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Selective sweeps and genetic lineages of Plasmodium falciparum multi-drug resistance (pfmdr1) gene in Kenya

BACKGROUND: There are concerns that resistance to artemisinin-based combination therapy might emerge in Kenya and sub-Saharan Africa (SSA) in the same pattern as was with chloroquine and sulfadoxine–pyrimethamine. Single nucleotide polymorphisms (SNPs) in critical alleles of pfmdr1 gene have been as...

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Autores principales: Muiruri, Peninah, Juma, Denis W., Ingasia, Luicer A., Chebon, Lorna J., Opot, Benjamin, Ngalah, Bidii S., Cheruiyot, Jelagat, Andagalu, Ben, Akala, Hoseah M., Nyambati, Venny C. S., Ng’ang’a, Joseph K., Kamau, Edwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6208105/
https://www.ncbi.nlm.nih.gov/pubmed/30376843
http://dx.doi.org/10.1186/s12936-018-2534-8
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author Muiruri, Peninah
Juma, Denis W.
Ingasia, Luicer A.
Chebon, Lorna J.
Opot, Benjamin
Ngalah, Bidii S.
Cheruiyot, Jelagat
Andagalu, Ben
Akala, Hoseah M.
Nyambati, Venny C. S.
Ng’ang’a, Joseph K.
Kamau, Edwin
author_facet Muiruri, Peninah
Juma, Denis W.
Ingasia, Luicer A.
Chebon, Lorna J.
Opot, Benjamin
Ngalah, Bidii S.
Cheruiyot, Jelagat
Andagalu, Ben
Akala, Hoseah M.
Nyambati, Venny C. S.
Ng’ang’a, Joseph K.
Kamau, Edwin
author_sort Muiruri, Peninah
collection PubMed
description BACKGROUND: There are concerns that resistance to artemisinin-based combination therapy might emerge in Kenya and sub-Saharan Africa (SSA) in the same pattern as was with chloroquine and sulfadoxine–pyrimethamine. Single nucleotide polymorphisms (SNPs) in critical alleles of pfmdr1 gene have been associated with resistance to artemisinin and its partner drugs. Microsatellite analysis of loci flanking genes associated with anti-malarial drug resistance has been used in defining the geographic origins, dissemination of resistant parasites and identifying regions in the genome that have been under selection. METHODS: This study set out to investigate evidence of selective sweep and genetic lineages in pfmdr1 genotypes associated with the use of artemether–lumefantrine (AL), as the first-line treatment in Kenya. Parasites (n = 252) from different regions in Kenya were assayed for SNPs at codons 86, 184 and 1246 and typed for 7 neutral microsatellites and 13 microsatellites loci flanking (± 99 kb) pfmdr1 in Plasmodium falciparum infections. RESULTS: The data showed differential site and region specific prevalence of SNPs associated with drug resistance in the pfmdr1 gene. The prevalence of pfmdr1 N86, 184F, and D1246 in western Kenya (Kisumu, Kericho and Kisii) compared to the coast of Kenya (Malindi) was 92.9% vs. 66.7%, 53.5% vs. to 24.2% and 96% vs. to 87.9%, respectively. The NFD haplotype which is consistent with AL selection was at 51% in western Kenya compared to 25% in coastal Kenya. CONCLUSION: Selection pressures were observed to be different in different regions of Kenya, especially the western region compared to the coastal region. The data showed independent genetic lineages for all the pfmdr1 alleles. The evidence of soft sweeps in pfmdr1 observed varied in direction from one region to another. This is challenging for malaria control programs in SSA which clearly indicate effective malaria control policies should be based on the region and not at a country wide level. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-018-2534-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-62081052018-11-16 Selective sweeps and genetic lineages of Plasmodium falciparum multi-drug resistance (pfmdr1) gene in Kenya Muiruri, Peninah Juma, Denis W. Ingasia, Luicer A. Chebon, Lorna J. Opot, Benjamin Ngalah, Bidii S. Cheruiyot, Jelagat Andagalu, Ben Akala, Hoseah M. Nyambati, Venny C. S. Ng’ang’a, Joseph K. Kamau, Edwin Malar J Research BACKGROUND: There are concerns that resistance to artemisinin-based combination therapy might emerge in Kenya and sub-Saharan Africa (SSA) in the same pattern as was with chloroquine and sulfadoxine–pyrimethamine. Single nucleotide polymorphisms (SNPs) in critical alleles of pfmdr1 gene have been associated with resistance to artemisinin and its partner drugs. Microsatellite analysis of loci flanking genes associated with anti-malarial drug resistance has been used in defining the geographic origins, dissemination of resistant parasites and identifying regions in the genome that have been under selection. METHODS: This study set out to investigate evidence of selective sweep and genetic lineages in pfmdr1 genotypes associated with the use of artemether–lumefantrine (AL), as the first-line treatment in Kenya. Parasites (n = 252) from different regions in Kenya were assayed for SNPs at codons 86, 184 and 1246 and typed for 7 neutral microsatellites and 13 microsatellites loci flanking (± 99 kb) pfmdr1 in Plasmodium falciparum infections. RESULTS: The data showed differential site and region specific prevalence of SNPs associated with drug resistance in the pfmdr1 gene. The prevalence of pfmdr1 N86, 184F, and D1246 in western Kenya (Kisumu, Kericho and Kisii) compared to the coast of Kenya (Malindi) was 92.9% vs. 66.7%, 53.5% vs. to 24.2% and 96% vs. to 87.9%, respectively. The NFD haplotype which is consistent with AL selection was at 51% in western Kenya compared to 25% in coastal Kenya. CONCLUSION: Selection pressures were observed to be different in different regions of Kenya, especially the western region compared to the coastal region. The data showed independent genetic lineages for all the pfmdr1 alleles. The evidence of soft sweeps in pfmdr1 observed varied in direction from one region to another. This is challenging for malaria control programs in SSA which clearly indicate effective malaria control policies should be based on the region and not at a country wide level. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-018-2534-8) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-30 /pmc/articles/PMC6208105/ /pubmed/30376843 http://dx.doi.org/10.1186/s12936-018-2534-8 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Muiruri, Peninah
Juma, Denis W.
Ingasia, Luicer A.
Chebon, Lorna J.
Opot, Benjamin
Ngalah, Bidii S.
Cheruiyot, Jelagat
Andagalu, Ben
Akala, Hoseah M.
Nyambati, Venny C. S.
Ng’ang’a, Joseph K.
Kamau, Edwin
Selective sweeps and genetic lineages of Plasmodium falciparum multi-drug resistance (pfmdr1) gene in Kenya
title Selective sweeps and genetic lineages of Plasmodium falciparum multi-drug resistance (pfmdr1) gene in Kenya
title_full Selective sweeps and genetic lineages of Plasmodium falciparum multi-drug resistance (pfmdr1) gene in Kenya
title_fullStr Selective sweeps and genetic lineages of Plasmodium falciparum multi-drug resistance (pfmdr1) gene in Kenya
title_full_unstemmed Selective sweeps and genetic lineages of Plasmodium falciparum multi-drug resistance (pfmdr1) gene in Kenya
title_short Selective sweeps and genetic lineages of Plasmodium falciparum multi-drug resistance (pfmdr1) gene in Kenya
title_sort selective sweeps and genetic lineages of plasmodium falciparum multi-drug resistance (pfmdr1) gene in kenya
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6208105/
https://www.ncbi.nlm.nih.gov/pubmed/30376843
http://dx.doi.org/10.1186/s12936-018-2534-8
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