Literature DB >> 17550470

The role of pfmdr1 in Plasmodium falciparum tolerance to artemether-lumefantrine in Africa.

Christin Sisowath1, Pedro E Ferreira, Leyla Y Bustamante, Sabina Dahlström, Andreas Mårtensson, Anders Björkman, Sanjeev Krishna, José P Gil.   

Abstract

OBJECTIVE: Artemether-lumefantrine (AL), presently the most favoured combination therapy against uncomplicated Plasmodium falciparum malaria in Africa, has recently shown to select for the pfmdr1 86N allele. The objective of this study was to search for the selection of other mutations potentially involved in artemether-lumefantrine tolerance and/or resistance, i.e. pfmdr1 gene amplification, pfmdr1 Y184F, S1034C, N1042D, D1246Y, pfcrt S163R and PfATP6 S769N.
METHODS: The above mentioned SNPs were analysed by PCR-restriction fragment length polymorphism and pfmdr1 gene amplification by real-time PCR based protocols in parasites from 200 children treated with AL for uncomplicated P. falciparum malaria in Zanzibar.
RESULTS: A statistically significant selection of pfmdr1 184F mostly in combination with 86N was seen in reinfections after treatment. No pfmdr1 gene amplification was found.
CONCLUSION: The results suggest that different pfmdr1 alleles are involved in the development of tolerance/resistance to lumefantrine.

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Year:  2007        PMID: 17550470     DOI: 10.1111/j.1365-3156.2007.01843.x

Source DB:  PubMed          Journal:  Trop Med Int Health        ISSN: 1360-2276            Impact factor:   2.622


  83 in total

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2.  Association between the pfmdr1 gene and in vitro artemether and lumefantrine sensitivity in Thai isolates of Plasmodium falciparum.

Authors:  Mathirut Mungthin; Rommanee Khositnithikul; Naruemon Sitthichot; Nantana Suwandittakul; Veerachai Wattanaveeradej; Stephen A Ward; Kesara Na-Bangchang
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3.  Rational deployment of antimalarial drugs in Africa: should first-line combination drugs be reserved for paediatric malaria cases?

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4.  Development, evaluation, and application of an in silico model for antimalarial drug treatment and failure.

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Review 6.  Artemisinin-based combination therapies: a vital tool in efforts to eliminate malaria.

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8.  In vitro activities of piperaquine, lumefantrine, and dihydroartemisinin in Kenyan Plasmodium falciparum isolates and polymorphisms in pfcrt and pfmdr1.

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9.  The perils of PCR: can we accurately 'correct' antimalarial trials?

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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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