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Substance P enhances lactic acid and tyramine production in Enterococcus faecalis V583 and promotes its cytotoxic effect on intestinal Caco-2/TC7 cells

BACKGROUND: Enterococcus faecalis, generally considered as a saprophytic bowel commensal, has recently emerged as an important nosocomial pathogen causing severe urinary tract infections, surgical wound infections, bacteremia, and bacterial endocarditis. This bacterium is capable of forming biofilms...

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Autores principales: Biaggini, Kelly, Borrel, Valérie, Szunerits, Sabine, Boukherroub, Rabah, N’Diaye, Awa, Zébré, Arthur, Bonnin-Jusserand, Maryse, Duflos, Guillaume, Feuilloley, Marc, Drider, Djamel, Déchelotte, Pierre, Connil, Nathalie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399405/
https://www.ncbi.nlm.nih.gov/pubmed/28439299
http://dx.doi.org/10.1186/s13099-017-0171-3
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author Biaggini, Kelly
Borrel, Valérie
Szunerits, Sabine
Boukherroub, Rabah
N’Diaye, Awa
Zébré, Arthur
Bonnin-Jusserand, Maryse
Duflos, Guillaume
Feuilloley, Marc
Drider, Djamel
Déchelotte, Pierre
Connil, Nathalie
author_facet Biaggini, Kelly
Borrel, Valérie
Szunerits, Sabine
Boukherroub, Rabah
N’Diaye, Awa
Zébré, Arthur
Bonnin-Jusserand, Maryse
Duflos, Guillaume
Feuilloley, Marc
Drider, Djamel
Déchelotte, Pierre
Connil, Nathalie
author_sort Biaggini, Kelly
collection PubMed
description BACKGROUND: Enterococcus faecalis, generally considered as a saprophytic bowel commensal, has recently emerged as an important nosocomial pathogen causing severe urinary tract infections, surgical wound infections, bacteremia, and bacterial endocarditis. This bacterium is capable of forming biofilms on various surfaces and its high level of antibiotic resistance contributes to its pathogenicity. The aim of this study was to evaluate the effect on E. faecalis, of Substance P (SP), an antimicrobial peptide that is produced in the gut and skin. RESULTS: We found that SP did not have antibacterial activity against E. faecalis V583 (MIC >1000 µg/ml). Conversely, SP stimulated aggregation, hydrophobicity, lactic acid and tyramine production in this bacterium. The cytotoxicity and bacterial translocation were also accelerated when E. faecalis V583 were pretreated with SP before infection of intestinal Caco-2/TC7 cells. CONCLUSION: SP can modulate the physiology of E. faecalis. Extensive studies are now needed to screen within the human microbiota which bacteria are responsive to host molecules, and to identify their sensors.
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spelling pubmed-53994052017-04-24 Substance P enhances lactic acid and tyramine production in Enterococcus faecalis V583 and promotes its cytotoxic effect on intestinal Caco-2/TC7 cells Biaggini, Kelly Borrel, Valérie Szunerits, Sabine Boukherroub, Rabah N’Diaye, Awa Zébré, Arthur Bonnin-Jusserand, Maryse Duflos, Guillaume Feuilloley, Marc Drider, Djamel Déchelotte, Pierre Connil, Nathalie Gut Pathog Research BACKGROUND: Enterococcus faecalis, generally considered as a saprophytic bowel commensal, has recently emerged as an important nosocomial pathogen causing severe urinary tract infections, surgical wound infections, bacteremia, and bacterial endocarditis. This bacterium is capable of forming biofilms on various surfaces and its high level of antibiotic resistance contributes to its pathogenicity. The aim of this study was to evaluate the effect on E. faecalis, of Substance P (SP), an antimicrobial peptide that is produced in the gut and skin. RESULTS: We found that SP did not have antibacterial activity against E. faecalis V583 (MIC >1000 µg/ml). Conversely, SP stimulated aggregation, hydrophobicity, lactic acid and tyramine production in this bacterium. The cytotoxicity and bacterial translocation were also accelerated when E. faecalis V583 were pretreated with SP before infection of intestinal Caco-2/TC7 cells. CONCLUSION: SP can modulate the physiology of E. faecalis. Extensive studies are now needed to screen within the human microbiota which bacteria are responsive to host molecules, and to identify their sensors. BioMed Central 2017-04-21 /pmc/articles/PMC5399405/ /pubmed/28439299 http://dx.doi.org/10.1186/s13099-017-0171-3 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Biaggini, Kelly
Borrel, Valérie
Szunerits, Sabine
Boukherroub, Rabah
N’Diaye, Awa
Zébré, Arthur
Bonnin-Jusserand, Maryse
Duflos, Guillaume
Feuilloley, Marc
Drider, Djamel
Déchelotte, Pierre
Connil, Nathalie
Substance P enhances lactic acid and tyramine production in Enterococcus faecalis V583 and promotes its cytotoxic effect on intestinal Caco-2/TC7 cells
title Substance P enhances lactic acid and tyramine production in Enterococcus faecalis V583 and promotes its cytotoxic effect on intestinal Caco-2/TC7 cells
title_full Substance P enhances lactic acid and tyramine production in Enterococcus faecalis V583 and promotes its cytotoxic effect on intestinal Caco-2/TC7 cells
title_fullStr Substance P enhances lactic acid and tyramine production in Enterococcus faecalis V583 and promotes its cytotoxic effect on intestinal Caco-2/TC7 cells
title_full_unstemmed Substance P enhances lactic acid and tyramine production in Enterococcus faecalis V583 and promotes its cytotoxic effect on intestinal Caco-2/TC7 cells
title_short Substance P enhances lactic acid and tyramine production in Enterococcus faecalis V583 and promotes its cytotoxic effect on intestinal Caco-2/TC7 cells
title_sort substance p enhances lactic acid and tyramine production in enterococcus faecalis v583 and promotes its cytotoxic effect on intestinal caco-2/tc7 cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399405/
https://www.ncbi.nlm.nih.gov/pubmed/28439299
http://dx.doi.org/10.1186/s13099-017-0171-3
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