Chen Wenxuan, Suo Jingxia, Kong Jiahua, Lu Chunxia, Ge Xiaomin, Yu Fang, Tang Xinming, Suo Xun, Liu Xianyong
State Key Laboratory of Veterinary Public Health and Safety; Key Laboratory of Animal Epidemiology and Zoonosis of Ministry of Agriculture, National Animal Protozoa Laboratory & College of Veterinary Medicine, China Agricultural University, Beijing, China.
Department of Basic Veterinary Medicine, College of Veterinary Medicine, China Agricultural University, Beijing, China.
NPJ Vaccines. 2025 Jul 24;10(1):167. doi: 10.1038/s41541-025-01223-9.
Rabbit coccidiosis and rabbit haemorrhagic disease (RHD) pose major threats to the rabbit industry, causing significant economic losses. Developing a multivalent vaccine to concurrently protect rabbits against Eimeria and RHDV infections would provide dual protection through a single immunization protocol. Here, we utilized a precocious line of E. magna (EmagPWT) as a vaccine vector to express P2 subdomain of RHDV capsid protein VP60. We constructed three transgenic parasites expressing (i) RHDV1-P2 subdomain, (ii) RHDV2-P2 subdomain, and (iii) 2 copies of P2 subdomains from both RHDV1 and RHDV2. We found that all transgenic parasites elicited detectable neutralizing antibodies and robust mucosal immune response following secondary immunization. In conclusion, our results indicate genetically manipulated precocious Eimeria parasite expressing heterologous antigens, such as P2 subdomain, holds promise as a vector for developing a multivalent vaccine against RHD and Eimeria infections in rabbits.
兔球虫病和兔出血性疾病(RHD)对养兔业构成重大威胁,造成巨大经济损失。开发一种多价疫苗以同时保护兔子免受艾美耳球虫和兔出血症病毒(RHDV)感染,将通过单一免疫方案提供双重保护。在此,我们利用巨型艾美耳球虫早熟株(EmagPWT)作为疫苗载体来表达RHDV衣壳蛋白VP60的P2亚结构域。我们构建了三种转基因寄生虫,分别表达(i)RHDV1 - P2亚结构域、(ii)RHDV2 - P2亚结构域以及(iii)来自RHDV1和RHDV2的2个拷贝的P2亚结构域。我们发现,所有转基因寄生虫在二次免疫后均引发了可检测到的中和抗体和强烈的黏膜免疫反应。总之,我们的结果表明,表达异源抗原(如P2亚结构域)的基因工程改造的早熟艾美耳球虫寄生虫有望作为开发针对兔RHD和艾美耳球虫感染的多价疫苗的载体。