Abstract
Chloroquine resistance in Plasmodium falciparum has recently been shown to result from mutations in the novel vacuolar transporter, PfCRT. Field studies have demonstrated the importance of these mutations in clinical resistance. Although a pfcrt ortholog has been identified in Plasmodiumvivax, there is no association between in vivo chloroquine resistance and codon mutations in the P. vivax gene. This is consistent with lines of evidence that suggest alternative mechanisms of chloroquine resistance among various malaria parasite species.
MeSH terms
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Animals
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Antimalarials / pharmacology*
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Antimalarials / therapeutic use
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Chloroquine / pharmacology*
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Chloroquine / therapeutic use
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Drug Resistance
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Humans
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Malaria, Falciparum / drug therapy
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Malaria, Falciparum / parasitology
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Membrane Proteins / genetics*
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Membrane Proteins / metabolism
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Membrane Transport Proteins
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Mutation
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Plasmodium falciparum / drug effects*
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Plasmodium falciparum / genetics
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Plasmodium falciparum / metabolism
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Protozoan Proteins
Substances
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Antimalarials
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Membrane Proteins
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Membrane Transport Proteins
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PfCRT protein, Plasmodium falciparum
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Protozoan Proteins
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Chloroquine