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Molecular markers of anti-malarial drug resistance in Lahj Governorate, Yemen: baseline data and implications

BACKGROUND: This is an investigation of anti-malarial molecular markers coupled with a therapeutic efficacy test of chloroquine (CQ) against falciparum malaria in an area of unstable malaria in Lahj Governorate, Yemen. The study was aimed at assessment of therapeutic response to CQ and elucidation o...

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Autores principales: Mubjer, Reem A, Adeel, Ahmed A, Chance, Michael L, Hassan, Amir A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3177815/
https://www.ncbi.nlm.nih.gov/pubmed/21854642
http://dx.doi.org/10.1186/1475-2875-10-245
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author Mubjer, Reem A
Adeel, Ahmed A
Chance, Michael L
Hassan, Amir A
author_facet Mubjer, Reem A
Adeel, Ahmed A
Chance, Michael L
Hassan, Amir A
author_sort Mubjer, Reem A
collection PubMed
description BACKGROUND: This is an investigation of anti-malarial molecular markers coupled with a therapeutic efficacy test of chloroquine (CQ) against falciparum malaria in an area of unstable malaria in Lahj Governorate, Yemen. The study was aimed at assessment of therapeutic response to CQ and elucidation of baseline information on molecular markers for Plasmodium falciparum resistance against CQ and sulphadoxine/pyrimethamine (SP). METHODS: Between 2002 and 2003 the field test was conducted according to the standard WHO protocol to evaluate the therapeutic efficacy of CQ in 124 patients with falciparum malaria in an endemic area in Lahj Governorate in Yemen. Blood samples collected during this study were analysed for P. falciparum chloroquine resistance transporter gene (pfcrt)-76 polymorphisms, mutation pfcrt-S163R and the antifolate resistance-associated mutations dihydrofolate reductase (dhfr)-C59R and dihydropteroate synthase (dhps)-K540E. Direct DNA sequencing of the pfcrt gene from three representative field samples was carried out after DNA amplification of the 13 exons of the pfcrt gene. RESULTS: Treatment failure was detected in 61% of the 122 cases that completed the 14-day follow-up. The prevalence of mutant pfcrt T76 was 98% in 112 amplified pre-treatment samples. The presence of pfcrt T76 was poorly predictive of in vivo CQ resistance (PPV = 61.8%, 95% CI = 52.7-70.9). The prevalence of dhfr Arg-59 mutation in 99 amplified samples was 5%, while the dhps Glu-540 was not detected in any of 119 amplified samples. Sequencing the pfcrt gene confirmed that Yemeni CQ resistant P. falciparum carry the old world (Asian and African) CQ resistant haplotype CVIETSESI at positions 72,73,74,75,76,220,271, 326 and 371. CONCLUSION: This is the first study to report baseline information on the characteristics and implications of anti-malarial drug resistance markers in Yemen. It is also the first report of the haplotype associated with CQR P. falciparum parasites from Yemen. Mutant pfcrtT76 is highly prevalent but it is a poor predictor of treatment failure in the study population. The prevalence of mutation dhfrArg59 is suggestive of emerging resistance to SP, which is currently a component of the recommended combination treatment of falciparum malaria in Yemen. More studies on these markers are recommended for surveillance of resistance in the study area.
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spelling pubmed-31778152011-09-22 Molecular markers of anti-malarial drug resistance in Lahj Governorate, Yemen: baseline data and implications Mubjer, Reem A Adeel, Ahmed A Chance, Michael L Hassan, Amir A Malar J Research BACKGROUND: This is an investigation of anti-malarial molecular markers coupled with a therapeutic efficacy test of chloroquine (CQ) against falciparum malaria in an area of unstable malaria in Lahj Governorate, Yemen. The study was aimed at assessment of therapeutic response to CQ and elucidation of baseline information on molecular markers for Plasmodium falciparum resistance against CQ and sulphadoxine/pyrimethamine (SP). METHODS: Between 2002 and 2003 the field test was conducted according to the standard WHO protocol to evaluate the therapeutic efficacy of CQ in 124 patients with falciparum malaria in an endemic area in Lahj Governorate in Yemen. Blood samples collected during this study were analysed for P. falciparum chloroquine resistance transporter gene (pfcrt)-76 polymorphisms, mutation pfcrt-S163R and the antifolate resistance-associated mutations dihydrofolate reductase (dhfr)-C59R and dihydropteroate synthase (dhps)-K540E. Direct DNA sequencing of the pfcrt gene from three representative field samples was carried out after DNA amplification of the 13 exons of the pfcrt gene. RESULTS: Treatment failure was detected in 61% of the 122 cases that completed the 14-day follow-up. The prevalence of mutant pfcrt T76 was 98% in 112 amplified pre-treatment samples. The presence of pfcrt T76 was poorly predictive of in vivo CQ resistance (PPV = 61.8%, 95% CI = 52.7-70.9). The prevalence of dhfr Arg-59 mutation in 99 amplified samples was 5%, while the dhps Glu-540 was not detected in any of 119 amplified samples. Sequencing the pfcrt gene confirmed that Yemeni CQ resistant P. falciparum carry the old world (Asian and African) CQ resistant haplotype CVIETSESI at positions 72,73,74,75,76,220,271, 326 and 371. CONCLUSION: This is the first study to report baseline information on the characteristics and implications of anti-malarial drug resistance markers in Yemen. It is also the first report of the haplotype associated with CQR P. falciparum parasites from Yemen. Mutant pfcrtT76 is highly prevalent but it is a poor predictor of treatment failure in the study population. The prevalence of mutation dhfrArg59 is suggestive of emerging resistance to SP, which is currently a component of the recommended combination treatment of falciparum malaria in Yemen. More studies on these markers are recommended for surveillance of resistance in the study area. BioMed Central 2011-08-21 /pmc/articles/PMC3177815/ /pubmed/21854642 http://dx.doi.org/10.1186/1475-2875-10-245 Text en Copyright ©2011 Mubjer et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Mubjer, Reem A
Adeel, Ahmed A
Chance, Michael L
Hassan, Amir A
Molecular markers of anti-malarial drug resistance in Lahj Governorate, Yemen: baseline data and implications
title Molecular markers of anti-malarial drug resistance in Lahj Governorate, Yemen: baseline data and implications
title_full Molecular markers of anti-malarial drug resistance in Lahj Governorate, Yemen: baseline data and implications
title_fullStr Molecular markers of anti-malarial drug resistance in Lahj Governorate, Yemen: baseline data and implications
title_full_unstemmed Molecular markers of anti-malarial drug resistance in Lahj Governorate, Yemen: baseline data and implications
title_short Molecular markers of anti-malarial drug resistance in Lahj Governorate, Yemen: baseline data and implications
title_sort molecular markers of anti-malarial drug resistance in lahj governorate, yemen: baseline data and implications
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3177815/
https://www.ncbi.nlm.nih.gov/pubmed/21854642
http://dx.doi.org/10.1186/1475-2875-10-245
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