Treatment Failure in a UK Malaria Patient Harboring Genetically Variant Plasmodium falciparum From Uganda With Reduced In Vitro Susceptibility to Artemisinin and Lumefantrine

Clin Infect Dis. 2024 Feb 17;78(2):445-452. doi: 10.1093/cid/ciad724.

Abstract

Background: Recent cases of clinical failure in malaria patients in the United Kingdom (UK) treated with artemether-lumefantrine have implications for malaria chemotherapy worldwide.

Methods: Parasites were isolated from an index case of confirmed Plasmodium falciparum treatment failure after standard treatment, and from comparable travel-acquired UK malaria cases. Drug susceptibility in vitro and genotypes at 6 resistance-associated loci were determined for all parasite isolates and compared with clinical outcomes for each parasite donor.

Results: A traveler, who returned to the UK from Uganda in 2022 with Plasmodium falciparum malaria, twice failed treatment with full courses of artemether-lumefantrine. Parasites from the patient exhibited significantly reduced susceptibility to artemisinin (ring-stage survival, 17.3% [95% confidence interval {CI}, 13.6%-21.1%]; P < .0001) and lumefantrine (effective concentration preventing 50% of growth = 259.4 nM [95% CI, 130.6-388.2 nM]; P = .001). Parasite genotyping identified an allele of pfk13 encoding both the A675V variant in the Pfk13 propeller domain and a novel L145V nonpropeller variant. In vitro susceptibility testing of 6 other P. falciparum lines of Ugandan origin identified reduced susceptibility to artemisinin and lumefantrine in 1 additional line, also from a 2022 treatment failure case. These parasites did not harbor a pfk13 propeller domain variant but rather the novel nonpropeller variant T349I. Variant alleles of pfubp1, pfap2mu, and pfcoronin were also identified among the 7 parasite lines.

Conclusions: We confirm, in a documented case of artemether-lumefantrine treatment failure imported from Uganda, the presence of pfk13 mutations encoding L145V and A675V. Parasites with reduced susceptibility to both artemisinin and lumefantrine may be emerging in Uganda.

Keywords: Plasmodium falciparum; Uganda; drug susceptibility; travelers’ malaria; treatment failure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antimalarials* / pharmacology
  • Antimalarials* / therapeutic use
  • Artemether / pharmacology
  • Artemether / therapeutic use
  • Artemether, Lumefantrine Drug Combination / pharmacology
  • Artemether, Lumefantrine Drug Combination / therapeutic use
  • Artemisinins* / pharmacology
  • Artemisinins* / therapeutic use
  • Drug Resistance
  • Humans
  • Lumefantrine / pharmacology
  • Lumefantrine / therapeutic use
  • Malaria* / drug therapy
  • Malaria, Falciparum* / drug therapy
  • Malaria, Falciparum* / parasitology
  • Plasmodium falciparum
  • Protozoan Proteins / genetics
  • Treatment Failure
  • Uganda
  • United Kingdom

Substances

  • Lumefantrine
  • Antimalarials
  • Artemether, Lumefantrine Drug Combination
  • Artemether
  • artemisinin
  • Artemisinins
  • Protozoan Proteins