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B-cell epitopes of African horse sickness virus serotype 4 recognised by immune horse sera

机译:免疫马血清识别的非洲马病病毒血清型4的B细胞表位

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摘要

Identifying antigenic proteins and mapping their epitopes is important for the development of diagnostic reagents and recombinant vaccines. B-cell epitopes of African horse sickness virus (AHSV) have previously been mapped on VP2, VP5, VP7 and NS1, using mouse, rabbit and chicken monoclonal antibodies. A comprehensive study of the humoral immune response of five vaccinated horses to AHSV-4 antigenic peptides was undertaken. A fragmented-genome phage display library expressing a repertoire of AHSV-4 peptides spanning the entire genome was constructed. The library was affinity selected for binders on immobilised polyclonal immunoglobulin G (IgG) isolated from horse sera collected pre- and post-immunisation with an attenuated AHSV-4 monovalent vaccine. The DNA inserts of binding phages were sequenced with Illumina high-throughput sequencing. The data were normalised using pre-immune IgG-selected sequences. More sequences mapped to the genes coding for NS3, VP6 and VP5 than to the other genes. However, VP2 and VP5 each had more antigenic regions than each of the other proteins. This study identified a number of epitopes to which the horse’s humoral immune system responds during immunisation with AHSV-4.
机译:鉴定抗原蛋白并定位其表位对于开发诊断试剂和重组疫苗很重要。先前已使用小鼠,兔和鸡的单克隆抗体将非洲马瘟病毒(AHSV)的B细胞表位定位在VP2,VP5,VP7和NS1上。进行了五只接种疫苗的马对AHSV-4抗原肽的体液免疫应答的综合研究。构建了片段化的基因组噬菌体展示文库,该文库表达了横跨整个基因组的AHSV-4肽库。选择文库中结合物的亲和力,该结合物是用减毒的AHSV-4单价疫苗免疫前和免疫后从马血清中分离的固定化多克隆免疫球蛋白G(IgG)。用Illumina高通量测序对结合噬菌体的DNA插入片段进行测序。使用免疫前IgG选择的序列将数据标准化。与编码其他基因相比,映射到编码NS3,VP6和VP5的基因的序列更多。但是,VP2和VP5各自具有比其他蛋白质更多的抗原区域。这项研究确定了在AHSV-4免疫过程中,马的体液免疫系统会对其做出反应的许多表位。

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