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Effects of long-term antibiotic treatment on mice urinary aromatic amino acid profiles
The gut microbiota–host co-metabolites are good indicators for representing the cross-talk between host and gut microbiota in a bi-direct manner. There is increasing evidence that levels of aromatic amino acids (AAAs) are associated with the alteration of intestinal microbial community though the ef...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7786327/ https://www.ncbi.nlm.nih.gov/pubmed/33269386 http://dx.doi.org/10.1042/BSR20203498 |
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author | Zhu, Xuehang Fu, Bin Dong, Manyuan Guo, Yangyang Cao, Zheng Wu, Junfang |
author_facet | Zhu, Xuehang Fu, Bin Dong, Manyuan Guo, Yangyang Cao, Zheng Wu, Junfang |
author_sort | Zhu, Xuehang |
collection | PubMed |
description | The gut microbiota–host co-metabolites are good indicators for representing the cross-talk between host and gut microbiota in a bi-direct manner. There is increasing evidence that levels of aromatic amino acids (AAAs) are associated with the alteration of intestinal microbial community though the effects of long-term microbial disturbance remain unclear. Here we monitored the gut microbiota composition and host–microbiota co-metabolites AAA profiles of mice after gentamicin and ceftriaxone treatments for nearly 4 months since their weaning to reveal the relationship between host and microbiome in long- term microbial disturbances. The study was performed employing targeted LC-MS measurement of AAA-related metabolites and 16S RNA sequence of mice cecal contents. The results showed obvious decreased gut microbial diversity and decreased Firmicutes/Bacteroidetes ratio in the cecal contents after long-term antibiotics treatment. The accumulated AAA (tyrosine, phenylalanine and tryptophan) and re-distribution of their downstreaming metabolites that produced under the existence of intestinal flora were found in mice treated with antibiotics for 4 months. Our results suggested that the long-term antibiotic treatment significantly changed the composition of the gut microbiota and destroyed the homeostasis in the intestinal metabolism. And the urinary AAA could be an indicator for exploring interactions between host and gut microbiota. |
format | Online Article Text |
id | pubmed-7786327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77863272021-01-13 Effects of long-term antibiotic treatment on mice urinary aromatic amino acid profiles Zhu, Xuehang Fu, Bin Dong, Manyuan Guo, Yangyang Cao, Zheng Wu, Junfang Biosci Rep Host-Microbe Interactions The gut microbiota–host co-metabolites are good indicators for representing the cross-talk between host and gut microbiota in a bi-direct manner. There is increasing evidence that levels of aromatic amino acids (AAAs) are associated with the alteration of intestinal microbial community though the effects of long-term microbial disturbance remain unclear. Here we monitored the gut microbiota composition and host–microbiota co-metabolites AAA profiles of mice after gentamicin and ceftriaxone treatments for nearly 4 months since their weaning to reveal the relationship between host and microbiome in long- term microbial disturbances. The study was performed employing targeted LC-MS measurement of AAA-related metabolites and 16S RNA sequence of mice cecal contents. The results showed obvious decreased gut microbial diversity and decreased Firmicutes/Bacteroidetes ratio in the cecal contents after long-term antibiotics treatment. The accumulated AAA (tyrosine, phenylalanine and tryptophan) and re-distribution of their downstreaming metabolites that produced under the existence of intestinal flora were found in mice treated with antibiotics for 4 months. Our results suggested that the long-term antibiotic treatment significantly changed the composition of the gut microbiota and destroyed the homeostasis in the intestinal metabolism. And the urinary AAA could be an indicator for exploring interactions between host and gut microbiota. Portland Press Ltd. 2021-01-05 /pmc/articles/PMC7786327/ /pubmed/33269386 http://dx.doi.org/10.1042/BSR20203498 Text en © 2021 The Author(s). https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Host-Microbe Interactions Zhu, Xuehang Fu, Bin Dong, Manyuan Guo, Yangyang Cao, Zheng Wu, Junfang Effects of long-term antibiotic treatment on mice urinary aromatic amino acid profiles |
title | Effects of long-term antibiotic treatment on mice urinary aromatic amino acid profiles |
title_full | Effects of long-term antibiotic treatment on mice urinary aromatic amino acid profiles |
title_fullStr | Effects of long-term antibiotic treatment on mice urinary aromatic amino acid profiles |
title_full_unstemmed | Effects of long-term antibiotic treatment on mice urinary aromatic amino acid profiles |
title_short | Effects of long-term antibiotic treatment on mice urinary aromatic amino acid profiles |
title_sort | effects of long-term antibiotic treatment on mice urinary aromatic amino acid profiles |
topic | Host-Microbe Interactions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7786327/ https://www.ncbi.nlm.nih.gov/pubmed/33269386 http://dx.doi.org/10.1042/BSR20203498 |
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