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鉴定一种新型 B 细胞表位的 ASFV pCP312R 识别使用单克隆抗体。

Identification of a novel B cell epitope of ASFV pCP312R recognized using a monoclonal antibody.

机构信息

Key Laboratory of Zoonosis Prevention and Control of Guangdong Province, College of Veterinary Medicine, South China Agricultural University, Guangzhou, China; African Swine Fever Regional Laboratory of China (Guangzhou), Guangzhou, China.

Key Laboratory of Zoonosis Prevention and Control of Guangdong Province, College of Veterinary Medicine, South China Agricultural University, Guangzhou, China; Guangdong Provincial Key Laboratory of Utilization and Conservation of Food and Medicinal Resources in the Northern Region, Shaoguan University, Shaoguan, China; African Swine Fever Regional Laboratory of China (Guangzhou), Guangzhou, China.

出版信息

Vet Microbiol. 2024 Nov;298:110247. doi: 10.1016/j.vetmic.2024.110247. Epub 2024 Sep 2.

Abstract

African swine fever (ASF) is an acute and devastating infectious disease that has caused significant economic losses to the global pig industry since it was first discovered and reported. African swine fever virus (ASFV) has a large genome encoding more than 160 proteins. The biological characteristics and functions of its various proteins still remain unclear; therefore, the efficacy of specific drugs and vaccines against ASFV remains limited. ASFV pCP312R is an important ASFV protein that exhibits good immunogenicity. In this study, five monoclonal antibodies (mAbs) targeting pCP312R were successfully prepared. Confocal microscopy observations showed that pCP312R was located in the viral factory at the late stage of ASFV infection, and was co-located with p30 and pK205R. These results suggested that pCP312R might be involved in ASFV assembly. Neutralization tests revealed that pCP312R mAb could not neutralize ASFV. Next, we identified the B cell epitopes of one of the most immunogenic mAbs and found a novel epitope of pCP312R, TIPPSTDEEVIR, which was conserved in different pCP312R strains. Overall, five ASFV pCP312R monoclonal antibodies were prepared, and the antigenic epitope of one strain was identified in this study, laying a foundation for further studies on ASFV pCP312R function and facilitating serological diagnosis vaccine development for ASFV.

摘要

非洲猪瘟(ASF)是一种急性、毁灭性的传染病,自首次发现并报告以来,已给全球养猪业造成了重大经济损失。非洲猪瘟病毒(ASFV)基因组庞大,编码超过 160 种蛋白质。其各种蛋白质的生物学特性和功能仍不清楚;因此,针对 ASFV 的特效药物和疫苗的疗效仍然有限。ASFV pCP312R 是一种重要的 ASFV 蛋白,具有良好的免疫原性。本研究成功制备了针对 pCP312R 的 5 株单克隆抗体(mAbs)。共聚焦显微镜观察显示,pCP312R 位于 ASFV 感染晚期的病毒工厂中,与 p30 和 pK205R 共定位。这些结果表明 pCP312R 可能参与 ASFV 的组装。中和试验表明,pCP312R mAb 不能中和 ASFV。接下来,我们鉴定了其中一种免疫原性最强的 mAb 的 B 细胞表位,并发现了 pCP312R 的一个新表位 TIPPSTDEEVIR,该表位在不同的 pCP312R 株中保守。总之,本研究成功制备了 5 株 ASFV pCP312R 单克隆抗体,并鉴定了一株单克隆抗体的抗原表位,为进一步研究 ASFV pCP312R 的功能奠定了基础,也为 ASFV 的血清学诊断和疫苗开发提供了便利。

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