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Antibiotics may increase triazine herbicide exposure risk via disturbing gut microbiota
BACKGROUND: Antibiotics are commonly used worldwide, and pesticide is a kind of xenobiotic to which humans are frequently exposed. The interactive impact of antibiotics on pesticides has rarely been studied. We aim to investigate the effects of antibiotics on the pesticide exposure risk and whether...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291969/ https://www.ncbi.nlm.nih.gov/pubmed/30545405 http://dx.doi.org/10.1186/s40168-018-0602-5 |
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author | Zhan, Jing Liang, Yiran Liu, Donghui Ma, Xiaoran Li, Peize Liu, Chang Liu, Xueke Wang, Peng Zhou, Zhiqiang |
author_facet | Zhan, Jing Liang, Yiran Liu, Donghui Ma, Xiaoran Li, Peize Liu, Chang Liu, Xueke Wang, Peng Zhou, Zhiqiang |
author_sort | Zhan, Jing |
collection | PubMed |
description | BACKGROUND: Antibiotics are commonly used worldwide, and pesticide is a kind of xenobiotic to which humans are frequently exposed. The interactive impact of antibiotics on pesticides has rarely been studied. We aim to investigate the effects of antibiotics on the pesticide exposure risk and whether gut microbiota altered by antibiotics has an influence on pesticide bioavailability. Furthermore, we explored the mechanisms of gut microbiota affecting the fate of pesticides in the host. RESULTS: The oral bioavailability of triazine herbicides significantly increased in the rats treated with ampicillin or antibiotic cocktails. The antibiotic-altered gut microbiota directly influenced the increased pesticide bioavailability through downregulating hepatic metabolic enzyme gene expression and upregulating intestinal absorption-related proteins. CONCLUSIONS: Antibiotics could increase the pesticide bioavailability and thereby may increase the pesticide exposure risk. The antibiotic-altered gut microbiota that could alter the hepatic metabolic enzyme gene expression and intestinal absorption-related proteome was a critical cause of the increased bioavailability. This study revealed an undiscovered potential health impact of antibiotics and reminded people to consider the co-exposed xenobiotics when taking antibiotics. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-018-0602-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6291969 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62919692018-12-17 Antibiotics may increase triazine herbicide exposure risk via disturbing gut microbiota Zhan, Jing Liang, Yiran Liu, Donghui Ma, Xiaoran Li, Peize Liu, Chang Liu, Xueke Wang, Peng Zhou, Zhiqiang Microbiome Research BACKGROUND: Antibiotics are commonly used worldwide, and pesticide is a kind of xenobiotic to which humans are frequently exposed. The interactive impact of antibiotics on pesticides has rarely been studied. We aim to investigate the effects of antibiotics on the pesticide exposure risk and whether gut microbiota altered by antibiotics has an influence on pesticide bioavailability. Furthermore, we explored the mechanisms of gut microbiota affecting the fate of pesticides in the host. RESULTS: The oral bioavailability of triazine herbicides significantly increased in the rats treated with ampicillin or antibiotic cocktails. The antibiotic-altered gut microbiota directly influenced the increased pesticide bioavailability through downregulating hepatic metabolic enzyme gene expression and upregulating intestinal absorption-related proteins. CONCLUSIONS: Antibiotics could increase the pesticide bioavailability and thereby may increase the pesticide exposure risk. The antibiotic-altered gut microbiota that could alter the hepatic metabolic enzyme gene expression and intestinal absorption-related proteome was a critical cause of the increased bioavailability. This study revealed an undiscovered potential health impact of antibiotics and reminded people to consider the co-exposed xenobiotics when taking antibiotics. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-018-0602-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-13 /pmc/articles/PMC6291969/ /pubmed/30545405 http://dx.doi.org/10.1186/s40168-018-0602-5 Text en © The Author(s). 2018 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 Zhan, Jing Liang, Yiran Liu, Donghui Ma, Xiaoran Li, Peize Liu, Chang Liu, Xueke Wang, Peng Zhou, Zhiqiang Antibiotics may increase triazine herbicide exposure risk via disturbing gut microbiota |
title | Antibiotics may increase triazine herbicide exposure risk via disturbing gut microbiota |
title_full | Antibiotics may increase triazine herbicide exposure risk via disturbing gut microbiota |
title_fullStr | Antibiotics may increase triazine herbicide exposure risk via disturbing gut microbiota |
title_full_unstemmed | Antibiotics may increase triazine herbicide exposure risk via disturbing gut microbiota |
title_short | Antibiotics may increase triazine herbicide exposure risk via disturbing gut microbiota |
title_sort | antibiotics may increase triazine herbicide exposure risk via disturbing gut microbiota |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291969/ https://www.ncbi.nlm.nih.gov/pubmed/30545405 http://dx.doi.org/10.1186/s40168-018-0602-5 |
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