Simultaneous transient expression assays of the trypanosomatid parasite Leishmania using /3-galacto- sidase and j&glucuronidase as reporter enzymes

We describe a transient transfection protocol for cultured Leishmania major promastigotes, utilizing Escherichia coli genes encoding /?-galactosidase and B-glucuronidase inserted into an expression vector derived from the dihydrofolate reductasethymidylate synthase locus. Less than 0.1 pg of either reporter enzyme can be detected with a simple fluorimetric assay, and transfection of 10 pg of either reporter construct yields activities at least lOO-fold over background. Simultaneous introduction of both constructs showed that the activity of each reporter gene was unaffected by the presence of the other, allowing one reporter construct to serve as a control for experimental variability in test gene constructs containing the second reporter gene. These results show that it is feasible to apply transient expression assays to the identification of c&acting elements of genes encoding nonabundant mRNAs in the genus Leishmania.