Zhang Yuanyuan, Cheng Jing, Liu Wenxiao, Zhou Linyi, Yang Chun, Li Yongqing, Du Enqi
College of Veterinary Medicine, Northwest A&F University, Yangling, China; Institute of Animal Husbandry and Veterinary Medicine, Beijing Academy of Agriculture and Forestry Sciences, Beijing, China; Research Center for Infectious Diseases in Livestock and Poultry, Beijing Academy of Agriculture and Forestry Sciences, Beijing, China; Sino-UK Joint Laboratory for Prevention & Control of Infectious Diseases in Livestock and Poultry, Beijing, China.
Institute of Animal Husbandry and Veterinary Medicine, Beijing Academy of Agriculture and Forestry Sciences, Beijing, China; Research Center for Infectious Diseases in Livestock and Poultry, Beijing Academy of Agriculture and Forestry Sciences, Beijing, China; Sino-UK Joint Laboratory for Prevention & Control of Infectious Diseases in Livestock and Poultry, Beijing, China.
Int J Biol Macromol. 2025 May;308(Pt 4):142767. doi: 10.1016/j.ijbiomac.2025.142767. Epub 2025 Apr 1.
Bovine viral diarrhea virus (BVDV) is a major pathogen in cattle herds, widely distributed across the globe and causing significant economic losses to the cattle industry. The nonstructural protein NS3 is highly conserved across BVDV subtypes. Identifying and screening epitopes on BVDV NS3 is crucial for developing sensitive, specific diagnostic tools. In this study, we obtained three monoclonal antibodies (mAbs) against the NS3 protein: 2F7, 3E8, and 4D6. Three novel linear B-cell epitope EYG, FLDIA, and EYGVK were identified through reactions of these mAbs with a series of continuous-truncated peptides and one of which a rare three-amino-acid B-cell epitope EYG. Critical amino acid residues were further characterized through alanine (A)-scanning mutagenesis. Sequence alignment revealed that EYG and EYGVK were highly conserved allowing mAbs 2F7 and 4D6 to recognize all BVDV subtypes. In contrast, FLDIA was specifically conserved in BVDV-1 and BVDV-3 enabling 3E8 mAb to differential diagnosis BVDV-2 from other BVDV subtypes. Additionally, preliminary diagnostic assays for BVDV were established by western blotting and peptide-based blocking ELISA. Moreover, we observed that these mAbs could inhibit the replication of BVDV. These findings provide a theoretical foundation for developing of therapeutic strategies for nonstructural protein and accurate diagnostic procedures.
牛病毒性腹泻病毒(BVDV)是牛群中的一种主要病原体,广泛分布于全球,给养牛业造成重大经济损失。非结构蛋白NS3在BVDV各亚型中高度保守。鉴定和筛选BVDV NS3上的表位对于开发灵敏、特异的诊断工具至关重要。在本研究中,我们获得了三种针对NS3蛋白的单克隆抗体(mAb):2F7、3E8和4D6。通过这些mAb与一系列连续截短肽的反应,鉴定出三个新的线性B细胞表位EYG、FLDIA和EYGVK,其中之一EYG是罕见的三氨基酸B细胞表位。通过丙氨酸(A)扫描诱变进一步鉴定关键氨基酸残基。序列比对显示,EYG和EYGVK高度保守,使mAb 2F7和4D6能够识别所有BVDV亚型。相比之下,FLDIA在BVDV-1和BVDV-3中特异性保守,使3E8 mAb能够将BVDV-2与其他BVDV亚型进行鉴别诊断。此外,通过蛋白质印迹法和基于肽的阻断ELISA建立了BVDV的初步诊断方法。此外,我们观察到这些mAb能够抑制BVDV的复制。这些发现为开发针对非结构蛋白的治疗策略和准确的诊断程序提供了理论基础。