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Evolutionary potential, cross-stress behavior and the genetic basis of acquired stress resistance in Escherichia coli
Bacterial populations have a remarkable capacity to cope with extreme environmental fluctuations in their natural environments. In certain cases, adaptation to one stressful environment provides a fitness advantage when cells are exposed to a second stressor, a phenomenon that has been coined as cro...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Molecular Biology Organization
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588905/ https://www.ncbi.nlm.nih.gov/pubmed/23385483 http://dx.doi.org/10.1038/msb.2012.76 |
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author | Dragosits, Martin Mozhayskiy, Vadim Quinones-Soto, Semarhy Park, Jiyeon Tagkopoulos, Ilias |
author_facet | Dragosits, Martin Mozhayskiy, Vadim Quinones-Soto, Semarhy Park, Jiyeon Tagkopoulos, Ilias |
author_sort | Dragosits, Martin |
collection | PubMed |
description | Bacterial populations have a remarkable capacity to cope with extreme environmental fluctuations in their natural environments. In certain cases, adaptation to one stressful environment provides a fitness advantage when cells are exposed to a second stressor, a phenomenon that has been coined as cross-stress protection. A tantalizing question in bacterial physiology is how the cross-stress behavior emerges during evolutionary adaptation and what the genetic basis of acquired stress resistance is. To address these questions, we evolved Escherichia coli cells over 500 generations in five environments that include four abiotic stressors. Through growth profiling and competition assays, we identified several cases of positive and negative cross-stress behavior that span all strain–stress combinations. Resequencing the genomes of the evolved strains resulted in the identification of several mutations and gene amplifications, whose fitness effect was further assessed by mutation reversal and competition assays. Transcriptional profiling of all strains under a specific stress, NaCl-induced osmotic stress, and integration with resequencing data further elucidated the regulatory responses and genes that are involved in this phenomenon. Our results suggest that cross-stress dependencies are ubiquitous, highly interconnected, and can emerge within short timeframes. The high adaptive potential that we observed argues that bacterial populations occupy a genotypic space that enables a high phenotypic plasticity during adaptation in fluctuating environments. |
format | Online Article Text |
id | pubmed-3588905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | European Molecular Biology Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-35889052013-03-06 Evolutionary potential, cross-stress behavior and the genetic basis of acquired stress resistance in Escherichia coli Dragosits, Martin Mozhayskiy, Vadim Quinones-Soto, Semarhy Park, Jiyeon Tagkopoulos, Ilias Mol Syst Biol Article Bacterial populations have a remarkable capacity to cope with extreme environmental fluctuations in their natural environments. In certain cases, adaptation to one stressful environment provides a fitness advantage when cells are exposed to a second stressor, a phenomenon that has been coined as cross-stress protection. A tantalizing question in bacterial physiology is how the cross-stress behavior emerges during evolutionary adaptation and what the genetic basis of acquired stress resistance is. To address these questions, we evolved Escherichia coli cells over 500 generations in five environments that include four abiotic stressors. Through growth profiling and competition assays, we identified several cases of positive and negative cross-stress behavior that span all strain–stress combinations. Resequencing the genomes of the evolved strains resulted in the identification of several mutations and gene amplifications, whose fitness effect was further assessed by mutation reversal and competition assays. Transcriptional profiling of all strains under a specific stress, NaCl-induced osmotic stress, and integration with resequencing data further elucidated the regulatory responses and genes that are involved in this phenomenon. Our results suggest that cross-stress dependencies are ubiquitous, highly interconnected, and can emerge within short timeframes. The high adaptive potential that we observed argues that bacterial populations occupy a genotypic space that enables a high phenotypic plasticity during adaptation in fluctuating environments. European Molecular Biology Organization 2013-02-05 /pmc/articles/PMC3588905/ /pubmed/23385483 http://dx.doi.org/10.1038/msb.2012.76 Text en Copyright © 2013, EMBO and Macmillan Publishers Limited https://creativecommons.org/licenses/by-nc-sa/3.0/This article is licensed under a Creative Commons Attribution Noncommercial Share Alike 3.0 Unported License. |
spellingShingle | Article Dragosits, Martin Mozhayskiy, Vadim Quinones-Soto, Semarhy Park, Jiyeon Tagkopoulos, Ilias Evolutionary potential, cross-stress behavior and the genetic basis of acquired stress resistance in Escherichia coli |
title | Evolutionary potential, cross-stress behavior and the genetic basis of acquired stress resistance in Escherichia coli |
title_full | Evolutionary potential, cross-stress behavior and the genetic basis of acquired stress resistance in Escherichia coli |
title_fullStr | Evolutionary potential, cross-stress behavior and the genetic basis of acquired stress resistance in Escherichia coli |
title_full_unstemmed | Evolutionary potential, cross-stress behavior and the genetic basis of acquired stress resistance in Escherichia coli |
title_short | Evolutionary potential, cross-stress behavior and the genetic basis of acquired stress resistance in Escherichia coli |
title_sort | evolutionary potential, cross-stress behavior and the genetic basis of acquired stress resistance in escherichia coli |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588905/ https://www.ncbi.nlm.nih.gov/pubmed/23385483 http://dx.doi.org/10.1038/msb.2012.76 |
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