The plasmid constructs producing shRNA corresponding to the conserved 3D polymerase of Foot and Mouth Disease virus protects guinea pigs against challenge …
DH Joyappa, S Sasi, KC Ashok, GR Reddy… - Veterinary research …, 2009 - Springer
DH Joyappa, S Sasi, KC Ashok, GR Reddy, VVS Suryanarayana
Veterinary research communications, 2009•SpringerRNA interference (RNAi) has been used as an effective antiviral strategy for its specific
silencing of viral gene expression in mammalian cells. In this study, shRNA targeting two
regions of Foot and Mouth Disease Virus (FMDV) ie 3D and 5′ UTR which are very
essential in virus replication were evaluated. The constructs were made using h7K RNA
polymerase III promoter. We investigated in vivo inhibitory effect of shRNA on FMDV
replication in BHK-21 cells and guinea pigs. The results showed that transfection of 3D …
silencing of viral gene expression in mammalian cells. In this study, shRNA targeting two
regions of Foot and Mouth Disease Virus (FMDV) ie 3D and 5′ UTR which are very
essential in virus replication were evaluated. The constructs were made using h7K RNA
polymerase III promoter. We investigated in vivo inhibitory effect of shRNA on FMDV
replication in BHK-21 cells and guinea pigs. The results showed that transfection of 3D …
Abstract
RNA interference (RNAi) has been used as an effective antiviral strategy for its specific silencing of viral gene expression in mammalian cells. In this study, shRNA targeting two regions of Foot and Mouth Disease Virus (FMDV) i.e. 3D and 5′UTR which are very essential in virus replication were evaluated. The constructs were made using h7K RNA polymerase III promoter. We investigated in vivo inhibitory effect of shRNA on FMDV replication in BHK-21 cells and guinea pigs. The results showed that transfection of 3D shRNA could reduce virus growth by three folds when cells were challenged with 102 TCID50 of FMDV. Pretreated guinea pigs with 3DshRNA were protected 80% with 103 GPID50 of FMDV. As a first report in guinea pigs which are recognized animal model for FMD vaccine potency testing, the study suggests that shRNA could be a viable therapeutic approach to control severity of FMD infection and spread.
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