Jiang Qian, Ma Zhigang, Min Fang, Ding Xiaojun, Liang Yumeng, Wang Jinquan, Liu Lu, Li Na, Sun Yawei, Zhong Qi, Yao Gang, Ma Xuelian
College of Veterinary Medicine, Xinjiang Agricultural University, Urumqi 830052, China.
Xinjiang Key Laboratory of New Drug Study and Creation for Herbivorous Animal (XJ-KLNDSCHA), Xinjiang Agricultural University, Urumqi 830052, China.
Transbound Emerg Dis. 2024 Jul 18;2024:5986893. doi: 10.1155/2024/5986893. eCollection 2024.
Bovine coronavirus (BCoV) is a causative agent of enteric and respiratory disease in cattle. BCoV has been reported to cause a variety of animal diseases and is closely related to human coronaviruses; moreover, it has attracted extensive attention from both cattle farmers and researchers. With the rise of BCoV, a vaccine that is prophylactic and immunotherapeutic has to be utilized for a preemptive and adroit therapeutic approach. The aim of this study was to develop a novel multiepitope-based BCoV vaccine that can induce an immune response using a silicon reverse vaccinology approach. In this study, an immunoinformatics approach was employed to identify potential vaccine targets against BCoV, and four candidate antigen proteins were selected to predict B-cell and T-cell epitopes. To identify dominant epitopes, we employed a variety of bioinformatics techniques, including antigenicity prediction, immunogenicity assessment, allergenicity analysis, conservative analysis, and toxicity assessment. Finally, six multiepitope vaccines were developed using dominant epitopes, suitable adjuvants, Pan HLADR-binding epitope (PADRE), and linkers. Then based on the antigenicity score, solubility analysis, allergenicity evaluation, physicochemical property assessment, and tertiary structure verification score, construct 6 was selected as the best candidate vaccine; it was named CY. Molecular modeling and structural validation ensured the high-quality 3D structure of construct CY. The immunogenicity and complex stability of the vaccine were evaluated by molecular docking and kinetic simulation. In silicon clones, the BCoV vaccine had high levels of gene expression in the insect expression system. These results may contribute to the development of experimental BCoV vaccines with higher potency and safety.
牛冠状病毒(BCoV)是牛肠道和呼吸道疾病的病原体。据报道,BCoV可引发多种动物疾病,且与人类冠状病毒密切相关;此外,它已引起养牛户和研究人员的广泛关注。随着BCoV的出现,必须使用一种具有预防和免疫治疗作用的疫苗来采取先发制人和巧妙的治疗方法。本研究的目的是利用硅反向疫苗学方法开发一种新型的基于多表位的BCoV疫苗,该疫苗能够诱导免疫反应。在本研究中,采用免疫信息学方法来确定针对BCoV的潜在疫苗靶点,并选择了四种候选抗原蛋白来预测B细胞和T细胞表位。为了确定优势表位,我们采用了多种生物信息学技术,包括抗原性预测、免疫原性评估、致敏性分析、保守性分析和毒性评估。最后,利用优势表位、合适的佐剂、泛HLA-DR结合表位(PADRE)和连接子开发了六种多表位疫苗。然后根据抗原性评分、溶解度分析、致敏性评估、理化性质评估和三级结构验证评分,选择构建体6作为最佳候选疫苗;将其命名为CY。分子建模和结构验证确保了构建体CY的高质量三维结构。通过分子对接和动力学模拟评估了疫苗的免疫原性和复合物稳定性。在硅克隆中,BCoV疫苗在昆虫表达系统中具有高水平的基因表达。这些结果可能有助于开发出效力更高、安全性更高的实验性BCoV疫苗。