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Parallel evolutionary pathways to antibiotic resistance selected by biocide exposure
OBJECTIVES: Biocides are widely used to prevent infection. We aimed to determine whether exposure of Salmonella to various biocides could act as a driver of antibiotic resistance. METHODS: Salmonella enterica serovar Typhimurium was exposed to four biocides with differing modes of action. Antibiotic...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4500774/ https://www.ncbi.nlm.nih.gov/pubmed/25953808 http://dx.doi.org/10.1093/jac/dkv109 |
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author | Webber, Mark A. Whitehead, Rebekah N. Mount, Manuella Loman, Nick J. Pallen, Mark J. Piddock, Laura J. V. |
author_facet | Webber, Mark A. Whitehead, Rebekah N. Mount, Manuella Loman, Nick J. Pallen, Mark J. Piddock, Laura J. V. |
author_sort | Webber, Mark A. |
collection | PubMed |
description | OBJECTIVES: Biocides are widely used to prevent infection. We aimed to determine whether exposure of Salmonella to various biocides could act as a driver of antibiotic resistance. METHODS: Salmonella enterica serovar Typhimurium was exposed to four biocides with differing modes of action. Antibiotic-resistant mutants were selected during exposure to all biocides and characterized phenotypically and genotypically to identify mechanisms of resistance. RESULTS: All biocides tested selected MDR mutants with decreased antibiotic susceptibility; these occurred randomly throughout the experiments. Mutations that resulted in de-repression of the multidrug efflux pump AcrAB-TolC were seen in MDR mutants. A novel mutation in rpoA was also selected and contributed to the MDR phenotype. Other mutants were highly resistant to both quinolone antibiotics and the biocide triclosan. CONCLUSIONS: This study shows that exposure of bacteria to biocides can select for antibiotic-resistant mutants and this is mediated by clinically relevant mechanisms of resistance prevalent in human pathogens. |
format | Online Article Text |
id | pubmed-4500774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45007742015-07-15 Parallel evolutionary pathways to antibiotic resistance selected by biocide exposure Webber, Mark A. Whitehead, Rebekah N. Mount, Manuella Loman, Nick J. Pallen, Mark J. Piddock, Laura J. V. J Antimicrob Chemother Original Research OBJECTIVES: Biocides are widely used to prevent infection. We aimed to determine whether exposure of Salmonella to various biocides could act as a driver of antibiotic resistance. METHODS: Salmonella enterica serovar Typhimurium was exposed to four biocides with differing modes of action. Antibiotic-resistant mutants were selected during exposure to all biocides and characterized phenotypically and genotypically to identify mechanisms of resistance. RESULTS: All biocides tested selected MDR mutants with decreased antibiotic susceptibility; these occurred randomly throughout the experiments. Mutations that resulted in de-repression of the multidrug efflux pump AcrAB-TolC were seen in MDR mutants. A novel mutation in rpoA was also selected and contributed to the MDR phenotype. Other mutants were highly resistant to both quinolone antibiotics and the biocide triclosan. CONCLUSIONS: This study shows that exposure of bacteria to biocides can select for antibiotic-resistant mutants and this is mediated by clinically relevant mechanisms of resistance prevalent in human pathogens. Oxford University Press 2015-08 2015-05-07 /pmc/articles/PMC4500774/ /pubmed/25953808 http://dx.doi.org/10.1093/jac/dkv109 Text en © The Author 2015. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Webber, Mark A. Whitehead, Rebekah N. Mount, Manuella Loman, Nick J. Pallen, Mark J. Piddock, Laura J. V. Parallel evolutionary pathways to antibiotic resistance selected by biocide exposure |
title | Parallel evolutionary pathways to antibiotic resistance selected by biocide exposure |
title_full | Parallel evolutionary pathways to antibiotic resistance selected by biocide exposure |
title_fullStr | Parallel evolutionary pathways to antibiotic resistance selected by biocide exposure |
title_full_unstemmed | Parallel evolutionary pathways to antibiotic resistance selected by biocide exposure |
title_short | Parallel evolutionary pathways to antibiotic resistance selected by biocide exposure |
title_sort | parallel evolutionary pathways to antibiotic resistance selected by biocide exposure |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4500774/ https://www.ncbi.nlm.nih.gov/pubmed/25953808 http://dx.doi.org/10.1093/jac/dkv109 |
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