High Prevalence of Markers for Sulfadoxine and Pyrimethamine Resistance in Plasmodium falciparum in the Absence of Drug Pressure in the Ashanti Region of Ghana
Open Access
- 1 March 2005
- journal article
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 49 (3) , 1101-1105
- https://doi.org/10.1128/aac.49.3.1101-1105.2005
Abstract
Markers of Plasmodium falciparum resistance to chloroquine (CQ) and pyrimethamine-sulfadoxine (PYR-SDX) are widespread in areas where malaria is endemic. In an area where the use PYR-SDX is negligible, the Ashanti Region of Ghana, West Africa, adult individuals were enrolled in an analysis of CQ- and PYR-SDX-associated molecular resistance markers in 2001 ( n = 177) and 2003 ( n = 180). Parasite prevalence, as assessed by PCR assays, were 56.5 and 48.8% in 2001 and 2003, respectively. A high frequency of CQ, PYR, and SDX resistance markers was observed, whereby, as a weak trend, the frequency was higher in 2003. The quintuple combination of three pfdhfr mutations and two pfdhps mutations has previously been recognized to be the most important determinant of PYR-SDX resistance. Approximately 60% of parasite carriers harbored fourfold mutated parasites, indicative of a considerable risk for a switch to high-level PYR-SDX resistance in an area where the rate of PYR-SDX use is low. Among the factors contributing to the high frequency of PYR-SDX resistance-associated mutations are background use of PYR-SDX, past use of PYR for malaria prophylaxis, cross-resistance of trimethoprim with PYR, and the sufficient biological fitness of resistant parasites in the absence of drug pressure.Keywords
This publication has 36 references indexed in Scilit:
- Genotyping of Plasmodium falciparum Pyrimethamine Resistance by Matrix-Assisted Laser Desorption-Ionization Time-of-Flight Mass SpectrometryAntimicrobial Agents and Chemotherapy, 2004
- Molecular characterization of antibiotic resistance in clinicalSalmonella typhiisolated in GhanaFEMS Microbiology Letters, 2002
- Review: Genetic diversity of Plasmodium falciparum: asexual stagesTropical Medicine & International Health, 2002
- Molecular Markers for Failure of Sulfadoxine‐Pyrimethamine and Chlorproguanil‐Dapsone Treatment ofPlasmodium falciparumMalariaThe Journal of Infectious Diseases, 2002
- Chloroquine‐Resistant MalariaThe Journal of Infectious Diseases, 2001
- A primary malarial infection is composed of a very wide range of genetically diverse but related parasites.Journal of Clinical Investigation, 1998
- Direct evidence that asparagine at position 108 of the Plasmodium falciparum dihydrofolate reductase is involved in resistance to antifolate drugs in TanzaniaTransactions of the Royal Society of Tropical Medicine and Hygiene, 1996
- Features of recrudescent chloroquine-resistant Plasmodium falciparum infections confer a survival advantage on parasites and have implications for disease controlTransactions of the Royal Society of Tropical Medicine and Hygiene, 1996
- The effects of chloroquine on the infectivity of chloroquine-sensitve and -resisant populations of Plasmodium yoelii nigeriensis to mosquitoesParasitology, 1990
- Infectivity of Chloroquine Resistant Plasmodium berghei to Anopheles stephensi enhanced by ChloroquineNature, 1969