Stabilization of a full-length infectious cDNA clone for duck Tembusu virus by insertion of an intron

被引:14
|
作者
Guo, Jiaqi [1 ]
He, Yu [1 ]
Wang, Xiaoli [1 ]
Jiang, Bowen [1 ]
Lin, Xiao [1 ]
Wang, Mingshu [1 ,2 ,3 ]
Jia, Renyong [1 ,2 ,3 ]
Zhu, Dekang [2 ,3 ]
Liu, Mafeng [1 ,2 ,3 ]
Zhao, Xinxin [1 ,2 ,3 ]
Yang, Qiao [1 ,2 ,3 ]
Wu, Ying [1 ,2 ,3 ]
Chen, Shun [1 ,2 ,3 ]
Cheng, Anchun [1 ,2 ,3 ]
机构
[1] Sichuan Agr Univ, Inst Prevent Vet Med, Chengdu 611130, Sichuan, Peoples R China
[2] Sichuan Agr Univ, Coll Vet Med, Res Ctr Avian Dis, Chengdu 611130, Sichuan, Peoples R China
[3] Sichuan Agr Univ, Key Lab Anim Dis & Human Hlth Sichuan Prov, Chengdu 611130, Sichuan, Peoples R China
关键词
Duck Tembusu virus; Reverse genetics system; Intron; CONSTRUCTION; FLAVIVIRUS; SYSTEMS;
D O I
10.1016/j.jviromet.2020.113922
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Duck Tembusu virus (DTMUV) belongs to the genus Flavivirus, family Flaviviridae. In our previously study, a full-length cDNA clone of DTMUV was constructed, however, it is prone to mutation during genetic engineering due to the prokaryotic toxicity of viral protein, which is also a common feature for flavivirus. In this study, we reported an intron-containing full-length cDNA clone for a clinical strain CQW1, the intro (133bp) was inserted into nonstructural protein 1 of DTMUV at 192 site. This intron-containing full-length cDNA clone was stably propagated in Escherichia coli without prokaryotic toxicity, and recombinant virus was produced by direct transfection of plasmids. Besides, this cDNA clone-derived recombinant virus showed similar properties in comparison with parent virus both in vitro and in vivo. It's convenient and efficient, making it a useful platform for the subsequent research of reverse genetics of flavivirus.
引用
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页数:6
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