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Plasmodium falciparum kelch 13 Mutations, 9 Countries in Africa, 2014–2018
The spread of drug resistance to antimalarial treatments poses a serious public health risk globally. To combat this risk, molecular surveillance of drug resistance is imperative. We report the prevalence of mutations in the Plasmodium falciparum kelch 13 propeller domain associated with partial art...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Centers for Disease Control and Prevention
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8237877/ https://www.ncbi.nlm.nih.gov/pubmed/34152946 http://dx.doi.org/10.3201/eid2707.203230 |
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author | Schmedes, Sarah E. Patel, Dhruviben Dhal, Simran Kelley, Julia Svigel, Samaly S. Dimbu, Pedro Rafael Adeothy, Adicatou-Laï Kahunu, Gauthier Mesia Nkoli, Papy Mandoko Beavogui, Abdoul Habib Kariuki, Simon Mathanga, Don P. Koita, Ousmane Ishengoma, Deus Mohamad, Ally Hawela, Moonga Moriarty, Leah F. Samuels, Aaron M. Gutman, Julie Plucinski, Mateusz M. Udhayakumar, Venkatachalam Zhou, Zhiyong Lucchi, Naomi W. Venkatesan, Meera Halsey, Eric S. Talundzic, Eldin |
author_facet | Schmedes, Sarah E. Patel, Dhruviben Dhal, Simran Kelley, Julia Svigel, Samaly S. Dimbu, Pedro Rafael Adeothy, Adicatou-Laï Kahunu, Gauthier Mesia Nkoli, Papy Mandoko Beavogui, Abdoul Habib Kariuki, Simon Mathanga, Don P. Koita, Ousmane Ishengoma, Deus Mohamad, Ally Hawela, Moonga Moriarty, Leah F. Samuels, Aaron M. Gutman, Julie Plucinski, Mateusz M. Udhayakumar, Venkatachalam Zhou, Zhiyong Lucchi, Naomi W. Venkatesan, Meera Halsey, Eric S. Talundzic, Eldin |
author_sort | Schmedes, Sarah E. |
collection | PubMed |
description | The spread of drug resistance to antimalarial treatments poses a serious public health risk globally. To combat this risk, molecular surveillance of drug resistance is imperative. We report the prevalence of mutations in the Plasmodium falciparum kelch 13 propeller domain associated with partial artemisinin resistance, which we determined by using Sanger sequencing samples from patients enrolled in therapeutic efficacy studies from 9 sub-Saharan countries during 2014–2018. Of the 2,865 samples successfully sequenced before treatment (day of enrollment) and on the day of treatment failure, 29 (1.0%) samples contained 11 unique nonsynonymous mutations and 83 (2.9%) samples contained 27 unique synonymous mutations. Two samples from Kenya contained the S522C mutation, which has been associated with delayed parasite clearance; however, no samples contained validated or candidate artemisinin-resistance mutations. |
format | Online Article Text |
id | pubmed-8237877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Centers for Disease Control and Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-82378772021-07-09 Plasmodium falciparum kelch 13 Mutations, 9 Countries in Africa, 2014–2018 Schmedes, Sarah E. Patel, Dhruviben Dhal, Simran Kelley, Julia Svigel, Samaly S. Dimbu, Pedro Rafael Adeothy, Adicatou-Laï Kahunu, Gauthier Mesia Nkoli, Papy Mandoko Beavogui, Abdoul Habib Kariuki, Simon Mathanga, Don P. Koita, Ousmane Ishengoma, Deus Mohamad, Ally Hawela, Moonga Moriarty, Leah F. Samuels, Aaron M. Gutman, Julie Plucinski, Mateusz M. Udhayakumar, Venkatachalam Zhou, Zhiyong Lucchi, Naomi W. Venkatesan, Meera Halsey, Eric S. Talundzic, Eldin Emerg Infect Dis Research The spread of drug resistance to antimalarial treatments poses a serious public health risk globally. To combat this risk, molecular surveillance of drug resistance is imperative. We report the prevalence of mutations in the Plasmodium falciparum kelch 13 propeller domain associated with partial artemisinin resistance, which we determined by using Sanger sequencing samples from patients enrolled in therapeutic efficacy studies from 9 sub-Saharan countries during 2014–2018. Of the 2,865 samples successfully sequenced before treatment (day of enrollment) and on the day of treatment failure, 29 (1.0%) samples contained 11 unique nonsynonymous mutations and 83 (2.9%) samples contained 27 unique synonymous mutations. Two samples from Kenya contained the S522C mutation, which has been associated with delayed parasite clearance; however, no samples contained validated or candidate artemisinin-resistance mutations. Centers for Disease Control and Prevention 2021-07 /pmc/articles/PMC8237877/ /pubmed/34152946 http://dx.doi.org/10.3201/eid2707.203230 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited. |
spellingShingle | Research Schmedes, Sarah E. Patel, Dhruviben Dhal, Simran Kelley, Julia Svigel, Samaly S. Dimbu, Pedro Rafael Adeothy, Adicatou-Laï Kahunu, Gauthier Mesia Nkoli, Papy Mandoko Beavogui, Abdoul Habib Kariuki, Simon Mathanga, Don P. Koita, Ousmane Ishengoma, Deus Mohamad, Ally Hawela, Moonga Moriarty, Leah F. Samuels, Aaron M. Gutman, Julie Plucinski, Mateusz M. Udhayakumar, Venkatachalam Zhou, Zhiyong Lucchi, Naomi W. Venkatesan, Meera Halsey, Eric S. Talundzic, Eldin Plasmodium falciparum kelch 13 Mutations, 9 Countries in Africa, 2014–2018 |
title | Plasmodium falciparum kelch
13 Mutations, 9 Countries in Africa, 2014–2018 |
title_full | Plasmodium falciparum kelch
13 Mutations, 9 Countries in Africa, 2014–2018 |
title_fullStr | Plasmodium falciparum kelch
13 Mutations, 9 Countries in Africa, 2014–2018 |
title_full_unstemmed | Plasmodium falciparum kelch
13 Mutations, 9 Countries in Africa, 2014–2018 |
title_short | Plasmodium falciparum kelch
13 Mutations, 9 Countries in Africa, 2014–2018 |
title_sort | plasmodium falciparum kelch
13 mutations, 9 countries in africa, 2014–2018 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8237877/ https://www.ncbi.nlm.nih.gov/pubmed/34152946 http://dx.doi.org/10.3201/eid2707.203230 |
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