Huang Benli, Chen Sheng, Wang Zhanxin, Feng Keyu, Teng Yutao, Li Ruoying, Shao Guanming, Rao Jiaqian, Zhang Xinheng, Xie Qingmei
State Key Laboratory of Swine and Poultry Breeding Industry & Heyuan Branch, Guangdong Provincial Laboratory of Lingnan Modern Agricultural Science and Technology, College of Animal Science, South China Agricultural University, Guangzhou, 510642, China; Guangdong Provincial Key Lab of AgroAnimal Genomics and Molecular Breeding, College of Animal Science, South China Agricultural University, Guangzhou, 510642, China; Guangdong Engineering Research Center for Vector Vaccine of Animal Virus, Guangzhou, 510642, China; Zhongshan Innovation Center of South China Agricultural University, Zhongshan, 528400, China.
Wens Foodstuff Group. CO., LTD, Guangdong, Yunfu, 527400, China.
Virol Sin. 2025 Jun;40(3):462-476. doi: 10.1016/j.virs.2025.03.008. Epub 2025 Mar 25.
Infectious bronchitis (IB), a highly contagious acute respiratory disease affecting avian species, poses significant challenges to poultry production. The causative agent, infectious bronchitis virus (IBV), exhibits a high mutation rate, leading to limited cross-protection by existing vaccines. This necessitates the development of novel vaccines. This study, based on preliminary investigations conducted by our research team, identified six potential strains (PYG QX1, ZQF QX2, FQH QX3, LYZ QX4, XXX QX5, and CSL strains) for vaccine development. Previous pathogenicity test and serum cross-neutralization experiments conducted in this study have demonstrated that the FQH QX3 strain exhibited the weakest pathogenicity and the broadest spectrum of serum neutralization, while the CSL strain showed the highest pathogenicity and was the most challenging to neutralize, posing the greatest difficulty in prevention and control. Subsequently, we constructed and rescued recombinant vaccine candidates, H120-FQH QX3, and H120-CSL, expressing the S1 and N proteins of the FQH QX3 and CSL strains, respectively. Immunization protection experiments indicated that the H120-CSL recombinant vaccine candidate exhibited the most effective immune protection, making it a promising candidate for further study and evaluation as a recombinant vaccine. The S1 and N genes of the CSL strain demonstrated strong immunogenicity, making them potential candidate antigen genes for future vaccine development.
传染性支气管炎(IB)是一种影响禽类的高度传染性急性呼吸道疾病,对家禽生产构成重大挑战。病原体传染性支气管炎病毒(IBV)具有很高的突变率,导致现有疫苗的交叉保护作用有限。这就需要开发新型疫苗。本研究基于我们研究团队进行的初步调查,确定了六种潜在的疫苗开发毒株(PYG QX1、ZQF QX2、FQH QX3、LYZ QX4、XXX QX5和CSL毒株)。本研究先前进行的致病性试验和血清交叉中和试验表明,FQH QX3毒株致病性最弱,血清中和谱最广,而CSL毒株致病性最强,最难中和,在预防和控制方面面临最大困难。随后,我们构建并拯救了重组疫苗候选株H120-FQH QX3和H120-CSL,分别表达FQH QX3和CSL毒株的S1和N蛋白。免疫保护实验表明,H120-CSL重组疫苗候选株表现出最有效的免疫保护作用,使其成为作为重组疫苗进行进一步研究和评估的有希望的候选株。CSL毒株的S1和N基因表现出很强的免疫原性,使其成为未来疫苗开发的潜在候选抗原基因。