Plasmodium falciparum kelch13 Mutations, 9 Countries in Africa, 2014–2018
Supporting Files
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July 2021
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File Language:
English
Details
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Alternative Title:Emerg Infect Dis
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Personal 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
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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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Subjects:
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Source:Emerg Infect Dis. 27(7):1902-1908
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Pubmed ID:34152946
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Pubmed Central ID:PMC8237877
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Document Type:
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Funding:
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Place as Subject:
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Volume:27
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Issue:7
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Collection(s):
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Main Document Checksum:urn:sha256:fa072df70c21db8c652debd3440dab7f6c0f5af1efc0a77edd4e75736e2a2ff0
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Download URL:
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File Type:
Supporting Files
File Language:
English
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