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Coffee Consumption Modulates Amoxicillin-Induced Dysbiosis in the Murine Gut Microbiome

The microbiome is essential for host health, and perturbations resulting from antibiotic use can lead to dysbiosis and disease. Diet can be a powerful modulator of microbiome composition and function, with the potential to mitigate the negative effects of antibiotic use. Thus, it is necessary to stu...

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Autores principales: Diamond, Emma, Hewlett, Katharine, Penumutchu, Swathi, Belenky, Alexei, Belenky, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8278525/
https://www.ncbi.nlm.nih.gov/pubmed/34276581
http://dx.doi.org/10.3389/fmicb.2021.637282
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author Diamond, Emma
Hewlett, Katharine
Penumutchu, Swathi
Belenky, Alexei
Belenky, Peter
author_facet Diamond, Emma
Hewlett, Katharine
Penumutchu, Swathi
Belenky, Alexei
Belenky, Peter
author_sort Diamond, Emma
collection PubMed
description The microbiome is essential for host health, and perturbations resulting from antibiotic use can lead to dysbiosis and disease. Diet can be a powerful modulator of microbiome composition and function, with the potential to mitigate the negative effects of antibiotic use. Thus, it is necessary to study the impacts of diet and drug interactions on the gut microbiome. Coffee is a commonly consumed beverage containing many compounds that have the potential to affect the microbiome, including caffeine, polyphenols, and fiber. We supplemented mice with caffeinated and decaffeinated coffee in conjunction with amoxicillin, and used 16S rRNA amplicon sequencing of fecal samples to investigate changes in diversity and composition of the murine fecal microbiome. We found that antibiotics, regardless of coffee supplementation, caused significant disruption to the murine fecal microbiome, enriching for Proteobacteria, Verrucomicrobia, and Bacteroidetes, but reducing Firmicutes. While we found that coffee alone did not have a significant impact on the composition of the fecal microbiome, coffee supplementation did significantly affect relative abundance metrics in mice treated with amoxicillin. After caffeinated coffee supplementation, mice treated with amoxicillin showed a smaller increase in Proteobacteria, specifically of the family Burkholderiaceae. Correspondingly we found that in vitro, Burkholderia cepacia was highly resistant to amoxicillin, and that it was inhibited by concentrations of caffeine and caffeinated coffee comparable to levels of caffeine in murine ceca. Overall, this work shows that coffee, and possibly the caffeine component, can impact both the microbiome and microbiome members during antibiotic exposure.
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spelling pubmed-82785252021-07-15 Coffee Consumption Modulates Amoxicillin-Induced Dysbiosis in the Murine Gut Microbiome Diamond, Emma Hewlett, Katharine Penumutchu, Swathi Belenky, Alexei Belenky, Peter Front Microbiol Microbiology The microbiome is essential for host health, and perturbations resulting from antibiotic use can lead to dysbiosis and disease. Diet can be a powerful modulator of microbiome composition and function, with the potential to mitigate the negative effects of antibiotic use. Thus, it is necessary to study the impacts of diet and drug interactions on the gut microbiome. Coffee is a commonly consumed beverage containing many compounds that have the potential to affect the microbiome, including caffeine, polyphenols, and fiber. We supplemented mice with caffeinated and decaffeinated coffee in conjunction with amoxicillin, and used 16S rRNA amplicon sequencing of fecal samples to investigate changes in diversity and composition of the murine fecal microbiome. We found that antibiotics, regardless of coffee supplementation, caused significant disruption to the murine fecal microbiome, enriching for Proteobacteria, Verrucomicrobia, and Bacteroidetes, but reducing Firmicutes. While we found that coffee alone did not have a significant impact on the composition of the fecal microbiome, coffee supplementation did significantly affect relative abundance metrics in mice treated with amoxicillin. After caffeinated coffee supplementation, mice treated with amoxicillin showed a smaller increase in Proteobacteria, specifically of the family Burkholderiaceae. Correspondingly we found that in vitro, Burkholderia cepacia was highly resistant to amoxicillin, and that it was inhibited by concentrations of caffeine and caffeinated coffee comparable to levels of caffeine in murine ceca. Overall, this work shows that coffee, and possibly the caffeine component, can impact both the microbiome and microbiome members during antibiotic exposure. Frontiers Media S.A. 2021-06-30 /pmc/articles/PMC8278525/ /pubmed/34276581 http://dx.doi.org/10.3389/fmicb.2021.637282 Text en Copyright © 2021 Diamond, Hewlett, Penumutchu, Belenky and Belenky. https://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
Diamond, Emma
Hewlett, Katharine
Penumutchu, Swathi
Belenky, Alexei
Belenky, Peter
Coffee Consumption Modulates Amoxicillin-Induced Dysbiosis in the Murine Gut Microbiome
title Coffee Consumption Modulates Amoxicillin-Induced Dysbiosis in the Murine Gut Microbiome
title_full Coffee Consumption Modulates Amoxicillin-Induced Dysbiosis in the Murine Gut Microbiome
title_fullStr Coffee Consumption Modulates Amoxicillin-Induced Dysbiosis in the Murine Gut Microbiome
title_full_unstemmed Coffee Consumption Modulates Amoxicillin-Induced Dysbiosis in the Murine Gut Microbiome
title_short Coffee Consumption Modulates Amoxicillin-Induced Dysbiosis in the Murine Gut Microbiome
title_sort coffee consumption modulates amoxicillin-induced dysbiosis in the murine gut microbiome
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8278525/
https://www.ncbi.nlm.nih.gov/pubmed/34276581
http://dx.doi.org/10.3389/fmicb.2021.637282
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