Ecological memory of prior nutrient exposure in the human gut microbiome.

Journal Article (Journal Article)

Many ecosystems have been shown to retain a memory of past conditions, which in turn affects how they respond to future stimuli. In microbial ecosystems, community disturbance has been associated with lasting impacts on microbiome structure. However, whether microbial communities alter their response to repeated stimulus remains incompletely understood. Using the human gut microbiome as a model, we show that bacterial communities retain an "ecological memory" of past carbohydrate exposures. Memory of the prebiotic inulin was encoded within a day of supplementation among a cohort of human study participants. Using in vitro gut microbial models, we demonstrated that the strength of ecological memory scales with nutrient dose and persists for days. We found evidence that memory is seeded by transcriptional changes among primary degraders of inulin within hours of nutrient exposure, and that subsequent changes in the activity and abundance of these taxa are sufficient to enhance overall community nutrient metabolism. We also observed that ecological memory of one carbohydrate species impacts microbiome response to other carbohydrates, and that an individual's habitual exposure to dietary fiber was associated with their gut microbiome's efficiency at digesting inulin. Together, these findings suggest that the human gut microbiome's metabolic potential reflects dietary exposures over preceding days and changes within hours of exposure to a novel nutrient. The dynamics of this ecological memory also highlight the potential for intra-individual microbiome variation to affect the design and interpretation of interventions involving the gut microbiome.

Full Text

Duke Authors

Cited Authors

  • Letourneau, J; Holmes, ZC; Dallow, EP; Durand, HK; Jiang, S; Carrion, VM; Gupta, SK; Mincey, AC; Muehlbauer, MJ; Bain, JR; David, LA

Published Date

  • November 2022

Published In

Volume / Issue

  • 16 / 11

Start / End Page

  • 2479 - 2490

PubMed ID

  • 35871250

Pubmed Central ID

  • PMC9563064

Electronic International Standard Serial Number (EISSN)

  • 1751-7370

Digital Object Identifier (DOI)

  • 10.1038/s41396-022-01292-x


  • eng

Conference Location

  • England