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Understanding Beta-Lactam-Induced Lysis at the Single-Cell Level
Mechanical rupture, or lysis, of the cytoplasmic membrane is a common cell death pathway in bacteria occurring in response to β-lactam antibiotics. A better understanding of the cellular design principles governing the susceptibility and response of individual cells to lysis could indicate methods o...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8372035/ https://www.ncbi.nlm.nih.gov/pubmed/34421870 http://dx.doi.org/10.3389/fmicb.2021.712007 |
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author | Wong, Felix Wilson, Sean Helbig, Ralf Hegde, Smitha Aftenieva, Olha Zheng, Hai Liu, Chenli Pilizota, Teuta Garner, Ethan C. Amir, Ariel Renner, Lars D. |
author_facet | Wong, Felix Wilson, Sean Helbig, Ralf Hegde, Smitha Aftenieva, Olha Zheng, Hai Liu, Chenli Pilizota, Teuta Garner, Ethan C. Amir, Ariel Renner, Lars D. |
author_sort | Wong, Felix |
collection | PubMed |
description | Mechanical rupture, or lysis, of the cytoplasmic membrane is a common cell death pathway in bacteria occurring in response to β-lactam antibiotics. A better understanding of the cellular design principles governing the susceptibility and response of individual cells to lysis could indicate methods of potentiating β-lactam antibiotics and clarify relevant aspects of cellular physiology. Here, we take a single-cell approach to bacterial cell lysis to examine three cellular features—turgor pressure, mechanosensitive channels, and cell shape changes—that are expected to modulate lysis. We develop a mechanical model of bacterial cell lysis and experimentally analyze the dynamics of lysis in hundreds of single Escherichia coli cells. We find that turgor pressure is the only factor, of these three cellular features, which robustly modulates lysis. We show that mechanosensitive channels do not modulate lysis due to insufficiently fast solute outflow, and that cell shape changes result in more severe cellular lesions but do not influence the dynamics of lysis. These results inform a single-cell view of bacterial cell lysis and underscore approaches of combatting antibiotic tolerance to β-lactams aimed at targeting cellular turgor. |
format | Online Article Text |
id | pubmed-8372035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83720352021-08-19 Understanding Beta-Lactam-Induced Lysis at the Single-Cell Level Wong, Felix Wilson, Sean Helbig, Ralf Hegde, Smitha Aftenieva, Olha Zheng, Hai Liu, Chenli Pilizota, Teuta Garner, Ethan C. Amir, Ariel Renner, Lars D. Front Microbiol Microbiology Mechanical rupture, or lysis, of the cytoplasmic membrane is a common cell death pathway in bacteria occurring in response to β-lactam antibiotics. A better understanding of the cellular design principles governing the susceptibility and response of individual cells to lysis could indicate methods of potentiating β-lactam antibiotics and clarify relevant aspects of cellular physiology. Here, we take a single-cell approach to bacterial cell lysis to examine three cellular features—turgor pressure, mechanosensitive channels, and cell shape changes—that are expected to modulate lysis. We develop a mechanical model of bacterial cell lysis and experimentally analyze the dynamics of lysis in hundreds of single Escherichia coli cells. We find that turgor pressure is the only factor, of these three cellular features, which robustly modulates lysis. We show that mechanosensitive channels do not modulate lysis due to insufficiently fast solute outflow, and that cell shape changes result in more severe cellular lesions but do not influence the dynamics of lysis. These results inform a single-cell view of bacterial cell lysis and underscore approaches of combatting antibiotic tolerance to β-lactams aimed at targeting cellular turgor. Frontiers Media S.A. 2021-07-27 /pmc/articles/PMC8372035/ /pubmed/34421870 http://dx.doi.org/10.3389/fmicb.2021.712007 Text en Copyright © 2021 Wong, Wilson, Helbig, Hegde, Aftenieva, Zheng, Liu, Pilizota, Garner, Amir and Renner. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Wong, Felix Wilson, Sean Helbig, Ralf Hegde, Smitha Aftenieva, Olha Zheng, Hai Liu, Chenli Pilizota, Teuta Garner, Ethan C. Amir, Ariel Renner, Lars D. Understanding Beta-Lactam-Induced Lysis at the Single-Cell Level |
title | Understanding Beta-Lactam-Induced Lysis at the Single-Cell Level |
title_full | Understanding Beta-Lactam-Induced Lysis at the Single-Cell Level |
title_fullStr | Understanding Beta-Lactam-Induced Lysis at the Single-Cell Level |
title_full_unstemmed | Understanding Beta-Lactam-Induced Lysis at the Single-Cell Level |
title_short | Understanding Beta-Lactam-Induced Lysis at the Single-Cell Level |
title_sort | understanding beta-lactam-induced lysis at the single-cell level |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8372035/ https://www.ncbi.nlm.nih.gov/pubmed/34421870 http://dx.doi.org/10.3389/fmicb.2021.712007 |
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