Prevalence of mutations associated with antimalarial drugs in <it>Plasmodium falciparum </it>isolates prior to the introduction of sulphadoxine-pyrimethamine as first-line treatment in Iran

<p>Abstract</p> <p>Background</p> <p>This work was carried out to assess the patterns and prevalence of resistance to chloroquine (CQ) and sulphadoxine-pyrimethamine (SP) in Iran.</p> <p>Methods</p> <p>The prevalence of <it>pfcrt </it>...

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Main Authors: Djadid Navid, Raeisi Ahmad, Afsharpad Mandana, Zakeri Sedigheh
Format: Article
Language:English
Published: BMC 2007-11-01
Series:Malaria Journal
Online Access:http://www.malariajournal.com/content/6/1/148
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author Djadid Navid
Raeisi Ahmad
Afsharpad Mandana
Zakeri Sedigheh
author_facet Djadid Navid
Raeisi Ahmad
Afsharpad Mandana
Zakeri Sedigheh
author_sort Djadid Navid
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>This work was carried out to assess the patterns and prevalence of resistance to chloroquine (CQ) and sulphadoxine-pyrimethamine (SP) in Iran.</p> <p>Methods</p> <p>The prevalence of <it>pfcrt </it>K76T, <it>pfmdr1 </it>N86Y, <it>pfdhfr </it>N51I, C59R, S108N/T and I164L and codons S436F/A, A437G, K540E, A581E, and A613S/T in <it>pfdhps </it>genes were genotyped by PCR/RFLP methods in 206 <it>Plasmodium falciparum </it>isolates from Chabahar and Sarbaz districts in Sistan and Baluchistan province, Iran, during 2003–2005.</p> <p>Results</p> <p>All <it>P. falciparum </it>isolates carried the 108N, while 98.5% parasite isolates carried the 59R mutation. 98.5% of patients carried both 108N and 59R. The prevalence of <it>pfdhps </it>437G mutation was 17% (Chabahar) and 33% (Sarbaz) isolates. 20.4% of samples presented the <it>pfdhfr </it>108N, 59R with <it>pfdhps </it>437G mutations. The frequency of allele <it>pfcrt </it>76T was 98%, while 41.4% (Chabahar) and 27.7% (Sarbaz) isolates carried <it>pfmdr1 </it>86Y allele. Eight distinct haplotypes were identified in all 206 samples, while the most prevalent haplotype was <b>T</b><sub>76/</sub>N<sub>86/</sub>N<sub>51</sub><b>R</b><sub>59</sub><b>N</b><sub>108/</sub>A<sub>437 </sub>among both study areas.</p> <p>Conclusion</p> <p>Finding the fixed level of CQ resistance polymorphisms (<it>pfcrt </it>76T) suggests that CQ must be withdrawn from the current treatment strategy in Iran, while SP may remain the treatment of choice for uncomplicated malaria.</p>
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spelling doaj.art-1163fee263954709bb9129e2b6a0e9842022-12-22T03:29:09ZengBMCMalaria Journal1475-28752007-11-016114810.1186/1475-2875-6-148Prevalence of mutations associated with antimalarial drugs in <it>Plasmodium falciparum </it>isolates prior to the introduction of sulphadoxine-pyrimethamine as first-line treatment in IranDjadid NavidRaeisi AhmadAfsharpad MandanaZakeri Sedigheh<p>Abstract</p> <p>Background</p> <p>This work was carried out to assess the patterns and prevalence of resistance to chloroquine (CQ) and sulphadoxine-pyrimethamine (SP) in Iran.</p> <p>Methods</p> <p>The prevalence of <it>pfcrt </it>K76T, <it>pfmdr1 </it>N86Y, <it>pfdhfr </it>N51I, C59R, S108N/T and I164L and codons S436F/A, A437G, K540E, A581E, and A613S/T in <it>pfdhps </it>genes were genotyped by PCR/RFLP methods in 206 <it>Plasmodium falciparum </it>isolates from Chabahar and Sarbaz districts in Sistan and Baluchistan province, Iran, during 2003–2005.</p> <p>Results</p> <p>All <it>P. falciparum </it>isolates carried the 108N, while 98.5% parasite isolates carried the 59R mutation. 98.5% of patients carried both 108N and 59R. The prevalence of <it>pfdhps </it>437G mutation was 17% (Chabahar) and 33% (Sarbaz) isolates. 20.4% of samples presented the <it>pfdhfr </it>108N, 59R with <it>pfdhps </it>437G mutations. The frequency of allele <it>pfcrt </it>76T was 98%, while 41.4% (Chabahar) and 27.7% (Sarbaz) isolates carried <it>pfmdr1 </it>86Y allele. Eight distinct haplotypes were identified in all 206 samples, while the most prevalent haplotype was <b>T</b><sub>76/</sub>N<sub>86/</sub>N<sub>51</sub><b>R</b><sub>59</sub><b>N</b><sub>108/</sub>A<sub>437 </sub>among both study areas.</p> <p>Conclusion</p> <p>Finding the fixed level of CQ resistance polymorphisms (<it>pfcrt </it>76T) suggests that CQ must be withdrawn from the current treatment strategy in Iran, while SP may remain the treatment of choice for uncomplicated malaria.</p>http://www.malariajournal.com/content/6/1/148
spellingShingle Djadid Navid
Raeisi Ahmad
Afsharpad Mandana
Zakeri Sedigheh
Prevalence of mutations associated with antimalarial drugs in <it>Plasmodium falciparum </it>isolates prior to the introduction of sulphadoxine-pyrimethamine as first-line treatment in Iran
Malaria Journal
title Prevalence of mutations associated with antimalarial drugs in <it>Plasmodium falciparum </it>isolates prior to the introduction of sulphadoxine-pyrimethamine as first-line treatment in Iran
title_full Prevalence of mutations associated with antimalarial drugs in <it>Plasmodium falciparum </it>isolates prior to the introduction of sulphadoxine-pyrimethamine as first-line treatment in Iran
title_fullStr Prevalence of mutations associated with antimalarial drugs in <it>Plasmodium falciparum </it>isolates prior to the introduction of sulphadoxine-pyrimethamine as first-line treatment in Iran
title_full_unstemmed Prevalence of mutations associated with antimalarial drugs in <it>Plasmodium falciparum </it>isolates prior to the introduction of sulphadoxine-pyrimethamine as first-line treatment in Iran
title_short Prevalence of mutations associated with antimalarial drugs in <it>Plasmodium falciparum </it>isolates prior to the introduction of sulphadoxine-pyrimethamine as first-line treatment in Iran
title_sort prevalence of mutations associated with antimalarial drugs in it plasmodium falciparum it isolates prior to the introduction of sulphadoxine pyrimethamine as first line treatment in iran
url http://www.malariajournal.com/content/6/1/148
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