Metabolic adaptations of Leishmania donovani in relation to differentiation, drug resistance, and drug pressure

Mol Microbiol. 2013 Oct;90(2):428-42. doi: 10.1111/mmi.12374. Epub 2013 Sep 11.

Abstract

Antimonial (sodium stibogluconate, SSG) resistance and differentiation have been shown to be closely linked in Leishmania donovani, with SSG-resistant strains showing an increased capacity to generate infectious (metacyclic) forms. This is the first untargeted LC-MS metabolomics study which integrated both phenomena in one experimental design and provided insights into metabolic differences between three clinical L. donovani strains with a similar genetic background but different SSG-susceptibilities. We performed this analysis at different stages during promastigote growth and in the absence or presence of drug pressure. When comparing SSG-resistant and SSG-sensitive strains, a number of metabolic changes appeared to be constitutively present in all growth stages, pointing towards a clear link with SSG-resistance, whereas most metabolic changes were only detected in the stationary stage. These changes reflect the close intertwinement between SSG-resistance and an increased metacyclogenesis in resistant parasites. The metabolic changes suggest that SSG-resistant parasites have (i) an increased capacity for protection against oxidative stress; (ii) a higher fluidity of the plasma membrane; and (iii) a metabolic survival kit to better endure infection. These changes were even more pronounced in a resistant strain kept under Sb(III) drug pressure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological*
  • Antimony Sodium Gluconate / pharmacology*
  • Antiprotozoal Agents / pharmacology*
  • Cell Differentiation
  • Cell Membrane / physiology
  • Chromatography, Liquid
  • Drug Resistance
  • Humans
  • Leishmania donovani / drug effects
  • Leishmania donovani / genetics
  • Leishmania donovani / growth & development
  • Leishmania donovani / metabolism*
  • Leishmaniasis, Visceral / parasitology
  • Mass Spectrometry
  • Membrane Fluidity
  • Metabolomics
  • Oxidative Stress
  • Phenotype
  • Signal Transduction

Substances

  • Antiprotozoal Agents
  • Antimony Sodium Gluconate