Bashir Shahbaz, Kossarev Andrey, Martin Violeta Cascon, Paeshuyse Jan
Laboratory of Host Pathogen Interaction in Livestock, Department of Biosystems, Division of Animal and Human Health Engineering, KU Leuven University, 3000 Leuven, Belgium.
Vet Sci. 2020 Oct 31;7(4):169. doi: 10.3390/vetsci7040169.
Bovine viral diarrhea virus (BVDV) is a (+) ssRNA virus that belongs to the family . BVDV is a significant animal pathogen causing substantial economic losses to the cattle industry worldwide through respiratory and gastrointestinal infections and abortion or birth of persistently infected calves. While the immunogenic profile of some of the BVDV proteins (i.e., E, E2 and NS3) is well established during viral pathogenesis, very little information is available about most of BVDV's non-structural proteins in this regard. In recent times, the NS4B protein has emerged as an interesting target of diagnostic, vaccination and therapeutic value in viral infections of other members of the family due to its key scaffold-like contribution in the viral replication complex. Although, BVDV-NS4B has a membrane topology alongside its role in induction of autophagosomes . However, information on its immunogenicity during BVDV pathogenesis and vaccination is scarce. To characterize the immunogenic profile of the NS4B, five cows were vaccinated with the live attenuated BVDV vaccine Bovela and blood samples were taken pre- and post-immunization for serum isolation. Virus neutralization assay (VNA) confirmed the presence of anti-BVDV antibodies in the sera of vaccinated cows. VNA also revealed pre-existing antibodies against BVDV in the pre-immunization sera of two cows. To identify BVDV-NS4B specific antibodies, the NS4B protein was expressed in mammalian cells by using the pCI-neo vector system. The sera from BVDV vaccinated cows were evaluated for the presence of BVDV-NS4B specific antibodies through western blot and indirect ELISA. Interestingly, t sera from cows with pre-existing immunity against BVDV were able to detect NS4B in western blot and ELISA, suggesting the presence of NS4B-specific antibodies. The obtained results provide the first indication of the immunogenic nature of BVDV-NS4B protein in sero-converted animals. These findings are consistent with the observation made for NS4B in other members and confirm this protein as an interesting target with diagnostic, vaccination and therapeutic value.
牛病毒性腹泻病毒(BVDV)是一种正链单股RNA病毒,属于黄病毒科。BVDV是一种重要的动物病原体,通过呼吸道和胃肠道感染以及流产或出生持续感染的犊牛,给全球养牛业造成巨大经济损失。虽然在病毒发病机制中,一些BVDV蛋白(即E、E2和NS3)的免疫原性特征已得到充分证实,但在这方面,关于大多数BVDV非结构蛋白的信息却非常少。近年来,由于NS4B蛋白在病毒复制复合体中起着关键的支架样作用,它已成为黄病毒科其他成员病毒感染中具有诊断、疫苗接种和治疗价值的有趣靶点。尽管BVDV-NS4B除了在诱导自噬体方面发挥作用外,还具有膜拓扑结构。然而,关于其在BVDV发病机制和疫苗接种过程中的免疫原性信息却很少。为了表征NS4B的免疫原性特征,用减毒活BVDV疫苗Bovela对五头奶牛进行了接种,并在免疫前和免疫后采集血样用于血清分离。病毒中和试验(VNA)证实了接种疫苗奶牛血清中存在抗BVDV抗体。VNA还显示,在两头奶牛的免疫前血清中存在针对BVDV的预先存在的抗体。为了鉴定BVDV-NS4B特异性抗体,使用pCI-neo载体系统在哺乳动物细胞中表达NS4B蛋白。通过蛋白质印迹法和间接ELISA法评估接种BVDV奶牛的血清中是否存在BVDV-NS4B特异性抗体。有趣的是,预先对BVDV具有免疫力的奶牛的血清能够在蛋白质印迹法和ELISA法中检测到NS4B,这表明存在NS4B特异性抗体。所获得的结果首次表明了BVDV-NS4B蛋白在血清转化动物中的免疫原性本质。这些发现与在其他黄病毒科成员中对NS4B的观察结果一致,并证实该蛋白是一个具有诊断、疫苗接种和治疗价值的有趣靶点。