4.7 Article

Social groups constrain the spatiotemporal dynamics of wild sifaka gut microbiomes

Journal

MOLECULAR ECOLOGY
Volume 30, Issue 24, Pages 6759-6775

Publisher

WILEY
DOI: 10.1111/mec.16193

Keywords

gut microbiome; lemur; longitudinal survey; Madagascar; primate; social network

Funding

  1. NIH MIDAS [U01GM087719-01]
  2. NSF [DEB-0749097, BCS-1719655]
  3. NSF Beacon Center for the Study of Evolution in Action [DBI-0939454]
  4. L.S.B. Leakey Foundation
  5. Primate Conservation, Inc.
  6. Campbell Foundation
  7. Margot Marsh Biodiversity Fund
  8. International Primatological Society
  9. American Society of Primatologists
  10. University of Texas at Austin

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The study found that permanent social groupings have a significant impact on the gut microbiome composition and dynamics of wild primates, with each social group maintaining unique gut microbial signatures. Individuals with unstable social ties or new immigrants exhibited faster rates of microbiome turnover across seasons.
Primates acquire gut microbiota from conspecifics through direct social contact and shared environmental exposures. Host behaviour is a prominent force in structuring gut microbial communities, yet the extent to which group or individual-level forces shape the long-term dynamics of gut microbiota is poorly understood. We investigated the effects of three aspects of host sociality (social groupings, dyadic interactions, and individual dispersal between groups) on gut microbiome composition and plasticity in 58 wild Verreaux's sifaka (Propithecus verreauxi) from six social groups. Over the course of three dry seasons in a 5-year period, the six social groups maintained distinct gut microbial signatures, with the taxonomic composition of individual communities changing in tandem among coresiding group members. Samples collected from group members during each season were more similar than samples collected from single individuals across different years. In addition, new immigrants and individuals with less stable social ties exhibited elevated rates of microbiome turnover across seasons. Our results suggest that permanent social groupings shape the changing composition of commensal and mutualistic gut microbial communities and thus may be important drivers of health and resilience in wild primate populations.

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