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Genetic confirmation of atovaquone-proguanil-resistant Plasmodium falciparum malaria acquired by a nonimmune traveler to East Africa.

Abstract
We report a case of atovaquone-proguanil-resistant Plasmodium falciparum malaria acquired by a nonimmune traveler to Kenya. Recurrent parasitemia occurred 30 days after directly observed therapy with a combination of atovaquone and proguanil. Treatment failure was confirmed by genetic fingerprinting and sequencing. The primary isolate had wild-type sequence of cytochrome b; however, the recrudescent isolate had a single mutation at position 268 (Tyr268Ser).
AuthorsEli Schwartz, Shay Bujanover, Kevin C Kain
JournalClinical infectious diseases : an official publication of the Infectious Diseases Society of America (Clin Infect Dis) Vol. 37 Issue 3 Pg. 450-1 (Aug 01 2003) ISSN: 1537-6591 [Electronic] United States
PMID12884171 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antimalarials
  • Cytochrome b Group
  • Naphthoquinones
  • Proguanil
  • Atovaquone
Topics
  • Adult
  • Animals
  • Antimalarials (therapeutic use)
  • Atovaquone
  • Cytochrome b Group (genetics, metabolism)
  • Drug Resistance (genetics)
  • Drug Therapy, Combination
  • Female
  • Humans
  • Kenya (epidemiology)
  • Malaria, Falciparum (drug therapy, epidemiology)
  • Naphthoquinones (therapeutic use)
  • Plasmodium falciparum (drug effects, genetics)
  • Proguanil (therapeutic use)
  • Travel
  • Treatment Failure

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