Preparation and characterization of a mouse polyclonal antibody against the truncated ORFV113 recombinant protein of Orf virus

IF 2.3 2区 农林科学 Q1 VETERINARY SCIENCES
Shaobo Liang, Qinqin Long, Feng Pang
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引用次数: 0

Abstract

Orf is a contagious zoonotic disease caused by Orf virus (ORFV), posing a threat to both animal and human health. The ORFV113 gene, located in the terminal variable region of the ORFV genome, has been demonstrated as a significant virulence gene, but its function remains largely unknown. In the study, we first amplified the truncated version of the ORFV113 gene (ORFV113t) by removing its transmembrane domain at the 5′ end. We then constructed the pET-32a-ORFV113t recombinant plasmid and expressed the truncated ORFV113 recombinant protein in Escherichia coli (E.coli). The purified ORFV113t fusion protein was used to immunize mice and generate a polyclonal antibody. This polyclonal antibody was subsequently used to detect the expression and subcellular localization of the ORFV113 protein. Additionally, virus neutralization test was utilized to determine the neutralizing titer of the polyclonal antibody. The results demonstrated that we successfully expressed the ORFV113t recombinant protein in a prokaryotic expression system and generated a mouse-derived polyclonal antibody targeting the ORFV113t recombinant protein with a titer of 1:204,800. This antibody exhibited specificity for detecting the ORFV113 protein expressed in both prokaryotic and eukaryotic cells. The ORFV113 protein was found to be localized in the cytoplasm of infected Lamb testis (LT) cells. Notably, the polyclonal antibody demonstrated neutralizing activity against ORFV in vitro, with a neutralizing titer of 1:32. The prepared mouse anti-ORFV113t protein polyclonal antibody can be utilized for further study on potential functions of the ORFV113 protein in viral pathogenesis.
针对截短的 Orf 病毒 ORFV113 重组蛋白的小鼠多克隆抗体的制备与表征。
奥尔夫病是由奥尔夫病毒(ORFV)引起的一种传染性人畜共患病,对动物和人类健康都构成威胁。ORFV113基因位于ORFV基因组的末端可变区,已被证实是一个重要的毒力基因,但其功能在很大程度上仍然未知。在这项研究中,我们首先扩增了ORFV113基因的截短版本(ORFV113t),去除了其5'端的跨膜结构域。然后,我们构建了 pET-32a-ORFV113t 重组质粒,并在大肠杆菌(E.coli)中表达了截短的 ORFV113 重组蛋白。纯化的 ORFV113t 融合蛋白被用来免疫小鼠并产生多克隆抗体。这种多克隆抗体随后被用来检测 ORFV113 蛋白的表达和亚细胞定位。此外,我们还利用病毒中和试验确定了多克隆抗体的中和滴度。结果表明,我们成功地在原核表达系统中表达了 ORFV113t 重组蛋白,并产生了针对 ORFV113t 重组蛋白的小鼠多克隆抗体,抗体滴度为 1:204,800。该抗体对检测原核细胞和真核细胞中表达的 ORFV113 蛋白均有特异性。研究发现,ORFV113 蛋白定位于受感染的羔羊睾丸(LT)细胞的细胞质中。值得注意的是,该多克隆抗体在体外对 ORFV 具有中和活性,中和滴度为 1:32。制备的小鼠抗 ORFV113t 蛋白多克隆抗体可用于进一步研究 ORFV113 蛋白在病毒致病过程中的潜在功能。
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来源期刊
Veterinary journal
Veterinary journal 农林科学-兽医学
CiteScore
4.10
自引率
4.50%
发文量
79
审稿时长
40 days
期刊介绍: The Veterinary Journal (established 1875) publishes worldwide contributions on all aspects of veterinary science and its related subjects. It provides regular book reviews and a short communications section. The journal regularly commissions topical reviews and commentaries on features of major importance. Research areas include infectious diseases, applied biochemistry, parasitology, endocrinology, microbiology, immunology, pathology, pharmacology, physiology, molecular biology, immunogenetics, surgery, ophthalmology, dermatology and oncology.
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