Pyrimethamine-Resistant Plasmodium Falciparum Parasites among Tanzanian Children: a Facility-Based Study using the Polymerase Chain Reaction

Dominic Edoh Ifakara Centre, Department Public Health and Epidemiology, Swiss Tropical Institute, Friedrich Miescher-Institut, Ifakara, Tanzania

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Hassan Mshinda Ifakara Centre, Department Public Health and Epidemiology, Swiss Tropical Institute, Friedrich Miescher-Institut, Ifakara, Tanzania

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Jennifer Jenkins Ifakara Centre, Department Public Health and Epidemiology, Swiss Tropical Institute, Friedrich Miescher-Institut, Ifakara, Tanzania

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Max Burger Ifakara Centre, Department Public Health and Epidemiology, Swiss Tropical Institute, Friedrich Miescher-Institut, Ifakara, Tanzania

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A mutation-specific polymerase chain reaction method was used to estimate the proportion of pyrimethamine-resistant parasites in 101 children reporting with malaria at the hospital in Ifakara, a town in southern Tanzania. The method is based on the observation that a point mutation (Asn-108) in the dihydroifolate reductase gene confers resistance to pyrimethamine. Twenty-eight percent of the examined 101 children had pyrimethamine-resistant parasites, 65% had pyrimethamine-sensitive parasites with the wild-type Ser-108 codon, and 9% had both alleles, suggesting a mixed infection. None of the 21 children with clinical malaria had pyrimethamine-resistant parasites. Currently, sulfadoxine-pyrimethamine is considered a potential first-line drug for malaria treatment in most African countries. We suggest that although sulfadoxine-pyrimethamine could still be effective against chloroquine-resistant malaria in this area, its judicious use is important so as to minimize the spread of resistance.

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