Figure 1.

Schematic construction of the full-length cDNA recombinant plasmid. The F1–F4 fragments covering the entire RABV genome of wtCVS-11 strain were amplified and inserted into pcDNA3.1. An eGFP gene from the eukaryotic expression vector pIRES2-eGFP was then cloned at the Bsiw I/Sac II sites to generate recombinant pCVS-11-eGFP.