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基于从噬菌体展示肽库获得的模拟表位鉴定牛病毒性腹泻病毒(BVDV)核心蛋白中的B细胞表位。

The identification of a B-cell epitope in bovine viral diarrhea virus (BVDV) core protein based on a mimotope obtained from a phage-displayed peptide library.

作者信息

Chen Xinye, Ding Xiuyan, Zhu Liqian, Zhang Gaiping

机构信息

College of Life Sciences, Hebei University, Baoding 071002, China; College of Veterinary Medicine, Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou 225009, China.

College of Life Sciences, Hebei University, Baoding 071002, China; College of Veterinary Medicine, Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou 225009, China.

出版信息

Int J Biol Macromol. 2021 Jul 31;183:2376-2386. doi: 10.1016/j.ijbiomac.2021.06.013. Epub 2021 Jun 7.

Abstract

Bovine pestivirus A and B, previously known as bovine viral diarrhea virus (BVDV)-1 and 2, respectively, are important pathogens of cattle worldwide, which causes significant economic losses. B-cell epitopes in BVDV glycoprotein E2 and nonstructural protein NS2/3 have been extensively identified. In this study, we screened a 12-mer phage display peptide library using commercial goat anti-BVDV serum, and identified a mimotope "LTPHKHHKHLHA" referred to as P3. With sequence alignment, a putative B-cell epitope "ESRKKLEKALLA" termed as P3-BVDV1/2 residing in BVDV core protein was identified. The synthesized peptides of both P3 and P3-BVDV1/2 show strong reactivity with BVDV serum in immune blot assay. Immunization of mice with these individual peptides leads to the production of antibody that cannot neutralize virus infectivity. Thus for the first time we identified a B-cell epitope, "ESRKKLEKALLA", in BVDV core protein. Interestingly, the epitope was highly conserved in Pestivirus A, B, C, D, as well as emerging Pestivirus E and I, but highly variable in Pestiviruses H, G, F, and J, as well as unclassified Pestivirus originated from non-ruminant animals. Whether this putative B-cell epitope is implicated in pestivirus pathogenesis or evolution needs further investigations once large numbers of isolates are available in the future.

摘要

牛瘟病毒A和B,以前分别称为牛病毒性腹泻病毒(BVDV)-1和2,是全球牛的重要病原体,会造成重大经济损失。BVDV糖蛋白E2和非结构蛋白NS2/3中的B细胞表位已被广泛鉴定。在本研究中,我们使用商业化山羊抗BVDV血清筛选了一个12肽噬菌体展示肽库,并鉴定出一个模拟表位“LTPHKHHKHLHA”,称为P3。通过序列比对,在BVDV核心蛋白中鉴定出一个假定的B细胞表位“ESRKKLEKALLA”,称为P3-BVDV1/2。P3和P3-BVDV1/2的合成肽在免疫印迹分析中与BVDV血清显示出强反应性。用这些单个肽免疫小鼠会导致产生不能中和病毒感染性的抗体。因此,我们首次在BVDV核心蛋白中鉴定出一个B细胞表位“ESRKKLEKALLA”。有趣的是,该表位在瘟病毒A、B、C、D以及新出现的瘟病毒E和I中高度保守,但在瘟病毒H、G、F和J以及源自非反刍动物的未分类瘟病毒中高度可变。一旦未来有大量分离株可用,这个假定的B细胞表位是否与瘟病毒发病机制或进化有关需要进一步研究。

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