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抗口疮病毒NA1/11株病毒粒子核心蛋白单克隆抗体的分离与鉴定:作为口疮病毒潜在的诊断工具

Isolation and Characterization of Monoclonal Antibodies Against a Virion Core Protein of Orf Virus Strain NA1/11 As Potential Diagnostic Tool for Orf Viruses.

作者信息

Wang Xiaoping, Zhang Jiafeng, Hao Wenbo, Peng Yongzheng, Li Hong, Li Wei, Li Ming, Luo Shuhong

机构信息

Institute of Antibody Engineering, School of Biotechnology, Southern Medical University , Guangzhou, People's Republic of China .

出版信息

Monoclon Antib Immunodiagn Immunother. 2015 Aug;34(4):233-45. doi: 10.1089/mab.2014.0101.

Abstract

Orf is caused by the orf virus (ORFV) and is a non-systemic, widespread disease afflicting sheep, goats, wild ruminants, and humans. Recent outbreaks in sheep and goats in Jilin and other northern Chinese provinces raise concerns about orf control in China. Thirty-five hybridoma clones were constructed from splenocytes of BALB/c mice immunized with natural orf virus protein. These hybridomas were used to produce antibodies targeting ORFV proteins. Immunological characterization of these monoclonal antibodies (MAb) showed that the 5F2D8 hybridoma line produced MAb that can recognize the 100, 70, and 20 kDa bands from total viral lysate. This hybridoma was further characterized by immunoprecipitation and peptide sequencing. The results indicate that 5F2D8 specifically recognizes orf virus encoded protein ORFV086, a late expression virion core protein that plays important roles in progeny virus particle assembly, morphogenesis, and maturity. Further experiments demonstrate that this MAb did not react with other viral proteins of ORFV orthopoxviruses, but reacted strongly to different field isolates of orf viruses from China. Additionally, this anti-ORFV086 MAb possesses ORFV neutralizing capability. Sequence alignments and phylogenetic analysis determined that ORFV086 of NA1/11, clustered together with NZ2 and IA82, is highly conserved and has structural similarities with the Vaccinia virus core protein P4a. As such, this MAb has great potential as a diagnostic tool for orf viruses, in the further exploration of orf pathogenesis, and in disease control and prevention.

摘要

羊口疮由羊口疮病毒(ORFV)引起,是一种非系统性、广泛传播的疾病,可感染绵羊、山羊、野生反刍动物和人类。中国北方吉林省及其他省份近期绵羊和山羊爆发羊口疮疫情,引发了对中国羊口疮防控的关注。用天然羊口疮病毒蛋白免疫BALB/c小鼠的脾细胞构建了35个杂交瘤克隆。这些杂交瘤用于生产靶向ORFV蛋白的抗体。对这些单克隆抗体(MAb)的免疫学特性分析表明,5F2D8杂交瘤细胞系产生的单克隆抗体可识别病毒总裂解物中的100、70和20 kDa条带。通过免疫沉淀和肽测序对该杂交瘤进行了进一步鉴定。结果表明,5F2D8特异性识别羊口疮病毒编码的蛋白ORFV086,这是一种晚期表达的病毒粒子核心蛋白,在子代病毒粒子组装、形态发生和成熟过程中起重要作用。进一步实验表明,该单克隆抗体不与ORFV正痘病毒的其他病毒蛋白反应,但与来自中国的不同羊口疮病毒野外分离株反应强烈。此外,这种抗ORFV086单克隆抗体具有ORFV中和能力。序列比对和系统发育分析确定,NA1/11的ORFV086与NZ2和IA82聚集在一起,高度保守,与痘苗病毒核心蛋白P4a具有结构相似性。因此,这种单克隆抗体在作为羊口疮病毒诊断工具、进一步探索羊口疮发病机制以及疾病控制和预防方面具有巨大潜力。

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