Huang Jing, Hu Yaping, Niu Zikang, Hao Wei, Ketema Hirpha, Wang Zhipeng, Xu Junjie, Sheng Le, Cai Yuze, Yu Zhenghong, Cai Yafei, Zhang Wei
College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Jinling Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing 210002, China.
Vet Sci. 2024 Aug 13;11(8):373. doi: 10.3390/vetsci11080373.
Bovine viral diarrhea virus (BVDV) is an RNA virus associated with severe economic losses in animal production. Effective vaccination and viral surveillance are urgent for the prevention and control of BVDV infection. However, the application of traditional modified live vaccines and inactivated vaccines is faced with tremendous challenges. In the present study, we describe the preclinical efficacy of two BVDV mRNA vaccines tested in mice and guinea pigs, followed by a field trial in goats, where they were compared to a commercial vaccine (formaldehyde inactivated). The two mRNAs were engineered to express the envelope protein E2 of BVDV-1, the most prevalent subtype across the world, through a 5' cap-dependent or independent fashion. Better titers of neutralizing antibodies against BVDV-1 were achieved using the capped RNA in the sera of mice and guinea pigs, with maximum values reaching 9.4 and 13.7 (by -log), respectively, on the 35th day post-vaccination. At the same time point, the antibody levels in goats were 9.1 and 10.2 for the capped and capless RNAs, respectively, and there were no significant differences compared to the commercial vaccine. The animals remained healthy throughout the experiment, as reflected by their normal leukogram profiles. Collectively, our findings demonstrate that mRNA vaccines have good safety and immunogenicity, and we laid a strong foundation for the further exploitation of efficient and safe BVDV vaccines.
牛病毒性腹泻病毒(BVDV)是一种RNA病毒,与动物生产中的严重经济损失相关。有效接种疫苗和进行病毒监测对于预防和控制BVDV感染至关重要。然而,传统的减毒活疫苗和灭活疫苗的应用面临巨大挑战。在本研究中,我们描述了两种BVDV mRNA疫苗在小鼠和豚鼠中进行的临床前效力测试,随后在山羊中进行了田间试验,并将它们与一种商业疫苗(甲醛灭活疫苗)进行比较。这两种mRNA被设计成通过5'帽依赖性或非依赖性方式表达世界上最普遍的亚型BVDV-1的包膜蛋白E2。使用加帽RNA在小鼠和豚鼠血清中获得了针对BVDV-1的更高中和抗体滴度,在接种疫苗后第35天,最大值分别达到9.4和13.7(以-log表示)。在同一时间点,加帽和无帽RNA在山羊中的抗体水平分别为9.1和10.2,与商业疫苗相比无显著差异。通过正常的白细胞图谱反映出,动物在整个实验过程中保持健康。总体而言,我们的研究结果表明mRNA疫苗具有良好的安全性和免疫原性,为进一步开发高效、安全的BVDV疫苗奠定了坚实基础。