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. Author manuscript; available in PMC: 2010 Sep 1.
Published in final edited form as: J Neuropathol Exp Neurol. 2009 Sep;68(9):1037–1048. doi: 10.1097/NEN.0b013e3181b5417e

Table 3.

Viral Load In Brain and Spinal Cord of Perforin-Competent and -Deficient Mice

Tissue dpi* Strain VP2 copy # Statistics^
Brain 7 PFP+/+
PFP−/−
6.6 ± 1.6
7.3 ± 1.1
p = 0.576
21 PFP+/+
PFP−/−
2.1 ± 2.1
5.7 ± 0.6
p = 0.035
45 PFP+/+
PFP−/−
0.6 ± 1.3
1.5 ± 3.0
p = 0.620
90 PFP+/+
PFP−/−
0.8 ± 1.4
0.8 ± 1.6
p = 0.978
180 PFP+/+
PFP−/−
0.6 ± 1.5
1.7 ± 1.8
p = 0.334
Spinal Cord 7 PFP+/+
PFP−/−
5.7 ± 0.2
5.4 ± 0.5
p = 0.382
21 PFP+/+
PFP−/−
5.2 ± 0.9
5.9 ± 0.5
p = 0.281
45 PFP+/+
PFP−/−
5.8 ± 0.2
5.1 ± 1.2
p = 0.301
90 PFP+/+
PFP−/−
5.6 ± 0.8
4.8 ± 0.3
p = 0.131
180 PFP+/+
PFP−/−
4.4 ± 1.3
5.4 ± 1.8
p = 0.444
*

Days post-infection

^

post-ANOVA pair-wise analysis

Viral RNA expression was analyzed at the indicated days post-infection in the brain and spinal cord of PFP+/+ and PFP−/− mice. Values are reported as mean log10 copy number ± 95% CI for 3 animals per group. The detection threshold for this assay is 0.61 ± 0.58 log10 copies, as measured in uninfected brain and spinal cord samples. The early difference in viral load observed in the brain (21 dpi) is compatible with delayed viral clearance associated with the lack of perforin effector function. Based on this difference two-way ANOVA identified a weak strain dependence on viral load in the brain (p = 0.048). By 45 dpi the virus was essentially cleared from the brain. In the spinal cord, there were no differences between the groups. Two-way ANOVA revealed no effect of strain on viral load in the spinal cord (p = 0.882). Levels of expression of control GAPDH RNA were not different between the groups at any time point.