A gut-microbiota-muscle axis that protects against age-related motor decline by regulating mitochondrial fission inC. elegans

Across diverse taxa, the composition of the microbiota is associated with lifelong host health. A mechanistic understanding of how microbial communities influence host physiology could lead to microbiota-based interventions for lifelong health. Here, we have developed a new host-microbiota model system utilising the model organismC. eleganscombined with a defined natural microbiota (DefNatMta) consisting of 11 bacteria isolated from wildC. elegans, to study host-microbiota interactions in a more natural setting. We show that DefNatMta colonises theC. elegansgut, forming a stable and distinct gut microbiota. Using DefNatMta, we find a gut microbiota-muscle axis by which the microbiota affects age-related motility and muscular strength and protects against age-related decline in motor function. The gut microbiota-muscle axis acts by altering metabolism and mitochondrial network dynamics in muscle, and requires dynamin-related protein 1 DRP-1, a regulator of mitochondrial fission to protect against age-related motility decline. Our study demonstrates a gut microbiota-muscle axis and microbiota-mitochondria communication affecting age-related muscle function.