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Artificial sweeteners stimulate horizontal transfer of extracellular antibiotic resistance genes through natural transformation
Antimicrobial resistance has emerged as a global threat to human health. Natural transformation is an important pathway for horizontal gene transfer, which facilitates the dissemination of antibiotic resistance genes (ARGs) among bacteria. Although it is suspected that artificial sweeteners could ex...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8776823/ https://www.ncbi.nlm.nih.gov/pubmed/34465899 http://dx.doi.org/10.1038/s41396-021-01095-6 |
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author | Yu, Zhigang Wang, Yue Henderson, Ian R. Guo, Jianhua |
author_facet | Yu, Zhigang Wang, Yue Henderson, Ian R. Guo, Jianhua |
author_sort | Yu, Zhigang |
collection | PubMed |
description | Antimicrobial resistance has emerged as a global threat to human health. Natural transformation is an important pathway for horizontal gene transfer, which facilitates the dissemination of antibiotic resistance genes (ARGs) among bacteria. Although it is suspected that artificial sweeteners could exert antimicrobial effects, little is known whether artificial sweeteners would also affect horizontal transfer of ARGs via transformation. Here we demonstrate that four commonly used artificial sweeteners (saccharin, sucralose, aspartame, and acesulfame potassium) promote transfer of ARGs via natural transformation in Acinetobacter baylyi ADP1, a model organism for studying competence and transformation. Such phenomenon was also found in a Gram-positive human pathogen Bacillus subtilis and mice faecal microbiome. We reveal that exposure to these sweeteners increases cell envelope permeability and results in an upregulation of genes encoding DNA uptake and translocation (Com) machinery. In addition, we find that artificial sweeteners induce an increase in plasmid persistence in transformants. We propose a mathematical model established to predict the long-term effects on transformation dynamics under exposure to these sweeteners. Collectively, our findings offer insights into natural transformation promoted by artificial sweeteners and highlight the need to evaluate these environmental contaminants for their antibiotic-like side effects. |
format | Online Article Text |
id | pubmed-8776823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87768232022-02-04 Artificial sweeteners stimulate horizontal transfer of extracellular antibiotic resistance genes through natural transformation Yu, Zhigang Wang, Yue Henderson, Ian R. Guo, Jianhua ISME J Article Antimicrobial resistance has emerged as a global threat to human health. Natural transformation is an important pathway for horizontal gene transfer, which facilitates the dissemination of antibiotic resistance genes (ARGs) among bacteria. Although it is suspected that artificial sweeteners could exert antimicrobial effects, little is known whether artificial sweeteners would also affect horizontal transfer of ARGs via transformation. Here we demonstrate that four commonly used artificial sweeteners (saccharin, sucralose, aspartame, and acesulfame potassium) promote transfer of ARGs via natural transformation in Acinetobacter baylyi ADP1, a model organism for studying competence and transformation. Such phenomenon was also found in a Gram-positive human pathogen Bacillus subtilis and mice faecal microbiome. We reveal that exposure to these sweeteners increases cell envelope permeability and results in an upregulation of genes encoding DNA uptake and translocation (Com) machinery. In addition, we find that artificial sweeteners induce an increase in plasmid persistence in transformants. We propose a mathematical model established to predict the long-term effects on transformation dynamics under exposure to these sweeteners. Collectively, our findings offer insights into natural transformation promoted by artificial sweeteners and highlight the need to evaluate these environmental contaminants for their antibiotic-like side effects. Nature Publishing Group UK 2021-09-01 2022-02 /pmc/articles/PMC8776823/ /pubmed/34465899 http://dx.doi.org/10.1038/s41396-021-01095-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yu, Zhigang Wang, Yue Henderson, Ian R. Guo, Jianhua Artificial sweeteners stimulate horizontal transfer of extracellular antibiotic resistance genes through natural transformation |
title | Artificial sweeteners stimulate horizontal transfer of extracellular antibiotic resistance genes through natural transformation |
title_full | Artificial sweeteners stimulate horizontal transfer of extracellular antibiotic resistance genes through natural transformation |
title_fullStr | Artificial sweeteners stimulate horizontal transfer of extracellular antibiotic resistance genes through natural transformation |
title_full_unstemmed | Artificial sweeteners stimulate horizontal transfer of extracellular antibiotic resistance genes through natural transformation |
title_short | Artificial sweeteners stimulate horizontal transfer of extracellular antibiotic resistance genes through natural transformation |
title_sort | artificial sweeteners stimulate horizontal transfer of extracellular antibiotic resistance genes through natural transformation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8776823/ https://www.ncbi.nlm.nih.gov/pubmed/34465899 http://dx.doi.org/10.1038/s41396-021-01095-6 |
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