4.8 Article

Microbiome stability and structure is governed by host phylogeny over diet and geography in woodrats (Neotoma spp.)

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.2108787118

Keywords

neutral model; DNA metabarcoding; phylosymbiosis; Neotoma; 16S rRNA

Funding

  1. NSF [1342615, 1656497]
  2. Ruth L. Kirschstein National Research Service Award [NIH T32AI055434]
  3. Genetics Training Grant NIH [5T32GM007464-38]
  4. Smithsonian-Mpala fellowship
  5. Division Of Integrative Organismal Systems
  6. Direct For Biological Sciences [1656497] Funding Source: National Science Foundation

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This study found that geography, diet, and host genetics account for nearly 50% of microbiome variation, with diet and microbiome diversity being correlated. Host genetic background is the most significant predictor of microbiome composition and stability, indicating the important role of genetics in shaping the microbiome structure in closely related hosts.
The microbiome is critical for host survival and fitness, but gaps remain in our understanding of how this symbiotic community is structured. Despite evidence that related hosts often harbor similar bacterial communities, it is unclear whether this pattern is due to genetic similarities between hosts or to common ecological selection pressures. Here, using herbivorous rodents in the genus Neotoma, we quantify how geography, diet, and host genetics, alongside neutral processes, influence microbiome structure and stability under natural and captive conditions. Using bacterial and plant metabarcoding, we first characterized dietary and microbiome compositions for animals from 25 populations, representing seven species from 19 sites across the southwestern United States. We then brought wild animals into captivity, reducing the influence of environmental variation. In nature, geography, diet, and phylogeny collectively explained similar to 50% of observed microbiome variation. Diet and microbiome diversity were correlated, with different toxin-enriched diets selecting for distinct microbial symbionts. Although diet and geography influenced natural microbiome structure, the effects of host phylogeny were stronger for both wild and captive animals. In captivity, gut microbiomes were altered; however, responses were species specific, indicating again that host genetic background is the most significant predictor of microbiome composition and stability. In captivity, diet effects declined and the effects of host genetic similarity increased. By bridging a critical divide between studies in wild and captive animals, this work underscores the extent to which genetics shape microbiome structure and stability in closely related hosts.

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