Literature DB >> 12543682

Genetics of mefloquine resistance in the rodent malaria parasite Plasmodium chabaudi.

Pedro V L Cravo1, Jane M-R Carlton, Paul Hunt, Laura Bisoni, Rose Ann Padua, David Walliker.   

Abstract

The genetic determinants of resistance to mefloquine in malaria parasites are unclear. Some studies have implied that amplification of, or mutations in, the multidrug resistance gene pfmdr1 in Plasmodium falciparum may be involved. Using the rodent malaria model Plasmodium chabaudi, we investigated the role of the orthologue of this gene, pcmdr1, in a stable mefloquine-resistant mutant, AS(15MF/3), selected from a sensitive clone. pcmdr1 exists as a single copy gene on chromosome 12 of the sensitive clone. In AS(15MF/3), the gene was found to have undergone duplication, with one copy translocating to chromosome 4. mRNA levels of pcmdr1 were higher in the mutant than in the parent sensitive clone. A partial genetic map of the translocation showed that other genes in addition to pcmdr1 had been cotranslocated. The sequences of both copies of pcmdr1 of AS(15MF/3) were identical to that of the parent sensitive clone. A cross was made between AS(15MF/3) and an unrelated mefloquine-sensitive clone, AJ. Phenotypic and molecular analysis of progeny clones showed that duplication and overexpression of the pcmdr1 gene was an important determinant of resistance. However, not all mefloquine-resistant progeny contained the duplicated gene, showing that at least one other gene was involved in resistance.

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Year:  2003        PMID: 12543682      PMCID: PMC151772          DOI: 10.1128/AAC.47.2.709-718.2003

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  49 in total

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Journal:  Mol Biochem Parasitol       Date:  1993-12       Impact factor: 1.759

9.  Amplification of pfmdr 1 associated with mefloquine and halofantrine resistance in Plasmodium falciparum from Thailand.

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Journal:  Antimicrob Agents Chemother       Date:  1999-12       Impact factor: 5.191

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  24 in total

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2.  Selection of Plasmodium falciparum pfmdr1 alleles following therapy with artemether-lumefantrine in an area of Uganda where malaria is highly endemic.

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Journal:  Antimicrob Agents Chemother       Date:  2006-05       Impact factor: 5.191

3.  Genomewide scan reveals amplification of mdr1 as a common denominator of resistance to mefloquine, lumefantrine, and artemisinin in Plasmodium chabaudi malaria parasites.

Authors:  Sofia Borges; Pedro Cravo; Alison Creasey; Richard Fawcett; Katarzyna Modrzynska; Louise Rodrigues; Axel Martinelli; Paul Hunt
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4.  Piperaquine and Lumefantrine resistance in Plasmodium berghei ANKA associated with increased expression of Ca2+/H+ antiporter and glutathione associated enzymes.

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5.  Protocol for production of a genetic cross of the rodent malaria parasites.

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6.  Experimental evolution of resistance to artemisinin combination therapy results in amplification of the mdr1 gene in a rodent malaria parasite.

Authors:  Louise A Rodrigues; Gisela Henriques; Sofia T Borges; Paul Hunt; Cecília P Sanchez; Axel Martinelli; Pedro Cravo
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7.  Experimental evolution, genetic analysis and genome re-sequencing reveal the mutation conferring artemisinin resistance in an isogenic lineage of malaria parasites.

Authors:  Paul Hunt; Axel Martinelli; Katarzyna Modrzynska; Sofia Borges; Alison Creasey; Louise Rodrigues; Dario Beraldi; Laurence Loewe; Richard Fawcett; Sujai Kumar; Marian Thomson; Urmi Trivedi; Thomas D Otto; Arnab Pain; Mark Blaxter; Pedro Cravo
Journal:  BMC Genomics       Date:  2010-09-16       Impact factor: 3.969

Review 8.  Large-scale genotyping and genetic mapping in Plasmodium parasites.

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Review 9.  Gene copy number and malaria biology.

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10.  Plasmodium berghei ANKA: selection of resistance to piperaquine and lumefantrine in a mouse model.

Authors:  D M Kiboi; B N Irungu; B Langat; S Wittlin; R Brun; J Chollet; O Abiodun; J K Nganga; V C S Nyambati; G M Rukunga; A Bell; A Nzila
Journal:  Exp Parasitol       Date:  2009-03-24       Impact factor: 2.011

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