Population Genomics ofPlasmodium malariaefrom Four African Countries

Author:

Popkin-Hall Zachary R.ORCID,Carey-Ewend KellyORCID,Aghakhanian FarhangORCID,Oriero Eniyou C.ORCID,Seth Misago D.ORCID,Kashamuka Melchior M.ORCID,Ngasala BillyORCID,Ali Innocent M.ORCID,Mukomena Eric SompweORCID,Mandara Celine I.ORCID,Kharabora Oksana,Sendor RachelORCID,Simkin AlfredORCID,Amambua-Ngwa AlfredORCID,Tshefu AntoinetteORCID,Fola Abebe A.ORCID,Ishengoma Deus S.ORCID,Bailey Jeffrey A.ORCID,Parr Jonathan B.ORCID,Lin Jessica T.ORCID,Juliano Jonathan J.ORCID

Abstract

AbstractPlasmodium malariaeis geographically widespread but neglected and may become more prevalent asP. falciparumdeclines. We completed the largest genomic study of AfricanP. malariaeto-date by performing hybrid capture and sequencing of 77 isolates from Cameroon (n=7), the Democratic Republic of the Congo (n=16), Nigeria (n=4), and Tanzania (n=50) collected between 2015 and 2021. There is no evidence of geographic population structure. Nucleotide diversity was significantly lower than in co-localizedP. falciparumisolates, while linkage disequilibrium was significantly higher. Genome-wide selection scans identified no erythrocyte invasion ligands or antimalarial resistance orthologs as top hits; however, targeted analyses of these loci revealed evidence of selective sweeps around four erythrocyte invasion ligands and six antimalarial resistance orthologs. Demographic inference modeling suggests that AfricanP. malariaeis recovering from a bottleneck. Altogether, these results suggest thatP. malariaeis genomically atypical among humanPlasmodiumspp. and panmictic in Africa.

Publisher

Cold Spring Harbor Laboratory

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