Language

English

Publication Date

12-31-2026

Journal

Gut Microbes

DOI

10.1080/19490976.2026.2691334

PMID

42359789

PMCID

PMC13313206

PubMedCentral® Posted Date

6-26-2026

PubMedCentral® Full Text Version

Post-print

Abstract

Akkermansia muciniphila is a key member of the gut microbiota and plays important roles in host metabolism and health. In the colon, A. muciniphila extracts nutrients from oligosaccharide-rich mucin glycans that comprise the mucosa. However, this environment is complex and shaped by dietary inputs, microbiome metabolism, and mucin glycan composition varying across hosts, gastrointestinal regions, and physiological states. How strains of A. muciniphila integrate these nutrient signals into growth initiation and niche colonization remains unclear. Here, we compare physiological responses of a human- and mouse-derived strain of A. muciniphila, finding that dietary sugars differentially affect these isolates, suggesting host-associated tuning of metabolic capacity. In contrast, several mucin-derived sugars impose a conserved, concentration-dependent delay in growth initiation, implicating the lag phase as a critical metabolic checkpoint for growth. Genetic suppressor analysis identified sugar kinases and a component of the tricarboxylic acid cycle as genetically encoded control points linking glycan sugar exposure to the energy balance required for growth. These findings demonstrate that mucin-derived sugars function as both nutrients and metabolic stressors, regulating growth initiation. We propose that A. muciniphila employs metabolic “brakes” to coordinate growth with mucin composition, putatively linking host glycan landscapes to microbial physiology and ecological fitness within the mucus layer.

Keywords

Mucins, Animals, Humans, Akkermansia, Mice, Gastrointestinal Microbiome, Polysaccharides, Dietary Sugars, Colon, Citric Acid Cycle, Verrucomicrobia, Akkermansia muciniphila, microbial metabolism, central carbon metabolism, lag phase, mucin, glycans, gut colonization

Published Open-Access

yes

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