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Occurrence of pfatpase6 Single Nucleotide Polymorphisms Associated with Artemisinin Resistance among Field Isolates of Plasmodium falciparum in North-Eastern Tanzania

We aimed to determine the current prevalence of four P. falciparum candidate artemisinin resistance biomarkers L263E, E431K, A623E, and S769N in the pfatpase6 gene in a high transmission area in Tanzania in a retrospective cross sectional study using 154 archived samples collected from three previou...

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Autores principales: Chilongola, Jaffu, Ndaro, Arnold, Tarimo, Hipolite, Shedrack, Tamara, Barthazary, Sakurani, Kaaya, Robert, Masokoto, Alutu, Kajeguka, Debora, Kavishe, Reginald A., Lusingu, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313681/
https://www.ncbi.nlm.nih.gov/pubmed/25685593
http://dx.doi.org/10.1155/2015/279028
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author Chilongola, Jaffu
Ndaro, Arnold
Tarimo, Hipolite
Shedrack, Tamara
Barthazary, Sakurani
Kaaya, Robert
Masokoto, Alutu
Kajeguka, Debora
Kavishe, Reginald A.
Lusingu, John
author_facet Chilongola, Jaffu
Ndaro, Arnold
Tarimo, Hipolite
Shedrack, Tamara
Barthazary, Sakurani
Kaaya, Robert
Masokoto, Alutu
Kajeguka, Debora
Kavishe, Reginald A.
Lusingu, John
author_sort Chilongola, Jaffu
collection PubMed
description We aimed to determine the current prevalence of four P. falciparum candidate artemisinin resistance biomarkers L263E, E431K, A623E, and S769N in the pfatpase6 gene in a high transmission area in Tanzania in a retrospective cross sectional study using 154 archived samples collected from three previous malaria studies in 2010, 2011 and 2013. Mutations in pfatpase6 gene were detected in parasite DNA isolated from Dried Blood Spots by using PCR-RFLP. We observed overall allelic frequencies for L263E, E431K, A623E, and S769N to be 5.8% (9/154), 16.2% (25/154), 0.0% (0/154), and 3.9% (6/154). The L263E mutation was not detected in 2010 but occurred at 3.9% and 2.6% in 2011 and 2013 respectively. The L263E mutation showed a significant change of frequency between 2010 and 2011, but not between 2011 and 2013 (P < 0.05). Frequency of E431K was highest of all without any clear trend whereas S769N increased from 2.2% in 2010 to 3.6% in 2011 and 5.1% in 2013. A623E mutation was not detected. The worrisome detection and the increase in the frequency of S769N and other mutations calls for urgent assessment of temporal changes of known artemisinin biomarkers in association with in vivo ACT efficacy.
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spelling pubmed-43136812015-02-15 Occurrence of pfatpase6 Single Nucleotide Polymorphisms Associated with Artemisinin Resistance among Field Isolates of Plasmodium falciparum in North-Eastern Tanzania Chilongola, Jaffu Ndaro, Arnold Tarimo, Hipolite Shedrack, Tamara Barthazary, Sakurani Kaaya, Robert Masokoto, Alutu Kajeguka, Debora Kavishe, Reginald A. Lusingu, John Malar Res Treat Research Article We aimed to determine the current prevalence of four P. falciparum candidate artemisinin resistance biomarkers L263E, E431K, A623E, and S769N in the pfatpase6 gene in a high transmission area in Tanzania in a retrospective cross sectional study using 154 archived samples collected from three previous malaria studies in 2010, 2011 and 2013. Mutations in pfatpase6 gene were detected in parasite DNA isolated from Dried Blood Spots by using PCR-RFLP. We observed overall allelic frequencies for L263E, E431K, A623E, and S769N to be 5.8% (9/154), 16.2% (25/154), 0.0% (0/154), and 3.9% (6/154). The L263E mutation was not detected in 2010 but occurred at 3.9% and 2.6% in 2011 and 2013 respectively. The L263E mutation showed a significant change of frequency between 2010 and 2011, but not between 2011 and 2013 (P < 0.05). Frequency of E431K was highest of all without any clear trend whereas S769N increased from 2.2% in 2010 to 3.6% in 2011 and 5.1% in 2013. A623E mutation was not detected. The worrisome detection and the increase in the frequency of S769N and other mutations calls for urgent assessment of temporal changes of known artemisinin biomarkers in association with in vivo ACT efficacy. Hindawi Publishing Corporation 2015 2015-01-05 /pmc/articles/PMC4313681/ /pubmed/25685593 http://dx.doi.org/10.1155/2015/279028 Text en Copyright © 2015 Jaffu Chilongola et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chilongola, Jaffu
Ndaro, Arnold
Tarimo, Hipolite
Shedrack, Tamara
Barthazary, Sakurani
Kaaya, Robert
Masokoto, Alutu
Kajeguka, Debora
Kavishe, Reginald A.
Lusingu, John
Occurrence of pfatpase6 Single Nucleotide Polymorphisms Associated with Artemisinin Resistance among Field Isolates of Plasmodium falciparum in North-Eastern Tanzania
title Occurrence of pfatpase6 Single Nucleotide Polymorphisms Associated with Artemisinin Resistance among Field Isolates of Plasmodium falciparum in North-Eastern Tanzania
title_full Occurrence of pfatpase6 Single Nucleotide Polymorphisms Associated with Artemisinin Resistance among Field Isolates of Plasmodium falciparum in North-Eastern Tanzania
title_fullStr Occurrence of pfatpase6 Single Nucleotide Polymorphisms Associated with Artemisinin Resistance among Field Isolates of Plasmodium falciparum in North-Eastern Tanzania
title_full_unstemmed Occurrence of pfatpase6 Single Nucleotide Polymorphisms Associated with Artemisinin Resistance among Field Isolates of Plasmodium falciparum in North-Eastern Tanzania
title_short Occurrence of pfatpase6 Single Nucleotide Polymorphisms Associated with Artemisinin Resistance among Field Isolates of Plasmodium falciparum in North-Eastern Tanzania
title_sort occurrence of pfatpase6 single nucleotide polymorphisms associated with artemisinin resistance among field isolates of plasmodium falciparum in north-eastern tanzania
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313681/
https://www.ncbi.nlm.nih.gov/pubmed/25685593
http://dx.doi.org/10.1155/2015/279028
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