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Prevalence of molecular markers of drug resistance in an area of seasonal malaria chemoprevention in children in Senegal

BACKGROUND: In sub-Saharan Africa, malaria is the leading cause of morbidity and mortality especially in children. In Senegal, seasonal malaria chemoprevention (SMC) previously referred to as intermittent preventive treatment in children (IPTc) is a new strategy for malaria control in areas of high...

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Autores principales: Lo, Aminata C, Faye, Babacar, Ba, El-Hadj, Cisse, Badara, Tine, Roger, Abiola, Annie, Ndiaye, Magatte, Ndiaye, Jean LA, Ndiaye, Daouda, Sokhna, Cheikh, Gomis, Jules F, Dieng, Yemou, Faye, Omar, Ndir, Omar, Milligan, Paul, Cairns, Matthew, Hallett, Rachel, Sutherland, Colin, Gaye, Oumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3652725/
https://www.ncbi.nlm.nih.gov/pubmed/23617576
http://dx.doi.org/10.1186/1475-2875-12-137
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author Lo, Aminata C
Faye, Babacar
Ba, El-Hadj
Cisse, Badara
Tine, Roger
Abiola, Annie
Ndiaye, Magatte
Ndiaye, Jean LA
Ndiaye, Daouda
Sokhna, Cheikh
Gomis, Jules F
Dieng, Yemou
Faye, Omar
Ndir, Omar
Milligan, Paul
Cairns, Matthew
Hallett, Rachel
Sutherland, Colin
Gaye, Oumar
author_facet Lo, Aminata C
Faye, Babacar
Ba, El-Hadj
Cisse, Badara
Tine, Roger
Abiola, Annie
Ndiaye, Magatte
Ndiaye, Jean LA
Ndiaye, Daouda
Sokhna, Cheikh
Gomis, Jules F
Dieng, Yemou
Faye, Omar
Ndir, Omar
Milligan, Paul
Cairns, Matthew
Hallett, Rachel
Sutherland, Colin
Gaye, Oumar
author_sort Lo, Aminata C
collection PubMed
description BACKGROUND: In sub-Saharan Africa, malaria is the leading cause of morbidity and mortality especially in children. In Senegal, seasonal malaria chemoprevention (SMC) previously referred to as intermittent preventive treatment in children (IPTc) is a new strategy for malaria control in areas of high seasonal transmission. An effectiveness study of SMC, using sulphadoxine-pyrimethamine (SP) plus amodiaquine (AQ), was conducted in central Senegal from 2008 to 2010 to obtain information about safety, feasibility of delivery, and cost effectiveness of SMC. Here are report the effect of SMC delivery on the prevalence of markers of resistance to SP and AQ. METHODS: This study was conducted in three health districts in Senegal with 54 health posts with a gradual introduction of SMC. Three administrations of the combination AQ + SP were made during the months of September, October and November of each year in children aged less than 10 years living in the area. Children were surveyed in December of each year and samples (filter paper and thick films) were made in 2008, 2009 and 2010. The prevalence of mutations in the pfdhfr, pfdhps, pfmdr1 and pfcrt genes was investigated by sequencing and RTPCR in samples positive by microscopy for Plasmodium falciparum. RESULTS: Mutations at codon 540 of pfdhps and codon 164 of pfdhfr were not detected in the study. Among children with parasitaemia at the end of the transmission seasons, the CVIET haplotypes of pfcrt and the 86Y polymorphism of pfmdr1 were more common among those that had received SMC, but the number of infections detected was very low and confidence intervals were wide. The overall prevalence of these mutations was lower in SMC areas than in control areas, reflecting the lower prevalence of parasitaemia in areas where SMC was delivered. CONCLUSION: The sensitivity of P. falciparum to SMC drugs should be regularly monitored in areas deploying this intervention. Overall the prevalence of genotypes associated with resistance to either SP or AQ was lower in SMC areas due to the reduced number of parasitaemia individuals.
