The human milk oligosaccharide 2′-fucosyllactose augments the adaptive response to extensive intestinal

Author:

Mezoff Ethan A.1,Hawkins Jennifer A.2,Ollberding Nicholas J.3,Karns Rebekah4,Morrow Ardythe L.5,Helmrath Michael A.2

Affiliation:

1. Cincinnati Children's Hospital Medical Center, Division of Gastroenterology, Hepatology, and Nutrition;

2. Cincinnati Children's Hospital Medical Center, Division of Pediatric General and Thoracic Surgery;

3. Cincinnati Children's Hospital Medical Center, Division of Biostatistics and Epidemiology;

4. Cincinnati Children's Hospital Medical Center, Division of Biomedical Informatics; and

5. Cincinnati Children's Hospital Medical Center, Division of Neonatology and Pulmonary Biology

Abstract

Intestinal resection resulting in short bowel syndrome (SBS) carries a heavy burden of long-term morbidity, mortality, and cost of care, which can be attenuated with strategies that improve intestinal adaptation. SBS infants fed human milk, compared with formula, have more rapid intestinal adaptation. We tested the hypothesis that the major noncaloric human milk oligosaccharide 2′-fucosyllactose (2′-FL) contributes to the adaptive response after intestinal resection. Using a previously described murine model of intestinal adaptation, we demonstrated increased weight gain from 21 to 56 days ( P < 0.001) and crypt depth at 56 days ( P < 0.0095) with 2′-FL supplementation after ileocecal resection. Furthermore, 2′-FL increased small bowel luminal content microbial alpha diversity following resection ( P < 0.005) and stimulated a bloom in organisms of the genus Parabacteroides (log2-fold = 4.1, P = 0.035). Finally, transcriptional analysis of the intestine revealed enriched ontologies and pathways related to antimicrobial peptides, metabolism, and energy processing. We conclude that 2′-FL supplementation following ileocecal resection increases weight gain, energy availability through microbial community modulation, and histological changes consistent with improved adaptation.

Funder

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

HHS | NIH | National Institute of Child Health and Human Development (NICHD)

Publisher

American Physiological Society

Subject

Physiology (medical),Gastroenterology,Hepatology,Physiology

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