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Pleiotropic actions of phenothiazine drugs are detrimental to Gram-negative bacterial persister cells

Bacterial persister cells are temporarily tolerant to bactericidal antibiotics but are not necessarily dormant and may exhibit physiological activities leading to cell damage. Based on the link between fluoroquinolone-mediated SOS responses and persister cell recovery, we screened chemicals that tar...

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Autores principales: Mohiuddin, Sayed Golam, Nguyen, Thao Vy, Orman, Mehmet A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8907348/
https://www.ncbi.nlm.nih.gov/pubmed/35264714
http://dx.doi.org/10.1038/s42003-022-03172-8
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author Mohiuddin, Sayed Golam
Nguyen, Thao Vy
Orman, Mehmet A.
author_facet Mohiuddin, Sayed Golam
Nguyen, Thao Vy
Orman, Mehmet A.
author_sort Mohiuddin, Sayed Golam
collection PubMed
description Bacterial persister cells are temporarily tolerant to bactericidal antibiotics but are not necessarily dormant and may exhibit physiological activities leading to cell damage. Based on the link between fluoroquinolone-mediated SOS responses and persister cell recovery, we screened chemicals that target fluoroquinolone persisters. Metabolic inhibitors (e.g., phenothiazines) combined with ofloxacin (OFX) perturbed persister levels in metabolically active cell populations. When metabolically stimulated, intrinsically tolerant stationary phase cells also became OFX-sensitive in the presence of phenothiazines. The effects of phenothiazines on cell metabolism and physiology are highly pleiotropic: at sublethal concentrations, phenothiazines reduce cellular metabolic, transcriptional, and translational activities; impair cell repair and recovery mechanisms; transiently perturb membrane integrity; and disrupt proton motive force by dissipating the proton concentration gradient across the cell membrane. Screening a subset of mutant strains lacking membrane-bound proteins revealed the pleiotropic effects of phenothiazines potentially rely on their ability to inhibit a wide range of critical metabolic proteins. Altogether, our study further highlights the complex roles of metabolism in persister cell formation, survival and recovery, and suggests metabolic inhibitors such as phenothiazines can be selectively detrimental to persister cells.
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spelling pubmed-89073482022-03-23 Pleiotropic actions of phenothiazine drugs are detrimental to Gram-negative bacterial persister cells Mohiuddin, Sayed Golam Nguyen, Thao Vy Orman, Mehmet A. Commun Biol Article Bacterial persister cells are temporarily tolerant to bactericidal antibiotics but are not necessarily dormant and may exhibit physiological activities leading to cell damage. Based on the link between fluoroquinolone-mediated SOS responses and persister cell recovery, we screened chemicals that target fluoroquinolone persisters. Metabolic inhibitors (e.g., phenothiazines) combined with ofloxacin (OFX) perturbed persister levels in metabolically active cell populations. When metabolically stimulated, intrinsically tolerant stationary phase cells also became OFX-sensitive in the presence of phenothiazines. The effects of phenothiazines on cell metabolism and physiology are highly pleiotropic: at sublethal concentrations, phenothiazines reduce cellular metabolic, transcriptional, and translational activities; impair cell repair and recovery mechanisms; transiently perturb membrane integrity; and disrupt proton motive force by dissipating the proton concentration gradient across the cell membrane. Screening a subset of mutant strains lacking membrane-bound proteins revealed the pleiotropic effects of phenothiazines potentially rely on their ability to inhibit a wide range of critical metabolic proteins. Altogether, our study further highlights the complex roles of metabolism in persister cell formation, survival and recovery, and suggests metabolic inhibitors such as phenothiazines can be selectively detrimental to persister cells. Nature Publishing Group UK 2022-03-09 /pmc/articles/PMC8907348/ /pubmed/35264714 http://dx.doi.org/10.1038/s42003-022-03172-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mohiuddin, Sayed Golam
Nguyen, Thao Vy
Orman, Mehmet A.
Pleiotropic actions of phenothiazine drugs are detrimental to Gram-negative bacterial persister cells
title Pleiotropic actions of phenothiazine drugs are detrimental to Gram-negative bacterial persister cells
title_full Pleiotropic actions of phenothiazine drugs are detrimental to Gram-negative bacterial persister cells
title_fullStr Pleiotropic actions of phenothiazine drugs are detrimental to Gram-negative bacterial persister cells
title_full_unstemmed Pleiotropic actions of phenothiazine drugs are detrimental to Gram-negative bacterial persister cells
title_short Pleiotropic actions of phenothiazine drugs are detrimental to Gram-negative bacterial persister cells
title_sort pleiotropic actions of phenothiazine drugs are detrimental to gram-negative bacterial persister cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8907348/
https://www.ncbi.nlm.nih.gov/pubmed/35264714
http://dx.doi.org/10.1038/s42003-022-03172-8
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