Wang Kai, Huang Qi, Yang Zhiwei, Qi Kezong, Liu Hongmei, Chen Hongjun
Shanghai Veterinary Research Institute, CAAS, Shanghai, 200241, China.
College of Animal Science and Technology, Anhui Agricultural University, Hefei, 230036, China.
Virus Genes. 2017 Aug;53(4):661-666. doi: 10.1007/s11262-017-1457-8. Epub 2017 Apr 22.
We generated an alternative reverse genetics (RG) system based on a synthesized swine 45S rRNA promoter to rescue the H3N2 subtype swine influenza virus. All eight flanking segment cassettes of A/swine/Henan/7/2010 (H3N2) were amplified with ambisense expression elements from RG plasmids. All segments were then recombined with the pHC2014 vector, which contained the synthesized swine 45S rRNA promoter (spol1) and its terminal sequence (t1) in a pcDNA3 backbone. As a result, we obtained a set of RG plasmids carrying the corresponding eight-segment cassettes. We efficiently generated the H3N2 virus after transfection into 293T/PK15, PK15, and 293T cells. The efficiency of spol1-driven influenza virus rescue in PK15 cells was similar to that in 293T cells by titration using the human pol1 RG system. Our approach suggests that an alternative spol1-based RG system can produce influenza viruses.
我们基于合成的猪45S rRNA启动子构建了一种替代性反向遗传学(RG)系统,以拯救H3N2亚型猪流感病毒。使用来自RG质粒的双义表达元件扩增了A/猪/河南/7/2010(H3N2)的所有八个侧翼片段盒。然后将所有片段与pHC2014载体重组,该载体在pcDNA3骨架中包含合成的猪45S rRNA启动子(spol1)及其末端序列(t1)。结果,我们获得了一组携带相应八个片段盒的RG质粒。将其转染到293T/PK15、PK15和293T细胞后,我们高效地产生了H3N2病毒。通过使用人pol1 RG系统进行滴定,spol1驱动的流感病毒在PK15细胞中的拯救效率与在293T细胞中的相似。我们的方法表明,基于spol1的替代性RG系统可以产生流感病毒。