Population genomics of Plasmodium ovale species in sub-Saharan Africa
Kelly Carey-EwendiD, Zachary R. Popkin-HalliD, Alfred SimkiniD, Meredith Muller, Christopher M. HennellyiD, Wenqiao HeiD, Kara A. MoseriD, Claudia GaitheriD, Karamoko NiaréiD, Farhang F. AghakhanianiD, Sindew Mekasha FelekeiD, Bokretsion Gidey BrhaneiD, Fernandine Phanzu, Kashamuka MwandagalirwaiD, Özkan AydemiriD, Colin J. SutherlandiD, Deus S. IshengomaiD, Innocent Mbulli AliiD, Billy NgasalaiD, Albert Ntumba KalonjiiD, Antoinette Kitoto TshefuiD, Jonathan B. ParriD, Jeffrey A. BaileyiD, Jonathan J. JulianoiD, Jessica T. LiniD
Abstract
Plasmodium ovale curtisi (Poc) and Plasmodium ovale wallikeri (Pow) are relapsing malaria parasites endemic to Africa and Asia that were previously thought to represent a single species. Amid increasing detection of ovale malaria in sub-Saharan Africa, we performed a population genomic study of both species across the continent. We conducted whole-genome sequencing of 25 isolates from Central and East Africa and analyzed them alongside 20 previously published African genomes. Isolates were predominantly monoclonal (43/45), with their genetic similarity aligning with geography. Pow showed lower average nucleotide diversity (1.8x10-4) across the genome compared to Poc (3.0x10-4) (p < 0.0001). Signatures of selective sweeps involving the dihydrofolate reductase gene were found in both species, as were signs of balancing selection at the merozoite surface protein 1 gene. Differences in the nucleotide diversity of Poc and Pow may reflect unique demographic history, even as similar selective forces facilitate their resilience to malaria control interventions.
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