Abstract
Conditions have been developed which induce axenically grown Leishmania pifanoi amastigotes to transform into the promastigote stage in a highly reproducible fashion. Transformation was induced by a temperature shift from 31 to 22°C, was inhibited by high cell concentration (≥40 × 106 cells/ml), and was unaffected by pH from 5.5-7.2. Morphologic transformation was first evident at 8 hr after induction, had occurred in >50% of cells by 24 hr, and was >90% complete by 48 hr. This system enabled study of the kinetics of mRNA expression during the transformation of Leishmania. The differentially expressed mRNAs for ATPase 1a and 1b. α- and β-tubulin, P100/11E, Pro-1, and pLm 2, 7, 14, and 16 exhibited complex patterns of temporal expression, suggesting a highly regulated process. Differentiation on the biochemical level was evident within an hour and continued throughout the course of morphologic transformation. In addition, transformed L. pifanoi promastigotes in the plateau growth phase expressed genes characteristic of metacyclic promastigotes. Axenically cultured L. pifanoi should provide an excellent model for the study of differentiation in Leishmania. © 1993 Academic press, Inc.
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CITATION STYLE
Campbell, S. M., & Rainey, P. M. (1993). Leishmania-pifanoi: Kinetics of messenger RNA expression during amastigote to promastigote transformation in vitro. Experimental Parasitology, 77(1), 1–12. https://doi.org/10.1006/expr.1993.1055
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