Abstract
Multidrug resistance is a major obstacle to the control of Plasmodium falciparum malaria, and its origins and modes of dissemination are imperfectly understood. In this study, haplotyping and microsatellite analysis of malaria from 5 regions of the South American Amazon support the conclusion that the parasite mutations conferring mid- and high-level resistance to the antifolate combination sulfadoxine-pyrimethamine have a common origin. Parasites harboring these mutations are also found to share drug-resistance alleles that confer a unique chloroquine resistance phenotype and to be similar at loci not linked to drug resistance, although not genetically identical. Since the 1980s, multidrug-resistant P. falciparum has spread in a north-northwest manner across the continent, from an origin likely in the lower Amazon. This study highlights the importance of continent-wide malaria-control policies and suggests that the containment of resistance to the next generation of therapies may be feasible.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Alleles
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Amino Acid Sequence
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Animals
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Antimalarials / pharmacology*
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Chloroquine / pharmacology
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Cloning, Molecular
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Drug Resistance, Multiple / genetics
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Folic Acid Antagonists / pharmacology
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Haplotypes
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Humans
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Malaria, Falciparum / epidemiology
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Malaria, Falciparum / parasitology*
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Microsatellite Repeats
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Molecular Sequence Data
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Multienzyme Complexes / genetics
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Mutation
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Plasmodium falciparum / drug effects*
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Plasmodium falciparum / enzymology
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Plasmodium falciparum / genetics
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Pyrimethamine / pharmacology
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South America / epidemiology
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Sulfadoxine / pharmacology
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Tetrahydrofolate Dehydrogenase / genetics
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Thymidylate Synthase / genetics
Substances
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6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase-7,8-dihydropteroate synthase
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Antimalarials
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Folic Acid Antagonists
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Multienzyme Complexes
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thymidylate synthase-dihydrofolate reductase
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Sulfadoxine
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Chloroquine
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Tetrahydrofolate Dehydrogenase
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Thymidylate Synthase
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Pyrimethamine