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Evolution of antibiotic resistance at low antibiotic concentrations including selection below the minimal selective concentration
Determining the selective potential of antibiotics at environmental concentrations is critical for designing effective strategies to limit selection for antibiotic resistance. This study determined the minimal selective concentrations (MSCs) for macrolide and fluoroquinolone antibiotics included on...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471295/ https://www.ncbi.nlm.nih.gov/pubmed/32884065 http://dx.doi.org/10.1038/s42003-020-01176-w |
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author | Stanton, Isobel C. Murray, Aimee K. Zhang, Lihong Snape, Jason Gaze, William H. |
author_facet | Stanton, Isobel C. Murray, Aimee K. Zhang, Lihong Snape, Jason Gaze, William H. |
author_sort | Stanton, Isobel C. |
collection | PubMed |
description | Determining the selective potential of antibiotics at environmental concentrations is critical for designing effective strategies to limit selection for antibiotic resistance. This study determined the minimal selective concentrations (MSCs) for macrolide and fluoroquinolone antibiotics included on the European Commissionʼs Water Framework Directive’s priority hazardous substances Watch List. The macrolides demonstrated positive selection for ermF at concentrations 1–2 orders of magnitude greater (>500 and <750 µg/L) than measured environmental concentrations (MECs). Ciprofloxacin illustrated positive selection for intI1 at concentrations similar to current MECs (>7.8 and <15.6 µg/L). This highlights the need for compound specific assessment of selective potential. In addition, a sub-MSC selective window defined by the minimal increased persistence concentration (MIPC) is described. Differential rates of negative selection (or persistence) were associated with elevated prevalence relative to the no antibiotic control below the MSC. This increased persistence leads to opportunities for further selection over time and risk of human exposure and environmental transmission. |
format | Online Article Text |
id | pubmed-7471295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74712952020-09-16 Evolution of antibiotic resistance at low antibiotic concentrations including selection below the minimal selective concentration Stanton, Isobel C. Murray, Aimee K. Zhang, Lihong Snape, Jason Gaze, William H. Commun Biol Article Determining the selective potential of antibiotics at environmental concentrations is critical for designing effective strategies to limit selection for antibiotic resistance. This study determined the minimal selective concentrations (MSCs) for macrolide and fluoroquinolone antibiotics included on the European Commissionʼs Water Framework Directive’s priority hazardous substances Watch List. The macrolides demonstrated positive selection for ermF at concentrations 1–2 orders of magnitude greater (>500 and <750 µg/L) than measured environmental concentrations (MECs). Ciprofloxacin illustrated positive selection for intI1 at concentrations similar to current MECs (>7.8 and <15.6 µg/L). This highlights the need for compound specific assessment of selective potential. In addition, a sub-MSC selective window defined by the minimal increased persistence concentration (MIPC) is described. Differential rates of negative selection (or persistence) were associated with elevated prevalence relative to the no antibiotic control below the MSC. This increased persistence leads to opportunities for further selection over time and risk of human exposure and environmental transmission. Nature Publishing Group UK 2020-09-03 /pmc/articles/PMC7471295/ /pubmed/32884065 http://dx.doi.org/10.1038/s42003-020-01176-w Text en © The Author(s) 2020 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/. |
spellingShingle | Article Stanton, Isobel C. Murray, Aimee K. Zhang, Lihong Snape, Jason Gaze, William H. Evolution of antibiotic resistance at low antibiotic concentrations including selection below the minimal selective concentration |
title | Evolution of antibiotic resistance at low antibiotic concentrations including selection below the minimal selective concentration |
title_full | Evolution of antibiotic resistance at low antibiotic concentrations including selection below the minimal selective concentration |
title_fullStr | Evolution of antibiotic resistance at low antibiotic concentrations including selection below the minimal selective concentration |
title_full_unstemmed | Evolution of antibiotic resistance at low antibiotic concentrations including selection below the minimal selective concentration |
title_short | Evolution of antibiotic resistance at low antibiotic concentrations including selection below the minimal selective concentration |
title_sort | evolution of antibiotic resistance at low antibiotic concentrations including selection below the minimal selective concentration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471295/ https://www.ncbi.nlm.nih.gov/pubmed/32884065 http://dx.doi.org/10.1038/s42003-020-01176-w |
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