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spelling pubmed-36527252013-05-14 Prevalence of molecular markers of drug resistance in an area of seasonal malaria chemoprevention in children in Senegal Lo, Aminata C Faye, Babacar Ba, El-Hadj Cisse, Badara Tine, Roger Abiola, Annie Ndiaye, Magatte Ndiaye, Jean LA Ndiaye, Daouda Sokhna, Cheikh Gomis, Jules F Dieng, Yemou Faye, Omar Ndir, Omar Milligan, Paul Cairns, Matthew Hallett, Rachel Sutherland, Colin Gaye, Oumar Malar J Research BACKGROUND: In sub-Saharan Africa, malaria is the leading cause of morbidity and mortality especially in children. In Senegal, seasonal malaria chemoprevention (SMC) previously referred to as intermittent preventive treatment in children (IPTc) is a new strategy for malaria control in areas of high seasonal transmission. An effectiveness study of SMC, using sulphadoxine-pyrimethamine (SP) plus amodiaquine (AQ), was conducted in central Senegal from 2008 to 2010 to obtain information about safety, feasibility of delivery, and cost effectiveness of SMC. Here are report the effect of SMC delivery on the prevalence of markers of resistance to SP and AQ. METHODS: This study was conducted in three health districts in Senegal with 54 health posts with a gradual introduction of SMC. Three administrations of the combination AQ + SP were made during the months of September, October and November of each year in children aged less than 10 years living in the area. Children were surveyed in December of each year and samples (filter paper and thick films) were made in 2008, 2009 and 2010. The prevalence of mutations in the pfdhfr, pfdhps, pfmdr1 and pfcrt genes was investigated by sequencing and RTPCR in samples positive by microscopy for Plasmodium falciparum. RESULTS: Mutations at codon 540 of pfdhps and codon 164 of pfdhfr were not detected in the study. Among children with parasitaemia at the end of the transmission seasons, the CVIET haplotypes of pfcrt and the 86Y polymorphism of pfmdr1 were more common among those that had received SMC, but the number of infections detected was very low and confidence intervals were wide. The overall prevalence of these mutations was lower in SMC areas than in control areas, reflecting the lower prevalence of parasitaemia in areas where SMC was delivered. CONCLUSION: The sensitivity of P. falciparum to SMC drugs should be regularly monitored in areas deploying this intervention. Overall the prevalence of genotypes associated with resistance to either SP or AQ was lower in SMC areas due to the reduced number of parasitaemia individuals. BioMed Central 2013-04-23 /pmc/articles/PMC3652725/ /pubmed/23617576 http://dx.doi.org/10.1186/1475-2875-12-137 Text en Copyright © 2013 Lo 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
Lo, Aminata C
Faye, Babacar
Ba, El-Hadj
Cisse, Badara
Tine, Roger
Abiola, Annie
Ndiaye, Magatte
Ndiaye, Jean LA
Ndiaye, Daouda
Sokhna, Cheikh
Gomis, Jules F
Dieng, Yemou
Faye, Omar
Ndir, Omar
Milligan, Paul
Cairns, Matthew
Hallett, Rachel
Sutherland, Colin
Gaye, Oumar
Prevalence of molecular markers of drug resistance in an area of seasonal malaria chemoprevention in children in Senegal
title Prevalence of molecular markers of drug resistance in an area of seasonal malaria chemoprevention in children in Senegal
title_full Prevalence of molecular markers of drug resistance in an area of seasonal malaria chemoprevention in children in Senegal
title_fullStr Prevalence of molecular markers of drug resistance in an area of seasonal malaria chemoprevention in children in Senegal
title_full_unstemmed Prevalence of molecular markers of drug resistance in an area of seasonal malaria chemoprevention in children in Senegal
title_short Prevalence of molecular markers of drug resistance in an area of seasonal malaria chemoprevention in children in Senegal
title_sort prevalence of molecular markers of drug resistance in an area of seasonal malaria chemoprevention in children in senegal
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3652725/
https://www.ncbi.nlm.nih.gov/pubmed/23617576
http://dx.doi.org/10.1186/1475-2875-12-137
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