Multiple local PfDHFR I164L haplotype expansions drive Plasmodium falciparum antifolate resistance in Uganda

Abstract Mutations in the Plasmodium falciparum genes, pfdhfr and pfdhps , drive antifolate resistance and threaten malaria control in regions where sulfadoxine-pyrimethamine (SP) is the primary chemoprevention strategy. The spatial patterns and evolutionary dynamics of these mutations in high-transmission settings remain incompletely understood. Here we genotyped 11 resistance-associated mutations in pfdhfr and pfdhps in 4,725 P. falciparum isolates collected from 16 Ugandan health facilities as part of annual surveillance between 2016 and 2022. Notably, we show that the frequency of PfDHFR I164L, which confers higher pyrimethamine resistance, increased over time from 19.4% to 32.4%. Using identity-by-descent, haplotype structure, and extended haplotype homozygosity analyses, we show that PfDHFR I164L is present on multiple haplotype backgrounds and undergoes localised expansions, without detectable signatures of recent positive selection at all but one site. Our results suggest that the evolution of antifolate resistance, driven by PfDHFR I164L, is spatially heterogeneous and complex in regions that primarily use SP chemoprevention programmes.

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Publication Details

Journal
Nature Communications
Published
2026-09-04
DOI
https://doi.org/10.1038/s41467-026-76826-4
Primary Topic
Malaria Research and Control
Type
article
Field-Weighted Citation Impact
0.00

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article

Multiple local PfDHFR I164L haplotype expansions drive Plasmodium falciparum antifolate resistance in Uganda

Karamoko Niaré, Victor Asua, Melissa D. Conrad, Jeffrey A. Bailey et al.
Nature Communications
Malaria Research and Control
article

Multiple local PfDHFR I164L haplotype expansions drive Plasmodium falciparum antifolate resistance in Uganda

Karamoko Niaré, Victor Asua, Melissa D. Conrad, Jeffrey A. Bailey, Thomas Katairo, Shreeya Garg, Isaac Ssewanyana, Jenny Legac, Steffen Borrmann, Rebecca M. Crudale, Stephen Tukwasibwe, Moses R. Kamya, Philip J. Rosenthal, Sam L. Nsobya, Grant Dorsey, Adoke Yeka, Jerry Mulondo, Alfred Simkin, Francis E. Bohissou
article en

Abstract

Abstract Mutations in the Plasmodium falciparum genes, pfdhfr and pfdhps , drive antifolate resistance and threaten malaria control in regions where sulfadoxine-pyrimethamine (SP) is the primary chemoprevention strategy. The spatial patterns and evolutionary dynamics of these mutations in high-transmission settings remain incompletely understood. Here we genotyped 11 resistance-associated mutations in pfdhfr and pfdhps in 4,725 P. falciparum isolates collected from 16 Ugandan health facilities as part of annual surveillance between 2016 and 2022. Notably, we show that the frequency of PfDHFR I164L, which confers higher pyrimethamine resistance, increased over time from 19.4% to 32.4%. Using identity-by-descent, haplotype structure, and extended haplotype homozygosity analyses, we show that PfDHFR I164L is present on multiple haplotype backgrounds and undergoes localised expansions, without detectable signatures of recent positive selection at all but one site. Our results suggest that the evolution of antifolate resistance, driven by PfDHFR I164L, is spatially heterogeneous and complex in regions that primarily use SP chemoprevention programmes.

Nature Communications
Johns Hopkins University (US), University of California, San Francisco (US), Brown University (US), German Center for Infection Research (DE), Infectious Diseases Research Collaboration (UG), Mali-Folkecenter (ML), Institut de Recherche en Sciences de la Santé (BF), Makerere University (UG), University of Tübingen (DE)
Bill and Melinda Gates Foundation, Styrelsen för Internationellt Utvecklingssamarbete, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, European Commission, National Institutes of Health, European and Developing Countries Clinical Trials Partnership
Good health and well-being
Openalex Percentile: Top 8%
Malaria Research and Control
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