Zhou Yulong, Zhang Jiawen, Wu Hailiang, Zhao Shuai, Ren Yachao, Chen Qiuhui, Zhang Zhe, Liao Xianmao, Mo Yuming, Zhong Yiming, Zhang Guohua
College of Animal Science and Veterinary Medicine, Heilongjiang Bayi Agricultural University, Daqing, 163319, China; Heilongjiang Provincial Technology Innovation Center for Bovine Disease Control and Prevention, Daqing, 163319, China; Heilongjiang Provincial Key Laboratory of Prevention and Control of Bovine Diseases, Daqing, 163319, China.
College of Animal Science and Veterinary Medicine, Heilongjiang Bayi Agricultural University, Daqing, 163319, China.
Virology. 2025 Sep;610:110581. doi: 10.1016/j.virol.2025.110581. Epub 2025 May 25.
Bovine coronavirus (BCoV) is an important pathogen that can cause diarrhea in calves, respiratory disease, and winter dysentery in adult dairy cows. BCoV nucleocapsid protein (N) is highly conserved structural proteins that stimulate a strong immune response in the host, inducing both humoral and cellular immune responses, and are key targets for early and rapid diagnosis of coronaviruses and vaccine development. Therefore, the identification and screening of epitopes on N proteins is essential for the development of sensitive and specific diagnostic methods. In this study, BALB/c mice were immunized with soluble recombinant BCoV N protein expressed with a prokaryotic expression system, and two N-specific monoclonal antibodies (mAbs): 2F9 and 7H6 were prepared that recognize the same linear B-cell epitope with the smallest fragment located at YQQQDG. Homology analysis of the amino acid sequences of the corresponding regions of nine typical BCoV strains from the different areas showed that the epitopes were high conservation. Homology analysis of the corresponding amino acid sequences of other animal-derived coronaviruses within the β coronavirus genus revealed that the homology of this epitope across different species was remarkably low. Intriguingly, it exhibited 100 % identity exclusively with human coronavirus OC43 and canine coronavirus CRCoV/BJ - 221. Such a finding offers crucial insights into viral evolution, transmission dynamics, and strategies for disease prevention and control, thereby highlighting its significance in advancing our understanding of coronaviruses. These findings fill the gaps in the study of BCoV N protein epitopes and promote the understanding of BCoV N protein structure, which is valuable for developing diagnostic methods for detecting BCoV and exploring the biological functions of BCoV N proteins.
牛冠状病毒(BCoV)是一种重要的病原体,可导致犊牛腹泻、呼吸道疾病以及成年奶牛的冬季痢疾。BCoV核衣壳蛋白(N)是高度保守的结构蛋白,可在宿主体内激发强烈的免疫反应,诱导体液免疫和细胞免疫反应,是冠状病毒早期快速诊断及疫苗研发的关键靶点。因此,鉴定和筛选N蛋白上的表位对于开发灵敏且特异的诊断方法至关重要。在本研究中,用原核表达系统表达的可溶性重组BCoV N蛋白免疫BALB/c小鼠,制备了两种N特异性单克隆抗体(mAb):2F9和7H6,它们识别相同的线性B细胞表位,最小片段位于YQQQDG。对来自不同地区的9株典型BCoV菌株相应区域的氨基酸序列进行同源性分析,结果表明这些表位具有高度保守性。对β冠状病毒属内其他动物源冠状病毒相应氨基酸序列进行同源性分析发现,该表位在不同物种间的同源性极低。有趣的是,它仅与人冠状病毒OC43和犬冠状病毒CRCoV/BJ - 221具有100%的同一性。这一发现为病毒进化、传播动态以及疾病预防控制策略提供了关键见解,从而凸显了其在增进我们对冠状病毒理解方面的重要性。这些发现填补了BCoV N蛋白表位研究的空白,促进了对BCoV N蛋白结构的理解,对于开发检测BCoV的诊断方法以及探索BCoV N蛋白的生物学功能具有重要价值。