Cargando…
Large-scale genome-wide analysis links lactic acid bacteria from food with the gut microbiome
Lactic acid bacteria (LAB) are fundamental in the production of fermented foods and several strains are regarded as probiotics. Large quantities of live LAB are consumed within fermented foods, but it is not yet known to what extent the LAB we ingest become members of the gut microbiome. By analysis...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248083/ https://www.ncbi.nlm.nih.gov/pubmed/32451391 http://dx.doi.org/10.1038/s41467-020-16438-8 |
_version_ | 1783538292153647104 |
---|---|
author | Pasolli, Edoardo De Filippis, Francesca Mauriello, Italia E. Cumbo, Fabio Walsh, Aaron M. Leech, John Cotter, Paul D. Segata, Nicola Ercolini, Danilo |
author_facet | Pasolli, Edoardo De Filippis, Francesca Mauriello, Italia E. Cumbo, Fabio Walsh, Aaron M. Leech, John Cotter, Paul D. Segata, Nicola Ercolini, Danilo |
author_sort | Pasolli, Edoardo |
collection | PubMed |
description | Lactic acid bacteria (LAB) are fundamental in the production of fermented foods and several strains are regarded as probiotics. Large quantities of live LAB are consumed within fermented foods, but it is not yet known to what extent the LAB we ingest become members of the gut microbiome. By analysis of 9445 metagenomes from human samples, we demonstrate that the prevalence and abundance of LAB species in stool samples is generally low and linked to age, lifestyle, and geography, with Streptococcus thermophilus and Lactococcus lactis being most prevalent. Moreover, we identify genome-based differences between food and gut microbes by considering 666 metagenome-assembled genomes (MAGs) newly reconstructed from fermented food microbiomes along with 154,723 human MAGs and 193,078 reference genomes. Our large-scale genome-wide analysis demonstrates that closely related LAB strains occur in both food and gut environments and provides unprecedented evidence that fermented foods can be indeed regarded as a possible source of LAB for the gut microbiome. |
format | Online Article Text |
id | pubmed-7248083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72480832020-06-03 Large-scale genome-wide analysis links lactic acid bacteria from food with the gut microbiome Pasolli, Edoardo De Filippis, Francesca Mauriello, Italia E. Cumbo, Fabio Walsh, Aaron M. Leech, John Cotter, Paul D. Segata, Nicola Ercolini, Danilo Nat Commun Article Lactic acid bacteria (LAB) are fundamental in the production of fermented foods and several strains are regarded as probiotics. Large quantities of live LAB are consumed within fermented foods, but it is not yet known to what extent the LAB we ingest become members of the gut microbiome. By analysis of 9445 metagenomes from human samples, we demonstrate that the prevalence and abundance of LAB species in stool samples is generally low and linked to age, lifestyle, and geography, with Streptococcus thermophilus and Lactococcus lactis being most prevalent. Moreover, we identify genome-based differences between food and gut microbes by considering 666 metagenome-assembled genomes (MAGs) newly reconstructed from fermented food microbiomes along with 154,723 human MAGs and 193,078 reference genomes. Our large-scale genome-wide analysis demonstrates that closely related LAB strains occur in both food and gut environments and provides unprecedented evidence that fermented foods can be indeed regarded as a possible source of LAB for the gut microbiome. Nature Publishing Group UK 2020-05-25 /pmc/articles/PMC7248083/ /pubmed/32451391 http://dx.doi.org/10.1038/s41467-020-16438-8 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 Pasolli, Edoardo De Filippis, Francesca Mauriello, Italia E. Cumbo, Fabio Walsh, Aaron M. Leech, John Cotter, Paul D. Segata, Nicola Ercolini, Danilo Large-scale genome-wide analysis links lactic acid bacteria from food with the gut microbiome |
title | Large-scale genome-wide analysis links lactic acid bacteria from food with the gut microbiome |
title_full | Large-scale genome-wide analysis links lactic acid bacteria from food with the gut microbiome |
title_fullStr | Large-scale genome-wide analysis links lactic acid bacteria from food with the gut microbiome |
title_full_unstemmed | Large-scale genome-wide analysis links lactic acid bacteria from food with the gut microbiome |
title_short | Large-scale genome-wide analysis links lactic acid bacteria from food with the gut microbiome |
title_sort | large-scale genome-wide analysis links lactic acid bacteria from food with the gut microbiome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248083/ https://www.ncbi.nlm.nih.gov/pubmed/32451391 http://dx.doi.org/10.1038/s41467-020-16438-8 |
work_keys_str_mv | AT pasolliedoardo largescalegenomewideanalysislinkslacticacidbacteriafromfoodwiththegutmicrobiome AT defilippisfrancesca largescalegenomewideanalysislinkslacticacidbacteriafromfoodwiththegutmicrobiome AT maurielloitaliae largescalegenomewideanalysislinkslacticacidbacteriafromfoodwiththegutmicrobiome AT cumbofabio largescalegenomewideanalysislinkslacticacidbacteriafromfoodwiththegutmicrobiome AT walshaaronm largescalegenomewideanalysislinkslacticacidbacteriafromfoodwiththegutmicrobiome AT leechjohn largescalegenomewideanalysislinkslacticacidbacteriafromfoodwiththegutmicrobiome AT cotterpauld largescalegenomewideanalysislinkslacticacidbacteriafromfoodwiththegutmicrobiome AT segatanicola largescalegenomewideanalysislinkslacticacidbacteriafromfoodwiththegutmicrobiome AT ercolinidanilo largescalegenomewideanalysislinkslacticacidbacteriafromfoodwiththegutmicrobiome |