Advanced science (Weinheim, Baden-Wurttemberg, Germany)Oct 4, 2026

Gene Roles in How Bacteroides thetaiotaomicron Uses Mucin for Survival

CRISPR Gene Editing Weekly Brief ↗PubMed ↗DOI ↗OA ↗

Updated Oct 5, 2026

Abstract

A total of 1,256 genes exhibited condition-dependent fitness divergence in the mucin-utilization network of Bacteroides thetaiotaomicron.

Mucin utilization is organized in a layered manner, reflecting different contributions to growth.
Enrichment for strains with repressed capsular polysaccharide loci indicates a mucin-specific fitness signature.
Specific capsules were found to impede growth on mucin, suggesting a trade-off related to surface accessibility.
Most genes involved in carbohydrate binding and glycan breakdown exhibited little impact on fitness, indicating redundancy in these functions.
Significant constraints were observed in downstream sugar catabolism, particularly with the galactose-utilization gene BT_0623.
Comparative analysis with murine colon data showed alignment with in vitro findings, while also revealing environment-specific differences.

Simplified

Host mucus is a major nutrient reservoir for gut Bacteroidota, yet the gene-level determinants of mucin utilization remain poorly defined. In this study, we used a genome-scale CRISPR interference library in Bacteroides thetaiotaomicron to systematically map fitness contributions across the mucin-utilization network, spanning surface accessibility, glycan degradation, and intracellular sugar assimilation. Our screen identified 1,256 genes with condition-dependent fitness divergence, which revealed a layered organization of mucin-dependent growth. A prominent mucin-specific fitness signature was enrichment of strains with repressed capsular polysaccharide loci. Subsequent competition and deletion experiments validated that specific capsules impede growth on mucin, supporting a surface-accessibility trade-off model. By contrast, most mucin-induced carbohydrate-binding and glycoside hydrolase genes showed negligible fitness contributions, consistent with functional redundancy in extracellular glycan capture and processing. Conversely, downstream sugar catabolism showed pronounced condition-specific constraints, with the galactose-utilization gene BT_0623, causing measurable fitness defects upon repression in both mucin- and galactose-containing media. Finally, comparison with murine colon CRISPRi data revealed broad concordance with the in vitro mucin fitness landscape, while also highlighting environment-specific differences, in CPS- and polysaccharide degradation-associated functions. Together, these results define mucin utilization as a layered fitness architecture governed by surface-accessibility costs, redundant extracellular glycan processing, and downstream metabolic constraints.

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Gene Roles in How Bacteroides thetaiotaomicron Uses Mucin for Survival

Abstract

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