Wang Yufei, Xu Siyi, Chen Xia, Dou Yunlong, Yang Xingzhu, Hu Zenglei, Wu Shuang, Wang Xiaoquan, Hu Jiao, Liu Xiufan
Key Laboratory of Avian Bioproducts Developmen, Ministry of Agriculture and Rural Affairs, China; Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonosis, Yangzhou University, Yangzhou, Jiangsu, China.
Joint International Research Laboratory of Agriculture and Agri-Product Safety, Ministry of Education of China, Yangzhou University, Yangzhou, China.
Poult Sci. 2025 Jan;104(1):104565. doi: 10.1016/j.psj.2024.104565. Epub 2024 Nov 26.
The novel duck reovirus (NDRV) disease causes high economic losses, resulting in substantial economic losses in waterfowl industry. However, currently, no commercial vaccines are available to alleviate NDRV infection throughout the world. Here, we developed two subunit vaccine candidates for NDRV based on the insect cell-baculovirus expression system (IC-BEVS). Two recombinant viruses, namely rBac-σB and rBac-σC, were successfully generated based on the consensus sequence of NDRV. Then, the σB and σC subunit vaccine candidates were prepared by directly inactivating the recombinant virus infected-Sf9 cell suspension. The double antibody-sandwich ELISA was used for quantitative of σB or σC protein in the inactivated crude antigen. Protective efficacy results revealed that, compared with the whole virus inactivated vaccine, a single dose of 160 ng σB or σC protein showed advantages in inducing serum antibodies, elevating weight, alleviating liver and spleen injury, restraining viral shedding and viral replication in ducklings. To be noted, the subunit σC or the combination of subunit σB and σC vaccine candidates had better protective efficacies, especially the combined σB and σC vaccine group. Therefore, our study provides useful information for developing effective vaccine against NDRV infection.
新型鸭呼肠孤病毒(NDRV)病造成了巨大的经济损失,给水禽产业带来了重大的经济损失。然而,目前全世界尚无商业疫苗可用于减轻NDRV感染。在此,我们基于昆虫细胞-杆状病毒表达系统(IC-BEVS)开发了两种针对NDRV的亚单位疫苗候选物。基于NDRV的共有序列成功构建了两种重组病毒,即rBac-σB和rBac-σC。然后,通过直接灭活感染重组病毒的Sf9细胞悬液制备了σB和σC亚单位疫苗候选物。采用双抗体夹心ELISA法定量灭活粗抗原中的σB或σC蛋白。保护性效力结果显示,与全病毒灭活疫苗相比,单剂量160 ng的σB或σC蛋白在诱导血清抗体、增加体重、减轻肝脏和脾脏损伤、抑制雏鸭病毒排泄和病毒复制方面具有优势。需要注意的是,亚单位σC或亚单位σB与σC的联合疫苗候选物具有更好的保护性效力,尤其是联合的σB和σC疫苗组。因此,我们的研究为开发针对NDRV感染的有效疫苗提供了有用信息。