TABLE 1.
Virus | IC50a (nM) of GS 4071
|
IC50 (nM) of zanamivir
|
||
---|---|---|---|---|
Culture assayb | Enzymatic assayc | Culture assay | Enzymatic assay | |
Laboratory strains | ||||
A/WS/33 (H1N1) | 22 | 1.0 | 19 | 0.7 |
A/FM/1/47 (H1N1) | 24 | NDd | 20 | ND |
A/Victoria/3/75 (H3N2) | 0.6 | 0.5 | 3.5 | 1.7 |
A/Port Chalmers/1/73 (H3N2) | 0.8 | 0.3 | 3.1 | 1.1 |
B/Mass/3/66 | 117 | 0.8 | 90 | 1.7 |
B/Hong Kong/5/72 | 155 | 1.7 | 150 | 1.0 |
Clinical isolates | ||||
A/Texas/36/91 (H1N1) | 94 | 0.5 | 70 | 0.3 |
A/Johannesburg/33/94 (H3N2) | 40 | 0.8 | 241 | 4.6 |
B/Harbin/07/94 | 91 | 2.0 | 30 | 2.1 |
IC50s are taken to be the concentration of compound necessary to reduce the plaque number or the extent of cell killing by 50% in tissue culture assays or the enzymatic activity by 50%, relative to duplicate samples assayed in the absence of inhibitor.
Replication in tissue culture was determined by a plaque reduction assay for the laboratory strains and by a CPE assay for the clinical isolates. Values represent the means obtained from at least three independent experiments except in the case of A/Johannesburg/33/94 (H3N2) which was tested only twice.
Enzymatic assays were performed as described in the text with tissue culture medium harvested from cultures in which full cell death occurred. Values represent the means of two independent experiments.
ND, not determined.