Publication:
Intrahost selection of Plasmodium falciparum pfmdr1 alleles after antimalarial treatment on the northwestern border of Thailand

dc.contributor.authorAnne Catrin Uhlemannen_US
dc.contributor.authorRose McGreadyen_US
dc.contributor.authorElizabeth A. Ashleyen_US
dc.contributor.authorAlan Brockmanen_US
dc.contributor.authorPratap Singhasivanonen_US
dc.contributor.authorSanjeev Krishnaen_US
dc.contributor.authorNicholas J. Whiteen_US
dc.contributor.authorFrançois Nostenen_US
dc.contributor.authorRic N. Priceen_US
dc.contributor.otherSt George's University of Londonen_US
dc.contributor.otherChurchill Hospitalen_US
dc.contributor.otherShoklo Malaria Research Uniten_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherMenzies School of Health Researchen_US
dc.date.accessioned2018-08-24T02:12:59Z
dc.date.available2018-08-24T02:12:59Z
dc.date.issued2007-01-01en_US
dc.description.abstractBackground. Increased pfmdr1 copy number is associated with reduced susceptibility to structurally unrelated antimalarial drugs. We assessed how administration of different antimalarial drugs altered pfmdr1 polymorphism in parasites from patients who experienced treatment failure. Methods. In studies conducted on the northwestern border of Thailand, amplifications and single-nucleotide polymorphisms in pfmdr1 were compared before and after antimalarial drug treatment. Results. Intrahost changes in pfmdr1 copy number were observed in 20% (26/132) of patients with recurrent infections. Among infections that recrudesced after mefloquine-containing regimens, increases in pfmdr1 copy number occurred in 68% (95% confidence interval [CI], 46%-85%), and decreases occurred in 2% (95% CI, 0.4%-11%) of isolates; corresponding proportions after artemether-lumefantrine were 25% (2/8) and 11% (2/19); after quinine, 50% (1/2) and 40% (4/10); and after artemisinins alone, 0% (0/10) and 19% (3/16) of isolates (overall P < .001). Conclusions. Intrahost selection based on pfmdr1 copy number occurs frequently in parasite populations within individual patients. Amplification confers multidrug resistance but probably imposes a significant fitness cost to the parasites. © 2006 by the Infectious Diseases Society of America. All rights reserved.en_US
dc.identifier.citationJournal of Infectious Diseases. Vol.195, No.1 (2007), 134-141en_US
dc.identifier.doi10.1086/509809en_US
dc.identifier.issn00221899en_US
dc.identifier.other2-s2.0-33845663264en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/25079
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33845663264&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleIntrahost selection of Plasmodium falciparum pfmdr1 alleles after antimalarial treatment on the northwestern border of Thailanden_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33845663264&origin=inwarden_US

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