Journal
JOURNAL OF INFECTIOUS DISEASES
Volume 202, Issue 5, Pages 801-808Publisher
OXFORD UNIV PRESS INC
DOI: 10.1086/655659
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Funding
- National Institutes of Health [K23AI059316, U01AI044824, R29AI040539, R01AI44824M01, RR 16500, K12RR023250]
- Doris Duke Charitable Foundation
- Howard Hughes Medical Institute
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The spread of drug-resistant Plasmodium falciparum malaria has been a major impediment to malaria control and threatens prospects for elimination. We recently demonstrated the return of chloroquine-susceptible malaria in Malawi after chloroquine use was abandoned. In this study, we trace the origins of chloroquine-resistant and chloroquine-susceptible parasites in Malawi by sequencing the P. falciparum chloroquine resistance transporter gene (pfcrt) and by genotyping microsatellites flanking this gene in isolates from infections that occurred in Malawi from 1992 through 2005. Malaria parasites from 2005 harbored the expected wildtype pfcrt haplotype associated with chloroquine susceptibility and have maintained high levels of diversity without linkage disequilibrium, which suggests that the return of chloroquine susceptibility is not the result of a back mutation in a formerly resistant parasite or a new selective sweep. Chloroquine-susceptible parasites that predominate in Malawi likely represent a reexpansion of the susceptible parasites that survived in the population despite widespread drug pressure in the region.
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