TABLE 1.
PG545 inhibits HSV-2 plaque-forming activity and inactivates infectivity of free virus particles
HSV-2 strain or clinical isolate | IC50 (μg/ml) as determined by plaque assay |
Virus-inactivation activitya at indicated concn (μg/ml) of agent |
||||||
---|---|---|---|---|---|---|---|---|
PG545 | Acyclovir | PG545 |
Acyclovir |
|||||
100 | 20 | 4 | 100 | 20 | 4 | |||
333 | 0.8 | 7.3 | 0.0 | 0.0 | 0.0 | 103.5 | 113.8 | 100.0 |
DE06-3942b | 0.4 | >100 | 0.0 | 0.0 | 0.0 | 85.3 | 100 | 88 |
DE07-6820b | 0.5 | >100 | 0.0 | 0.0 | 2.8 | 108.7 | 104.9 | 102.9 |
VI03-1678c | 0.6 | 3.6 | 0.0 | 0.0 | 0.0 | 113.4 | 104.9 | 108.5 |
90-036 | 0.4 | 3.0 | 0.0 | 0.0 | 52.2 | 99.4 | 108.5 | 100 |
90-306 | 0.4 | 2.3 | 0.0 | 0.0 | 73.6 | 99.4 | 103.2 | 93.6 |
Virus-inactivating activity is expressed as the percentage of residual infectivity found with PG545- or acyclovir-treated virus relative to that of the mock-treated virus control.
Clinical isolate of HSV-2 resistant to acyclovir.
Clinical isolate of HSV-2 from routine diagnostics.