Human milk microbiota, oligosaccharide profiles, and infant gut microbiome in preterm infants diagnosed with necrotizing enterocolitis

Necrotizing enterocolitis (NEC) is a severe intestinal disease of very preterm infants with mother's own milk (MOM) providing protection, but the contribution of the MOM microbiota to NEC risk has not been explored. Here, we analyze MOM of 110 preterm infants (48 NEC, 62 control) in a cross-sectional study. Breast milk contains viable bacteria, but there is no significant difference in MOM microbiota between NEC and controls. Integrative analysis between MOM microbiota, human milk oligosaccharides (HMOs), and the infant gut microbiota shows positive correlations only between Acinetobacter in the infant gut and Acinetobacter and Staphylococcus in MOM. This study suggests that NEC protection from MOM is not modulated through the MOM microbiota. Thus, "'restoring" the MOM microbiota in donor human milk is unlikely to reduce NEC, and emphasis should instead focus on increasing fresh maternal human milk intake and researching different therapies for NEC prevention.

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Publication Details

Journal
Cell Reports Medicine
Published
2024-08-30
DOI
https://doi.org/10.1016/j.xcrm.2024.101708
Citations
16
Primary Topic
Infant Nutrition and Health
Type
article
Field-Weighted Citation Impact
4.95

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article

Human milk microbiota, oligosaccharide profiles, and infant gut microbiome in preterm infants diagnosed with necrotizing enterocolitis

John D. Perry, Claire Granger, Christopher James Stewart, Lauren C. Beck et al.
16 citations
Cell Reports Medicine
Infant Nutrition and Health
4.95
article

Human milk microbiota, oligosaccharide profiles, and infant gut microbiome in preterm infants diagnosed with necrotizing enterocolitis

John D. Perry, Claire Granger, Christopher James Stewart, Lauren C. Beck, Nicholas David Embleton, Janet Berrington, Gregory R. Young, A Masi, Lars Bode, Alice Hiorns
article en
16 citations

Abstract

Necrotizing enterocolitis (NEC) is a severe intestinal disease of very preterm infants with mother's own milk (MOM) providing protection, but the contribution of the MOM microbiota to NEC risk has not been explored. Here, we analyze MOM of 110 preterm infants (48 NEC, 62 control) in a cross-sectional study. Breast milk contains viable bacteria, but there is no significant difference in MOM microbiota between NEC and controls. Integrative analysis between MOM microbiota, human milk oligosaccharides (HMOs), and the infant gut microbiota shows positive correlations only between Acinetobacter in the infant gut and Acinetobacter and Staphylococcus in MOM. This study suggests that NEC protection from MOM is not modulated through the MOM microbiota. Thus, "'restoring" the MOM microbiota in donor human milk is unlikely to reduce NEC, and emphasis should instead focus on increasing fresh maternal human milk intake and researching different therapies for NEC prevention.

Cell Reports MedicineVol. 5(9)
Freeman Hospital (GB), Newcastle upon Tyne Hospital (GB), NIHR Newcastle Biomedical Research Centre (GB), Mothers’ Milk Bank (US), Newcastle University (GB)
Wellcome Trust, Royal Society, Newcastle University, Lister Institute of Preventive Medicine
Zero hunger
Openalex Percentile: Top 4%
Infant Nutrition and Health
4.95
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