After sequencing, we amplified and cloned foot-and-mouth disease virus (FMDV) O/QYYS/s/06 whole genome by three fragments. These three fragments were cloned into vector P43 one by one to construct recombinant plasmid P43C, which carried the full-length cDNA of FMDV O/QYYS/s/06. Then, plasmid P43C and plasmid T7 expressing T7 RNA polymerase were co-transfected into BHK-21 cells. After 48 h, we harvested the culture broth from transfected BHK-21 cells and inoculated into 2-3 day-old sucking mice. After four generation passage, the virus harvested from sucking mice was confirmed to be type O FMDV by the indirect hemagglutination test, sucking mice’s neutralization test and sequencing. The results showed that we have successfully constructed the full-length cDNA clone of FMDV O/QYYS/s/06 strain.
卢受昇,赵启祖,刘湘涛,孙彦伟,任涛,张桂红,亓文宝,查云峰,孔令辰,张翰,樊惠英,廖明. 口蹄疫病毒O/QYYS/s/06株感染性克隆的构建[J]. Chinese Journal of Biotechnology, 2009, 25(7): 982-986
Copy

WeChat ID
Mobile Terminal ® 2026 All Rights Reserved



