TABLE 1.
Drug | Mean EC50 (μM) ± SD (RI)b |
||
---|---|---|---|
pUCNEO | LABCG2 | LABCG2rev 90D | |
SbIII | 16.02 ± 2.63 | 118.84 ± 11.50 (7.4)* | 11.53 ± 0.69 (0.7) |
AsIII | 0.99 ± 0.30 | 6.02 ± 1.50 (6.0)* | 1.32 ± 0.02 (1.3) |
Amphotericin B | 2.27 ± 0.73 | 2.33 ± 0.45 (1.0) | — |
Miltefosine | 18.25 ± 0.22 | 17.64 ± 1.70 (0.9) | — |
Pentamidine | 0.66 ± 0.11 | 1.03 ± 0.11 (1.6)* | 0.83 ± 0.03 (1.3) |
Tafenoquine | 12.87 ± 3.16 | 15.92 ± 7.50 (1.2) | — |
Sitamaquine | 21.88 ± 5.43 | 18.02 ± 0.82 (0.8) | — |
Primaquine | 5.43 ± 0.32 | 6.11 ± 0.05 (1.1) | — |
Chloroquine | 10.99 ± 0.53 | 9.37 ± 1.67 (0.8) | — |
Daunomycin | 0.56 ± 0.09 | 1.06 ± 0.16 (1.9)* | 0.67 ± 0.06 (1.2) |
Mefloquine | 2.02 ± 0.19 | 3.04 ± 0.34 (1.5) | — |
Quinine | 23.62 ± 2.84 | 29.69 ± 0.26 (1.3) | — |
Perifosine | 20.99 ± 1.95 | 20.96 ± 1.27 (1.0) | — |
Vinblastine | 10.31 ± 2.16 | 13.25 ± 2.65 (1.3) | — |
Promastigotes of Leishmania lines were grown for 72 h at 28°C in the presence of increasing concentrations of drugs. Cell viability was determined by using an MTT-based assay as described in Materials and Methods. Bold font represents significant resistance.
Resistance indexes (RI) were calculated by dividing the EC50 for the Leishmania line overexpressing LABCG2 and LABCG2rev 90D by that for the Leishmania control line (pUCNEO). Data are the means ± standard deviations of results from three independent experiments. Significant differences were determined by using the Student t test (*, P < 0.01). —, not determined.