Prevalence of <it>pfmdr1</it>, <it>pfcrt</it>, <it>pfdhfr </it>and <it>pfdhps </it>mutations associated with drug resistance, in Luanda, Angola

<p>Abstract</p> <p>Background</p> <p>Malaria is the infectious disease causing the highest morbidity and mortality in Angola and due to widespread chloroquine (CQ) resistance, the country has recently changed its first-line treatment recommendations for uncomplicated ma...

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Main Authors: Varandas Luís, do Rosário Virgílio E, Bernardino Luís, Lopes Dinora, Benchimol Carla, Figueiredo Paula, Nogueira Fátima
Format: Article
Language:English
Published: BMC 2008-11-01
Series:Malaria Journal
Online Access:http://www.malariajournal.com/content/7/1/236
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spelling doaj-765056b2d1a14799adc934d91d8ba6632020-11-25T00:26:35ZengBMCMalaria Journal1475-28752008-11-017123610.1186/1475-2875-7-236Prevalence of <it>pfmdr1</it>, <it>pfcrt</it>, <it>pfdhfr </it>and <it>pfdhps </it>mutations associated with drug resistance, in Luanda, AngolaVarandas Luísdo Rosário Virgílio EBernardino LuísLopes DinoraBenchimol CarlaFigueiredo PaulaNogueira Fátima<p>Abstract</p> <p>Background</p> <p>Malaria is the infectious disease causing the highest morbidity and mortality in Angola and due to widespread chloroquine (CQ) resistance, the country has recently changed its first-line treatment recommendations for uncomplicated malaria, from CQ to artemisinin combination therapies (ACT) in adults, and sulphadoxine/pyrimethamine (S/P) in pregnant women. Loss of SP sensitivity is, however, progressing rapidly in Africa and, in this study, were investigated a number of molecular markers associated to CQ and S/P.</p> <p>Methods</p> <p>Blood samples were collected from 245 children with uncomplicated malaria, admitted at the Pediatric Hospital Dr. David Bernardino (HPDB), Angola, and the occurrence of mutations in <it>Plasmodium falciparum </it>was investigated in the <it>pfmdr1 </it>(N86Y) and <it>pfcrt </it>(K76T) genes, associated with CQ resistance, as well as in <it>pfdhfr </it>(C59R) and <it>pfdhps </it>(K540E), conferring SP resistance.</p> <p>Results</p> <p>The frequencies of <it>pfmdr1 </it>mutations in codon 86 were 28.6% N, 61.3% Y and 10.1% mixed infections (NY). The frequency of <it>pfcrt </it>mutations in codon 76 were 93.9% K, 5.7% T and 0.4% mixed infections (KT). For <it>pfdhfr </it>the results were in codon 59, 60.6% C, 20.6% R and 18.8% mixed infections (CR). Concerning <it>pfdhps</it>, 6.3% of the isolates were bearers of the mutation 540E and 5.4% mixed infections (K540E).</p> <p>Conclusion</p> <p>The results of this epidemiologic study showed high presence of CQ resistance markers while for SP a much lower prevalence was detected for the markers under study.</p> http://www.malariajournal.com/content/7/1/236
collection DOAJ
language English
format Article
sources DOAJ
author Varandas Luís
do Rosário Virgílio E
Bernardino Luís
Lopes Dinora
Benchimol Carla
Figueiredo Paula
Nogueira Fátima
spellingShingle Varandas Luís
do Rosário Virgílio E
Bernardino Luís
Lopes Dinora
Benchimol Carla
Figueiredo Paula
Nogueira Fátima
Prevalence of <it>pfmdr1</it>, <it>pfcrt</it>, <it>pfdhfr </it>and <it>pfdhps </it>mutations associated with drug resistance, in Luanda, Angola
Malaria Journal
author_facet Varandas Luís
do Rosário Virgílio E
Bernardino Luís
Lopes Dinora
Benchimol Carla
Figueiredo Paula
Nogueira Fátima
author_sort Varandas Luís
title Prevalence of <it>pfmdr1</it>, <it>pfcrt</it>, <it>pfdhfr </it>and <it>pfdhps </it>mutations associated with drug resistance, in Luanda, Angola
title_short Prevalence of <it>pfmdr1</it>, <it>pfcrt</it>, <it>pfdhfr </it>and <it>pfdhps </it>mutations associated with drug resistance, in Luanda, Angola
title_full Prevalence of <it>pfmdr1</it>, <it>pfcrt</it>, <it>pfdhfr </it>and <it>pfdhps </it>mutations associated with drug resistance, in Luanda, Angola
title_fullStr Prevalence of <it>pfmdr1</it>, <it>pfcrt</it>, <it>pfdhfr </it>and <it>pfdhps </it>mutations associated with drug resistance, in Luanda, Angola
title_full_unstemmed Prevalence of <it>pfmdr1</it>, <it>pfcrt</it>, <it>pfdhfr </it>and <it>pfdhps </it>mutations associated with drug resistance, in Luanda, Angola
title_sort prevalence of <it>pfmdr1</it>, <it>pfcrt</it>, <it>pfdhfr </it>and <it>pfdhps </it>mutations associated with drug resistance, in luanda, angola
publisher BMC
series Malaria Journal
issn 1475-2875
publishDate 2008-11-01
description <p>Abstract</p> <p>Background</p> <p>Malaria is the infectious disease causing the highest morbidity and mortality in Angola and due to widespread chloroquine (CQ) resistance, the country has recently changed its first-line treatment recommendations for uncomplicated malaria, from CQ to artemisinin combination therapies (ACT) in adults, and sulphadoxine/pyrimethamine (S/P) in pregnant women. Loss of SP sensitivity is, however, progressing rapidly in Africa and, in this study, were investigated a number of molecular markers associated to CQ and S/P.</p> <p>Methods</p> <p>Blood samples were collected from 245 children with uncomplicated malaria, admitted at the Pediatric Hospital Dr. David Bernardino (HPDB), Angola, and the occurrence of mutations in <it>Plasmodium falciparum </it>was investigated in the <it>pfmdr1 </it>(N86Y) and <it>pfcrt </it>(K76T) genes, associated with CQ resistance, as well as in <it>pfdhfr </it>(C59R) and <it>pfdhps </it>(K540E), conferring SP resistance.</p> <p>Results</p> <p>The frequencies of <it>pfmdr1 </it>mutations in codon 86 were 28.6% N, 61.3% Y and 10.1% mixed infections (NY). The frequency of <it>pfcrt </it>mutations in codon 76 were 93.9% K, 5.7% T and 0.4% mixed infections (KT). For <it>pfdhfr </it>the results were in codon 59, 60.6% C, 20.6% R and 18.8% mixed infections (CR). Concerning <it>pfdhps</it>, 6.3% of the isolates were bearers of the mutation 540E and 5.4% mixed infections (K540E).</p> <p>Conclusion</p> <p>The results of this epidemiologic study showed high presence of CQ resistance markers while for SP a much lower prevalence was detected for the markers under study.</p>
url http://www.malariajournal.com/content/7/1/236
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