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. 2007 Aug;88(Pt 8):2091–2100. doi: 10.1099/vir.0.82940-0

Fig. 2.

Fig. 2.

Analysis of the effect of poxvirus infection on MNV replication. (a) BHK cells were mock-infected (M) or infected with either VACV (MVA-T7) or FWPV (FPV-T7) expressing T7 RNA polymerase and subsequently transfected with MNV VPg-linked RNA. Levels of the viral RNA-dependent RNA polymerase (NS7) and minor capsid protein (VP2) were analysed by Western blotting with rabbit polyclonal antisera. In parallel, the virus yield was determined and expressed as TCID50 per 35 mm dish. Transfections were carried out in triplicate; error bars represent sd. (b) BHK cells were either mock-infected (M) or infected with MVA-T7 or FPV-T7 and subsequently transfected with a cDNA construct containing the entire MNV genome under the control of a T7 RNA polymerase promoter (pT7 : MNV-G). NS7 expression levels were subsequently analysed by Western blotting.