Genome sequencing of Plasmodium malariae identifies continental segregation and mutations associated with reduced pyrimethamine susceptibility

Plasmodium malariae parasites are widely observed across the tropics and sub-tropics. This slow-growing species, known to maintain chronic asymptomatic infections, has been associated with reduced antimalarial susceptibility. We analyse 251 P. malariae genomes from 28 countries, and leveraging 131,601 high-quality SNPs, demonstrate segregation of African and Asian isolates. Signals of recent evolutionary selection were identified in genes encoding putative surface proteins (pmmsp1) and putative erythrocyte invasion proteins (pmdpap3, pmrbp2, pmnif4). Amino acid substitutions were identified in orthologs of genes associated with antimalarial susceptibility including 2 amino acid substitutions in pmdhfr aligning with pyrimethamine resistance mutations in P. falciparum. Additionally, we characterise pmdhfr mutation F57L and demonstrate its involvement in reduced susceptibility to pyrimethamine in an in vitro parasite assay. We validate CRISPR-Cas9 mediated ortholog replacement in P. knowlesi parasites to determine the function of pmdhfr mutations and demonstrate that circulating pmdhfr genotypes are less susceptible to pyrimethamine.

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Publication Details

Journal
Nature Communications
Published
2024-12-30
DOI
https://doi.org/10.1038/s41467-024-55102-3
Citations
6
Primary Topic
Malaria Research and Control
Type
article
Field-Weighted Citation Impact
3.26

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article

Genome sequencing of Plasmodium malariae identifies continental segregation and mutations associated with reduced pyrimethamine susceptibility

Mohammad Shafiul Alam, Debbie Nolder, Susana Campino, Sílvia Maria Di Santi et al.
6 citations
Nature Communications
Malaria Research and Control
3.26
article

Genome sequencing of Plasmodium malariae identifies continental segregation and mutations associated with reduced pyrimethamine susceptibility

Mohammad Shafiul Alam, Debbie Nolder, Susana Campino, Sílvia Maria Di Santi, Franziska Mohring, Amy Ibrahim, Colin J. Sutherland, Donelly A. van Schalkwyk, Taane Gregory Clark, Jody Phelan, Emilia Mańko, Robert William Moon, Steffen Borrmann, Ayôla Akim Adégnika, Dinesh Mondal, François Henry Nosten
article en
6 citations

Abstract

Plasmodium malariae parasites are widely observed across the tropics and sub-tropics. This slow-growing species, known to maintain chronic asymptomatic infections, has been associated with reduced antimalarial susceptibility. We analyse 251 P. malariae genomes from 28 countries, and leveraging 131,601 high-quality SNPs, demonstrate segregation of African and Asian isolates. Signals of recent evolutionary selection were identified in genes encoding putative surface proteins (pmmsp1) and putative erythrocyte invasion proteins (pmdpap3, pmrbp2, pmnif4). Amino acid substitutions were identified in orthologs of genes associated with antimalarial susceptibility including 2 amino acid substitutions in pmdhfr aligning with pyrimethamine resistance mutations in P. falciparum. Additionally, we characterise pmdhfr mutation F57L and demonstrate its involvement in reduced susceptibility to pyrimethamine in an in vitro parasite assay. We validate CRISPR-Cas9 mediated ortholog replacement in P. knowlesi parasites to determine the function of pmdhfr mutations and demonstrate that circulating pmdhfr genotypes are less susceptible to pyrimethamine.

Nature CommunicationsVol. 15(1)
Universidade de São Paulo (BR), International Centre for Diarrhoeal Disease Research (BD), Mahidol University (TH), Public Health England (GB), London School of Hygiene & Tropical Medicine (GB), Shoklo Malaria Research Unit (TH), Centre de Recherche Médicales de Lambaréné (GA), German Center for Infection Research (DE), Mahidol Oxford Tropical Medicine Research Unit (TH), University of Tübingen (DE)
Wellcome, Wellcome Trust, UK Research and Innovation, Department for International Development, Medical Research Council, Engineering and Physical Sciences Research Council
Openalex Percentile: Top 7%
Malaria Research and Control
3.26
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