» Articles » PMID: 39804931

Genomic Exploration of the Journey of Plasmodium Vivax in Latin America

Abstract

Plasmodium vivax is the predominant malaria parasite in Latin America. Its colonization history in the region is rich and complex, and is still highly debated, especially about its origin(s). Our study employed cutting-edge population genomic techniques to analyze whole genome variation from 620 P. vivax isolates, including 107 newly sequenced samples from West Africa, Middle East, and Latin America. This sampling represents nearly all potential source populations worldwide currently available. Analyses of the genetic structure, diversity, ancestry, coalescent-based inferences, including demographic scenario testing using Approximate Bayesian Computation, have revealed a more complex evolutionary history than previously envisioned. Indeed, our analyses suggest that the current American P. vivax populations predominantly stemmed from a now-extinct European lineage, with the potential contribution also from unsampled populations, most likely of West African origin. We also found evidence that P. vivax arrived in Latin America in multiple waves, initially during early European contact and later through post-colonial human migration waves in the late 19th-century. This study provides a fresh perspective on P. vivax's intricate evolutionary journey and brings insights into the possible contribution of West African P. vivax populations to the colonization history of Latin America.

References
1.
Battle K, Lucas T, Nguyen M, Howes R, Nandi A, Twohig K . Mapping the global endemicity and clinical burden of Plasmodium vivax, 2000-17: a spatial and temporal modelling study. Lancet. 2019; 394(10195):332-343. PMC: 6675736. DOI: 10.1016/S0140-6736(19)31096-7. View

2.
Sutanto E, Pava Z, Echeverry D, Lopera-Mesa T, Montenegro L, Yasnot-Acosta M . Genomics of Plasmodium vivax in Colombia reveals evidence of local bottle-necking and inter-country connectivity in the Americas. Sci Rep. 2023; 13(1):19779. PMC: 10643449. DOI: 10.1038/s41598-023-46076-1. View

3.
Cowell A, Loy D, Sundararaman S, Valdivia H, Fisch K, Lescano A . Selective Whole-Genome Amplification Is a Robust Method That Enables Scalable Whole-Genome Sequencing of Plasmodium vivax from Unprocessed Clinical Samples. mBio. 2017; 8(1). PMC: 5296604. DOI: 10.1128/mBio.02257-16. View

4.
Adam I, Alam M, Alemu S, Amaratunga C, Amato R, Andrianaranjaka V . An open dataset of genome variation in 1,895 worldwide samples. Wellcome Open Res. 2022; 7:136. PMC: 9127374. DOI: 10.12688/wellcomeopenres.17795.1. View

5.
Rougeron V, Elguero E, Arnathau C, Hidalgo B, Durand P, Houze S . Human Plasmodium vivax diversity, population structure and evolutionary origin. PLoS Negl Trop Dis. 2020; 14(3):e0008072. PMC: 7082039. DOI: 10.1371/journal.pntd.0008072. View