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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 2021
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.
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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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