Wang Wenjie, Bi Zhenwei, Liu Yakun, Xia Xingxia, Qian Jing, Tan Yeping, Zhu Yumei, Song Suquan, Yan Liping
Institute of Veterinary Medicine, Jiangsu Academy of Agricultural Sciences, Key Laboratory of Veterinary Biological Engineering and Technology, Ministry of Agriculture and Rural Affairs, Nanjing, Jiangsu 210014, China; MOE Joint International Research Laboratory of Animal Health and Food Safety, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, Jiangsu 210095, China.
Institute of Veterinary Medicine, Jiangsu Academy of Agricultural Sciences, Key Laboratory of Veterinary Biological Engineering and Technology, Ministry of Agriculture and Rural Affairs, Nanjing, Jiangsu 210014, China; GuoTai (Taizhou) Center of Technology Innovation for Veterinary Biologicals, Taizhou, Jiangsu 225300, China.
Int J Biol Macromol. 2023 Aug 15;246:125584. doi: 10.1016/j.ijbiomac.2023.125584. Epub 2023 Jun 29.
Canine distemper virus (CDV) is an economically important virus responsible for canine distemper (CD), a highly contagious disease that afflicts various animal species worldwide. The hemagglutinin (H) protein is the major neutralizing target of virus. Therefore, it is often considered as immunogen to prepare neutralizing antibodies. The accurate identification of neutralizing epitope will provide important antigenic information and extend the knowledge of mechanisms of virus neutralization. In this study, we generated a neutralizing monoclonal antibody (mAb) 4C6 against CDV H protein, and defined the minimal linear epitope 238DIEREFDT245, which was highly conserved in America-1 genotype of CDV strains (vaccines). The mAb 4C6 could not react with a CDV strain that had two substitutions of D238Y and R241G in the epitope, which appeared in most CDV strains of the other genotypes. Besides, a few different amino acid mutations in the epitope were also included. Collectively, the epitope 238DIEREFDT245 was variable in the other genotypes of CDV strains. The epitope 238DIEREFDT245 was exposed to the surface of CDV H protein, showing good antigenicity. These data will provide insights into structure, function and antigenicity of H protein and lay the foundation for the development of diagnostic technologies and vaccine design for CDV.
犬瘟热病毒(CDV)是一种具有重要经济意义的病毒,可引发犬瘟热(CD),这是一种在全球范围内感染多种动物物种的高度传染性疾病。血凝素(H)蛋白是该病毒的主要中和靶点。因此,它常被视为制备中和抗体的免疫原。准确鉴定中和表位将提供重要的抗原信息,并拓展对病毒中和机制的认识。在本研究中,我们制备了一种针对CDV H蛋白的中和单克隆抗体(mAb)4C6,并确定了最小线性表位238DIEREFDT245,该表位在CDV毒株(疫苗)的美洲-1基因型中高度保守。mAb 4C6不能与一株在表位中有D238Y和R241G两个替换的CDV毒株反应,这两个替换出现在大多数其他基因型的CDV毒株中。此外,该表位中还存在一些不同的氨基酸突变。总体而言,表位238DIEREFDT245在其他基因型的CDV毒株中具有变异性。表位238DIEREFDT245暴露于CDV H蛋白表面,具有良好的抗原性。这些数据将为深入了解H蛋白的结构、功能和抗原性提供见解,并为犬瘟热病毒诊断技术的开发和疫苗设计奠定基础。