Microbiome dynamics in the congregate environment of U.S. Army Infantry training

Within military training and operational environments, individuals from diverse backgrounds share common spaces, follow structured routines and diets, and engage in physically demanding tasks. While there has been interest in leveraging microbiome features to predict and improve military health and performance, the longitudinal convergence of microbiomes in such constrained environments has not been established. To assess the degree of microbiome convergence, we performed shotgun metagenomic sequencing on swab samples from a military trainee cohort. Samples were taken across four different body sites, three timepoints, and two spatially distinct platoons. We observed evidence of convergence in one platoon, whereby similarity in microbiome composition increased over time, with numerous differentially abundant species. We found no indication of strain transfer between individuals, suggesting that convergence was influenced by external environmental factors, diet, and lifestyle. Microbial shifts observed in the convergence process included a decrease in fungal species, such as <i>Malassezia restricta</i> in nasal cavities, and a decrease in <i>Prevotella</i> species at inguinal regions across time. Shifts in multiple <i>Corynebacterium</i> species were also observed with varying magnitudes depending on the body site. Overall, we provide preliminary evidence of convergence of host microbial communities in military-associated environments that were distinguishable using shotgun metagenomic sequencing approaches. The data presented here on microbiome convergence, dynamics, and stability may inform risk-based mitigation in congregate military settings facilitating development of targeted microbial, dietary, or other interventions to optimize health and performance of military populations.<b>IMPORTANCE</b>Microbiome convergence in deployed environments could impact the health and readiness of the warfighter, with potential implications for susceptibility to biothreats. This study describes a shotgun metagenomic approach used to study the microbiomes of swab samples collected at different body sites in a military trainee cohort. The results presented here provide a foundation for developing future microbiome-based interventions and protocols to enhance operational readiness.

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Publication Details

Journal
Microbiology Spectrum
Published
2025-12-17
DOI
https://doi.org/10.1128/spectrum.00474-25
Primary Topic
Gut microbiota and health
Type
article
Field-Weighted Citation Impact
0.00
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article

Microbiome dynamics in the congregate environment of U.S. Army Infantry training

Jeffrey A. Kimbrel, Katrin Mende, James B. Thissen, M Leigh Carson et al.
Microbiology Spectrum
Gut microbiota and health
article

Microbiome dynamics in the congregate environment of U.S. Army Infantry training

Jeffrey A. Kimbrel, Katrin Mende, James B. Thissen, M Leigh Carson, Car Reen Kok, Nicholas A. Be, Shalini Mabery, Michael D. Morrison, Jason W. Bennett, Eugene V. Millar, David R. Tribble
article en

Abstract

Within military training and operational environments, individuals from diverse backgrounds share common spaces, follow structured routines and diets, and engage in physically demanding tasks. While there has been interest in leveraging microbiome features to predict and improve military health and performance, the longitudinal convergence of microbiomes in such constrained environments has not been established. To assess the degree of microbiome convergence, we performed shotgun metagenomic sequencing on swab samples from a military trainee cohort. Samples were taken across four different body sites, three timepoints, and two spatially distinct platoons. We observed evidence of convergence in one platoon, whereby similarity in microbiome composition increased over time, with numerous differentially abundant species. We found no indication of strain transfer between individuals, suggesting that convergence was influenced by external environmental factors, diet, and lifestyle. Microbial shifts observed in the convergence process included a decrease in fungal species, such as <i>Malassezia restricta</i> in nasal cavities, and a decrease in <i>Prevotella</i> species at inguinal regions across time. Shifts in multiple <i>Corynebacterium</i> species were also observed with varying magnitudes depending on the body site. Overall, we provide preliminary evidence of convergence of host microbial communities in military-associated environments that were distinguishable using shotgun metagenomic sequencing approaches. The data presented here on microbiome convergence, dynamics, and stability may inform risk-based mitigation in congregate military settings facilitating development of targeted microbial, dietary, or other interventions to optimize health and performance of military populations.<b>IMPORTANCE</b>Microbiome convergence in deployed environments could impact the health and readiness of the warfighter, with potential implications for susceptibility to biothreats. This study describes a shotgun metagenomic approach used to study the microbiomes of swab samples collected at different body sites in a military trainee cohort. The results presented here provide a foundation for developing future microbiome-based interventions and protocols to enhance operational readiness.

Microbiology SpectrumVol. 14(2)
Henry M. Jackson Foundation (US), Lawrence Livermore National Laboratory (US), Uniformed Services University of the Health Sciences (US), Joint Base San Antonio (US), Walter Reed Army Institute of Research (US)
Openalex Percentile: Top 63%
Gut microbiota and health
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