Abstract | BACKGROUND: METHODS: In samples from 86 patients with uncomplicated Plasmodium falciparum malaria from Mbeya and Matema, Mbeya region, south-western Tanzania, the occurrence of mutations was investigated in the pfcrt and pfmdr1 genes which are associated with CQ resistance and in pfdhfr and pfdhps, conferring SP resistance, as well in cytb which is linked to resistance to atovaquone. RESULTS: Pfcrt T76 occurs in 50% and pfmdr1 Y86 in 51.7%. Pfdhfr triple mutations coexisting with pfdhps double mutations were detected in 64.3% of the P. falciparum isolates. This quintuple mutation is seen as a possible predictive molecular marker for SP treatment failure. Mutations of the cytb gene were not detected. CONCLUSION: These findings of a high prevalence of mutations conferring SP resistance correspond to data of in vivo SP efficacy studies in other regions of Tanzania and underline the recommendation of changing first-line treatment to artemisinin-based combination therapy.
|
Authors | Mirjam Schönfeld, Isabel Barreto Miranda, Mirjam Schunk, Ibrahim Maduhu, Leonard Maboko, Michael Hoelscher, Nicole Berens-Riha, Andrew Kitua, Thomas Löscher |
Journal | Malaria journal
(Malar J)
Vol. 6
Pg. 2
(Jan 15 2007)
ISSN: 1475-2875 [Electronic] England |
PMID | 17224049
(Publication Type: Journal Article)
|
Chemical References |
- Antimalarials
- Drug Combinations
- fanasil, pyrimethamine drug combination
- Sulfadoxine
- Tetrahydrofolate Dehydrogenase
- Dihydropteroate Synthase
- Pyrimethamine
|
Topics |
- Adolescent
- Adult
- Animals
- Antimalarials
(pharmacology)
- Child
- Child, Preschool
- Dihydropteroate Synthase
(genetics)
- Drug Combinations
- Drug Resistance
(genetics)
- Female
- Humans
- Infant
- Malaria, Falciparum
(drug therapy, epidemiology, parasitology)
- Male
- Middle Aged
- Parasitic Sensitivity Tests
- Plasmodium falciparum
(drug effects, genetics)
- Point Mutation
- Pyrimethamine
(pharmacology)
- Sulfadoxine
(pharmacology)
- Tanzania
(epidemiology)
- Tetrahydrofolate Dehydrogenase
(genetics)
|