| Autor: |
Sykes ML; Discovery Biology, Centre for Cellular Phenomics, Griffith University, Nathan, QLD 4111, Australia.; School of Environment & Science, Griffith University, Nathan, QLD 4111, Australia., Kennedy EK; Discovery Biology, Centre for Cellular Phenomics, Griffith University, Nathan, QLD 4111, Australia., Avery VM; Discovery Biology, Centre for Cellular Phenomics, Griffith University, Nathan, QLD 4111, Australia.; School of Environment & Science, Griffith University, Nathan, QLD 4111, Australia. |
| Abstrakt: |
Chagas disease is caused by infection with the protozoan parasite, Trypanosoma cruzi . The disease causes ~12,000 deaths annually and is one of the world's 20 neglected tropical diseases, as defined by the World Health Organisation. The drug discovery pipeline for Chagas disease currently has few new clinical candidates, with high attrition rates an ongoing issue. To determine if the Trypanosoma cruzi strain utilised to assess in vitro compound activity impacts activity, a comparison of laboratory-adapted T. cruzi strains from differing geographical locations was undertaken for a selection of compounds with anti- T. cruzi activity. To minimise the possible effect of differences in experimental methodology, the same host cell and multiplicity of infection were utilised. To determine whether the compound exposure time influenced results, activity was determined following exposure for 48 and 72 h of incubation. To ascertain whether replication rates affected outcomes, comparative rates of replication of the T. cruzi strains were investigated, using the nucleoside analogue, 5-ethynyl-2'-deoxyuridine. Minimal differences in the in vitro activity of compounds between strains were observed following 48 h incubation, whereas significant differences were observed following 72 h incubation, in particular for the cytochrome P450 inhibitors tested and the cell cycle inhibitor, camptothecin. Thus, the use of panels of laboratory adapted strains in vitro may be dependent on the speed of action that is prioritised. For the identification of fast-acting compounds, an initial shorter duration assay using a single strain may be used. A longer incubation to identify compound activity may alternatively require profiling of compounds against multiple T. cruzi strains. |
