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Malarone treatment failure not associated with previously described mutations in the cytochrome b gene

Malarone(® )(atovaquone-proguanil) is an effective drug for the treatment and prophylaxis of multidrug-resistant falciparum malaria. However, first cases of resistance have been reported, which are associated with mutations at codon 268 of the parasite's cytochrome b gene. We report the first c...

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Autores principales: Wichmann, Ole, Muehlen, Marion, Gruss, Holger, Mockenhaupt, Frank P, Suttorp, Norbert, Jelinek, Tomas
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC425592/
https://www.ncbi.nlm.nih.gov/pubmed/15186499
http://dx.doi.org/10.1186/1475-2875-3-14
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author Wichmann, Ole
Muehlen, Marion
Gruss, Holger
Mockenhaupt, Frank P
Suttorp, Norbert
Jelinek, Tomas
author_facet Wichmann, Ole
Muehlen, Marion
Gruss, Holger
Mockenhaupt, Frank P
Suttorp, Norbert
Jelinek, Tomas
author_sort Wichmann, Ole
collection PubMed
description Malarone(® )(atovaquone-proguanil) is an effective drug for the treatment and prophylaxis of multidrug-resistant falciparum malaria. However, first cases of resistance have been reported, which are associated with mutations at codon 268 of the parasite's cytochrome b gene. We report the first case of Malarone(® )treatment failure from Central Africa. Drug concentration was well within curative range. Pre- and post-treatment Plasmodium falciparum isolates revealed codon 268 wild-type alleles, and no other mutations of the putative atovaquone-binding domain. These findings illustrate the spread of atovaquone-proguanil-resistance in Africa and question the usefulness of codon 268 as the only target for the surveillance of its emergence.
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spelling pubmed-4255922004-06-18 Malarone treatment failure not associated with previously described mutations in the cytochrome b gene Wichmann, Ole Muehlen, Marion Gruss, Holger Mockenhaupt, Frank P Suttorp, Norbert Jelinek, Tomas Malar J Case Report Malarone(® )(atovaquone-proguanil) is an effective drug for the treatment and prophylaxis of multidrug-resistant falciparum malaria. However, first cases of resistance have been reported, which are associated with mutations at codon 268 of the parasite's cytochrome b gene. We report the first case of Malarone(® )treatment failure from Central Africa. Drug concentration was well within curative range. Pre- and post-treatment Plasmodium falciparum isolates revealed codon 268 wild-type alleles, and no other mutations of the putative atovaquone-binding domain. These findings illustrate the spread of atovaquone-proguanil-resistance in Africa and question the usefulness of codon 268 as the only target for the surveillance of its emergence. BioMed Central 2004-06-08 /pmc/articles/PMC425592/ /pubmed/15186499 http://dx.doi.org/10.1186/1475-2875-3-14 Text en Copyright © 2004 Wichmann et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Case Report
Wichmann, Ole
Muehlen, Marion
Gruss, Holger
Mockenhaupt, Frank P
Suttorp, Norbert
Jelinek, Tomas
Malarone treatment failure not associated with previously described mutations in the cytochrome b gene
title Malarone treatment failure not associated with previously described mutations in the cytochrome b gene
title_full Malarone treatment failure not associated with previously described mutations in the cytochrome b gene
title_fullStr Malarone treatment failure not associated with previously described mutations in the cytochrome b gene
title_full_unstemmed Malarone treatment failure not associated with previously described mutations in the cytochrome b gene
title_short Malarone treatment failure not associated with previously described mutations in the cytochrome b gene
title_sort malarone treatment failure not associated with previously described mutations in the cytochrome b gene
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC425592/
https://www.ncbi.nlm.nih.gov/pubmed/15186499
http://dx.doi.org/10.1186/1475-2875-3-14
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