Rapid fluorescent assay for screening drugs on Leishmania amastigotes

Orly Shimony, Charles L. Jaffe*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

54 Scopus citations

Abstract

A rapid fluorescent viability assay employing alamarBlue was optimized for use with Leishmania axenic amastigotes, the stage of the parasite responsible for disease pathology. The activity of two protein kinase inhibitors, Staurosporine and H-89, as well as Amphotericin B, on promastigotes and amastigotes of Leishmania donovani and Leishmania tropica was compared. Both protein kinase inhibitors inhibited promastigote growth at lower concentrations than amastigotes, while the GI50 for Amphotericin B on both stages was similar. This assay only requires a limited number of axenic amastigotes (50,000 cells/well) and can be used to rapidly screen large chemical or natural product libraries for activity against amastigotes.

Original languageEnglish
Pages (from-to)196-200
Number of pages5
JournalJournal of Microbiological Methods
Volume75
Issue number2
DOIs
StatePublished - Oct 2008

Keywords

  • AlamarBlue
  • Amphotericin B
  • Leishmania donovani
  • Leishmania tropica
  • Protein kinase inhibitors
  • Staurosporine

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