Human milk oligosaccharide mediates mutualism between Escherichia coli and Bifidobacterium bifidum

Infant gut microbiota development involves frequent colonization by Enterobacteriaceae, particularly Escherichia coli, yet their ecological role in healthy infants is unclear. Here, we analyse longitudinal stool samples from healthy, term-born, breastfed infants (n = 41) and related mothers (n = 30) using shotgun metagenomics and novel computational approaches. Strain-resolved profiling indicates that Bifidobacterium species are frequently shared within families, whereas E. coli derive from external sources, but often persist within individuals. Despite differing ecological strategies, these genera co-exist and share evolutionary adaptations related to lactose acquisition in the infant gut. In vitro, we demonstrate that interactions between E. coli and Bifidobacterium bifidum are mutualistic in co-culture, where E. coli supplies cysteine to its auxotrophic partner, facilitating cooperative degradation of 2'-fucosyllactose, the predominant human milk oligosaccharide. In turn, the liberated monosaccharides sustain E. coli growth, highlighting a cooperative cross-feeding interaction that may contribute to regulating E. coli abundance within the infant host.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2026-04-22
DOI
https://doi.org/10.1038/s41467-026-71764-7
Primary Topic
Infant Nutrition and Health
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Human milk oligosaccharide mediates mutualism between Escherichia coli and Bifidobacterium bifidum

Magdalena Kujawska, Shaul Pollak, Peter T. Chivers, Antia Acuna-Gonzalez et al.
Nature Communications
Infant Nutrition and Health
article

Human milk oligosaccharide mediates mutualism between Escherichia coli and Bifidobacterium bifidum

Magdalena Kujawska, Shaul Pollak, Peter T. Chivers, Antia Acuna-Gonzalez, Lindsay J. Hall, John Penders, Raymond Kiu, Monique Mommers, Lucy I. Crouch, Cassie R. Bakshani, Nils van Best
article en

Abstract

Infant gut microbiota development involves frequent colonization by Enterobacteriaceae, particularly Escherichia coli, yet their ecological role in healthy infants is unclear. Here, we analyse longitudinal stool samples from healthy, term-born, breastfed infants (n = 41) and related mothers (n = 30) using shotgun metagenomics and novel computational approaches. Strain-resolved profiling indicates that Bifidobacterium species are frequently shared within families, whereas E. coli derive from external sources, but often persist within individuals. Despite differing ecological strategies, these genera co-exist and share evolutionary adaptations related to lactose acquisition in the infant gut. In vitro, we demonstrate that interactions between E. coli and Bifidobacterium bifidum are mutualistic in co-culture, where E. coli supplies cysteine to its auxotrophic partner, facilitating cooperative degradation of 2'-fucosyllactose, the predominant human milk oligosaccharide. In turn, the liberated monosaccharides sustain E. coli growth, highlighting a cooperative cross-feeding interaction that may contribute to regulating E. coli abundance within the infant host.

Nature CommunicationsVol. 17(1)
University of East Anglia (GB), University of Vienna (AT), Durham University (GB), Maastricht University Medical Centre (NL), Quadram Institute (GB), Maastricht University (NL), Department of Health (TW), Leibniz-Institute for Food Systems Biology at the Technical University of Munich (DE), University of Birmingham (GB)
Wellcome, Wellcome Trust, Austrian Science Fund, Directorate for Biological Sciences, Biotechnology and Biological Sciences Research Council
Openalex Percentile: Top 22%
Infant Nutrition and Health
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.