A Novel Antiparasitic Compound Kills Ring-Stage Plasmodium falciparum and Retains Activity Against Artemisinin-Resistant Parasites

J Infect Dis. 2020 Mar 2;221(6):956-962. doi: 10.1093/infdis/jiz534.

Abstract

Spreading antimalarial resistance threatens effective treatment of malaria, an infectious disease caused by Plasmodium parasites. We identified a compound, BCH070, that inhibits asexual growth of multiple antimalarial-resistant strains of Plasmodium falciparum (half maximal inhibitory concentration [IC50] = 1-2 µM), suggesting that BCH070 acts via a novel mechanism of action. BCH070 preferentially kills early ring-form trophozoites, and, importantly, equally inhibits ring-stage survival of wild-type and artemisinin-resistant parasites harboring the PfKelch13:C580Y mutation. Metabolomic analysis demonstrates that BCH070 likely targets multiple pathways in the parasite. BCH070 is a promising lead compound for development of new antimalarial combination therapy that retains activity against artemisinin-resistant parasites.

Keywords: Plasmodium falciparum; antimalarial; artemisinin resistance; malaria; ring-stage survival.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antimalarials / administration & dosage
  • Antimalarials / chemistry
  • Antimalarials / pharmacology*
  • Artemisinins / pharmacology*
  • Cells, Cultured
  • Drug Resistance
  • Fibroblasts / parasitology
  • Humans
  • Molecular Structure
  • Plasmodium falciparum / drug effects*
  • Structure-Activity Relationship
  • Trypanosoma cruzi / drug effects

Substances

  • Antimalarials
  • Artemisinins
  • artemisinin