Abstract
We have developed a new pharmacological screening assay for epimastigotes of Trypanosoma cruzi (clone CL-B5) that express the Escherichia coli LacZ gene. The assay is based on determining the activity of the cytoplasmic β-galactosidase released into the culture on membrane lysis in the presence of the substrate chlorophenol red β-d-galactopyranoside (CPRG). The experimental conditions were adjusted to find those in which the relationship between epimastigote number and CPRG absorbance was linear over the widest possible range. Absorbance was significantly correlated with the number epimastigote from 5×103 to 1.2×106 parasites/ml (r=0.98, P<0.01). The optimal final concentration of CPRG was 200 µM and the optimal incubation period was 6 h when parasites were incubated for 3 days. Once the assay was standardized, the trypanocidal activities of nifurtimox and benznidazole were determined both by CPRG assay and microscopic counting, demonstrating the methods utility for drug-screening. The efficacy obtained was comparable to that obtained with the manual method.
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Vega, C., Rolón, M., Martínez-Fernández, A.R. et al. A new pharmacological screening assay with Trypanosoma cruzi epimastigotes expressing β-galactosidase. Parasitol Res 95, 296–298 (2005). https://doi.org/10.1007/s00436-005-1300-3
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DOI: https://doi.org/10.1007/s00436-005-1300-3