Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Webber, Mark A., Whitehead, Rebekah N., Mount, Manuella, Loman, Nick J., Pallen, Mark J., Piddock, Laura J. V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
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
_version_ 1782380950328442880
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
work_keys_str_mv AT webbermarka parallelevolutionarypathwaystoantibioticresistanceselectedbybiocideexposure
AT whiteheadrebekahn parallelevolutionarypathwaystoantibioticresistanceselectedbybiocideexposure
AT mountmanuella parallelevolutionarypathwaystoantibioticresistanceselectedbybiocideexposure
AT lomannickj parallelevolutionarypathwaystoantibioticresistanceselectedbybiocideexposure
AT pallenmarkj parallelevolutionarypathwaystoantibioticresistanceselectedbybiocideexposure
AT piddocklaurajv parallelevolutionarypathwaystoantibioticresistanceselectedbybiocideexposure