Social and environmental predictors of gut microbiome age in wild baboons

Mammalian gut microbiomes are highly dynamic communities that shape and are shaped by host aging, including age-related changes to host immunity, metabolism, and behavior. As such, gut microbial composition may provide valuable information on host biological age. Here, we test this idea by creating a microbiome-based age predictor using 13,563 gut microbial profiles from 479 wild baboons collected over 14 years. The resulting 'microbiome clock' predicts host chronological age. Deviations from the clock's predictions are linked to some demographic and socio-environmental factors that predict baboon health and survival: animals who appear old-for-age tend to be male, sampled in the dry season (for females), and have high social status (both sexes). However, an individual's 'microbiome age' does not predict the attainment of developmental milestones or lifespan. Hence, in our host population, gut microbiome age largely reflects current, as opposed to past, social and environmental conditions, and does not predict the pace of host development or host mortality risk. We add to a growing understanding of how age is reflected in different host phenotypes and what forces modify biological age in primates.

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Publication Details

Journal
eLife
Published
2024-10-28
DOI
https://doi.org/10.7554/elife.102166
Citations
4
Primary Topic
Gut microbiota and health
Type
article
Field-Weighted Citation Impact
0.94
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article

Social and environmental predictors of gut microbiome age in wild baboons

Susan C. Alberts, Ran Blekhman, Sayan Mukherjee, Kimberly Roche et al.
4 citations
eLife
Gut microbiota and health
0.94
article

Social and environmental predictors of gut microbiome age in wild baboons

Susan C. Alberts, Ran Blekhman, Sayan Mukherjee, Kimberly Roche, Jordan A. Anderson, Elizabeth A. Archie, Jack A. Gilbert, David Jansen, Jenny Tung, Mauna Dasari
article en
4 citations

Abstract

Mammalian gut microbiomes are highly dynamic communities that shape and are shaped by host aging, including age-related changes to host immunity, metabolism, and behavior. As such, gut microbial composition may provide valuable information on host biological age. Here, we test this idea by creating a microbiome-based age predictor using 13,563 gut microbial profiles from 479 wild baboons collected over 14 years. The resulting 'microbiome clock' predicts host chronological age. Deviations from the clock's predictions are linked to some demographic and socio-environmental factors that predict baboon health and survival: animals who appear old-for-age tend to be male, sampled in the dry season (for females), and have high social status (both sexes). However, an individual's 'microbiome age' does not predict the attainment of developmental milestones or lifespan. Hence, in our host population, gut microbiome age largely reflects current, as opposed to past, social and environmental conditions, and does not predict the pace of host development or host mortality risk. We add to a growing understanding of how age is reflected in different host phenotypes and what forces modify biological age in primates.

eLifeVol. 13
University of Notre Dame (US), Canadian Institute for Advanced Research (CA), Scripps Institution of Oceanography (US), University of Pittsburgh (US), Duke University (US), California Academy of Sciences (US), University of California San Diego (US), University of Chicago (US), Max Planck Institute for Evolutionary Anthropology (DE), Max Planck Institute for Mathematics (DE), Center for Scalable Data Analytics and Artificial Intelligence (DE), Leipzig University (DE)
Openalex Percentile: Top 25%
Gut microbiota and health
0.94
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