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Antidepressants promote the spread of extracellular antibiotic resistance genes via transformation

The development of antibiotic resistance as an unavoidable consequence of the application of antimicrobials is a significant concern for human health. Antidepressants are being increasingly consumed globally. Human gut microbial communities are frequently exposed to antidepressants, yet little is kn...

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Autores principales: Lu, Ji, Ding, Pengbo, Wang, Yue, Guo, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330934/
https://www.ncbi.nlm.nih.gov/pubmed/37938640
http://dx.doi.org/10.1038/s43705-022-00147-y
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author Lu, Ji
Ding, Pengbo
Wang, Yue
Guo, Jianhua
author_facet Lu, Ji
Ding, Pengbo
Wang, Yue
Guo, Jianhua
author_sort Lu, Ji
collection PubMed
description The development of antibiotic resistance as an unavoidable consequence of the application of antimicrobials is a significant concern for human health. Antidepressants are being increasingly consumed globally. Human gut microbial communities are frequently exposed to antidepressants, yet little is known about the interaction between antidepressants and antibiotic resistance. This study aimed to investigate whether antidepressants can accelerate the dissemination of antibiotic resistance by increasing the rate of the horizontal transfer of antibiotic resistance genes (ARGs). Results demonstrated that some of the commonly-prescribed antidepressants (Duloxetine, Sertraline, Fluoxetine and Bupropion) at clinically relevant concentrations can significantly (n = 9; p(adj) < 0.01) promote the transformation of extracellular ARGs into Acinetobacter baylyi ADP1 for a maximum of 2.3-fold, which is primarily associated with the overproduction of reactive oxygen species. The increased cell membrane permeability and porosity, stimulated transcription and translation of competence, SOS response, universal stress response and ATP synthesis-related genes are also associated with antidepressants-enhanced transformation. This study demonstrated that some antidepressants can speed up the spread of antibiotic resistance by promoting the transformation of ARGs, which emphasizes the necessity to assess the potential risks of antidepressants in spreading antibiotic resistance during clinical antidepressant applications.
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spelling pubmed-93309342022-07-28 Antidepressants promote the spread of extracellular antibiotic resistance genes via transformation Lu, Ji Ding, Pengbo Wang, Yue Guo, Jianhua ISME Commun Article The development of antibiotic resistance as an unavoidable consequence of the application of antimicrobials is a significant concern for human health. Antidepressants are being increasingly consumed globally. Human gut microbial communities are frequently exposed to antidepressants, yet little is known about the interaction between antidepressants and antibiotic resistance. This study aimed to investigate whether antidepressants can accelerate the dissemination of antibiotic resistance by increasing the rate of the horizontal transfer of antibiotic resistance genes (ARGs). Results demonstrated that some of the commonly-prescribed antidepressants (Duloxetine, Sertraline, Fluoxetine and Bupropion) at clinically relevant concentrations can significantly (n = 9; p(adj) < 0.01) promote the transformation of extracellular ARGs into Acinetobacter baylyi ADP1 for a maximum of 2.3-fold, which is primarily associated with the overproduction of reactive oxygen species. The increased cell membrane permeability and porosity, stimulated transcription and translation of competence, SOS response, universal stress response and ATP synthesis-related genes are also associated with antidepressants-enhanced transformation. This study demonstrated that some antidepressants can speed up the spread of antibiotic resistance by promoting the transformation of ARGs, which emphasizes the necessity to assess the potential risks of antidepressants in spreading antibiotic resistance during clinical antidepressant applications. Nature Publishing Group UK 2022-07-28 /pmc/articles/PMC9330934/ /pubmed/37938640 http://dx.doi.org/10.1038/s43705-022-00147-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lu, Ji
Ding, Pengbo
Wang, Yue
Guo, Jianhua
Antidepressants promote the spread of extracellular antibiotic resistance genes via transformation
title Antidepressants promote the spread of extracellular antibiotic resistance genes via transformation
title_full Antidepressants promote the spread of extracellular antibiotic resistance genes via transformation
title_fullStr Antidepressants promote the spread of extracellular antibiotic resistance genes via transformation
title_full_unstemmed Antidepressants promote the spread of extracellular antibiotic resistance genes via transformation
title_short Antidepressants promote the spread of extracellular antibiotic resistance genes via transformation
title_sort antidepressants promote the spread of extracellular antibiotic resistance genes via transformation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330934/
https://www.ncbi.nlm.nih.gov/pubmed/37938640
http://dx.doi.org/10.1038/s43705-022-00147-y
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