Identification of two novel epitopes targeting glycoprotein E of pseudorabies virus using monoclonal antibodies

文献类型： 外文期刊

第一作者： Xu, Jing-jing

作者： Xu, Jing-jing;Wu, Ji-qiang;Cheng, Xue-fei;Tong, Wu;Zheng, Hao;Zhu, Hao-jie;Liu, Yu-ting;Jiang, Yi-feng;Gao, Fei;Yu, Hai;Shan, Tong-ling;Li, Guo-xin;Tong, Guang-zhi;Li, Guo-xin;Tong, Guang-zhi

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关键词： Pseudorabies virus; gE; Monoclonal antibody; Epitopes

期刊名称：BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS （ 影响因子：3.575； 五年影响因子：3.381 ）

ISSN： 0006-291X

年卷期： 2019 年 519 卷 2 期

页码：

收录情况： SCI

摘要： Pseudorabies virus (PRV), the agent of pseudorabies, has raised considerable attention since 2011 due to the outbreak of emerging PRV variants in China. In the present study, we obtained two monoclonal antibodies (mAbs) known as 2E5 and 5C3 against the glycoprotein E (gE) of a PRV variant (JS-2012 strain). The two mAbs reacted with wild PRV but not the vaccine strain (gE-deleted virus). The 2E5 was located in (RLRRE165)-R-161, which was conserved in almost of all PRV strains, while 5C3 in (148)EMGIGDY(154) was different from almost of all genotype I PRV, in which the 149th amino acid is methionine (M) instead of arginine (R). The two epitopes peptides located in the hydrophilic region and reacted with positive sera against genotype II PRV (JS-2012), which suggests they were likely dominant B-cell epitopes. Furthermore, the mutant peptide (148)ERGIGDY(154) (genotype I) did not react with the mAb 5C3 or positive sera against genotype II PRV (JS-2012). In conclusion, both mAb 2E5 and 5C3 could be used to identify wild PRV strains from vaccine strains, and mAb 5C3 and the epitope peptide of 5C3 might be used for epidemiological investigation to distinguish genotype II from genotype I PRV. (C) 2019 Elsevier Inc. All rights reserved.

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