4.8 Article

Ancient Hybridization and Adaptive Introgression of an Invadolysin Gene in Schistosome Parasites

Journal

MOLECULAR BIOLOGY AND EVOLUTION
Volume 36, Issue 10, Pages 2127-2142

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/molbev/msz154

Keywords

Schistosoma haematobium; Schistosoma bovis; parasite; adaptation; M8 metalloprotease

Funding

  1. National Institute of Allergy and Infectious Diseases [NIAD R01 AI097576-01, NIAD 5R21AI096277-01]
  2. National Center for Advancing Translational Sciences [UL1TR001120]
  3. Texas Biomedical Research Institute Forum [0467]
  4. National Center for Research Resources [C06 RR013556, RR017515]
  5. Wellcome Trust [104958/Z/14/Z]
  6. Gates Foundation [RR374-053/5054146, RR374-053/4785426]
  7. ZELS research grant (BBSRC) [BB/L018985/1]
  8. ZELS research grant (MRC) [BB/L018985/1]
  9. ZELS research grant (ESRC) [BB/L018985/1]
  10. ZELS research grant (NERC) [BB/L018985/1]
  11. ZELS research grant (DSTL) [BB/L018985/1]
  12. ZELS research grant (DFID) [BB/L018985/1]
  13. Cowles Fellowship
  14. BBSRC [BB/L018985/1] Funding Source: UKRI

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Introgression among parasite species has the potential to transfer traits of biomedical importance across species boundaries. The parasitic blood fluke Schistosoma haematobium causes urogenital schistosomiasis in humans across sub-Saharan Africa. Hybridization with other schistosome species is assumed to occur commonly, because genetic crosses between S. haematobium and livestock schistosomes, including S. bovis, can be staged in the laboratory, and sequencing of mtDNA and rDNA amplified from microscopic miracidia larvae frequently reveals markers from different species. However, the frequency, direction, age, and genomic consequences of hybridization are unknown. We hatched miracidia from eggs and sequenced the exomes from 96 individual S. haematobium miracidia from infected patients from Niger and the Zanzibar archipelago. These data revealed no evidence for contemporary hybridization between S. bovis and S. haematobium in our samples. However, all Nigerien S. haematobium genomes sampled show hybrid ancestry, with 3.3-8.2% of their nuclear genomes derived from S. bovis, providing evidence of an ancient introgression event that occurred at least 108-613 generations ago. Some S. bovis-derived alleles have spread to high frequency or reached fixation and show strong signatures of directional selection; the strongest signal spans a single gene in the invadolysin gene family (Chr. 4). Our results suggest that S. bovis/S. haematobium hybridization occurs rarely but demonstrate profound consequences of ancient introgression from a livestock parasite into the genome of S. haematobium, the most prevalent schistosome species infecting humans.

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