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Updated: Jan 25, 2026

Murine Fecal Isolation and Microbiota Transplantation
Published on: May 26, 2023
Fecal microbiota dysbiosis in macaques and humans within a shared environment
Erica T Grant1, Randall C Kyes2, Pensri Kyes2
1Center for One Health Research, Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington, United States of America.
Abstract:
Traditional zoonotic disease research focuses on detection of recognized pathogens and may miss opportunities to understand broader microbial transmission dynamics between humans, animals, and the environment. We studied human-macaque microbiome overlap in Kosum Phisai District, Maha Sarakham Province, Thailand, where a growing population of long-tailed macaques (Macaca fascicularis) in Kosumpee Forest Park interact with humans from an adjacent village. We surveyed workers in or near the park with elevated exposure to macaques to characterize tasks resulting in exposure to macaque feces in addition to dietary and lifestyle factors that influence gut microbiome composition. Fecal samples were collected from 12 exposed workers and 6 controls without macaque exposure, as well as 8 macaques from Kosumpee Forest Park and 4 from an isolated forest patch with minimal human contact. The V4 region of the 16S rRNA gene from fecal sample extracted DNA was amplified and sequenced using Illumina MiSeq to characterize the microbial community. A permuted betadisper test on the weighted UniFrac distances revealed significant differences in the dispersion patterns of gut microbiota from exposed and control macaques (p = 0.03). The high variance in gut microbiota composition of macaques in contact with humans has potential implications for gut microbiome stability and susceptibility to disease, described by the Anna Karenina principle (AKP). Human samples had homogenous variance in beta diversity but different spatial medians between groups (p = 0.02), indicating a shift in microbial composition that may be explained by fundamental lifestyle differences between the groups unrelated to exposure status. SourceTracker was used to estimate the percent of gut taxa in exposed humans that was contributed by macaques. While one worker showed evidence of elevated contribution, the overall trend was not significant. Task observations among workers revealed opportunities to employ protective measures or training to reduce exposure to occupational hazards. These results suggest the potential for hygiene measures to mitigate negative aspects of contact between humans and macaques in order to optimize the health of both populations.
Insights
Human and macaque gut microbes show overlap, with macaques exposed to humans exhibiting altered gut microbiome diversity. Hygiene measures can reduce risks associated with human-primate contact, benefiting both populations.
Area of Science:
- Microbiome research
- Zoonotic disease dynamics
- Human-animal interaction
Background:
- Traditional zoonotic disease research often overlooks broader microbial transmission dynamics between humans, animals, and the environment.
- Human-macaque interactions in Thailand present a unique model for studying microbiome overlap and potential pathogen transmission.
Purpose of the Study:
- To investigate the microbiome overlap between humans and long-tailed macaques (Macaca fascicularis) in Thailand.
- To characterize the impact of human contact on macaque gut microbiota and assess potential microbial transfer to exposed humans.
Main Methods:
- Fecal samples were collected from exposed workers, control individuals, and macaques from both high and low human-contact environments.
- 16S rRNA gene sequencing (Illumina MiSeq) was used to analyze gut microbial communities.
- Statistical analyses, including permuted betadisper and SourceTracker, were employed to assess microbial diversity and identify potential sources of microbial transfer.
Main Results:
- Macaques with higher human contact showed significantly different gut microbiota dispersion patterns compared to control macaques.
- Human gut microbiota exhibited homogenous variance but distinct spatial medians between exposed and control groups.
- While some individual human workers showed macaque-derived microbial contributions, overall transfer was not statistically significant.
Conclusions:
- Increased human contact alters macaque gut microbiome stability, potentially increasing disease susceptibility.
- Lifestyle differences, rather than direct exposure, may primarily drive human gut microbiome variations.
- Implementing hygiene measures is crucial for mitigating health risks associated with human-macaque interactions and optimizing the health of both populations.
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