Cargando…

Human Milk Glycomics and Gut Microbial Genomics in Infant Feces Show a Correlation between Human Milk Oligosaccharides and Gut Microbiota: A Proof-of-Concept Study

[Image: see text] Human milk oligosaccharides (HMOs) play a key role in shaping and maintaining a healthy infant gut microbiota. This article demonstrates the potential of combining recent advances in glycomics and genomics to correlate abundances of fecal microbes and fecal HMOs. Serial fecal speci...

Descripción completa

Detalles Bibliográficos
Autores principales: De Leoz, Maria Lorna A., Kalanetra, Karen M., Bokulich, Nicholas A., Strum, John S., Underwood, Mark A., German, J. Bruce, Mills, David A., Lebrilla, Carlito B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4286166/
https://www.ncbi.nlm.nih.gov/pubmed/25300177
http://dx.doi.org/10.1021/pr500759e
_version_ 1782351648625000448
author De Leoz, Maria Lorna A.
Kalanetra, Karen M.
Bokulich, Nicholas A.
Strum, John S.
Underwood, Mark A.
German, J. Bruce
Mills, David A.
Lebrilla, Carlito B.
author_facet De Leoz, Maria Lorna A.
Kalanetra, Karen M.
Bokulich, Nicholas A.
Strum, John S.
Underwood, Mark A.
German, J. Bruce
Mills, David A.
Lebrilla, Carlito B.
author_sort De Leoz, Maria Lorna A.
collection PubMed
description [Image: see text] Human milk oligosaccharides (HMOs) play a key role in shaping and maintaining a healthy infant gut microbiota. This article demonstrates the potential of combining recent advances in glycomics and genomics to correlate abundances of fecal microbes and fecal HMOs. Serial fecal specimens from two healthy breast-fed infants were analyzed by bacterial DNA sequencing to characterize the microbiota and by mass spectrometry to determine abundances of specific HMOs that passed through the intestinal tract without being consumed by the luminal bacteria. In both infants, the fecal bacterial population shifted from non-HMO-consuming microbes to HMO-consuming bacteria during the first few weeks of life. An initial rise in fecal HMOs corresponded with bacterial populations composed primarily of non-HMO-consuming Enterobacteriaceae and Staphylococcaeae. This was followed by decreases in fecal HMOs as the proportion of HMO-consuming Bacteroidaceae and Bifidobacteriaceae increased. Analysis of HMO structures with isomer differentiation revealed that HMO consumption is highly structure-specific, with unique isomers being consumed and others passing through the gut unaltered. These results represent a proof-of-concept and are consistent with the highly selective, prebiotic effect of HMOs in shaping the gut microbiota in the first weeks of life. The analysis of selective fecal bacterial substrates as a measure of alterations in the gut microbiota may be a potential marker of dysbiosis.
format Online
Article
Text
id pubmed-4286166
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-42861662015-10-10 Human Milk Glycomics and Gut Microbial Genomics in Infant Feces Show a Correlation between Human Milk Oligosaccharides and Gut Microbiota: A Proof-of-Concept Study De Leoz, Maria Lorna A. Kalanetra, Karen M. Bokulich, Nicholas A. Strum, John S. Underwood, Mark A. German, J. Bruce Mills, David A. Lebrilla, Carlito B. J Proteome Res [Image: see text] Human milk oligosaccharides (HMOs) play a key role in shaping and maintaining a healthy infant gut microbiota. This article demonstrates the potential of combining recent advances in glycomics and genomics to correlate abundances of fecal microbes and fecal HMOs. Serial fecal specimens from two healthy breast-fed infants were analyzed by bacterial DNA sequencing to characterize the microbiota and by mass spectrometry to determine abundances of specific HMOs that passed through the intestinal tract without being consumed by the luminal bacteria. In both infants, the fecal bacterial population shifted