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Intraspecific Diversity of Microbial Anti-Inflammatory Molecule (MAM) from Faecalibacterium prausnitzii
The commensal bacterium Faecalibacterium prausnitzii has unique anti-inflammatory properties, at least some of which have been attributed to its production of MAM, the Microbial Anti-inflammatory Molecule. Previous phylogenetic studies of F. prausnitzii strains have revealed the existence of various...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836110/ https://www.ncbi.nlm.nih.gov/pubmed/35163630 http://dx.doi.org/10.3390/ijms23031705 |
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author | Auger, Sandrine Kropp, Camille Borras-Nogues, Esther Chanput, Wasaporn Andre-Leroux, Gwenaelle Gitton-Quent, Oscar Benevides, Leandro Breyner, Natalia Azevedo, Vasco Langella, Philippe Chatel, Jean-Marc |
author_facet | Auger, Sandrine Kropp, Camille Borras-Nogues, Esther Chanput, Wasaporn Andre-Leroux, Gwenaelle Gitton-Quent, Oscar Benevides, Leandro Breyner, Natalia Azevedo, Vasco Langella, Philippe Chatel, Jean-Marc |
author_sort | Auger, Sandrine |
collection | PubMed |
description | The commensal bacterium Faecalibacterium prausnitzii has unique anti-inflammatory properties, at least some of which have been attributed to its production of MAM, the Microbial Anti-inflammatory Molecule. Previous phylogenetic studies of F. prausnitzii strains have revealed the existence of various phylogroups. In this work, we address the question of whether MAMs from different phylogroups display distinct anti-inflammatory properties. We first performed wide-scale identification, classification, and phylogenetic analysis of MAM-like proteins encoded in different genomes of F. prausnitzii. When combined with a gene context analysis, this approach distinguished at least 10 distinct clusters of MAMs, providing evidence for functional diversity within this protein. We then selected 11 MAMs from various clusters and evaluated their anti-inflammatory capacities in vitro. A wide range of anti-inflammatory activity was detected. MAM from the M21/2 strain had the highest inhibitory effect (96% inhibition), while MAM from reference strain A2-165 demonstrated only 56% inhibition, and MAM from strain CNCM4541 was almost inactive. These results were confirmed in vivo in murine models of acute and chronic colitis. This study provides insights into the family of MAM proteins and generates clues regarding the choice of F. prausnitzii strains as probiotics for use in targeting chronic inflammatory diseases. |
format | Online Article Text |
id | pubmed-8836110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88361102022-02-12 Intraspecific Diversity of Microbial Anti-Inflammatory Molecule (MAM) from Faecalibacterium prausnitzii Auger, Sandrine Kropp, Camille Borras-Nogues, Esther Chanput, Wasaporn Andre-Leroux, Gwenaelle Gitton-Quent, Oscar Benevides, Leandro Breyner, Natalia Azevedo, Vasco Langella, Philippe Chatel, Jean-Marc Int J Mol Sci Article The commensal bacterium Faecalibacterium prausnitzii has unique anti-inflammatory properties, at least some of which have been attributed to its production of MAM, the Microbial Anti-inflammatory Molecule. Previous phylogenetic studies of F. prausnitzii strains have revealed the existence of various phylogroups. In this work, we address the question of whether MAMs from different phylogroups display distinct anti-inflammatory properties. We first performed wide-scale identification, classification, and phylogenetic analysis of MAM-like proteins encoded in different genomes of F. prausnitzii. When combined with a gene context analysis, this approach distinguished at least 10 distinct clusters of MAMs, providing evidence for functional diversity within this protein. We then selected 11 MAMs from various clusters and evaluated their anti-inflammatory capacities in vitro. A wide range of anti-inflammatory activity was detected. MAM from the M21/2 strain had the highest inhibitory effect (96% inhibition), while MAM from reference strain A2-165 demonstrated only 56% inhibition, and MAM from strain CNCM4541 was almost inactive. These results were confirmed in vivo in murine models of acute and chronic colitis. This study provides insights into the family of MAM proteins and generates clues regarding the choice of F. prausnitzii strains as probiotics for use in targeting chronic inflammatory diseases. MDPI 2022-02-01 /pmc/articles/PMC8836110/ /pubmed/35163630 http://dx.doi.org/10.3390/ijms23031705 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 Auger, Sandrine Kropp, Camille Borras-Nogues, Esther Chanput, Wasaporn Andre-Leroux, Gwenaelle Gitton-Quent, Oscar Benevides, Leandro Breyner, Natalia Azevedo, Vasco Langella, Philippe Chatel, Jean-Marc Intraspecific Diversity of Microbial Anti-Inflammatory Molecule (MAM) from Faecalibacterium prausnitzii |
title | Intraspecific Diversity of Microbial Anti-Inflammatory Molecule (MAM) from Faecalibacterium prausnitzii |
title_full | Intraspecific Diversity of Microbial Anti-Inflammatory Molecule (MAM) from Faecalibacterium prausnitzii |
title_fullStr | Intraspecific Diversity of Microbial Anti-Inflammatory Molecule (MAM) from Faecalibacterium prausnitzii |
title_full_unstemmed | Intraspecific Diversity of Microbial Anti-Inflammatory Molecule (MAM) from Faecalibacterium prausnitzii |
title_short | Intraspecific Diversity of Microbial Anti-Inflammatory Molecule (MAM) from Faecalibacterium prausnitzii |
title_sort | intraspecific diversity of microbial anti-inflammatory molecule (mam) from faecalibacterium prausnitzii |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836110/ https://www.ncbi.nlm.nih.gov/pubmed/35163630 http://dx.doi.org/10.3390/ijms23031705 |
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