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Linking Human Milk Oligosaccharides, Infant Fecal Community Types, and Later Risk To Require Antibiotics
Human milk oligosaccharides (HMOs) may provide health benefits to infants partly by shaping the development of the early-life intestinal microbiota. In a randomized double-blinded controlled multicentric clinical trial, healthy term infants received either infant formula (control) or the same formul...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7078481/ https://www.ncbi.nlm.nih.gov/pubmed/32184252 http://dx.doi.org/10.1128/mBio.03196-19 |
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author | Berger, Bernard Porta, Nadine Foata, Francis Grathwohl, Dominik Delley, Michèle Moine, Deborah Charpagne, Aline Siegwald, Léa Descombes, Patrick Alliet, Philippe Puccio, Giuseppe Steenhout, Philippe Mercenier, Annick Sprenger, Norbert |
author_facet | Berger, Bernard Porta, Nadine Foata, Francis Grathwohl, Dominik Delley, Michèle Moine, Deborah Charpagne, Aline Siegwald, Léa Descombes, Patrick Alliet, Philippe Puccio, Giuseppe Steenhout, Philippe Mercenier, Annick Sprenger, Norbert |
author_sort | Berger, Bernard |
collection | PubMed |
description | Human milk oligosaccharides (HMOs) may provide health benefits to infants partly by shaping the development of the early-life intestinal microbiota. In a randomized double-blinded controlled multicentric clinical trial, healthy term infants received either infant formula (control) or the same formula with two HMOs (2′-fucosyllactose and lacto-N-neotetraose; test) from enrollment (0 to 14 days) to 6 months. Then, all infants received the same follow-up formula without HMOs until 12 months of age. Breastfed infants (BF) served as a reference group. Stool microbiota at 3 and 12 months, analyzed by 16S rRNA gene sequencing, clustered into seven fecal community types (FCTs) with marked differences in total microbial abundances. Three of the four 12-month FCTs were likely precursors of the adult enterotypes. At 3 months, microbiota composition in the test group (n = 58) appeared closer to that of BF (n = 35) than control (n = 63) by microbiota alpha (within group) and beta (between groups) diversity analyses and distribution of FCTs. While bifidobacteriaceae dominated two FCTs, its abundance was significantly higher in one (FCT BiH for Bifidobacteriaceae at high abundance) than in the other (FCT Bi for Bifidobacteriaceae). HMO supplementation increased the number of infants with FCT BiH (predominant in BF) at the expense of FCT Bi (predominant in control). We explored the association of the FCTs with reported morbidities and medication use up to 12 months. Formula-fed infants with FCT BiH at 3 months were significantly less likely to require antibiotics during the first year than those with FCT Bi. Previously reported lower rates of infection-related medication use with HMOs may therefore be linked to gut microbiota community types. (This study has been registered at ClinicalTrials.gov under registration number NCT01715246.) |
format | Online Article Text |
id | pubmed-7078481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-70784812020-03-31 Linking Human Milk Oligosaccharides, Infant Fecal Community Types, and Later Risk To Require Antibiotics Berger, Bernard Porta, Nadine Foata, Francis Grathwohl, Dominik Delley, Michèle Moine, Deborah Charpagne, Aline Siegwald, Léa Descombes, Patrick Alliet, Philippe Puccio, Giuseppe Steenhout, Philippe Mercenier, Annick Sprenger, Norbert mBio Research Article Human milk oligosaccharides (HMOs) may provide health benefits to infants partly by shaping the development of the early-life intestinal microbiota. In a randomized double-blinded controlled multicentric clinical trial, healthy term infants received either infant formula (control) or the same formula with two HMOs (2′-fucosyllactose and lacto-N-neotetraose; test) from enrollment (0 to 14 days) to 6 months. Then, all infants received the same follow-up formula without HMOs until 12 months of age. Breastfed infants (BF) served as a reference group. Stool microbiota at 3 and 12 months, analyzed by 16S rRNA gene sequencing, clustered into seven fecal community types (FCTs) with marked differences in total microbial abundances. Three of the four 12-month FCTs were likely precursors of the adult enterotypes. At 3 months, microbiota composition in the test group (n = 58) appeared closer to that of BF (n = 35) than control (n = 63) by microbiota alpha (within group) and beta (between groups) diversity analyses and distribution of FCTs. While bifidobacteriaceae dominated two FCTs, its abundance was significantly higher in one (FCT BiH for Bifidobacteriaceae at high abundance) than in the other (FCT Bi for Bifidobacteriaceae). HMO supplementation increased the number of infants with FCT BiH (predominant in BF) at the expense of FCT Bi (predominant in control). We explored the association of the FCTs with reported morbidities and medication use up to 12 months. Formula-fed infants with FCT BiH at 3 months were significantly less likely to require antibiotics during the first year than those with FCT Bi. Previously reported lower rates of infection-related medication use with HMOs may therefore be linked to gut microbiota community types. (This study has been registered at ClinicalTrials.gov under registration number NCT01715246.) American Society for Microbiology 2020-03-17 /pmc/articles/PMC7078481/ /pubmed/32184252 http://dx.doi.org/10.1128/mBio.03196-19 Text en Copyright © 2020 Berger et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Berger, Bernard Porta, Nadine Foata, Francis Grathwohl, Dominik Delley, Michèle Moine, Deborah Charpagne, Aline Siegwald, Léa Descombes, Patrick Alliet, Philippe Puccio, Giuseppe Steenhout, Philippe Mercenier, Annick Sprenger, Norbert Linking Human Milk Oligosaccharides, Infant Fecal Community Types, and Later Risk To Require Antibiotics |
title | Linking Human Milk Oligosaccharides, Infant Fecal Community Types, and Later Risk To Require Antibiotics |
title_full | Linking Human Milk Oligosaccharides, Infant Fecal Community Types, and Later Risk To Require Antibiotics |
title_fullStr | Linking Human Milk Oligosaccharides, Infant Fecal Community Types, and Later Risk To Require Antibiotics |
title_full_unstemmed | Linking Human Milk Oligosaccharides, Infant Fecal Community Types, and Later Risk To Require Antibiotics |
title_short | Linking Human Milk Oligosaccharides, Infant Fecal Community Types, and Later Risk To Require Antibiotics |
title_sort | linking human milk oligosaccharides, infant fecal community types, and later risk to require antibiotics |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7078481/ https://www.ncbi.nlm.nih.gov/pubmed/32184252 http://dx.doi.org/10.1128/mBio.03196-19 |
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