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Food-grade cationic antimicrobial ε-polylysine transiently alters the gut microbial community and predicted metagenome function in CD-1 mice

Diet is an important factor influencing the composition and function of the gut microbiome, but the effect of antimicrobial agents present within foods is currently not understood. In this study, we investigated the effect of the food-grade cationic antimicrobial ε-polylysine on the gut microbiome s...

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Autores principales: You, Xiaomeng, Einson, Jonah E., Lopez-Pena, Cynthia Lyliam, Song, Mingyue, Xiao, Hang, McClements, David Julian, Sela, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6550245/
https://www.ncbi.nlm.nih.gov/pubmed/31304250
http://dx.doi.org/10.1038/s41538-017-0006-0
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author You, Xiaomeng
Einson, Jonah E.
Lopez-Pena, Cynthia Lyliam
Song, Mingyue
Xiao, Hang
McClements, David Julian
Sela, David A.
author_facet You, Xiaomeng
Einson, Jonah E.
Lopez-Pena, Cynthia Lyliam
Song, Mingyue
Xiao, Hang
McClements, David Julian
Sela, David A.
author_sort You, Xiaomeng
collection PubMed
description Diet is an important factor influencing the composition and function of the gut microbiome, but the effect of antimicrobial agents present within foods is currently not understood. In this study, we investigated the effect of the food-grade cationic antimicrobial ε-polylysine on the gut microbiome structure and predicted metagenomic function in a mouse model. The relative abundances of predominant phyla and genera, as well as the overall community structure, were perturbed in response to the incorporation of dietary ε-polylysine. Unexpectedly, this modification to the gut microbiome was experienced transiently and resolved to the initial basal composition at the final sampling point. In addition, a differential non-random assembly was observed in the microbiomes characterized from male and female co-housed animals, although their perturbation trajectories in response to diet remain consistent. In conclusion, antimicrobial ε-polylysine incorporated into food systems transiently alters gut microbial communities in mice, as well as their predicted function. This indicates a dynamic but resilient microbiome that adapts to microbial-active dietary components.
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spelling pubmed-65502452019-07-12 Food-grade cationic antimicrobial ε-polylysine transiently alters the gut microbial community and predicted metagenome function in CD-1 mice You, Xiaomeng Einson, Jonah E. Lopez-Pena, Cynthia Lyliam Song, Mingyue Xiao, Hang McClements, David Julian Sela, David A. NPJ Sci Food Article Diet is an important factor influencing the composition and function of the gut microbiome, but the effect of antimicrobial agents present within foods is currently not understood. In this study, we investigated the effect of the food-grade cationic antimicrobial ε-polylysine on the gut microbiome structure and predicted metagenomic function in a mouse model. The relative abundances of predominant phyla and genera, as well as the overall community structure, were perturbed in response to the incorporation of dietary ε-polylysine. Unexpectedly, this modification to the gut microbiome was experienced transiently and resolved to the initial basal composition at the final sampling point. In addition, a differential non-random assembly was observed in the microbiomes characterized from male and female co-housed animals, although their perturbation trajectories in response to diet remain consistent. In conclusion, antimicrobial ε-polylysine incorporated into food systems transiently alters gut microbial communities in mice, as well as their predicted function. This indicates a dynamic but resilient microbiome that adapts to microbial-active dietary components. Nature Publishing Group UK 2017-12-18 /pmc/articles/PMC6550245/ /pubmed/31304250 http://dx.doi.org/10.1038/s41538-017-0006-0 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
You, Xiaomeng
Einson, Jonah E.
Lopez-Pena, Cynthia Lyliam
Song, Mingyue
Xiao, Hang
McClements, David Julian
Sela, David A.
Food-grade cationic antimicrobial ε-polylysine transiently alters the gut microbial community and predicted metagenome function in CD-1 mice
title Food-grade cationic antimicrobial ε-polylysine transiently alters the gut microbial community and predicted metagenome function in CD-1 mice
title_full Food-grade cationic antimicrobial ε-polylysine transiently alters the gut microbial community and predicted metagenome function in CD-1 mice
title_fullStr Food-grade cationic antimicrobial ε-polylysine transiently alters the gut microbial community and predicted metagenome function in CD-1 mice
title_full_unstemmed Food-grade cationic antimicrobial ε-polylysine transiently alters the gut microbial community and predicted metagenome function in CD-1 mice
title_short Food-grade cationic antimicrobial ε-polylysine transiently alters the gut microbial community and predicted metagenome function in CD-1 mice
title_sort food-grade cationic antimicrobial ε-polylysine transiently alters the gut microbial community and predicted metagenome function in cd-1 mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6550245/
https://www.ncbi.nlm.nih.gov/pubmed/31304250
http://dx.doi.org/10.1038/s41538-017-0006-0
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