4.8 Article

Biodiversity of protists and nematodes in the wild nonhuman primate gut

Journal

ISME JOURNAL
Volume 14, Issue 2, Pages 609-622

Publisher

SPRINGERNATURE
DOI: 10.1038/s41396-019-0551-4

Keywords

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Funding

  1. US NSF [BCS-0922465]
  2. NSF [BCS-0935349]
  3. NIH [TW009237]
  4. UK Economic Social Research Council [ES/J011266/1]
  5. Primate Conservation Inc.
  6. University of Texas at Austin
  7. American Association of Physical Anthropologists
  8. Hunter College of City University of New York
  9. Rowe-Wright Primate Fund
  10. Leaky Foundation
  11. University of Arizona
  12. University of Colorado-Boulder
  13. International Primatological Society
  14. Margot Marsh Biodiversity Foundation
  15. St. Louis Zoological Park [FRC 06-1]
  16. Banting Postdoctoral Fellowship
  17. Human Frontier in Science Program [RGY0078/2015]

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Documenting the natural diversity of eukaryotic organisms in the nonhuman primate (NHP) gut is important for understanding the evolution of the mammalian gut microbiome, its role in digestion, health and disease, and the consequences of anthropogenic change on primate biology and conservation. Despite the ecological significance of gut-associated eukaryotes, little is known about the factors that influence their assembly and diversity in mammals. In this study, we used an 18S rRNA gene fragment metabarcoding approach to assess the eukaryotic assemblage of 62 individuals representing 16 NHP species. We find that cercopithecoids, and especially the cercopithecines, have substantially higher alpha diversity than other NHP groups. Gut-associated protists and nematodes are widespread among NHPs, consistent with their ancient association with NHP hosts. However, we do not find a consistent signal of phylosymbiosis or host-species specificity. Rather, gut eukaryotes are only weakly structured by primate phylogeny with minimal signal from diet, in contrast to previous reports of NHP gut bacteria. The results of this study indicate that gut-associated eukaryotes offer different information than gut-associated bacteria and add to our understanding of the structure of the gut microbiome.

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