from non-HMO-consuming microbes to HMO-consuming bacteria during the first few weeks of life. An initial rise in fecal HMOs corresponded with bacterial populations composed primarily of non-HMO-consuming Enterobacteriaceae and Staphylococcaeae. This was followed by decreases in fecal HMOs as the proportion of HMO-consuming Bacteroidaceae and Bifidobacteriaceae increased. Analysis of HMO structures with isomer differentiation revealed that HMO consumption is highly structure-specific, with unique isomers being consumed and others passing through the gut unaltered. These results represent a proof-of-concept and are consistent with the highly selective, prebiotic effect of HMOs in shaping the gut microbiota in the first weeks of life. The analysis of selective fecal bacterial substrates as a measure of alterations in the gut microbiota may be a potential marker of dysbiosis. American Chemical Society 2014-10-10 2015-01-02 /pmc/articles/PMC4286166/ /pubmed/25300177 http://dx.doi.org/10.1021/pr500759e Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle De Leoz, Maria Lorna A.
Kalanetra, Karen M.
Bokulich, Nicholas A.
Strum, John S.
Underwood, Mark A.
German, J. Bruce
Mills, David A.
Lebrilla, Carlito B.
Human Milk Glycomics and Gut Microbial Genomics in Infant Feces Show a Correlation between Human Milk Oligosaccharides and Gut Microbiota: A Proof-of-Concept Study
title Human Milk Glycomics and Gut Microbial Genomics in Infant Feces Show a Correlation between Human Milk Oligosaccharides and Gut Microbiota: A Proof-of-Concept Study
title_full Human Milk Glycomics and Gut Microbial Genomics in Infant Feces Show a Correlation between Human Milk Oligosaccharides and Gut Microbiota: A Proof-of-Concept Study
title_fullStr Human Milk Glycomics and Gut Microbial Genomics in Infant Feces Show a Correlation between Human Milk Oligosaccharides and Gut Microbiota: A Proof-of-Concept Study
title_full_unstemmed Human Milk Glycomics and Gut Microbial Genomics in Infant Feces Show a Correlation between Human Milk Oligosaccharides and Gut Microbiota: A Proof-of-Concept Study
title_short Human Milk Glycomics and Gut Microbial Genomics in Infant Feces Show a Correlation between Human Milk Oligosaccharides and Gut Microbiota: A Proof-of-Concept Study
title_sort human milk glycomics and gut microbial genomics in infant feces show a correlation between human milk oligosaccharides and gut microbiota: a proof-of-concept study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4286166/
https://www.ncbi.nlm.nih.gov/pubmed/25300177
http://dx.doi.org/10.1021/pr500759e
work_keys_str_mv AT deleozmarialornaa humanmilkglycomicsandgutmicrobialgenomicsininfantfecesshowacorrelationbetweenhumanmilkoligosaccharidesandgutmicrobiotaaproofofconceptstudy
AT kalanetrakarenm humanmilkglycomicsandgutmicrobialgenomicsininfantfecesshowacorrelationbetweenhumanmilkoligosaccharidesandgutmicrobiotaaproofofconceptstudy
AT bokulichnicholasa humanmilkglycomicsandgutmicrobialgenomicsininfantfecesshowacorrelationbetweenhumanmilkoligosaccharidesandgutmicrobiotaaproofofconceptstudy
AT strumjohns humanmilkglycomicsandgutmicrobialgenomicsininfantfecesshowacorrelationbetweenhumanmilkoligosaccharidesandgutmicrobiotaaproofofconceptstudy
AT underwoodmarka humanmilkglycomicsandgutmicrobialgenomicsininfantfecesshowacorrelationbetweenhumanmilkoligosaccharidesandgutmicrobiotaaproofofconceptstudy
AT germanjbruce humanmilkglycomicsandgutmicrobialgenomicsininfantfecesshowacorrelationbetweenhumanmilkoligosaccharidesandgutmicrobiotaaproofofconceptstudy
AT millsdavida humanmilkglycomicsandgutmicrobialgenomicsininfantfecesshowacorrelationbetweenhumanmilkoligosaccharidesandgutmicrobiotaaproofofconceptstudy
AT lebrillacarlitob humanmilkglycomicsandgutmicrobialgenomicsininfantfecesshowacorrelationbetweenhumanmilkoligosaccharidesandgutmicrobiotaaproofofconceptstudy