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Examining the Early Distribution of the Artemisinin-Resistant Plasmodium falciparum kelch13 R561H Mutation in Areas of Higher Transmission in Rwanda

BACKGROUND: Artemisinin resistance mutations in Plasmodium falciparum kelch13 (Pfk13) have begun to emerge in Africa, with Pfk13-R561H being the first reported in Rwanda in 2014, but limited sampling left questions about its early distribution and origin. METHODS: We genotyped P. falciparum positive...

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Detalles Bibliográficos
Autores principales: Kirby, Rebecca, Giesbrecht, David, Karema, Corine, Watson, Oliver, Lewis, Savannah, Munyaneza, Tharcisse, Butera, Jean De Dieu, Juliano, Jonathan J, Bailey, Jeffrey A, Mazarati, Jean-Baptiste
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10122489/
https://www.ncbi.nlm.nih.gov/pubmed/37096145
http://dx.doi.org/10.1093/ofid/ofad149
Descripción
Sumario:BACKGROUND: Artemisinin resistance mutations in Plasmodium falciparum kelch13 (Pfk13) have begun to emerge in Africa, with Pfk13-R561H being the first reported in Rwanda in 2014, but limited sampling left questions about its early distribution and origin. METHODS: We genotyped P. falciparum positive dried blood spot (DBS) samples from a nationally representative 2014–2015 Rwanda Demographic Health Surveys (DHS) HIV study. DBS were subsampled from DHS sampling clusters with >15% P. falciparum prevalence, as determined by rapid testing or microscopy done during the DHS study (n clusters = 67, n samples = 1873). RESULTS: We detected 476 parasitemias among 1873 residual blood spots from a 2014–2015 Rwanda Demographic Health Survey. We sequenced 351 samples: 341/351 were wild-type (97.03% weighted), and 4 samples (1.34% weighted) harbored R561H that were significantly spatially clustered. Other nonsynonymous mutations found were V555A (3), C532W (1), and G533A (1). CONCLUSIONS: Our study better defines the early distribution of R561H in Rwanda. Previous studies only observed the mutation in Masaka as of 2014, but our study indicates its presence in higher-transmission regions in the southeast of the country at that time.