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Lipoteichoic acid from Bifidobacterium animalis subsp. lactis BPL1: a novel postbiotic that reduces fat deposition via IGF‐1 pathway

Obesity and its related metabolic disorders, such as diabetes and cardiovascular disease, are major risk factors for morbidity and mortality in the world population. In this context, supplementation with the probiotic strain Bifidobacterium animalis subsp. lactis BPL1 (CECT8145) has been shown to am...

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Autores principales: Balaguer, Ferran, Enrique, María, Llopis, Silvia, Barrena, Marta, Navarro, Verónica, Álvarez, Beatriz, Chenoll, Empar, Ramón, Daniel, Tortajada, Marta, Martorell, Patricia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8913875/
https://www.ncbi.nlm.nih.gov/pubmed/33620143
http://dx.doi.org/10.1111/1751-7915.13769
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author Balaguer, Ferran
Enrique, María
Llopis, Silvia
Barrena, Marta
Navarro, Verónica
Álvarez, Beatriz
Chenoll, Empar
Ramón, Daniel
Tortajada, Marta
Martorell, Patricia
author_facet Balaguer, Ferran
Enrique, María
Llopis, Silvia
Barrena, Marta
Navarro, Verónica
Álvarez, Beatriz
Chenoll, Empar
Ramón, Daniel
Tortajada, Marta
Martorell, Patricia
author_sort Balaguer, Ferran
collection PubMed
description Obesity and its related metabolic disorders, such as diabetes and cardiovascular disease, are major risk factors for morbidity and mortality in the world population. In this context, supplementation with the probiotic strain Bifidobacterium animalis subsp. lactis BPL1 (CECT8145) has been shown to ameliorate obesity biomarkers. Analyzing the basis of this observation and using the pre‐clinical model Caenorhabditis elegans, we have found that lipoteichoic acid (LTA) of BPL1 is responsible for its fat‐reducing properties and that this attribute is preserved under hyperglycaemic conditions. This fat‐reducing capacity of both BPL1 and LTA‐BPL1 is abolished under glucose restriction, as a result of changes in LTA chemical composition. Moreover, we have demonstrated that LTA exerts this function through the IGF‐1 pathway, as does BPL1 strain. These results open the possibility of using LTA as a novel postbiotic, whose beneficial properties can be applied therapeutically and/or preventively in metabolic syndrome and diabetes‐related disorders.
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spelling pubmed-89138752022-03-17 Lipoteichoic acid from Bifidobacterium animalis subsp. lactis BPL1: a novel postbiotic that reduces fat deposition via IGF‐1 pathway Balaguer, Ferran Enrique, María Llopis, Silvia Barrena, Marta Navarro, Verónica Álvarez, Beatriz Chenoll, Empar Ramón, Daniel Tortajada, Marta Martorell, Patricia Microb Biotechnol Research Articles Obesity and its related metabolic disorders, such as diabetes and cardiovascular disease, are major risk factors for morbidity and mortality in the world population. In this context, supplementation with the probiotic strain Bifidobacterium animalis subsp. lactis BPL1 (CECT8145) has been shown to ameliorate obesity biomarkers. Analyzing the basis of this observation and using the pre‐clinical model Caenorhabditis elegans, we have found that lipoteichoic acid (LTA) of BPL1 is responsible for its fat‐reducing properties and that this attribute is preserved under hyperglycaemic conditions. This fat‐reducing capacity of both BPL1 and LTA‐BPL1 is abolished under glucose restriction, as a result of changes in LTA chemical composition. Moreover, we have demonstrated that LTA exerts this function through the IGF‐1 pathway, as does BPL1 strain. These results open the possibility of using LTA as a novel postbiotic, whose beneficial properties can be applied therapeutically and/or preventively in metabolic syndrome and diabetes‐related disorders. John Wiley and Sons Inc. 2021-02-23 /pmc/articles/PMC8913875/ /pubmed/33620143 http://dx.doi.org/10.1111/1751-7915.13769 Text en © 2021 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Balaguer, Ferran
Enrique, María
Llopis, Silvia
Barrena, Marta
Navarro, Verónica
Álvarez, Beatriz
Chenoll, Empar
Ramón, Daniel
Tortajada, Marta
Martorell, Patricia
Lipoteichoic acid from Bifidobacterium animalis subsp. lactis BPL1: a novel postbiotic that reduces fat deposition via IGF‐1 pathway
title Lipoteichoic acid from Bifidobacterium animalis subsp. lactis BPL1: a novel postbiotic that reduces fat deposition via IGF‐1 pathway
title_full Lipoteichoic acid from Bifidobacterium animalis subsp. lactis BPL1: a novel postbiotic that reduces fat deposition via IGF‐1 pathway
title_fullStr Lipoteichoic acid from Bifidobacterium animalis subsp. lactis BPL1: a novel postbiotic that reduces fat deposition via IGF‐1 pathway
title_full_unstemmed Lipoteichoic acid from Bifidobacterium animalis subsp. lactis BPL1: a novel postbiotic that reduces fat deposition via IGF‐1 pathway
title_short Lipoteichoic acid from Bifidobacterium animalis subsp. lactis BPL1: a novel postbiotic that reduces fat deposition via IGF‐1 pathway
title_sort lipoteichoic acid from bifidobacterium animalis subsp. lactis bpl1: a novel postbiotic that reduces fat deposition via igf‐1 pathway
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8913875/
https://www.ncbi.nlm.nih.gov/pubmed/33620143
http://dx.doi.org/10.1111/1751-7915.13769
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