Yang Huiqiang, Li Zhushi, Lin Hua, Wang Wei, Yang Jian, Liu Lina, Zeng Xianwu, Wu Yonglin, Yu Yongxin, Li Yuhua
Department of Viral Vaccine, Chengdu Institute of Biological Products Co., Ltd, China National Biotech Group, Chengdu, 610023, People's Republic of China.
Department of Microbiology and Immunology, North Sichuan Medical College, Nanchong, 637007, People's Republic of China.
Arch Virol. 2016 Jun;161(6):1517-26. doi: 10.1007/s00705-016-2817-8. Epub 2016 Mar 15.
To develop a potential dengue vaccine candidate, a full-length cDNA clone of a novel chimeric virus was constructed using recombinant DNA technology, with Japanese encephalitis virus (JEV) vaccine strain SA14-14-2 as the backbone, with its premembrane (prM) and envelope (E) genes substituted by their counterparts from dengue virus type 1 (DENV1). The chimeric virus (JEV/DENV1) was successfully recovered from primary hamster kidney (PHK) cells by transfection with the in vitro transcription products of JEV/DENV1 cDNA and was identified by complete genome sequencing and immunofluorescent staining. No neuroinvasiveness of this chimeric virus was observed in mice inoculated by the subcutaneous route (s.c.) or by the intraperitoneal route (i.p.), while some neurovirulence was displayed in mice that were inoculated directly by the intracerebral route (i.c.). The chimeric virus was able to stimulate high-titer production of antibodies against DENV1 and provided protection against lethal challenge with neuroadapted dengue virus in mice. These results suggest that the chimeric virus is a promising dengue vaccine candidate.
为研发一种潜在的登革热疫苗候选物,利用重组DNA技术构建了一种新型嵌合病毒的全长cDNA克隆,以日本脑炎病毒(JEV)疫苗株SA14 - 14 - 2为骨架,其前膜(prM)和包膜(E)基因被1型登革病毒(DENV1)的相应基因所取代。通过用JEV/DENV1 cDNA的体外转录产物转染,从原代仓鼠肾(PHK)细胞中成功拯救出嵌合病毒(JEV/DENV1),并通过全基因组测序和免疫荧光染色进行鉴定。在通过皮下途径(s.c.)或腹腔途径(i.p.)接种的小鼠中未观察到这种嵌合病毒的神经侵袭性,而在通过脑内途径(i.c.)直接接种的小鼠中显示出一些神经毒力。该嵌合病毒能够刺激产生高滴度的抗DENV1抗体,并为小鼠提供针对神经适应性登革病毒致死性攻击的保护。这些结果表明该嵌合病毒是一种有前景的登革热疫苗候选物。