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Resistance/fitness trade-off is a barrier to the evolution of MarR inactivation mutants in Escherichia coli

BACKGROUND: Mutations that inactivate MarR reduce susceptibility to ciprofloxacin and competitive growth fitness in Escherichia coli. Both phenotypes are caused by overexpression of the MarA regulon, which includes the AcrAB-TolC drug efflux pump. OBJECTIVES: We asked whether compensatory evolution...

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Autores principales: Praski Alzrigat, Lisa, Huseby, Douglas L, Brandis, Gerrit, Hughes, Diarmaid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729382/
https://www.ncbi.nlm.nih.gov/pubmed/33089314
http://dx.doi.org/10.1093/jac/dkaa417
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author Praski Alzrigat, Lisa
Huseby, Douglas L
Brandis, Gerrit
Hughes, Diarmaid
author_facet Praski Alzrigat, Lisa
Huseby, Douglas L
Brandis, Gerrit
Hughes, Diarmaid
author_sort Praski Alzrigat, Lisa
collection PubMed
description BACKGROUND: Mutations that inactivate MarR reduce susceptibility to ciprofloxacin and competitive growth fitness in Escherichia coli. Both phenotypes are caused by overexpression of the MarA regulon, which includes the AcrAB-TolC drug efflux pump. OBJECTIVES: We asked whether compensatory evolution could reduce the fitness cost of MarR-inactivating mutations without affecting resistance to ciprofloxacin. METHODS: The cost of overexpressing the AcrAB-TolC efflux pump was measured independently of MarA overexpression. Experimental evolution of MarR-inactive strains was used to select mutants with increased fitness. The acquired mutations were identified and their effects on drug susceptibility were measured. RESULTS: Overexpression of the AcrAB-TolC efflux pump was found not to contribute to the fitness cost of MarA regulon overexpression. Fitness-compensatory mutations were selected in marA and lon. The mutations reduced the level of MarA protein thus reducing expression of the MarA regulon. They restored growth fitness but also reduced resistance to ciprofloxacin. CONCLUSIONS: The fitness cost caused by overexpression of the MarA regulon has multiple contributing factors. Experimental evolution did not identify any single pump-independent cost factor. Instead, efficient fitness compensation occurred only by mechanisms that reduce MarA concentration, which simultaneously reduce the drug resistance phenotype. This resistance/fitness trade-off is a barrier to the successful spread of MarR inactivation mutations in clinical isolates where growth fitness is essential.
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spelling pubmed-77293822020-12-16 Resistance/fitness trade-off is a barrier to the evolution of MarR inactivation mutants in Escherichia coli Praski Alzrigat, Lisa Huseby, Douglas L Brandis, Gerrit Hughes, Diarmaid J Antimicrob Chemother Original Research BACKGROUND: Mutations that inactivate MarR reduce susceptibility to ciprofloxacin and competitive growth fitness in Escherichia coli. Both phenotypes are caused by overexpression of the MarA regulon, which includes the AcrAB-TolC drug efflux pump. OBJECTIVES: We asked whether compensatory evolution could reduce the fitness cost of MarR-inactivating mutations without affecting resistance to ciprofloxacin. METHODS: The cost of overexpressing the AcrAB-TolC efflux pump was measured independently of MarA overexpression. Experimental evolution of MarR-inactive strains was used to select mutants with increased fitness. The acquired mutations were identified and their effects on drug susceptibility were measured. RESULTS: Overexpression of the AcrAB-TolC efflux pump was found not to contribute to the fitness cost of MarA regulon overexpression. Fitness-compensatory mutations were selected in marA and lon. The mutations reduced the level of MarA protein thus reducing expression of the MarA regulon. They restored growth fitness but also reduced resistance to ciprofloxacin. CONCLUSIONS: The fitness cost caused by overexpression of the MarA regulon has multiple contributing factors. Experimental evolution did not identify any single pump-independent cost factor. Instead, efficient fitness compensation occurred only by mechanisms that reduce MarA concentration, which simultaneously reduce the drug resistance phenotype. This resistance/fitness trade-off is a barrier to the successful spread of MarR inactivation mutations in clinical isolates where growth fitness is essential. Oxford University Press 2020-10-22 /pmc/articles/PMC7729382/ /pubmed/33089314 http://dx.doi.org/10.1093/jac/dkaa417 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Research
Praski Alzrigat, Lisa
Huseby, Douglas L
Brandis, Gerrit
Hughes, Diarmaid
Resistance/fitness trade-off is a barrier to the evolution of MarR inactivation mutants in Escherichia coli
title Resistance/fitness trade-off is a barrier to the evolution of MarR inactivation mutants in Escherichia coli
title_full Resistance/fitness trade-off is a barrier to the evolution of MarR inactivation mutants in Escherichia coli
title_fullStr Resistance/fitness trade-off is a barrier to the evolution of MarR inactivation mutants in Escherichia coli
title_full_unstemmed Resistance/fitness trade-off is a barrier to the evolution of MarR inactivation mutants in Escherichia coli
title_short Resistance/fitness trade-off is a barrier to the evolution of MarR inactivation mutants in Escherichia coli
title_sort resistance/fitness trade-off is a barrier to the evolution of marr inactivation mutants in escherichia coli
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729382/
https://www.ncbi.nlm.nih.gov/pubmed/33089314
http://dx.doi.org/10.1093/jac/dkaa417
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