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Fitness cost constrains the spectrum of marR mutations in ciprofloxacin-resistant Escherichia coli

OBJECTIVES: To determine whether the spectrum of mutations in marR in ciprofloxacin-resistant clinical isolates of Escherichia coli shows evidence of selection bias, either to reduce fitness costs, or to increase drug resistance. MarR is a repressor protein that regulates, via MarA, expression of th...

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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 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890708/
https://www.ncbi.nlm.nih.gov/pubmed/28962020
http://dx.doi.org/10.1093/jac/dkx270
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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 OBJECTIVES: To determine whether the spectrum of mutations in marR in ciprofloxacin-resistant clinical isolates of Escherichia coli shows evidence of selection bias, either to reduce fitness costs, or to increase drug resistance. MarR is a repressor protein that regulates, via MarA, expression of the Mar regulon, including the multidrug efflux pump AcrAB-TolC. METHODS: Isogenic strains carrying 36 different marR alleles identified in resistant clinical isolates, or selected for resistance in vitro, were constructed. Drug susceptibility and relative fitness in growth competition assays were measured for all strains. The expression level of marA, and of various efflux pump components, as a function of specific mutations in marR, was measured by qPCR. RESULTS: The spectrum of genetic alterations in marR in clinical isolates is strongly biased against inactivating mutations. In general, the alleles found in clinical isolates conferred a lower level of resistance and imposed a lower growth fitness cost than mutations selected in vitro. The level of expression of MarA correlated well with the MIC of ciprofloxacin. This supports the functional connection between mutations in marR and reduced susceptibility to ciprofloxacin. CONCLUSIONS: Mutations in marR selected in ciprofloxacin-resistant clinical isolates are strongly biased against inactivating mutations. Selection favours mutant alleles that have the lowest fitness costs, even though these cause only modest reductions in drug susceptibility. This suggests that selection for high relative fitness is more important than selection for increased resistance in determining which alleles of marR will be selected in resistant clinical isolates.
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spelling pubmed-58907082018-04-13 Fitness cost constrains the spectrum of marR mutations in ciprofloxacin-resistant Escherichia coli Praski Alzrigat, Lisa Huseby, Douglas L Brandis, Gerrit Hughes, Diarmaid J Antimicrob Chemother Original Research OBJECTIVES: To determine whether the spectrum of mutations in marR in ciprofloxacin-resistant clinical isolates of Escherichia coli shows evidence of selection bias, either to reduce fitness costs, or to increase drug resistance. MarR is a repressor protein that regulates, via MarA, expression of the Mar regulon, including the multidrug efflux pump AcrAB-TolC. METHODS: Isogenic strains carrying 36 different marR alleles identified in resistant clinical isolates, or selected for resistance in vitro, were constructed. Drug susceptibility and relative fitness in growth competition assays were measured for all strains. The expression level of marA, and of various efflux pump components, as a function of specific mutations in marR, was measured by qPCR. RESULTS: The spectrum of genetic alterations in marR in clinical isolates is strongly biased against inactivating mutations. In general, the alleles found in clinical isolates conferred a lower level of resistance and imposed a lower growth fitness cost than mutations selected in vitro. The level of expression of MarA correlated well with the MIC of ciprofloxacin. This supports the functional connection between mutations in marR and reduced susceptibility to ciprofloxacin. CONCLUSIONS: Mutations in marR selected in ciprofloxacin-resistant clinical isolates are strongly biased against inactivating mutations. Selection favours mutant alleles that have the lowest fitness costs, even though these cause only modest reductions in drug susceptibility. This suggests that selection for high relative fitness is more important than selection for increased resistance in determining which alleles of marR will be selected in resistant clinical isolates. Oxford University Press 2017-11 2017-08-17 /pmc/articles/PMC5890708/ /pubmed/28962020 http://dx.doi.org/10.1093/jac/dkx270 Text en © The Author 2017. 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
Fitness cost constrains the spectrum of marR mutations in ciprofloxacin-resistant Escherichia coli
title Fitness cost constrains the spectrum of marR mutations in ciprofloxacin-resistant Escherichia coli
title_full Fitness cost constrains the spectrum of marR mutations in ciprofloxacin-resistant Escherichia coli
title_fullStr Fitness cost constrains the spectrum of marR mutations in ciprofloxacin-resistant Escherichia coli
title_full_unstemmed Fitness cost constrains the spectrum of marR mutations in ciprofloxacin-resistant Escherichia coli
title_short Fitness cost constrains the spectrum of marR mutations in ciprofloxacin-resistant Escherichia coli
title_sort fitness cost constrains the spectrum of marr mutations in ciprofloxacin-resistant escherichia coli
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890708/
https://www.ncbi.nlm.nih.gov/pubmed/28962020
http://dx.doi.org/10.1093/jac/dkx270
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