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Polymorphism in plasmodium falciparum drug transporter proteins and reversal of in vitro chloroquine resistance by a 9,10-dihydroethanoanthracene derivative.
- Source :
-
Antimicrobial agents and chemotherapy [Antimicrob Agents Chemother] 2004 Dec; Vol. 48 (12), pp. 4869-72. - Publication Year :
- 2004
-
Abstract
- BG958 reverses resistance in chloroquine-resistant isolates from different countries. Five mutations in the Plasmodium falciparum crt (pfcrt) gene resulting in the amino acid changes K76T, M74I, N75E, A220S, and R371I are systematically identified in resistance-reversed Asian, African, and Brazilian parasites which possess the pfcrt (CIET) haplotype. In combination with BG958, the activity of chloroquine is increased in parasites with the N86Y mutation in pfmdr1.
- Subjects :
- Animals
DNA, Protozoan genetics
DNA, Protozoan isolation & purification
Drug Resistance
Drug Synergism
Genes, MDR genetics
Humans
Malaria, Falciparum parasitology
Membrane Proteins genetics
Membrane Transport Proteins
Mutation genetics
Plasmodium falciparum drug effects
Plasmodium falciparum metabolism
Protozoan Proteins
RNA, Protozoan genetics
RNA, Protozoan isolation & purification
Reverse Transcriptase Polymerase Chain Reaction
Anthracenes pharmacology
Antimalarials pharmacology
Carrier Proteins genetics
Chloroquine pharmacology
Plasmodium falciparum genetics
Polymorphism, Genetic genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0066-4804
- Volume :
- 48
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Antimicrobial agents and chemotherapy
- Publication Type :
- Academic Journal
- Accession number :
- 15561869
- Full Text :
- https://doi.org/10.1128/AAC.48.12.4869-4872.2004