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. 2000 Feb;74(4):2052–2056. doi: 10.1128/jvi.74.4.2052-2056.2000

TABLE 1.

Effects of IFN-α and cell type on plaque formation efficiency of different virusesa

Virus (strain) Gene inactivated −IFN-α/+IFN-α ratio
Vero cells U2OS cells
KOS 5.5 3.9
4 4.6
5.8 4.8
6.2
17syn+ 7 2.2
2.5 1.9
2.4
2.0
n212 (KOS) ICP0 230 10.9
207 10
285 8.5
260
dlX3.1 (KOS) ICP0 1,550 4.4
>1,200 5.1
7134 (KOS) ICP0 300 1.6
>200
dl1403 (17syn+) ICP0 320 3
200
in1814 (17syn+) VP16 14 2.9
22 3.8
10.9
V422 (KOS) VP16 16 10
45 28
d13lacZ (KOS) UL13 4 5.4
d22lacZ (KOS) ICP22 5 10
ΔSma (KOS) vhs 5.8 4.4
VSV >20,000 6.7
a

Vero and U2OS cells were mock treated or pretreated for 16 h with 1,000 U of human lymphoblastoid IFN-α (Sigma) per ml prior to infection. Results from individual experiments are reported for each virus in each cell line, with the ratio determined by dividing the viral titer in the absence versus presence of IFN-α pretreatment. The symbol > indicates that no plaques were visible at the lowest dilution of virus tested in the presence of IFN-α, and thus the exact level of inhibition is unknown in that experiment.