A diet of U.S. military food rations alters gut microbiota composition and does not increase intestinal permeability

Abstract

Interactions between gut microbes and dietary components modulate intestinal permeability (IP) and inflammation. Recent studies have reported altered fecal microbiota composition together with increased IP and inflammation in individuals consuming military food rations in austere environments, but could not isolate effects of the diet from environmental factors. To determine how the U.S. Meal, Ready-to-Eat food ration affects fecal microbiota composition, IP and inflammation, 60 adults (95 male,1861 years) were randomized to consume their usual ad libitum diet for 31 days (CON) or a strictly controlled Meal, Ready-to-Eat-only diet for 21 days followed by their usual diet for 10 days (MRE). In both groups, fecal microbiota composition was measured before, during (INT, days 121) and after the intervention period. IP and inflammation [high-sensitivity C-reactive protein (hsCRP)] were measured on days 0, 10, 21 and 31. Longitudinal changes in fecal microbiota composition differed between groups (P=.005), and fecal samples collected from MRE during INT were identified with 88 accuracy using random forest models. The genera making the strongest contribution to that prediction accuracy included multiple lactic acid bacteria (Lactobacillus, Lactococcus, Leuconostoc), which demonstrated lower relative abundance in MRE, and several genera known to dominate the ileal microbiota (Streptococcus, Veillonella, Clostridium), the latter two demonstrating higher relative abundance in MRE. IP and hsCRP were both lower (34 and 41 , respectively) in MRE relative to CON on day 21 (P<.05) but did not differ otherwise. Findings demonstrate that a Meal, Ready-to-Eat ration diet alters fecal microbiota composition and does not increase IP or inflammation.

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Document Details

Document Type
Technical Report
Publication Date
Jul 30, 2019
Accession Number
AD1100203

Entities

People

  • Holly L. Mcclung
  • J Philip Karl
  • Jason W. Soares
  • Jennifer C Rood
  • Kenneth Racicot
  • Nicholes J. Armstrong
  • Robert A. Player
  • Scott J. Montain

Organizations

  • United States Army Natick Soldier Research, Development and Engineering Center

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Accuracy
  • Bacteria
  • Body Weight
  • Cellular Structures
  • Chemistry
  • Digestive System Processes
  • Epithelial Cells
  • Glucose Metabolism Disorders
  • Gut Microbiome
  • Immunoproteins
  • Intestines
  • Liver Diseases
  • Meals
  • Medical Personnel
  • Microbiomes
  • Microorganisms
  • Military Personnel

Fields of Study

  • Biology
  • Environmental science

Readers

  • Gulf War Illness and Chronic Multisymptom Illness in Veterans.
  • Microbial Pathology
  • Toxicology/Environmental Toxicology