The stepwise selection for ketoconazole resistance induces upregulation of C14-demethylase (CYP51) in Leishmania amazonensis

Mem Inst Oswaldo Cruz. 2012 May;107(3):416-9. doi: 10.1590/s0074-02762012000300018.

Abstract

Ketoconazole is a clinically safe antifungal agent that also inhibits the growth of Leishmania spp. A study was undertaken to determine whether Leishmania parasites are prone to becoming resistant to ketoconazole by upregulating C14-demethylase after stepwise pharmacological pressure. Leishmania amazonensis promastigotes [inhibitory concentration (IC)₅₀ = 2 µM] were subjected to stepwise selection with ketoconazole and two resistant lines were obtained, La8 (IC₅₀ = 8 µM) and La10 (IC₅₀ = 10 µM). As a result, we found that the resistance level was directly proportional to the C14-demethylase mRNA expression level; we also observed that expression levels were six and 12 times higher in La8 and La10, respectively. This is the first demonstration that L. amazonensis can up-regulate C14-demethylase in response to drug pressure and this report contributes to the understanding of the mechanisms of parasite resistance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiprotozoal Agents / pharmacology*
  • Inhibitory Concentration 50
  • Ketoconazole / pharmacology*
  • Leishmania mexicana / drug effects*
  • Leishmania mexicana / enzymology*
  • Parasitic Sensitivity Tests
  • RNA, Messenger / analysis
  • RNA, Protozoan / analysis
  • Real-Time Polymerase Chain Reaction
  • Sterol 14-Demethylase / genetics
  • Sterol 14-Demethylase / metabolism*
  • Up-Regulation / drug effects*

Substances

  • Antiprotozoal Agents
  • RNA, Messenger
  • RNA, Protozoan
  • Sterol 14-Demethylase
  • Ketoconazole