Screening for mutations related to atovaquone/proguanil resistance in treatment failures and other imported isolates of Plasmodium falciparum in Europe

J Infect Dis. 2004 Nov 1;190(9):1541-6. doi: 10.1086/424469. Epub 2004 Sep 28.

Abstract

Background: Two single-point mutations of the Plasmodium falciparum cytochrome b gene (Tyr268Asn and Tyr268Ser) were recently reported in cases of atovaquone/proguanil (Malarone) treatment failure. However, little is known about the prevalence of codon-268 mutations and their quantitative association with treatment failure.

Methods: We set out to assess the prevalence of codon-268 mutations in P. falciparum isolates imported into Europe and to quantify their association with atovaquone/proguanil treatment failure. Isolates of P. falciparum collected by the European Network on Imported Infectious Disease Surveillance between April 2000 and August 2003 were analyzed for codon-268 mutations, by use of polymerase chain reaction-restriction fragment-length polymorphism.

Results: We successfully screened 504 samples for the presence of either Tyr268Ser or Tyr268Asn. One case of Ser268 and no cases of Asn268 were detected. Therefore, we can be 95% confident that the prevalence of Ser268 in the European patient pool does not exceed 0.96% and that Asn268 is less frequent than 0.77%. In 58 patients treated with atovaquone/proguanil, Tyr268Ser was present in 1 of 5 patients with treatment failure but in 0 of 53 successfully treated patients.

Conclusions: Tyr268Ser seems to be a sufficient, but not a necessary, cause for atovaquone/proguanil treatment failure. The prevalence of both codon-268 mutations is currently unlikely to be >1% in the European patient pool.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Amino Acid Substitution
  • Animals
  • Antimalarials / pharmacology*
  • Atovaquone
  • Codon
  • Cytochromes b / genetics
  • Cytochromes b / physiology
  • DNA, Protozoan / analysis
  • DNA, Protozoan / isolation & purification
  • Drug Combinations
  • Drug Resistance / genetics
  • Europe
  • Female
  • Genes, Protozoan
  • Humans
  • Malaria, Falciparum / drug therapy
  • Malaria, Falciparum / parasitology*
  • Male
  • Middle Aged
  • Molecular Epidemiology
  • Mutation, Missense
  • Naphthoquinones / pharmacology*
  • Naphthoquinones / therapeutic use
  • Plasmodium falciparum / drug effects*
  • Plasmodium falciparum / genetics*
  • Plasmodium falciparum / isolation & purification
  • Point Mutation*
  • Polymorphism, Restriction Fragment Length
  • Proguanil / pharmacology*
  • Proguanil / therapeutic use
  • Protozoan Proteins / genetics
  • Protozoan Proteins / physiology
  • Treatment Failure

Substances

  • Antimalarials
  • Codon
  • DNA, Protozoan
  • Drug Combinations
  • Naphthoquinones
  • Protozoan Proteins
  • atovaquone, proguanil drug combination
  • Cytochromes b
  • Proguanil
  • Atovaquone