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The T76 mutation in the pfcrt gene has been linked to chloroquine (CQ) resistance in Plasmodium falciparum. PCR-based analysis of pfcrt alleles was performed on pre-treatment samples from 107 individuals who had P. falciparum infections and lived in Papua, Indonesia. The results of a 28-day, in-vivo test revealed clinical resistance to CQ in 79 (74%) of the samples. The crude sensitivity of the pfcrt T76 assay for detecting the CQ-resistant infections in the samples was 96% and the crude specificity 52%. Discordance between pfcrt genotype and in-vivo phenotype was analysed either by genotyping of the merozoite surface protein-2 (to distinguish re-infection from recrudescence) or by amplification of the P. falciparum-specific small-subunit ribosomal RNA (ssrRNA) gene, using nested PCR (to detect any sub-patent but resistant parasites in infections misclassified as sensitive by the in-vivo test). When adjusting for the results of these analyses, the sensitivity and specificity of the pfcrt T76 assay for detecting the CQ-resistant infections became 93% and 82%, respectively. Overall, the present results indicate that the pfcrt T76 assay may be used to forecast therapeutic failure caused by CQ resistance. Validation requires exploration of the phenotype classifications based on the results of in-vivo tests, using genetic analyses that distinguish re-infection from recrudescence and detect microscopically subpatent parasitaemias.

Original publication

DOI

10.1080/00034980120092516

Type

Journal article

Journal

Ann Trop Med Parasitol

Publication Date

09/2001

Volume

95

Pages

559 - 572

Keywords

Adult, Alleles, Animals, Antigens, Protozoan, Antimalarials, Child, Chloroquine, Drug Resistance, Genes, Protozoan, Genotype, Humans, Malaria, Falciparum, Membrane Proteins, Membrane Transport Proteins, Mutation, Phenotype, Plasmodium falciparum, Polymerase Chain Reaction, Predictive Value of Tests, Prospective Studies, Protozoan Proteins, RNA, Ribosomal, Sensitivity and Specificity