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Bifidobacterium longum subsp. infantis CECT 7210 Reduces Inflammatory Cytokine Secretion in Caco-2 Cells Cultured in the Presence of Escherichia coli CECT 515

Previous works have described the activity of Bifidobacterium longum subsp. infantis CECT 7210 (also commercially named B. infantis IM-1(®)) against rotavirus in mice and intestinal pathogens in piglets, as well as its diarrhea-reducing effect on healthy term infants. In the present work, we focused...

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Autores principales: Álvarez-Mercado, Ana I., Plaza-Díaz, Julio, de Almagro, M. Cristina, Gil, Ángel, Moreno-Muñoz, José Antonio, Fontana, Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503999/
https://www.ncbi.nlm.nih.gov/pubmed/36142723
http://dx.doi.org/10.3390/ijms231810813
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author Álvarez-Mercado, Ana I.
Plaza-Díaz, Julio
de Almagro, M. Cristina
Gil, Ángel
Moreno-Muñoz, José Antonio
Fontana, Luis
author_facet Álvarez-Mercado, Ana I.
Plaza-Díaz, Julio
de Almagro, M. Cristina
Gil, Ángel
Moreno-Muñoz, José Antonio
Fontana, Luis
author_sort Álvarez-Mercado, Ana I.
collection PubMed
description Previous works have described the activity of Bifidobacterium longum subsp. infantis CECT 7210 (also commercially named B. infantis IM-1(®)) against rotavirus in mice and intestinal pathogens in piglets, as well as its diarrhea-reducing effect on healthy term infants. In the present work, we focused on the intestinal immunomodulatory effects of B. infantis IM-1(®) and for this purpose we used the epithelial cell line isolated from colorectal adenocarcinoma Caco-2 and a co-culture system of human dendritic cells (DCs) from peripheral blood together with Caco-2 cells. Single Caco-2 cultures and Caco-2: DC co-cultures were incubated with B. infantis IM-1(®) or its supernatant either in the presence or absence of Escherichia coli CECT 515. The B. infantis IM-1(®) supernatant exerted a protective effect against the cytotoxicity caused by Escherichia coli CECT 515 on single cultures of Caco-2 cells as viability reached the values of untreated cells. B. infantis IM-1(®) and its supernatant also decreased the secretion of pro-inflammatory cytokines by Caco-2 cells and the co-cultures incubated in the presence of E. coli CECT 515, with the response being more modest in the latter, which suggests that DCs modulate the activity of Caco-2 cells. Overall, the results obtained point to the immunomodulatory activity of this probiotic strain, which might underlie its previously reported beneficial effects.
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spelling pubmed-95039992022-09-24 Bifidobacterium longum subsp. infantis CECT 7210 Reduces Inflammatory Cytokine Secretion in Caco-2 Cells Cultured in the Presence of Escherichia coli CECT 515 Álvarez-Mercado, Ana I. Plaza-Díaz, Julio de Almagro, M. Cristina Gil, Ángel Moreno-Muñoz, José Antonio Fontana, Luis Int J Mol Sci Article Previous works have described the activity of Bifidobacterium longum subsp. infantis CECT 7210 (also commercially named B. infantis IM-1(®)) against rotavirus in mice and intestinal pathogens in piglets, as well as its diarrhea-reducing effect on healthy term infants. In the present work, we focused on the intestinal immunomodulatory effects of B. infantis IM-1(®) and for this purpose we used the epithelial cell line isolated from colorectal adenocarcinoma Caco-2 and a co-culture system of human dendritic cells (DCs) from peripheral blood together with Caco-2 cells. Single Caco-2 cultures and Caco-2: DC co-cultures were incubated with B. infantis IM-1(®) or its supernatant either in the presence or absence of Escherichia coli CECT 515. The B. infantis IM-1(®) supernatant exerted a protective effect against the cytotoxicity caused by Escherichia coli CECT 515 on single cultures of Caco-2 cells as viability reached the values of untreated cells. B. infantis IM-1(®) and its supernatant also decreased the secretion of pro-inflammatory cytokines by Caco-2 cells and the co-cultures incubated in the presence of E. coli CECT 515, with the response being more modest in the latter, which suggests that DCs modulate the activity of Caco-2 cells. Overall, the results obtained point to the immunomodulatory activity of this probiotic strain, which might underlie its previously reported beneficial effects. MDPI 2022-09-16 /pmc/articles/PMC9503999/ /pubmed/36142723 http://dx.doi.org/10.3390/ijms231810813 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Álvarez-Mercado, Ana I.
Plaza-Díaz, Julio
de Almagro, M. Cristina
Gil, Ángel
Moreno-Muñoz, José Antonio
Fontana, Luis
Bifidobacterium longum subsp. infantis CECT 7210 Reduces Inflammatory Cytokine Secretion in Caco-2 Cells Cultured in the Presence of Escherichia coli CECT 515
title Bifidobacterium longum subsp. infantis CECT 7210 Reduces Inflammatory Cytokine Secretion in Caco-2 Cells Cultured in the Presence of Escherichia coli CECT 515
title_full Bifidobacterium longum subsp. infantis CECT 7210 Reduces Inflammatory Cytokine Secretion in Caco-2 Cells Cultured in the Presence of Escherichia coli CECT 515
title_fullStr Bifidobacterium longum subsp. infantis CECT 7210 Reduces Inflammatory Cytokine Secretion in Caco-2 Cells Cultured in the Presence of Escherichia coli CECT 515
title_full_unstemmed Bifidobacterium longum subsp. infantis CECT 7210 Reduces Inflammatory Cytokine Secretion in Caco-2 Cells Cultured in the Presence of Escherichia coli CECT 515
title_short Bifidobacterium longum subsp. infantis CECT 7210 Reduces Inflammatory Cytokine Secretion in Caco-2 Cells Cultured in the Presence of Escherichia coli CECT 515
title_sort bifidobacterium longum subsp. infantis cect 7210 reduces inflammatory cytokine secretion in caco-2 cells cultured in the presence of escherichia coli cect 515
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503999/
https://www.ncbi.nlm.nih.gov/pubmed/36142723
http://dx.doi.org/10.3390/ijms231810813
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