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A Nutrient-Tunable Bistable Switch Controls Motility in Salmonella enterica Serovar Typhimurium
Many bacteria are motile only when nutrients are scarce. In contrast, Salmonella enterica serovar Typhimurium is motile only when nutrients are plentiful, suggesting that this bacterium uses motility for purposes other than foraging, most likely for host colonization. In this study, we investigated...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Microbiology
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173784/ https://www.ncbi.nlm.nih.gov/pubmed/25161191 http://dx.doi.org/10.1128/mBio.01611-14 |
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author | Koirala, Santosh Mears, Patrick Sim, Martin Golding, Ido Chemla, Yann R. Aldridge, Phillip D. Rao, Christopher V. |
author_facet | Koirala, Santosh Mears, Patrick Sim, Martin Golding, Ido Chemla, Yann R. Aldridge, Phillip D. Rao, Christopher V. |
author_sort | Koirala, Santosh |
collection | PubMed |
description | Many bacteria are motile only when nutrients are scarce. In contrast, Salmonella enterica serovar Typhimurium is motile only when nutrients are plentiful, suggesting that this bacterium uses motility for purposes other than foraging, most likely for host colonization. In this study, we investigated how nutrients affect motility in S. enterica and found that they tune the fraction of motile cells. In particular, we observed coexisting populations of motile and nonmotile cells, with the distribution being determined by the concentration of nutrients in the growth medium. Interestingly, S. enterica responds not to a single nutrient but apparently to a complex mixture of them. Using a combination of experimentation and mathematical modeling, we investigated the mechanism governing this behavior and found that it results from two antagonizing regulatory proteins, FliZ and YdiV. We also found that a positive feedback loop involving the alternate sigma factor FliA is required, although its role appears solely to amplify FliZ expression. We further demonstrate that the response is bistable: that is, genetically identical cells can exhibit different phenotypes under identical growth conditions. Together, these results uncover a new facet of the regulation of the flagellar genes in S. enterica and further demonstrate how bacteria employ phenotypic diversity as a general mechanism for adapting to change in their environment. |
format | Online Article Text |
id | pubmed-4173784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Society of Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-41737842014-10-06 A Nutrient-Tunable Bistable Switch Controls Motility in Salmonella enterica Serovar Typhimurium Koirala, Santosh Mears, Patrick Sim, Martin Golding, Ido Chemla, Yann R. Aldridge, Phillip D. Rao, Christopher V. mBio Research Article Many bacteria are motile only when nutrients are scarce. In contrast, Salmonella enterica serovar Typhimurium is motile only when nutrients are plentiful, suggesting that this bacterium uses motility for purposes other than foraging, most likely for host colonization. In this study, we investigated how nutrients affect motility in S. enterica and found that they tune the fraction of motile cells. In particular, we observed coexisting populations of motile and nonmotile cells, with the distribution being determined by the concentration of nutrients in the growth medium. Interestingly, S. enterica responds not to a single nutrient but apparently to a complex mixture of them. Using a combination of experimentation and mathematical modeling, we investigated the mechanism governing this behavior and found that it results from two antagonizing regulatory proteins, FliZ and YdiV. We also found that a positive feedback loop involving the alternate sigma factor FliA is required, although its role appears solely to amplify FliZ expression. We further demonstrate that the response is bistable: that is, genetically identical cells can exhibit different phenotypes under identical growth conditions. Together, these results uncover a new facet of the regulation of the flagellar genes in S. enterica and further demonstrate how bacteria employ phenotypic diversity as a general mechanism for adapting to change in their environment. American Society of Microbiology 2014-08-26 /pmc/articles/PMC4173784/ /pubmed/25161191 http://dx.doi.org/10.1128/mBio.01611-14 Text en Copyright © 2014 Koirala et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 3.0 Unported license (http://creativecommons.org/licenses/by/3.0/) . |
spellingShingle | Research Article Koirala, Santosh Mears, Patrick Sim, Martin Golding, Ido Chemla, Yann R. Aldridge, Phillip D. Rao, Christopher V. A Nutrient-Tunable Bistable Switch Controls Motility in Salmonella enterica Serovar Typhimurium |
title | A Nutrient-Tunable Bistable Switch Controls Motility in Salmonella enterica Serovar Typhimurium |
title_full | A Nutrient-Tunable Bistable Switch Controls Motility in Salmonella enterica Serovar Typhimurium |
title_fullStr | A Nutrient-Tunable Bistable Switch Controls Motility in Salmonella enterica Serovar Typhimurium |
title_full_unstemmed | A Nutrient-Tunable Bistable Switch Controls Motility in Salmonella enterica Serovar Typhimurium |
title_short | A Nutrient-Tunable Bistable Switch Controls Motility in Salmonella enterica Serovar Typhimurium |
title_sort | nutrient-tunable bistable switch controls motility in salmonella enterica serovar typhimurium |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173784/ https://www.ncbi.nlm.nih.gov/pubmed/25161191 http://dx.doi.org/10.1128/mBio.01611-14 |
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