Dalton Kevin P, Alvarado Carmen, Reytor Edel, Del Carmen Nuñez Maria, Podadera Ana, Martínez-Alonso Diego, Alonso Jose Manuel Martin, Nicieza Ines, Gómez-Sebastián Silvia, Dalton Romy M, Parra Francisco, Escribano José M
Instituto Universitario de Biotecnología de Asturias, Departamento de Bioquímica y Biología Molecular, Campus El Cristo, Universidad de Oviedo, Edificio Santiago Gascón, 33006 Oviedo, Spain.
Alternative Gene Expression S.L. Ronda de Poniente 14, Tres Cantos, 28760 Madrid, Spain.
Vaccines (Basel). 2021 Sep 9;9(9):1005. doi: 10.3390/vaccines9091005.
The VP60 capsid protein from rabbit haemorrhagic disease virus (RHDV), the causative agent of one of the most economically important disease in rabbits worldwide, forms virus-like particles (VLPs) when expressed using heterologous protein expression systems such as recombinant baculovirus, yeasts, plants or mammalian cell cultures. To prevent RHDV dissemination, it would be beneficial to develop a bivalent vaccine including both RHDV GI.1- and RHDV GI.2-derived VLPs to achieve robust immunisation against both serotypes. In the present work, we developed a strategy of production of a dual-serving RHDV vaccine co-expressing the VP60 proteins from the two RHDV predominant serotypes using CrisBio technology, which uses insect pupae as natural bioreactors, which are programmed by recombinant baculovirus vectors. Co-infecting the insect pupae with two baculovirus vectors expressing the RHDV GI.1- and RHDV GI.2-derived VP60 proteins, we obtained chimeric VLPs incorporating both proteins as determined by using serotype-specific monoclonal antibodies. The resulting VLPs showed the typical size and shape of this calicivirus as determined by electron microscopy. Rabbits immunised with the chimeric VLPs were fully protected against a lethal challenge infection with the two RHDV serotypes. This study demonstrates that it is possible to generate a dual cost-effective vaccine against this virus using a single production and purification process, greatly simplifying vaccine manufacturing.
兔出血症病毒(RHDV)是全球兔子中最具经济重要性的疾病之一的病原体,其VP60衣壳蛋白在使用重组杆状病毒、酵母、植物或哺乳动物细胞培养等异源蛋白表达系统表达时会形成病毒样颗粒(VLPs)。为防止RHDV传播,开发一种包含RHDV GI.1型和RHDV GI.2型来源的VLPs的二价疫苗以实现对两种血清型的有效免疫将是有益的。在本研究中,我们利用CrisBio技术开发了一种生产双效RHDV疫苗的策略,该技术使用昆虫蛹作为天然生物反应器,由重组杆状病毒载体进行编程。用两种表达RHDV GI.1型和RHDV GI.2型来源的VP60蛋白的杆状病毒载体共感染昆虫蛹,我们通过使用血清型特异性单克隆抗体确定获得了包含这两种蛋白的嵌合VLPs。通过电子显微镜观察,所得VLPs呈现出这种杯状病毒的典型大小和形状。用嵌合VLPs免疫的兔子对两种RHDV血清型的致死性攻击感染具有完全的抵抗力。这项研究表明,使用单一的生产和纯化过程来生产针对这种病毒的双效经济高效疫苗是可行的,这极大地简化了疫苗生产。