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. 2007 Dec 19;82(5):2427–2436. doi: 10.1128/JVI.02158-07

FIG. 6.

FIG. 6.

MDBK-E1*E2p7* cells have a defect at the level of BVDV entry. (A) MDBK-E1*E2p7* and pBabe cells were infected with NADLJiv90 luc in the presence of a BVDV polymerase inhibitor (4). At each time point, cells were harvested for luciferase assays. Each bar represents the mean value of duplicate wells; error bars show the standard errors of the means. The dashed line indicates the background level of the assay from naïve MDBK cells. (B) MDBK-E1*E2p7* and pBabe cells were electroporated with in vitro-transcribed BVDV NADLJiv90 luc RNA. At each time point, supernatants from electroporated cells were harvested and titers were determined on MDBK cells. Each point represents the mean titer of duplicate wells; error bars show the standard errors of the means.