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Akkermansia muciniphila uses human milk oligosaccharides to thrive in the early life conditions in vitro
Akkermansia muciniphila is a well-studied anaerobic bacterium specialized in mucus degradation and associated with human health. Because of the structural resemblance of mucus glycans and free human milk oligosaccharides (HMOs), we studied the ability of A. muciniphila to utilize human milk oligosac...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459334/ https://www.ncbi.nlm.nih.gov/pubmed/32868839 http://dx.doi.org/10.1038/s41598-020-71113-8 |
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author | Kostopoulos, Ioannis Elzinga, Janneke Ottman, Noora Klievink, Jay T. Blijenberg, Bernadet Aalvink, Steven Boeren, Sjef Mank, Marko Knol, Jan de Vos, Willem M. Belzer, Clara |
author_facet | Kostopoulos, Ioannis Elzinga, Janneke Ottman, Noora Klievink, Jay T. Blijenberg, Bernadet Aalvink, Steven Boeren, Sjef Mank, Marko Knol, Jan de Vos, Willem M. Belzer, Clara |
author_sort | Kostopoulos, Ioannis |
collection | PubMed |
description | Akkermansia muciniphila is a well-studied anaerobic bacterium specialized in mucus degradation and associated with human health. Because of the structural resemblance of mucus glycans and free human milk oligosaccharides (HMOs), we studied the ability of A. muciniphila to utilize human milk oligosaccharides. We found that A. muciniphila was able to grow on human milk and degrade HMOs. Analyses of the proteome of A. muciniphila indicated that key-glycan degrading enzymes were expressed when the bacterium was grown on human milk. Our results display the functionality of the key-glycan degrading enzymes (α-l-fucosidases, β-galactosidases, exo-α-sialidases and β-acetylhexosaminidases) to degrade the HMO-structures 2′-FL, LNT, lactose, and LNT2. The hydrolysation of the host-derived glycan structures allows A. muciniphila to promote syntrophy with other beneficial bacteria, contributing in that way to a microbial ecological network in the gut. Thus, the capacity of A. muciniphila to utilize human milk will enable its survival in the early life intestine and colonization of the mucosal layer in early life, warranting later life mucosal and metabolic health. |
format | Online Article Text |
id | pubmed-7459334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74593342020-09-01 Akkermansia muciniphila uses human milk oligosaccharides to thrive in the early life conditions in vitro Kostopoulos, Ioannis Elzinga, Janneke Ottman, Noora Klievink, Jay T. Blijenberg, Bernadet Aalvink, Steven Boeren, Sjef Mank, Marko Knol, Jan de Vos, Willem M. Belzer, Clara Sci Rep Article Akkermansia muciniphila is a well-studied anaerobic bacterium specialized in mucus degradation and associated with human health. Because of the structural resemblance of mucus glycans and free human milk oligosaccharides (HMOs), we studied the ability of A. muciniphila to utilize human milk oligosaccharides. We found that A. muciniphila was able to grow on human milk and degrade HMOs. Analyses of the proteome of A. muciniphila indicated that key-glycan degrading enzymes were expressed when the bacterium was grown on human milk. Our results display the functionality of the key-glycan degrading enzymes (α-l-fucosidases, β-galactosidases, exo-α-sialidases and β-acetylhexosaminidases) to degrade the HMO-structures 2′-FL, LNT, lactose, and LNT2. The hydrolysation of the host-derived glycan structures allows A. muciniphila to promote syntrophy with other beneficial bacteria, contributing in that way to a microbial ecological network in the gut. Thus, the capacity of A. muciniphila to utilize human milk will enable its survival in the early life intestine and colonization of the mucosal layer in early life, warranting later life mucosal and metabolic health. Nature Publishing Group UK 2020-08-31 /pmc/articles/PMC7459334/ /pubmed/32868839 http://dx.doi.org/10.1038/s41598-020-71113-8 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 Kostopoulos, Ioannis Elzinga, Janneke Ottman, Noora Klievink, Jay T. Blijenberg, Bernadet Aalvink, Steven Boeren, Sjef Mank, Marko Knol, Jan de Vos, Willem M. Belzer, Clara Akkermansia muciniphila uses human milk oligosaccharides to thrive in the early life conditions in vitro |
title | Akkermansia muciniphila uses human milk oligosaccharides to thrive in the early life conditions in vitro |
title_full | Akkermansia muciniphila uses human milk oligosaccharides to thrive in the early life conditions in vitro |
title_fullStr | Akkermansia muciniphila uses human milk oligosaccharides to thrive in the early life conditions in vitro |
title_full_unstemmed | Akkermansia muciniphila uses human milk oligosaccharides to thrive in the early life conditions in vitro |
title_short | Akkermansia muciniphila uses human milk oligosaccharides to thrive in the early life conditions in vitro |
title_sort | akkermansia muciniphila uses human milk oligosaccharides to thrive in the early life conditions in vitro |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459334/ https://www.ncbi.nlm.nih.gov/pubmed/32868839 http://dx.doi.org/10.1038/s41598-020-71113-8 |
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