4.7 Article

Genomic analysis of a parasite invasion: Colonization of the Americas by the blood fluke Schistosoma mansoni

Journal

MOLECULAR ECOLOGY
Volume 31, Issue 8, Pages 2242-2263

Publisher

WILEY
DOI: 10.1111/mec.16395

Keywords

Africa; Brazil; codispersal; exome; human parasite; migration

Funding

  1. Wellcome Trust [104958/Z/14/Z]
  2. Bill and Melinda Gates Foundation [RR374-053/4785426, RR374-053/5054146]
  3. Division of Intramural Research, National Institute of Allergy and Infectious Diseases [5R21AI096277-01, R01 AI097576-01]
  4. Texas Biomedical Research Institute Forum [0467]
  5. EU [FP6]

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The blood fluke parasite, Schistosoma mansoni, was introduced into the Americas from Africa during the Trans-Atlantic slave trade. Research shows that the parasite successfully adapted to the snail intermediate host in South America, without facing significant population bottlenecks or barriers to colonization. Furthermore, genetic analysis indicates differences in gene selection between the Americas and Africa, suggesting adaptation during colonization.
Schistosoma mansoni, a snail-borne, blood fluke that infects humans, was introduced into the Americas from Africa during the Trans-Atlantic slave trade. As this parasite shows strong specificity to the snail intermediate host, we expected that adaptation to South American Biomphalaria spp. snails would result in population bottlenecks and strong signatures of selection. We scored 475,081 single nucleotide variants in 143 S. mansoni from the Americas (Brazil, Guadeloupe and Puerto Rico) and Africa (Cameroon, Niger, Senegal, Tanzania, and Uganda), and used these data to ask: (i) Was there a population bottleneck during colonization? (ii) Can we identify signatures of selection associated with colonization? (iii) What were the source populations for colonizing parasites? We found a 2.4- to 2.9-fold reduction in diversity and much slower decay in linkage disequilibrium (LD) in parasites from East to West Africa. However, we observed similar nuclear diversity and LD in West Africa and Brazil, suggesting no strong bottlenecks and limited barriers to colonization. We identified five genome regions showing selection in the Americas, compared with three in West Africa and none in East Africa, which we speculate may reflect adaptation during colonization. Finally, we infer that unsampled populations from central African regions between Benin and Angola, with contributions from Niger, are probably the major source(s) for Brazilian S. mansoni. The absence of a bottleneck suggests that this is a rare case of a serendipitous invasion, where S. mansoni parasites were pre-adapted to the Americas and able to establish with relative ease.

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