| Literature DB >> 26927704 |
Akiko Takenaka-Uema1, Keita Sugiura2, Norasuthi Bangphoomi3, Chieko Shioda4, Kazuyuki Uchida5, Kentaro Kato6, Takeshi Haga7, Shin Murakami8, Hiroomi Akashi9, Taisuke Horimoto10.
Abstract
Akabane disease, caused by the insect-transmitted Akabane virus (AKAV), affects livestock by causing life-threatening deformities or mortality of fetuses. Therefore, Akabane disease has led to notable economic losses in numerous countries, including Japan. In this short communication, a new T7 RNA polymerase-based AKAV reverse genetics system was developed. Using this system, in which three plasmids transcribing antigenomic RNAs were transfected into cells stably expressing T7 polymerase, we successfully reconstituted the live attenuated vaccine TS-C2 strain (named rTTT), and also generated a mutant AKAV (rTTTΔNSs) that lacked the gene encoding the nonstructural NSs protein, which is regarded as a virulence factor. Analysis of growth kinetics revealed that rTTTΔNSs grew at a much slower rate than the rTTT and TS-C2 virus. These results suggest that our established reverse genetics system is a powerful tool that can be used for AKAV vaccine studies with gene-manipulated viruses.Entities:
Keywords: Akabane virus; Reverse genetics; Vaccine
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Year: 2016 PMID: 26927704 DOI: 10.1016/j.jviromet.2015.12.014
Source DB: PubMed Journal: J Virol Methods ISSN: 0166-0934 Impact factor: 2.014