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. 2008 Oct 8;82(24):12520–12534. doi: 10.1128/JVI.01528-08

FIG. 2.

FIG. 2.

Resistance properties of plaque-purified HPMPDAPR VACV (strain Lederle). HEL cells were grown to confluence in 96-well dishes, infected with 50 PFU of each cloned virus (nine HPMPDAPR [○] and five wild-type [•] viruses), and incubated for 3 to 4 days with serial dilutions of each test compound. At least four independent experiments were performed for each test compound. The data are presented as the EC50,CPE for the HPMPDAPR clones versus the EC50,CPE for the parent VACV clones (strain Lederle). Unpaired t tests were used to compare mean EC50,CPE values of the HPMPDAPR and wild-type clones for each compound as described in Materials and Methods. P values of <0.01 were considered to be highly significant (**), P values of <0.05 were considered to be significant (*), and P values of >0.05 were considered to not be significant. The changes in mean EC50,CPE values between wild-type and HPMPDAPR strains are also shown. Low levels of resistance (change in the range of 2.5- to 7.0-fold and with a P value of <0.05) are indicated by “L,” and high levels of resistance (change of more than sevenfold and a P value of <0.05) are indicated by an “H.” “∼wt” indicates that drug sensitivity was not significantly difference from that of the wild type. The EC50,CPE values, P values, and changes in EC50,CPE values are summarized in Table S1 in the supplemental material.