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Dynamic Boolean modelling reveals the influence of energy supply on bacterial efflux pump expression

Antimicrobial resistance (AMR) is a global health issue. One key factor contributing to AMR is the ability of bacteria to export drugs through efflux pumps, which relies on the ATP-dependent expression and interaction of several controlling genes. Recent studies have shown that significant cell-to-c...

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Autores principales: Kerr, Ryan, Jabbari, Sara, Blair, Jessica M. A., Johnston, Iain G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790346/
https://www.ncbi.nlm.nih.gov/pubmed/35078338
http://dx.doi.org/10.1098/rsif.2021.0771
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author Kerr, Ryan
Jabbari, Sara
Blair, Jessica M. A.
Johnston, Iain G.
author_facet Kerr, Ryan
Jabbari, Sara
Blair, Jessica M. A.
Johnston, Iain G.
author_sort Kerr, Ryan
collection PubMed
description Antimicrobial resistance (AMR) is a global health issue. One key factor contributing to AMR is the ability of bacteria to export drugs through efflux pumps, which relies on the ATP-dependent expression and interaction of several controlling genes. Recent studies have shown that significant cell-to-cell ATP variability exists within clonal bacterial populations, but the contribution of intrinsic cell-to-cell ATP heterogeneity is generally overlooked in understanding efflux pumps. Here, we consider how ATP variability influences gene regulatory networks controlling expression of efflux pump genes in two bacterial species. We develop and apply a generalizable Boolean modelling framework, developed to incorporate the dependence of gene expression dynamics on available cellular energy supply. Theoretical results show that differences in energy availability can cause pronounced downstream heterogeneity in efflux gene expression. Cells with higher energy availability have a superior response to stressors. Furthermore, in the absence of stress, model bacteria develop heterogeneous pulses of efflux pump gene expression which contribute to a sustained sub-population of cells with increased efflux expression activity, potentially conferring a continuous pool of intrinsically resistant bacteria. This modelling approach thus reveals an important source of heterogeneity in cell responses to antimicrobials and sheds light on potentially targetable aspects of efflux pump-related antimicrobial resistance.
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spelling pubmed-87903462022-02-03 Dynamic Boolean modelling reveals the influence of energy supply on bacterial efflux pump expression Kerr, Ryan Jabbari, Sara Blair, Jessica M. A. Johnston, Iain G. J R Soc Interface Life Sciences–Mathematics interface Antimicrobial resistance (AMR) is a global health issue. One key factor contributing to AMR is the ability of bacteria to export drugs through efflux pumps, which relies on the ATP-dependent expression and interaction of several controlling genes. Recent studies have shown that significant cell-to-cell ATP variability exists within clonal bacterial populations, but the contribution of intrinsic cell-to-cell ATP heterogeneity is generally overlooked in understanding efflux pumps. Here, we consider how ATP variability influences gene regulatory networks controlling expression of efflux pump genes in two bacterial species. We develop and apply a generalizable Boolean modelling framework, developed to incorporate the dependence of gene expression dynamics on available cellular energy supply. Theoretical results show that differences in energy availability can cause pronounced downstream heterogeneity in efflux gene expression. Cells with higher energy availability have a superior response to stressors. Furthermore, in the absence of stress, model bacteria develop heterogeneous pulses of efflux pump gene expression which contribute to a sustained sub-population of cells with increased efflux expression activity, potentially conferring a continuous pool of intrinsically resistant bacteria. This modelling approach thus reveals an important source of heterogeneity in cell responses to antimicrobials and sheds light on potentially targetable aspects of efflux pump-related antimicrobial resistance. The Royal Society 2022-01-26 /pmc/articles/PMC8790346/ /pubmed/35078338 http://dx.doi.org/10.1098/rsif.2021.0771 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Life Sciences–Mathematics interface
Kerr, Ryan
Jabbari, Sara
Blair, Jessica M. A.
Johnston, Iain G.
Dynamic Boolean modelling reveals the influence of energy supply on bacterial efflux pump expression
title Dynamic Boolean modelling reveals the influence of energy supply on bacterial efflux pump expression
title_full Dynamic Boolean modelling reveals the influence of energy supply on bacterial efflux pump expression
title_fullStr Dynamic Boolean modelling reveals the influence of energy supply on bacterial efflux pump expression
title_full_unstemmed Dynamic Boolean modelling reveals the influence of energy supply on bacterial efflux pump expression
title_short Dynamic Boolean modelling reveals the influence of energy supply on bacterial efflux pump expression
title_sort dynamic boolean modelling reveals the influence of energy supply on bacterial efflux pump expression
topic Life Sciences–Mathematics interface
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790346/
https://www.ncbi.nlm.nih.gov/pubmed/35078338
http://dx.doi.org/10.1098/rsif.2021.0771
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