Cargando…
L. rhamnosus CNCM I-3690 survival, adaptation, and small bowel microbiome impact in human
Fermented foods and beverages are a significant source of dietary bacteria that enter the gastrointestinal (GI) tract. However, little is known about how these microbes survive and adapt to the small intestinal environment. Colony-forming units (CFU) enumeration and viability qPCR of Lacticaseibacil...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10438856/ https://www.ncbi.nlm.nih.gov/pubmed/37589280 http://dx.doi.org/10.1080/19490976.2023.2244720 |
_version_ | 1785092815121809408 |
---|---|
author | Zaccaria, Edoardo Klaassen, Tim Alleleyn, Annick M.E. Boekhorst, Jos Chervaux, Christian Smokvina, Tamara Troost, Freddy J. Kleerebezem, Michiel |
author_facet | Zaccaria, Edoardo Klaassen, Tim Alleleyn, Annick M.E. Boekhorst, Jos Chervaux, Christian Smokvina, Tamara Troost, Freddy J. Kleerebezem, Michiel |
author_sort | Zaccaria, Edoardo |
collection | PubMed |
description | Fermented foods and beverages are a significant source of dietary bacteria that enter the gastrointestinal (GI) tract. However, little is known about how these microbes survive and adapt to the small intestinal environment. Colony-forming units (CFU) enumeration and viability qPCR of Lacticaseibacillus rhamnosus CNCM I-3690 in the ileal effluent of 10 ileostomy subjects during 12-h post consumption of a dairy product fermented with this strain demonstrated the high level of survival of this strain during human small intestine passage. Metatranscriptome analyses revealed the in situ transcriptome of L. rhamnosus in the small intestine, which was contrasted with transcriptome data obtained from in vitro cultivation. These comparative analyses revealed substantial metabolic adaptations of L. rhamnosus during small intestine transit, including adjustments of carbohydrate metabolism, surface-protein expression, and translation machinery. The prominent presence of L. rhamnosus in the effluent samples did not elicit an appreciable effect on the composition of the endogenous small intestine microbiome, but significantly altered the ecosystem’s overall activity profile, particularly of pathways associated with carbohydrate metabolism. Strikingly, two of the previously recognized gut-brain metabolic modules expressed in situ by L. rhamnosus (inositol degradation and glutamate synthesis II) are among the most dominantly enriched activities in the ecosystem’s activity profile. This study establishes the survival capacity of L. rhamnosus in the human small intestine and highlights its functional adjustment in situ, which we postulate to play a role in the probiotic effects associated with this strain. |
format | Online Article Text |
id | pubmed-10438856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-104388562023-08-19 L. rhamnosus CNCM I-3690 survival, adaptation, and small bowel microbiome impact in human Zaccaria, Edoardo Klaassen, Tim Alleleyn, Annick M.E. Boekhorst, Jos Chervaux, Christian Smokvina, Tamara Troost, Freddy J. Kleerebezem, Michiel Gut Microbes Research Paper Fermented foods and beverages are a significant source of dietary bacteria that enter the gastrointestinal (GI) tract. However, little is known about how these microbes survive and adapt to the small intestinal environment. Colony-forming units (CFU) enumeration and viability qPCR of Lacticaseibacillus rhamnosus CNCM I-3690 in the ileal effluent of 10 ileostomy subjects during 12-h post consumption of a dairy product fermented with this strain demonstrated the high level of survival of this strain during human small intestine passage. Metatranscriptome analyses revealed the in situ transcriptome of L. rhamnosus in the small intestine, which was contrasted with transcriptome data obtained from in vitro cultivation. These comparative analyses revealed substantial metabolic adaptations of L. rhamnosus during small intestine transit, including adjustments of carbohydrate metabolism, surface-protein expression, and translation machinery. The prominent presence of L. rhamnosus in the effluent samples did not elicit an appreciable effect on the composition of the endogenous small intestine microbiome, but significantly altered the ecosystem’s overall activity profile, particularly of pathways associated with carbohydrate metabolism. Strikingly, two of the previously recognized gut-brain metabolic modules expressed in situ by L. rhamnosus (inositol degradation and glutamate synthesis II) are among the most dominantly enriched activities in the ecosystem’s activity profile. This study establishes the survival capacity of L. rhamnosus in the human small intestine and highlights its functional adjustment in situ, which we postulate to play a role in the probiotic effects associated with this strain. Taylor & Francis 2023-08-17 /pmc/articles/PMC10438856/ /pubmed/37589280 http://dx.doi.org/10.1080/19490976.2023.2244720 Text en © 2023 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent. |
spellingShingle | Research Paper Zaccaria, Edoardo Klaassen, Tim Alleleyn, Annick M.E. Boekhorst, Jos Chervaux, Christian Smokvina, Tamara Troost, Freddy J. Kleerebezem, Michiel L. rhamnosus CNCM I-3690 survival, adaptation, and small bowel microbiome impact in human |
title | L. rhamnosus CNCM I-3690 survival, adaptation, and small bowel microbiome impact in human |
title_full | L. rhamnosus CNCM I-3690 survival, adaptation, and small bowel microbiome impact in human |
title_fullStr | L. rhamnosus CNCM I-3690 survival, adaptation, and small bowel microbiome impact in human |
title_full_unstemmed | L. rhamnosus CNCM I-3690 survival, adaptation, and small bowel microbiome impact in human |
title_short | L. rhamnosus CNCM I-3690 survival, adaptation, and small bowel microbiome impact in human |
title_sort | l. rhamnosus cncm i-3690 survival, adaptation, and small bowel microbiome impact in human |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10438856/ https://www.ncbi.nlm.nih.gov/pubmed/37589280 http://dx.doi.org/10.1080/19490976.2023.2244720 |
work_keys_str_mv | AT zaccariaedoardo lrhamnosuscncmi3690survivaladaptationandsmallbowelmicrobiomeimpactinhuman AT klaassentim lrhamnosuscncmi3690survivaladaptationandsmallbowelmicrobiomeimpactinhuman AT alleleynannickme lrhamnosuscncmi3690survivaladaptationandsmallbowelmicrobiomeimpactinhuman AT boekhorstjos lrhamnosuscncmi3690survivaladaptationandsmallbowelmicrobiomeimpactinhuman AT chervauxchristian lrhamnosuscncmi3690survivaladaptationandsmallbowelmicrobiomeimpactinhuman AT smokvinatamara lrhamnosuscncmi3690survivaladaptationandsmallbowelmicrobiomeimpactinhuman AT troostfreddyj lrhamnosuscncmi3690survivaladaptationandsmallbowelmicrobiomeimpactinhuman AT kleerebezemmichiel lrhamnosuscncmi3690survivaladaptationandsmallbowelmicrobiomeimpactinhuman |