Characterisation of antimony-resistant Leishmania donovani isolates: biochemical and biophysical studies and interaction with host cells

Int J Parasitol. 2011 Nov;41(13-14):1311-21. doi: 10.1016/j.ijpara.2011.07.013. Epub 2011 Sep 7.


Recent clinical isolates of Leishmania donovani from the hyperendemic zone of Bihar were characterised in vitro in terms of their sensitivity towards sodium stibogluconate in a macrophage culture system. The resulting half maximal effective concentration (EC(50)) values were compared with those of known sensitive isolates. Fifteen of the isolates showed decreased sensitivity towards SSG with an average EC(50) of 25.7 ± 4.5 μg/ml pentavalent antimony (defined as antimony resistant), whereas nine showed considerable sensitivity with an average EC(50) of 4.6 ± 1.7 μg/ml (defined as antimony sensitive). Out of those nine, seven were recent clinical isolates and the remaining two were known sensitive isolates. Compared with the antimony sensitive, resistant isolates showed enhanced expression of thiol metabolising enzymes in varying degrees coupled with increased intracellular non-protein thiol content, decreased fluorescence anisotropy (inversely proportional with membrane fluidity) and over-expression of the terminal glycoconjugates (N-acetyl-d-galactosaminyl residue). Macrophages infected with resistant but not with sensitive showed up-regulation of the ATP Binding Cassette transporter multidrug resistance protein 1 and permeability glycoprotein, while the supernatant contained abundant IL-10. The above results reinforce the notion that antimony resistant parasites have undergone a number of biochemical and biophysical changes as part of their adaptation to ensure their survival in the host.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Animals
  • Antimony Sodium Gluconate / pharmacology*
  • Antiprotozoal Agents / pharmacology*
  • Child
  • Cricetinae
  • Drug Resistance*
  • Female
  • Gene Expression Regulation
  • Host-Parasite Interactions*
  • Humans
  • India
  • Leishmania donovani / chemistry*
  • Leishmania donovani / drug effects*
  • Leishmania donovani / genetics
  • Leishmania donovani / metabolism
  • Leishmaniasis, Visceral / parasitology*
  • Male
  • Mesocricetus
  • Mice
  • Mice, Inbred BALB C
  • Middle Aged
  • Protozoan Proteins / genetics
  • Protozoan Proteins / metabolism
  • Young Adult


  • Antiprotozoal Agents
  • Protozoan Proteins
  • Antimony Sodium Gluconate