
生物化学
作者
Chao He,Hua Wang,Hongfei Wei,Youyou Yan,Tiesuo Zhao,Xiaoping Hu,Ping Luo,Liying Wang,Yongli Yu
出处
期刊:Vaccine
[Elsevier]
日期:2010-04-01
卷期号:28 (19): 3435-3439
被引量:23
标识
DOI:10.1016/j.vaccine.2010.02.072
摘要
To distinguish the antibodies induced by Foot-and-mouth disease virus (FMDV) infection from those induced by vaccination, a recombinant N-terminal truncated FMDV non-structural protein (NSP) of 3AB, designated as r3aB, was constructed by deleting 80 amino acids displayed about 30% homology to transposase IS4 family protein of Escherichia coli, expressed in E. coli BL21 (DE3) and then purified. The r3aB was majorly expressed in soluble fraction and presented as homogeneous monomers after purification. Using r3aB as coating antigen, an indirect ELISA was established to specifically identify antibodies induced by FMDV infection but not those induced by vaccination. Compared with 3AB, r3aB was more specific to catch antibodies against NSP. The performance of this assay was validated by two commercial FMDV NSP ELISA kits. The result suggested that the r3aB coated ELISA could be developed into a kit to better distinguish between infected and vaccinated cattle.
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