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Effect of Phorate on the Development of Hyperglycaemia in Mouse and Resistance Genes in Intestinal Microbiota
Phorate is a systemic, broad-spectrum organophosphorus insecticide. Although it is commonly used worldwide, phorate, like other pesticides, not only causes environmental pollution but also poses serious threats to human and animal health. Herein, we measured the blood glucose concentrations of high-...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686891/ https://www.ncbi.nlm.nih.gov/pubmed/36358236 http://dx.doi.org/10.3390/antibiotics11111584 |
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author | Cao, Tingting Guo, Yajie Wang, Dan Liu, Zhiyang Huang, Suli Peng, Changfeng Wang, Shaolin Wang, Yang Lu, Qi Xiao, Fan Liang, Zhaoyi Zheng, Sijia Shen, Jianzhong Wu, Yongning Lv, Ziquan Ke, Yuebin |
author_facet | Cao, Tingting Guo, Yajie Wang, Dan Liu, Zhiyang Huang, Suli Peng, Changfeng Wang, Shaolin Wang, Yang Lu, Qi Xiao, Fan Liang, Zhaoyi Zheng, Sijia Shen, Jianzhong Wu, Yongning Lv, Ziquan Ke, Yuebin |
author_sort | Cao, Tingting |
collection | PubMed |
description | Phorate is a systemic, broad-spectrum organophosphorus insecticide. Although it is commonly used worldwide, phorate, like other pesticides, not only causes environmental pollution but also poses serious threats to human and animal health. Herein, we measured the blood glucose concentrations of high-fat-diet-fed mice exposed to various concentrations of phorate (0, 0.005, 0.05, or 0.5 mg/kg); we also assessed the blood glucose concentrations of high-fat-diet-fed mice exposed to phorate; we also assessed the distribution characteristics of the resistance genes in the intestinal microbiota of these mice. We found that 0.005 and 0.5 mg/kg of phorate induced obvious hyperglycaemia in the high-fat-diet-fed mice. Exposure to phorate markedly reduced the abundance of Akkermansia muciniphila in the mouse intestine. The resistance genes vanRG, tetW/N/W, acrD, and evgS were significantly upregulated in the test group compared with the control group. Efflux pumping was the primary mechanism of drug resistance in the Firmicutes, Proteobacteria, Bacteroidetes, Verrucomicrobia, Synergistetes, Spirochaetes, and Actinobacteria found in the mouse intestine. Our findings indicate that changes in the abundance of the intestinal microbiota are closely related to the presence of antibiotic-resistant bacteria in the intestinal tract and the metabolic health of the host. |
format | Online Article Text |
id | pubmed-9686891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96868912022-11-25 Effect of Phorate on the Development of Hyperglycaemia in Mouse and Resistance Genes in Intestinal Microbiota Cao, Tingting Guo, Yajie Wang, Dan Liu, Zhiyang Huang, Suli Peng, Changfeng Wang, Shaolin Wang, Yang Lu, Qi Xiao, Fan Liang, Zhaoyi Zheng, Sijia Shen, Jianzhong Wu, Yongning Lv, Ziquan Ke, Yuebin Antibiotics (Basel) Communication Phorate is a systemic, broad-spectrum organophosphorus insecticide. Although it is commonly used worldwide, phorate, like other pesticides, not only causes environmental pollution but also poses serious threats to human and animal health. Herein, we measured the blood glucose concentrations of high-fat-diet-fed mice exposed to various concentrations of phorate (0, 0.005, 0.05, or 0.5 mg/kg); we also assessed the blood glucose concentrations of high-fat-diet-fed mice exposed to phorate; we also assessed the distribution characteristics of the resistance genes in the intestinal microbiota of these mice. We found that 0.005 and 0.5 mg/kg of phorate induced obvious hyperglycaemia in the high-fat-diet-fed mice. Exposure to phorate markedly reduced the abundance of Akkermansia muciniphila in the mouse intestine. The resistance genes vanRG, tetW/N/W, acrD, and evgS were significantly upregulated in the test group compared with the control group. Efflux pumping was the primary mechanism of drug resistance in the Firmicutes, Proteobacteria, Bacteroidetes, Verrucomicrobia, Synergistetes, Spirochaetes, and Actinobacteria found in the mouse intestine. Our findings indicate that changes in the abundance of the intestinal microbiota are closely related to the presence of antibiotic-resistant bacteria in the intestinal tract and the metabolic health of the host. MDPI 2022-11-09 /pmc/articles/PMC9686891/ /pubmed/36358236 http://dx.doi.org/10.3390/antibiotics11111584 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Cao, Tingting Guo, Yajie Wang, Dan Liu, Zhiyang Huang, Suli Peng, Changfeng Wang, Shaolin Wang, Yang Lu, Qi Xiao, Fan Liang, Zhaoyi Zheng, Sijia Shen, Jianzhong Wu, Yongning Lv, Ziquan Ke, Yuebin Effect of Phorate on the Development of Hyperglycaemia in Mouse and Resistance Genes in Intestinal Microbiota |
title | Effect of Phorate on the Development of Hyperglycaemia in Mouse and Resistance Genes in Intestinal Microbiota |
title_full | Effect of Phorate on the Development of Hyperglycaemia in Mouse and Resistance Genes in Intestinal Microbiota |
title_fullStr | Effect of Phorate on the Development of Hyperglycaemia in Mouse and Resistance Genes in Intestinal Microbiota |
title_full_unstemmed | Effect of Phorate on the Development of Hyperglycaemia in Mouse and Resistance Genes in Intestinal Microbiota |
title_short | Effect of Phorate on the Development of Hyperglycaemia in Mouse and Resistance Genes in Intestinal Microbiota |
title_sort | effect of phorate on the development of hyperglycaemia in mouse and resistance genes in intestinal microbiota |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686891/ https://www.ncbi.nlm.nih.gov/pubmed/36358236 http://dx.doi.org/10.3390/antibiotics11111584 |
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