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The protected physiological state of intracellular Salmonella enterica persisters reduces host cell-imposed stress
During infectious diseases, small subpopulations of bacterial pathogens enter a non-replicating (NR) state tolerant to antibiotics. After phagocytosis, intracellular Salmonella enterica serovar Typhimurium (STM) forms persisters able to subvert immune defenses of the host. Physiological state and se...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8096953/ https://www.ncbi.nlm.nih.gov/pubmed/33947954 http://dx.doi.org/10.1038/s42003-021-02049-6 |
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author | Schulte, Marc Olschewski, Katharina Hensel, Michael |
author_facet | Schulte, Marc Olschewski, Katharina Hensel, Michael |
author_sort | Schulte, Marc |
collection | PubMed |
description | During infectious diseases, small subpopulations of bacterial pathogens enter a non-replicating (NR) state tolerant to antibiotics. After phagocytosis, intracellular Salmonella enterica serovar Typhimurium (STM) forms persisters able to subvert immune defenses of the host. Physiological state and sensing properties of persisters are difficult to analyze, thus poorly understood. Here we deploy fluorescent protein reporters to detect intracellular NR persister cells, and to monitor their stress response on single cell level. We determined metabolic properties of NR STM during infection and demonstrate that NR STM persisters sense their environment and respond to stressors. Since persisters showed a lower stress response compared to replicating (R) STM, which was not consequence of lower metabolic capacity, the persistent state of STM serves as protective niche. Up to 95% of NR STM were metabolically active at beginning of infection, very similar to metabolic capacity of R STM. Sensing and reacting to stress with constant metabolic activity supports STM to create a more permissive environment for recurrent infections. Stress sensing and response of persister may be targeted by new antimicrobial approaches. |
format | Online Article Text |
id | pubmed-8096953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80969532021-05-05 The protected physiological state of intracellular Salmonella enterica persisters reduces host cell-imposed stress Schulte, Marc Olschewski, Katharina Hensel, Michael Commun Biol Article During infectious diseases, small subpopulations of bacterial pathogens enter a non-replicating (NR) state tolerant to antibiotics. After phagocytosis, intracellular Salmonella enterica serovar Typhimurium (STM) forms persisters able to subvert immune defenses of the host. Physiological state and sensing properties of persisters are difficult to analyze, thus poorly understood. Here we deploy fluorescent protein reporters to detect intracellular NR persister cells, and to monitor their stress response on single cell level. We determined metabolic properties of NR STM during infection and demonstrate that NR STM persisters sense their environment and respond to stressors. Since persisters showed a lower stress response compared to replicating (R) STM, which was not consequence of lower metabolic capacity, the persistent state of STM serves as protective niche. Up to 95% of NR STM were metabolically active at beginning of infection, very similar to metabolic capacity of R STM. Sensing and reacting to stress with constant metabolic activity supports STM to create a more permissive environment for recurrent infections. Stress sensing and response of persister may be targeted by new antimicrobial approaches. Nature Publishing Group UK 2021-05-04 /pmc/articles/PMC8096953/ /pubmed/33947954 http://dx.doi.org/10.1038/s42003-021-02049-6 Text en © The Author(s) 2021 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 Schulte, Marc Olschewski, Katharina Hensel, Michael The protected physiological state of intracellular Salmonella enterica persisters reduces host cell-imposed stress |
title | The protected physiological state of intracellular Salmonella enterica persisters reduces host cell-imposed stress |
title_full | The protected physiological state of intracellular Salmonella enterica persisters reduces host cell-imposed stress |
title_fullStr | The protected physiological state of intracellular Salmonella enterica persisters reduces host cell-imposed stress |
title_full_unstemmed | The protected physiological state of intracellular Salmonella enterica persisters reduces host cell-imposed stress |
title_short | The protected physiological state of intracellular Salmonella enterica persisters reduces host cell-imposed stress |
title_sort | protected physiological state of intracellular salmonella enterica persisters reduces host cell-imposed stress |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8096953/ https://www.ncbi.nlm.nih.gov/pubmed/33947954 http://dx.doi.org/10.1038/s42003-021-02049-6 |
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