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The importation of drug-resistant malaria is a growing public health problem in non-endemic countries. The combination of atovaquone and proguanil (MalaroneTM) has become established as an agent of choice to prevent and treat chloroquine-resistant Plasmodium falciparum malaria in travelers. We describe the first reported case in North America of genetically confirmed atovaquone/proguanil-resistant P. falciparum malaria. Polymerase chain reaction and sequence analysis of the primary and recrudescent isolates confirmed the acquisition of a point mutation (Tyr268Ser) in the cytochrome b gene of the recrudescent isolate known to confer high-level resistance to atovaquone. Suboptimal therapy may have played a contributory role in the emergence of resistance.
Received May 7, 2004. Accepted for publication September 17, 2004.
Financial support: This work was supported by the Canadian Institutes of Health Research (CIHR, MT-13721). Kevin C. Kain is supported by a Career Scientist Award from the Ontario Ministry of Health and a Canada Research Chair (CIHR).
Disclosure: Susan Kuhn is on the speakers bureau for GlaxoSmith-Kine, which produces MalaroneTM. This statement is made in the interest of full disclosure, and not because the author considers this a conflict of interest.
Authors addresses: Susan Kuhn and M. John Gill, Department of Pediatrics, Medicine, Medical Microbiology & Infectious Diseases, University of Calgary, Calgary T2N 1N4, Alberta, Canada. Kevin C. Kain, Toronto General Hospital, 200 Elizabeth Street, ES 9-412, Toronto M5G 2C4, Ontario, Canada, Telephone: 416-340-3535, Fax: 416-595-5826, E-mail: Kevin.Kain{at}uhn.on.ca.
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