摘要： 为检测Ⅰ型IBDVVP2蛋白线性B细胞抗原表位肽PJ14和PJ5的免疫原性,将人工合成并纯化的PJ14和PJ5分别与牛血清白蛋白(BSA)和卵清白蛋白(OVA)偶联;将与BSA偶联的PJ14和PJ5分别免疫BALB/c小鼠,然后以与OVA偶联的PJ14和PJ5作为间接酶联免疫吸附试验抗原,分别测定免疫鼠血清中抗相应多肽的抗体。结果显示,免疫小鼠产生了抗PJ14和PJ5的抗体,抗体持续期达21周。表明PJ14和PJ5具有免疫原性。

关键词: IBDV, VP2蛋白, 合成肽, 抗原表位, 免疫

Abstract: The peptides of the linear B-cell epitopes PJ14 and PJ5 on the VP2 protein of infectious bursal disease virus(IBDV)were synthesized and purified,then were conjugated to carrier protein BSA or OVA respectively.The BSA-conjugated PJ14 and PJ5 were inoculated into the BALB/c mice respectively.The OVA-conjugated PJ14 was used as the antigen to detect the anti-PJ14 antibody in the serum of the immunized mice,and so was the OVA-conjugated PJ5.The results showed that the PJ14 and PJ5 after the conjugation to BSA stimulated the production of the anti-PJ14 and anti-PJ5 antibody respectively,and that the antibodies lasted for twenty-one weeks.It indicated the immunogenicity of the PJ14 and PJ5.

Key words: IBDV, VP2 protein, B-cellepitope, Peptidesynthesis, Immunization

中图分类号: 

• S852.4