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. 2017 Jun 16;6:79–90. doi: 10.1016/j.omtm.2017.06.001

Figure 3.

Figure 3

GFP Expression from JΔNI7GFPΔB and JΔNI8GFPΔB in Infected HDFs and DRGs

(A) Schematic diagram of the genomic structure of the JΔNI8GFPΔB vector derived from JΔNI7GFP18 by deletion of the vhs (UL41) gene. Like JΔNI7GFP, JΔNI8GFP contains a CAG promoter-eGFP expression cassette in the LAT intron between an enhancer-like LAT region (LAP2 or LATP2)4, 46, 47 and CTRL2. (B) GFP fluorescence and (C) relative GFP mRNA levels in JΔNI7GFPΔB- and JΔNI8GFPΔB-infected HDFs (25,000 gc/cell) at 7 and 14 dpi. GFP qRT-PCR data were normalized to viral gc in the same samples and are presented as expression relative to that in JΔNI7GFPΔB infected cells at 7 dpi. (D) GFP fluorescence and (E) relative GFP mRNA levels in JΔNI7GFPΔB- and JΔNI8GFPΔB-infected rDRGs (3,000 gc/cell) at 7 and 14 dpi. Data in (C) and (E) represent averages ±SD of two independent experiments.