Identification of the B-cell epitopes on N protein of type 2 porcine reproductive and respiratory syndrome virus, using monoclonal antibodies

被引:8
作者
Zhang, Gaiping [1 ,2 ]
Li, Ning [1 ]
Chen, Yumei [1 ]
Zhou, Jingming [1 ]
Liu, Hongliang [1 ]
Qi, Yanhua [1 ]
Liu, Yankai [1 ]
Peng, Yayun [1 ]
Sun, Huanping [1 ]
Wang, Aiping [1 ]
机构
[1] Zhengzhou Univ, Sch Life Sci, Zhengzhou 450001, Henan, Peoples R China
[2] Henan Zhongze Biol Engn Co Ltd, Zhengzhou 450002, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
PRRSV; N protein; Epitope; Monoclonal antibody; NUCLEOCAPSID PROTEIN; NORTH-AMERICAN;
D O I
10.1016/j.ijbiomac.2019.02.140
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Porcine reproductive and respiratory syndrome virus (PRRSV) nucleocapsid protein (N) is the immunodominant region of PRRSV viral proteins. However, B cell epitopes present on N protein have not been well characterized. In this study, The ORF7 gene was amplified by RT-PCR and inserted into the expression vector pET-28a, the constructed pET-28a-N was transformed into Escherichia coli BL21. After expression, purification and identification, the recombined N protein was used as the target to generate monoclonal antibody (mAb). Strains of hybridoma cells secreting anti-N mAbs were obtained by the hybridoma technique. Three of them (named 1G4, 106, 3D11) were specifically reacted with PRRSV by IPMA and IFA. To identify the B-cell epitopes within PRRSV N protein, six serial overlapping synthesized peptides (P1-P6) covering the whole region of N were used to define the epitopes recognized by 1G4,106, 3D11. Importantly, after the identification of dot-ELISA and indirect ELISA, we found that 1-15aa was a new epitope which had never been reported before and that it was highly conserved among some HP-PRRSV isolates of type 2 PRRSV. The results of this study might open new perspectives on the detection of PRRSV and have important implications for studing the structure of the N protein. (C) 2019 Published by Elsevier B.V.
引用
收藏
页码:300 / 306
页数:7
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