| Literature DB >> 26976137 |
Huiqiang Yang1, Zhushi Li1, Hua Lin1, Wei Wang1, Jian Yang1,2, Lina Liu1, Xianwu Zeng1, Yonglin Wu3, Yongxin Yu4, Yuhua Li5.
Abstract
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.Entities:
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Year: 2016 PMID: 26976137 DOI: 10.1007/s00705-016-2817-8
Source DB: PubMed Journal: Arch Virol ISSN: 0304-8608 Impact factor: 2.574