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Genomic exploration of the journey of Plasmodium vivax in Latin America

  • Margaux J.M. Lefebvre
  • , Fanny Degrugillier
  • , Céline Arnathau
  • , Gustavo A. Fontecha
  • , Oscar Noya
  • , Sandrine Houzé
  • , Carlo Severini
  • , Bruno Pradines
  • , Antoine Berry
  • , Jean François Trape
  • , Fabian E. Sáenz
  • , Franck Prugnolle
  • , Michael C. Fontaine
  • , Virginie Rougeron

Research output: Contribution to journalArticlepeer-review

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.

Original languageEnglish
Article numbere1012811
Pages (from-to)e1012811
JournalPLoS Pathogens
Volume21
Issue number1
DOIs
StatePublished - 13 Jan 2025

Bibliographical note

Copyright: © 2025 Lefebvre et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Funding

This work was supported by the French National Research Agency (anr.fr): JCJC GENAD ANR-20-CE35-0003 to V.R.; MICETRAL ANR-19-CE350010 to F.P.). It was also supported by the French Institute for Public Health Surveillance (santepubliquefrance.fr): grant No CNR Paludisme to B. P. The collection of samples in Ecuador was funded by Pontificia Universidad Católica del Ecuador (www.puce.edu.ec): grants M131416 and N131416 to F.E.S. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

FundersFunder number
Institut de veille sanitaire
ANR-19-CE350010, JCJC GENAD ANR-20-CE35-0003
Pontifical Catholic University of EcuadorN131416, M131416

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Plasmodium vivax/genetics
    • Humans
    • Malaria, Vivax/parasitology
    • Latin America/epidemiology
    • Genetic Variation
    • Genome, Protozoan
    • Phylogeny
    • Genomics

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