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High Resistance of Plasmodium falciparum to Sulphadoxine/Pyrimethamine in Northern Tanzania andthe Emergence of dhps Resistance Mutation at Codon 581.

Authors :
Gesase, Samwel
Gosling, Roly D.
Hashim, Ramadhan
Ord, Rosalynn
Naidoo, Inbarani
Madebe, Rashid
Mosha, Jacklin F.
Joho, Angel
Mandia, Victor
Mrema, Hedwiga
Mapunda, Ephraim
Savael, Zacharia
Lemnge, Martha
Mosha, Frank W.
Greenwood, Brian
Roper, Cally
Chandramohan, Daniel
Source :
PLoS ONE; 2009, Vol. 4 Issue 2, p1-13, 13p, 1 Diagram, 6 Charts, 3 Graphs
Publication Year :
2009

Abstract

Background: Sulphadoxine-pyrimethamine (SP) a widely used treatment for uncomplicated malaria and recommended for intermittent preventive treatment of malaria in pregnancy, is being investigated for intermittent preventive treatment of malaria in infants (IPTi). High levels of drug resistance to SP have been reported from north-eastern Tanzania associated with mutations in parasite genes. This study compared the in vivo efficacy of SP in symptomatic 6-59 month children with uncomplicated malaria and in asymptomatic 2-10 month old infants. Methodology and Principal Findings: An open label single arm (SP) standard 28 day in vivo WHO antimalarial efficacy protocol was used in 6 to 59 months old symptomatic children and a modified protocol used in 2 to 10 months old asymptomatic infants. Enrolment was stopped early (87 in the symptomatic and 25 in the asymptomatic studies) due to the high failure rate. Molecular markers were examined for recrudescence, re-infection and markers of drug resistance and a review of literature of studies looking for the 581G dhps mutation was carried out. In symptomatic children PCR-corrected early treatment failure was 38.8% (95% CI 26.8-50.8) and total failures by day 28 were 82.2% (95% CI 72.5-92.0). There was no significant difference in treatment failures between asymptomatic and symptomatic children. 96% of samples carried parasites with mutations at codons 51, 59 and 108 in the dhfr gene and 63% carried a double mutation at codons 437 and 540. 55% carried a third mutation with the addition of a mutation at codon 581 in the dhps gene. This triple: triple haplotype maybe associated with earlier treatment failure. Conclusion: In northern Tanzania SP is a failed drug for treatment and its utility for prophylaxis is doubtful. The study found a new combination of parasite mutations that maybe associated with increased and earlier failure. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
19326203
Volume :
4
Issue :
2
Database :
Complementary Index
Journal :
PLoS ONE
Publication Type :
Academic Journal
Accession number :
55666616
Full Text :
https://doi.org/10.1371/journal.pone.0004569