» Articles » PMID: 30057296

Establishment of a Reverse Genetics System for Duck Tembusu Virus to Study Virulence and Screen Antiviral Genes

Overview
Journal Antiviral Res
Publisher Elsevier
Date 2018 Jul 31
PMID 30057296
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Recently, a newly emerged avian flavivirus, duck Tembusu virus (TMUV), was identified as the causative agent of a serious duck viral disease in Asia. Its rapid spread and expanded host range have raised substantial concerns regarding its potential threat to non-avian hosts, including humans. In this study, we report an infectious cDNA clone for a clinical strain CQW1 isolated from Southwest China, which is representative of the disease outbreak in the Chinese mainland. We generated a full-length cDNA clone pACYC FL-TMUV, which is infectious, and this cDNA clone-derived recombinant TMUV (rTMUV) showed comparative growth kinetics in both BHK21 cells and DEF cells compared with parental TMUV (pTMUV). In addition, rTMUV also showed the same high virulence in 9-day-old duck embryos as that in pTMUV, suggesting that rTMUV possessed similar properties to the natural virus both in vitro and in vivo. Based on the cDNA-clone, we first generated a reporter TMUV (TMUV-RLuc) carrying a Renilla luciferase (RLuc) gene. The luciferase kinetics of TMUV-RLuc were determined both in BHK21 and DEF cells. It seems that TMUV-RLuc grew well in vitro; however, the insertion of the RLuc gene attenuated viral replication in vitro. The higher viral titres of TMUV-RLuc were observed in BHK21 compared with that in DEF cells. The antiviral effects of exogenous-expressed duck RIG-I, MDA5, STING, MAVS, TBK1, IFNα and IFNγ were studied in vitro by using TMUV-RLuc. Our reverse genetics system will provide a multicomponent platform for the pathogenesis study of duck TMUV and the development of molecular countermeasures against duck TMUV infection.

Citing Articles

Duck Tembusu virus NS3 protein induces apoptosis by activating the PERK/PKR pathway and mitochondrial pathway.

Pan Y, Cai W, Cheng A, Wang M, Huang J, Chen S J Virol. 2023; 97(11):e0149723.

PMID: 37877719 PMC: 10688375. DOI: 10.1128/jvi.01497-23.


Comparative study of the pathogenicity of the mosquito origin strain and duck origin strain of Tembusu virus in ducklings and three-week-old mice.

Wang X, He Y, Guo J, Wu Z, Merits A, Wang M Virol Sin. 2023; 38(5):827-831.

PMID: 37544649 PMC: 10590687. DOI: 10.1016/j.virs.2023.07.006.


Attenuation of Avian Flavivirus by Rewiring the Leucine and Serine Codons of Its E-NS1 Protein toward Stop Mutation To Redirect Virus Evolution.

Guo J, He Y, Wang X, Merits A, Wang M, Jia R Microbiol Spectr. 2023; 11(1):e0292122.

PMID: 36625643 PMC: 9927255. DOI: 10.1128/spectrum.02921-22.


Stem-Loop I of the Tembusu Virus 3'-Untranslated Region Is Responsible for Viral Host-Specific Adaptation and the Pathogenicity of the Virus in Mice.

Mao L, He Y, Wu Z, Wang X, Guo J, Zhang S Microbiol Spectr. 2022; 10(5):e0244922.

PMID: 36214697 PMC: 9602528. DOI: 10.1128/spectrum.02449-22.


Duck Tembusu virus infection induces mitochondrial-mediated and death receptor-mediated apoptosis in duck embryo fibroblasts.

Pan Y, Cai W, Cheng A, Wang M, Chen S, Huang J Vet Res. 2022; 53(1):53.

PMID: 35799206 PMC: 9264590. DOI: 10.1186/s13567-022-01070-9.