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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2022
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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. |
format | Online Article Text |
id | pubmed-8790346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
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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