Utomo Doddy Irawan Setyo, Pambudi Sabar, Park Enoch Y
Laboratory of Biotechnology, Department of Bioscience, Graduate School of Science and Technology, Shizuoka University, 836 Ohya, Suruga-ku, Shizuoka, 422-8529, Japan.
Center of Pharmaceutical and Medical Technology, National Research and Innovation Agency (BRIN), Jl. Kawasan Puspiptek, Gedung I LAPTIAB, Kota Tangerang Selatan, Banten, 15314, Indonesia.
AMB Express. 2022 Jan 31;12(1):8. doi: 10.1186/s13568-022-01353-6.
Dengue is an arboviral disease, which threatens almost half the global population, and has emerged as the most significant of current global public health challenges. In this study, we prepared dengue virus-like particles (DENV-LPs) consisting of Capsid-premembrane-envelope (CprME) and premembrane-envelope (prME) polypeptides from serotype 1 and 4, which were expressed in the silkworms using Bombyx mori nucleopolyhedrovirus (BmNPV) bacmid. 1CprME, 1prME, 4CprME, and 4prME expressed proteins in hemolymph, and the molecular weight of the purified proteins was 55 kDa, respectively. The purified polypeptides formed spherical Dengue virus-like particles (DENV-LPs) with ~ 30-55 nm in diameter. The immunoelectron microscopy (IEM) images revealed antigens to the surface of a lipid bilayer of DENV-LPs. The heparin-binding assay shows a positive relationship between absorbance and E protein domain III (EDIII) quantity, which is supported by the isothermal titration calorimetry assay. This indicates a moderate binding affinity between heparin and DENV-LP. The high correlation between patient sera and DENV-LP reactivities revealed that these DENV-LPs shared similar epitopes with the natural dengue virus. IgG elicitation studies in mice have demonstrated that DENV-LPs/CPrMEs elicit a stronger immune response than DENV-LP/prMEs, which lends credence to this claim.
登革热是一种虫媒病毒病,威胁着全球近一半的人口,已成为当前全球公共卫生面临的最重大挑战。在本研究中,我们制备了由1型和4型的衣壳-前膜-包膜(CprME)和前膜-包膜(prME)多肽组成的登革病毒样颗粒(DENV-LPs),这些多肽利用家蚕核多角体病毒(BmNPV)杆粒在家蚕中表达。1CprME、1prME、4CprME和4prME在血淋巴中表达蛋白,纯化后的蛋白分子量均为55 kDa。纯化后的多肽形成了直径约为30 - 55 nm的球形登革病毒样颗粒(DENV-LPs)。免疫电子显微镜(IEM)图像显示DENV-LPs脂质双层表面存在抗原。肝素结合试验表明吸光度与E蛋白结构域III(EDIII)数量呈正相关,等温滴定量热法试验也证实了这一点。这表明肝素与DENV-LP之间具有中等结合亲和力。患者血清与DENV-LP反应性之间的高度相关性表明,这些DENV-LPs与天然登革病毒具有相似的表位。在小鼠中进行的IgG诱导研究表明,DENV-LPs/CPrMEs比DENV-LP/prMEs引发更强的免疫反应,这支持了这一说法。