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Saccharomyces boulardii CNCM I-745 Modulates the Fecal Bile Acids Metabolism During Antimicrobial Therapy in Healthy Volunteers

Saccharomyces boulardii CNCM I-745 (SB) is a probiotic yeast used to lower the incidence of antibiotic-associated Clostridium difficile (C. difficile) infection, though its mechanism of action remains unclear. Cholic acid is a primary bile acid, which triggers the germination and promotes the growth...

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Autores principales: Kelly, Ciaran Patrick, Chong Nguyen, Caroline, Palmieri, Lola Jade, Pallav, Kumar, Dowd, Scot E., Humbert, Lydie, Seksik, Philippe, Bado, Andre, Coffin, Benoit, Rainteau, Dominique, Kabbani, Toufic, Duboc, Henri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407479/
https://www.ncbi.nlm.nih.gov/pubmed/30881353
http://dx.doi.org/10.3389/fmicb.2019.00336
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author Kelly, Ciaran Patrick
Chong Nguyen, Caroline
Palmieri, Lola Jade
Pallav, Kumar
Dowd, Scot E.
Humbert, Lydie
Seksik, Philippe
Bado, Andre
Coffin, Benoit
Rainteau, Dominique
Kabbani, Toufic
Duboc, Henri
author_facet Kelly, Ciaran Patrick
Chong Nguyen, Caroline
Palmieri, Lola Jade
Pallav, Kumar
Dowd, Scot E.
Humbert, Lydie
Seksik, Philippe
Bado, Andre
Coffin, Benoit
Rainteau, Dominique
Kabbani, Toufic
Duboc, Henri
author_sort Kelly, Ciaran Patrick
collection PubMed
description Saccharomyces boulardii CNCM I-745 (SB) is a probiotic yeast used to lower the incidence of antibiotic-associated Clostridium difficile (C. difficile) infection, though its mechanism of action remains unclear. Cholic acid is a primary bile acid, which triggers the germination and promotes the growth of C. difficile. The intestinal microbiota transforms primary into secondary bile acids. This study examined (1) the antimicrobial-induced alteration of fecal bile acid content, and (2) whether the concomitant administration of SB influences this transformation. This is an ancillary work from a randomized study, which revealed that SB modulates fecal microbiota dysbiosis during antibiotic treatment. Healthy subjects were randomly assigned to (1) SB only, (2) amoxicillin-clavulanate (AC), (3) SB plus AC, or (4) no treatment. We analyzed fecal concentrations of BA by high performance liquid chromatography/tandem mass spectrometry. Compared to the untreated or the SB-treated groups, AC decreased the percentage of fecal secondary BA significantly (days 3 and 7). When SB and AC were administered concomitantly, this decrease in secondary BA was no longer significant. Following treatment with AC, a significant peak of fecal CA was measured on days 3 and 7, which was prevented by the concomitant administration of SB. AC administered to healthy volunteers altered the microbial transformation of primary BA, decreased secondary BA, and increased CA. The latter was prevented by the concomitant administration of SB and AC, suggesting a potent mechanism protection conferred by SB against post-antimicrobial C. difficile infection. Clinical Trial Registration: www.ClinicalTrials.gov, identifier NCT01473368.
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spelling pubmed-64074792019-03-15 Saccharomyces boulardii CNCM I-745 Modulates the Fecal Bile Acids Metabolism During Antimicrobial Therapy in Healthy Volunteers Kelly, Ciaran Patrick Chong Nguyen, Caroline Palmieri, Lola Jade Pallav, Kumar Dowd, Scot E. Humbert, Lydie Seksik, Philippe Bado, Andre Coffin, Benoit Rainteau, Dominique Kabbani, Toufic Duboc, Henri Front Microbiol Microbiology Saccharomyces boulardii CNCM I-745 (SB) is a probiotic yeast used to lower the incidence of antibiotic-associated Clostridium difficile (C. difficile) infection, though its mechanism of action remains unclear. Cholic acid is a primary bile acid, which triggers the germination and promotes the growth of C. difficile. The intestinal microbiota transforms primary into secondary bile acids. This study examined (1) the antimicrobial-induced alteration of fecal bile acid content, and (2) whether the concomitant administration of SB influences this transformation. This is an ancillary work from a randomized study, which revealed that SB modulates fecal microbiota dysbiosis during antibiotic treatment. Healthy subjects were randomly assigned to (1) SB only, (2) amoxicillin-clavulanate (AC), (3) SB plus AC, or (4) no treatment. We analyzed fecal concentrations of BA by high performance liquid chromatography/tandem mass spectrometry. Compared to the untreated or the SB-treated groups, AC decreased the percentage of fecal secondary BA significantly (days 3 and 7). When SB and AC were administered concomitantly, this decrease in secondary BA was no longer significant. Following treatment with AC, a significant peak of fecal CA was measured on days 3 and 7, which was prevented by the concomitant administration of SB. AC administered to healthy volunteers altered the microbial transformation of primary BA, decreased secondary BA, and increased CA. The latter was prevented by the concomitant administration of SB and AC, suggesting a potent mechanism protection conferred by SB against post-antimicrobial C. difficile infection. Clinical Trial Registration: www.ClinicalTrials.gov, identifier NCT01473368. Frontiers Media S.A. 2019-03-04 /pmc/articles/PMC6407479/ /pubmed/30881353 http://dx.doi.org/10.3389/fmicb.2019.00336 Text en Copyright © 2019 Kelly, Chong Nguyen, Palmieri, Pallav, Dowd, Humbert, Seksik, Bado, Coffin, Rainteau, Kabbani and Duboc. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Kelly, Ciaran Patrick
Chong Nguyen, Caroline
Palmieri, Lola Jade
Pallav, Kumar
Dowd, Scot E.
Humbert, Lydie
Seksik, Philippe
Bado, Andre
Coffin, Benoit
Rainteau, Dominique
Kabbani, Toufic
Duboc, Henri
Saccharomyces boulardii CNCM I-745 Modulates the Fecal Bile Acids Metabolism During Antimicrobial Therapy in Healthy Volunteers
title Saccharomyces boulardii CNCM I-745 Modulates the Fecal Bile Acids Metabolism During Antimicrobial Therapy in Healthy Volunteers
title_full Saccharomyces boulardii CNCM I-745 Modulates the Fecal Bile Acids Metabolism During Antimicrobial Therapy in Healthy Volunteers
title_fullStr Saccharomyces boulardii CNCM I-745 Modulates the Fecal Bile Acids Metabolism During Antimicrobial Therapy in Healthy Volunteers
title_full_unstemmed Saccharomyces boulardii CNCM I-745 Modulates the Fecal Bile Acids Metabolism During Antimicrobial Therapy in Healthy Volunteers
title_short Saccharomyces boulardii CNCM I-745 Modulates the Fecal Bile Acids Metabolism During Antimicrobial Therapy in Healthy Volunteers
title_sort saccharomyces boulardii cncm i-745 modulates the fecal bile acids metabolism during antimicrobial therapy in healthy volunteers
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407479/
https://www.ncbi.nlm.nih.gov/pubmed/30881353
http://dx.doi.org/10.3389/fmicb.2019.00336
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