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Identification of an analgesic lipopeptide produced by the probiotic Escherichia coli strain Nissle 1917
Administration of the probiotic Escherichia coli strain Nissle 1917 (EcN) decreases visceral pain associated with irritable bowel syndrome. Mutation of clbA, a gene involved in the biosynthesis of secondary metabolites, including colibactin, was previously shown to abrogate EcN probiotic activity. H...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670229/ https://www.ncbi.nlm.nih.gov/pubmed/29101366 http://dx.doi.org/10.1038/s41467-017-01403-9 |
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author | Pérez-Berezo, Teresa Pujo, Julien Martin, Patricia Le Faouder, Pauline Galano, Jean-Marie Guy, Alexandre Knauf, Claude Tabet, Jean Claude Tronnet, Sophie Barreau, Frederick Heuillet, Maud Dietrich, Gilles Bertrand-Michel, Justine Durand, Thierry Oswald, Eric Cenac, Nicolas |
author_facet | Pérez-Berezo, Teresa Pujo, Julien Martin, Patricia Le Faouder, Pauline Galano, Jean-Marie Guy, Alexandre Knauf, Claude Tabet, Jean Claude Tronnet, Sophie Barreau, Frederick Heuillet, Maud Dietrich, Gilles Bertrand-Michel, Justine Durand, Thierry Oswald, Eric Cenac, Nicolas |
author_sort | Pérez-Berezo, Teresa |
collection | PubMed |
description | Administration of the probiotic Escherichia coli strain Nissle 1917 (EcN) decreases visceral pain associated with irritable bowel syndrome. Mutation of clbA, a gene involved in the biosynthesis of secondary metabolites, including colibactin, was previously shown to abrogate EcN probiotic activity. Here, we show that EcN, but not an isogenic clbA mutant, produces an analgesic lipopeptide. We characterize lipoamino acids and lipopeptides produced by EcN but not by the mutant by online liquid chromatography mass spectrometry. One of these lipopeptides, C12AsnGABAOH, is able to cross the epithelial barrier and to inhibit calcium flux induced by nociceptor activation in sensory neurons via the GABA(B) receptor. C12AsnGABAOH inhibits visceral hypersensitivity induced by nociceptor activation in mice. Thus, EcN produces a visceral analgesic, which could be the basis for the development of new visceral pain therapies. |
format | Online Article Text |
id | pubmed-5670229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56702292017-11-07 Identification of an analgesic lipopeptide produced by the probiotic Escherichia coli strain Nissle 1917 Pérez-Berezo, Teresa Pujo, Julien Martin, Patricia Le Faouder, Pauline Galano, Jean-Marie Guy, Alexandre Knauf, Claude Tabet, Jean Claude Tronnet, Sophie Barreau, Frederick Heuillet, Maud Dietrich, Gilles Bertrand-Michel, Justine Durand, Thierry Oswald, Eric Cenac, Nicolas Nat Commun Article Administration of the probiotic Escherichia coli strain Nissle 1917 (EcN) decreases visceral pain associated with irritable bowel syndrome. Mutation of clbA, a gene involved in the biosynthesis of secondary metabolites, including colibactin, was previously shown to abrogate EcN probiotic activity. Here, we show that EcN, but not an isogenic clbA mutant, produces an analgesic lipopeptide. We characterize lipoamino acids and lipopeptides produced by EcN but not by the mutant by online liquid chromatography mass spectrometry. One of these lipopeptides, C12AsnGABAOH, is able to cross the epithelial barrier and to inhibit calcium flux induced by nociceptor activation in sensory neurons via the GABA(B) receptor. C12AsnGABAOH inhibits visceral hypersensitivity induced by nociceptor activation in mice. Thus, EcN produces a visceral analgesic, which could be the basis for the development of new visceral pain therapies. Nature Publishing Group UK 2017-11-03 /pmc/articles/PMC5670229/ /pubmed/29101366 http://dx.doi.org/10.1038/s41467-017-01403-9 Text en © The Author(s) 2017 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 Pérez-Berezo, Teresa Pujo, Julien Martin, Patricia Le Faouder, Pauline Galano, Jean-Marie Guy, Alexandre Knauf, Claude Tabet, Jean Claude Tronnet, Sophie Barreau, Frederick Heuillet, Maud Dietrich, Gilles Bertrand-Michel, Justine Durand, Thierry Oswald, Eric Cenac, Nicolas Identification of an analgesic lipopeptide produced by the probiotic Escherichia coli strain Nissle 1917 |
title | Identification of an analgesic lipopeptide produced by the probiotic Escherichia coli strain Nissle 1917 |
title_full | Identification of an analgesic lipopeptide produced by the probiotic Escherichia coli strain Nissle 1917 |
title_fullStr | Identification of an analgesic lipopeptide produced by the probiotic Escherichia coli strain Nissle 1917 |
title_full_unstemmed | Identification of an analgesic lipopeptide produced by the probiotic Escherichia coli strain Nissle 1917 |
title_short | Identification of an analgesic lipopeptide produced by the probiotic Escherichia coli strain Nissle 1917 |
title_sort | identification of an analgesic lipopeptide produced by the probiotic escherichia coli strain nissle 1917 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670229/ https://www.ncbi.nlm.nih.gov/pubmed/29101366 http://dx.doi.org/10.1038/s41467-017-01403-9 |
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