The gut microbiome regulates thermogenic performance in high-altitude deer mice

Abstract

High altitude is one of the most extreme environments inhabited by endotherms, where cold temperatures demand high rates of thermogenesis to maintain body temperature (Tb) but hypoxia constrains aerobic metabolism. Recent findings suggest that the gut microbiome contributes to whole-body thermogenesis, but its significance for coping in cold environments remains poorly understood. We hypothesized that the gut microbiome contributes to adaptive increases in thermogenic performance in deer mice native to high altitude. Mice from populations native to high altitude and low altitude were born and raised to adulthood in common lab conditions. Adults from both populations were then acclimated to warm (25°C) normoxia or cold (5°C) hypoxia (12 kPa O2) for 6 weeks, and a subset of mice in each group were treated with antibiotics to disrupt the gut microbiome. Thermogenic endurance was then measured as the duration that Tb could be maintained during acute cold challenge. Antibiotic treatment strongly diminished thermogenic endurance in highlanders, but led to only minor reductions in thermogenic endurance in lowlanders. These differences could not be fully explained by impairments in aerobic heat production by host thermogenic tissues, because antibiotic treatment had only modest effects on cold-induced increases in O2 consumption rate and the abundance of UCP-1 protein and oxidative phosphorylation complexes in brown adipose tissue. Therefore, our findings suggest that the gut microbiome plays an increased role in regulating thermogenesis in high-altitude deer mice, and that changes in host-microbe interactions contribute to high-altitude adaptation. Funded by NSERC of Canada. This is the full abstract presented at the American Physiology Summit 2024 meeting and is only available in HTML format. There are no additional versions or additional content available for this abstract. Physiology was not involved in the peer review process.