Rapid manipulation of the porcine epidemic diarrhea virus genome by CRISPR/Cas9 technology

被引:29
|
作者
Peng, Qi [1 ,2 ]
Fang, Liurong [1 ,2 ]
Ding, Zhen [1 ,2 ,3 ]
Wang, Dang [1 ,2 ]
Peng, Guiqing [1 ,2 ]
Xiao, Shaobo [1 ,2 ]
机构
[1] Huazhong Agr Univ, Coll Vet Med, State Key Lab Agr Microbiol, Wuhan 430070, Peoples R China
[2] Cooperat Innovat Ctr Sustainable Pig Prod, Key Lab Prevent Vet Med Hubei Prov, Wuhan 430070, Peoples R China
[3] Jiangxi Agr Univ, Coll Anim Sci & Technol, Jiangxi Prov Key Lab Anim Sci & Technol, Nanchang 330045, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Porcine epidemic diarrhea virus; Reverse genetics system; CRISPR/Cas9; PROTEIN; CORONAVIRUSES;
D O I
10.1016/j.jviromet.2019.113772
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Porcine epidemic diarrhea virus (PEDV) is a highly pathogenic enteric coronavirus causing lethal watery diarrhea in suckling piglets. Reverse genetics is a valuable tool to study the functions of viral genes and to generate vaccine candidates. In this study, a full-length infectious cDNA clone of the highly virulent PEDV strain AJ1102 was assembled in a bacterial artificial chromosome (BAC). The rescued virus (rAJ1102) exhibited similar proliferation characteristics in vitro to the wildtype AJ1102. Using CRISPR/Cas9 technology, a recombinant virus rAJ1102-Delta ORF3-EGFP in which the ORF3 gene was replaced with an EGFP gene, was successfully generated, and its proliferation characteristics were compared with the parental rAJ1102. Importantly, it just took one week to construct the recombinant PEDV rAJ1102-Delta ORF3-EGFP using this method, providing a more efficient platform for PEDV genome manipulation, which could also be applied to other RNA viruses.
引用
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页数:8
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