Abstract
Giardia canis can be infected with a double-stranded RNA virus, that is giardiavirus ( G. canis virus, GCV). In this study, green fluorescent protein (GFP) was stably expressed in G. canis mediated by GCV. The plasmid pNEO/GDH/MCS/ GFP, containing the neomycin phosphotransferase (NEO) encoding region flanked by the 636 nt of 5′-terminus and the 2174 nt of 3′-terminus from GCV positive strand RNA, was constructed by inserting GFP gene into downstream from the NEO gene and glutamate dehydrogenase (GDH) 5′-terminus uncoding regions on a single plasmid, and its in vitro transcript was introduced into GCV-infected G. canis by electroporation. The transfectants expressed GFP persistently under G418 selection. This stable transfection system should provide a valuable tool for genetic study of G. canis.
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