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Human milk and mucosa-associated disaccharides impact on cultured infant fecal microbiota

Human milk oligosaccharides (HMOs) are a mixture of structurally diverse carbohydrates that contribute to shape a healthy gut microbiota composition. The great diversity of the HMOs structures does not allow the attribution of specific prebiotic characteristics to single milk oligosaccharides. We an...

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Autores principales: Rubio-del-Campo, Antonio, Alcántara, Cristina, Collado, María Carmen, Rodríguez-Díaz, Jesús, Yebra, María J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7366668/
https://www.ncbi.nlm.nih.gov/pubmed/32678209
http://dx.doi.org/10.1038/s41598-020-68718-4
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author Rubio-del-Campo, Antonio
Alcántara, Cristina
Collado, María Carmen
Rodríguez-Díaz, Jesús
Yebra, María J.
author_facet Rubio-del-Campo, Antonio
Alcántara, Cristina
Collado, María Carmen
Rodríguez-Díaz, Jesús
Yebra, María J.
author_sort Rubio-del-Campo, Antonio
collection PubMed
description Human milk oligosaccharides (HMOs) are a mixture of structurally diverse carbohydrates that contribute to shape a healthy gut microbiota composition. The great diversity of the HMOs structures does not allow the attribution of specific prebiotic characteristics to single milk oligosaccharides. We analyze here the utilization of four disaccharides, lacto-N-biose (LNB), galacto-N-biose (GNB), fucosyl-α1,3-GlcNAc (3FN) and fucosyl-α1,6-GlcNAc (6FN), that form part of HMOs and glycoprotein structures, by the infant fecal microbiota. LNB significantly increased the total levels of bifidobacteria and the species Bifidobacterium breve and Bifidobacterium bifidum. The Lactobacillus genus levels were increased by 3FN fermentation and B. breve by GNB and 3FN. There was a significant reduction of Blautia coccoides group with LNB and 3FN. In addition, 6FN significantly reduced the levels of Enterobacteriaceae family members. Significantly higher concentrations of lactate, formate and acetate were produced in cultures containing either LNB or GNB in comparison with control cultures. Additionally, after fermentation of the oligosaccharides by the fecal microbiota, several Bifidobacterium strains were isolated and identified. The results presented here indicated that each, LNB, GNB and 3FN disaccharide, might have a specific beneficial effect in the infant gut microbiota and they are potential prebiotics for application in infant foods.
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spelling pubmed-73666682020-07-17 Human milk and mucosa-associated disaccharides impact on cultured infant fecal microbiota Rubio-del-Campo, Antonio Alcántara, Cristina Collado, María Carmen Rodríguez-Díaz, Jesús Yebra, María J. Sci Rep Article Human milk oligosaccharides (HMOs) are a mixture of structurally diverse carbohydrates that contribute to shape a healthy gut microbiota composition. The great diversity of the HMOs structures does not allow the attribution of specific prebiotic characteristics to single milk oligosaccharides. We analyze here the utilization of four disaccharides, lacto-N-biose (LNB), galacto-N-biose (GNB), fucosyl-α1,3-GlcNAc (3FN) and fucosyl-α1,6-GlcNAc (6FN), that form part of HMOs and glycoprotein structures, by the infant fecal microbiota. LNB significantly increased the total levels of bifidobacteria and the species Bifidobacterium breve and Bifidobacterium bifidum. The Lactobacillus genus levels were increased by 3FN fermentation and B. breve by GNB and 3FN. There was a significant reduction of Blautia coccoides group with LNB and 3FN. In addition, 6FN significantly reduced the levels of Enterobacteriaceae family members. Significantly higher concentrations of lactate, formate and acetate were produced in cultures containing either LNB or GNB in comparison with control cultures. Additionally, after fermentation of the oligosaccharides by the fecal microbiota, several Bifidobacterium strains were isolated and identified. The results presented here indicated that each, LNB, GNB and 3FN disaccharide, might have a specific beneficial effect in the infant gut microbiota and they are potential prebiotics for application in infant foods. Nature Publishing Group UK 2020-07-16 /pmc/articles/PMC7366668/ /pubmed/32678209 http://dx.doi.org/10.1038/s41598-020-68718-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Rubio-del-Campo, Antonio
Alcántara, Cristina
Collado, María Carmen
Rodríguez-Díaz, Jesús
Yebra, María J.
Human milk and mucosa-associated disaccharides impact on cultured infant fecal microbiota
title Human milk and mucosa-associated disaccharides impact on cultured infant fecal microbiota
title_full Human milk and mucosa-associated disaccharides impact on cultured infant fecal microbiota
title_fullStr Human milk and mucosa-associated disaccharides impact on cultured infant fecal microbiota
title_full_unstemmed Human milk and mucosa-associated disaccharides impact on cultured infant fecal microbiota
title_short Human milk and mucosa-associated disaccharides impact on cultured infant fecal microbiota
title_sort human milk and mucosa-associated disaccharides impact on cultured infant fecal microbiota
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7366668/
https://www.ncbi.nlm.nih.gov/pubmed/32678209
http://dx.doi.org/10.1038/s41598-020-68718-4
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