Human milk oligosaccharide metabolism and antibiotic resistance in early gut colonizers: Insights from bifidobacteria and lactobacilli in the maternal-infant microbiome

Samarra, Anna, Renwick, Simone, Arzamasov, Aleksandr A., Rodionov, Dmitry A., Spann, Kennedy, Cabrera-Rubio, Raul, Acuna-Gonzalez, Antia, Martínez-Costa, Cecilia, Hall, Lindsay, Segata, Nicola, Osterman, Andrei L., Bode, Lars and Collado, MCarmen (2025) Human milk oligosaccharide metabolism and antibiotic resistance in early gut colonizers: Insights from bifidobacteria and lactobacilli in the maternal-infant microbiome. Gut Microbes, 17 (1). ISSN 1949-0976

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Abstract

Breast milk, rich in human milk oligosaccharides (HMOs), supports the early-life colonization of beneficial bacteria such as bifidobacteria and lactobacilli, potentially reducing early-life antibiotic resistance. However, antibiotic treatment may interfere with the beneficial functions of HMO-degrading bacteria. This study investigated the metabolism of HMOs by bifidobacteria and lactobacilli isolated from human milk and mother-infant paired fecal samples, along with their antibiotic resistance profiles. Understanding these species- and sample-type-specific interactions will provide valuable insights into how bioactive components in human milk may shape the infant resistome during early life. A total of 39 Bifidobacterium and 14 Lactobacillaceae strains were isolated from paired mother-infant fecal and breast milk samples. Whole genome sequencing (WGS) allowed functional predictions on the HMO metabolism abilities and the resistance genotype of each strain. In vitro HMO utilization was assessed using growth kinetics assays combined with HMO glycoprofiling in culture supernatant. The minimum inhibitory concentration (MIC) was also determined for each strain. HMO metabolism by the bifidobacteria was species-specific. Bifidobacterium bifidum (B. bifidum) and Bifidobacterium longum subsp. infantis (B. infantis) exhibited the highest capacity for HMO degradation, consistent with genomic predictions. In contrast, lactobacilli were unable to degrade HMOs in vitro but were predicted to metabolize the by-products of HMO degradation. Phenotypic analysis revealed that B. bifidum strains had the lowest levels of antibiotic resistance, while Bifidobacterium animalis subsp. lactis (B. lactis) strains were resistant to most tested antibiotics. Overall, B. bifidum demonstrated the strongest HMO-degrading ability while remaining the most antibiotic-susceptible species. Early-life colonizing bifidobacterial species possess the essential machinery required to degrade HMOs and are highly susceptible to antibiotics. A better understanding of these dynamics could inform clinical strategies to protect and restore the infant gut microbiome, particularly in neonates exposed to antibiotics.

Item Type: Article
Additional Information: Data availability statement: Genome sequences of all isolates have been deposited in the National Center for Biotechnology Information (NCBI) under accession PRJNA1190840. Funding information: The authors acknowledge the Generalitat Valenciana-European Social Fund (ACIF/2021) for the predoctoral fellowship grant to Anna Samarra. SR is the MOMI CORE Milk and Microbes Fellow, a program endowed by the Family Larsson-Rosenquist Foundation, Switzerland. RC-R is funded by the Plan GenT project [CDEIGENT 2020]. LJH is supported by a Wellcome Trust Investigator Award 220876/Z/20/Z and the Biotechnology and Biological Sciences Research Council (BBSRC); funded by the BBSRC Institute Strategic Programme Food Microbiome and Health BB/X011054/1 and its constituent project BBS/E/QU/230001B. AAA, DAR, and ALO were supported by the National Institutes of Health [DK030292]. LB is the UC San Diego Chair of Collaborative Human Milk Research, endowed by the Family Larsson-Rosenquist Foundation, Switzerland. MCC acknowledges the support from H2020-ERC Starting Grant [MAMI, ref. 639226], Spanish Ministry of Science and Innovation (MCIN) research grant (MAMI+, ref. PID2022-139475OB-I00) and also, Excellence Research Group-Generalitat Valenciana (GVA) Prometeo Programme (NeoHealth ref. PROMETEO2020/12 & Microglocal ref. CIPROM2023/030). IATA-CSIC authors would like to acknowledge the award of the Spanish government MCIN/AEI to the IATA‐CSIC as Center of Excellence Accreditation Severo Ochoa (CEX2021‐001189‐S/MCIN/AEI/10.13039/501100011033).
Uncontrolled Keywords: antibiotic resistance,bifidobacteria,human milk,infant,mother,oligosaccharides,microbiology,microbiology (medical),gastroenterology,infectious diseases,sdg 3 - good health and well-being ,/dk/atira/pure/subjectarea/asjc/2400/2404
Faculty \ School: Faculty of Medicine and Health Sciences > Norwich Medical School
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Depositing User: LivePure Connector
Date Deposited: 18 Jun 2025 11:30
Last Modified: 23 Jun 2025 16:30
URI: https://ueaeprints.uea.ac.uk/id/eprint/99619
DOI: 10.1080/19490976.2025.2501192

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