Kalliope
Senior Member (Voting Rights)
Meta-omics analysis of elite athletes identifies a performance-enhancing microbe that functions via lactate metabolism - Jonathan Scheiman et al
The human gut microbiome is linked to many states of human health and disease1. The metabolic repertoire of the gut micro-biome is vast, but the health implications of these bacterial pathways are poorly understood.
In this study, we identify a link between members of the genus Veillonella and exercise performance. We observed an increase in Veillonella relative abundance in marathon runners postmarathon and isolated a strain of Veillonella atypica from stool samples.
Inoculation of this strain into mice significantly increased exhaustive tread-mill run time. Veillonella utilize lactate as their sole carbon source, which prompted us to perform a shotgun metage-nomic analysis in a cohort of elite athletes, finding that every gene in a major pathway metabolizing lactate to propionate is at higher relative abundance postexercise.
Using 13C3-labeled lactate in mice, we demonstrate that serum lactate crosses the epithelial barrier into the lumen of the gut. We also show that intrarectal instillation of propionate is sufficient to repro-duce the increased treadmill run time performance observed with V. atypica gavage.
Taken together, these studies reveal that V. atypica improves run time via its metabolic conversion of exercise-induced lactate into propionate, thereby identify-ing a natural, microbiome-encoded enzymatic process that enhances athletic performance.
The human gut microbiome is linked to many states of human health and disease1. The metabolic repertoire of the gut micro-biome is vast, but the health implications of these bacterial pathways are poorly understood.
In this study, we identify a link between members of the genus Veillonella and exercise performance. We observed an increase in Veillonella relative abundance in marathon runners postmarathon and isolated a strain of Veillonella atypica from stool samples.
Inoculation of this strain into mice significantly increased exhaustive tread-mill run time. Veillonella utilize lactate as their sole carbon source, which prompted us to perform a shotgun metage-nomic analysis in a cohort of elite athletes, finding that every gene in a major pathway metabolizing lactate to propionate is at higher relative abundance postexercise.
Using 13C3-labeled lactate in mice, we demonstrate that serum lactate crosses the epithelial barrier into the lumen of the gut. We also show that intrarectal instillation of propionate is sufficient to repro-duce the increased treadmill run time performance observed with V. atypica gavage.
Taken together, these studies reveal that V. atypica improves run time via its metabolic conversion of exercise-induced lactate into propionate, thereby identify-ing a natural, microbiome-encoded enzymatic process that enhances athletic performance.