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New Roles for Two-Component System Response Regulators of Salmonella enterica Serovar Typhi during Host Cell Interactions

In order to survive external stresses, bacteria need to adapt quickly to changes in their environment. One adaptive mechanism is to coordinate and alter their gene expression by using two-component systems (TCS). TCS are composed of a sensor kinase that activates a transcriptional response regulator...

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Autores principales: Murret-Labarthe, Claudie, Kerhoas, Maud, Dufresne, Karine, Daigle, France
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7285189/
https://www.ncbi.nlm.nih.gov/pubmed/32413972
http://dx.doi.org/10.3390/microorganisms8050722
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author Murret-Labarthe, Claudie
Kerhoas, Maud
Dufresne, Karine
Daigle, France
author_facet Murret-Labarthe, Claudie
Kerhoas, Maud
Dufresne, Karine
Daigle, France
author_sort Murret-Labarthe, Claudie
collection PubMed
description In order to survive external stresses, bacteria need to adapt quickly to changes in their environment. One adaptive mechanism is to coordinate and alter their gene expression by using two-component systems (TCS). TCS are composed of a sensor kinase that activates a transcriptional response regulator by phosphorylation. TCS are involved in motility, virulence, nutrient acquisition, and envelope stress in many bacteria. The pathogenic bacteria Salmonella enterica serovar Typhi (S. Typhi) possess 30 TCSs, is specific to humans, and causes typhoid fever. Here, we have individually deleted each of the 30 response regulators. We have determined their role during interaction with host cells (epithelial cells and macrophages). Deletion of most of the systems (24 out of 30) resulted in a significant change during infection. We have identified 32 new phenotypes associated with TCS of S. Typhi. Some previously known phenotypes associated with TCSs in Salmonella were also confirmed. We have also uncovered phenotypic divergence between Salmonella serovars, as distinct phenotypes between S. Typhi and S. Typhimurium were identified for cpxR. This finding highlights the importance of specifically studying S. Typhi to understand its pathogenesis mechanisms and to develop strategies to potentially reduce typhoid infections.
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spelling pubmed-72851892020-06-18 New Roles for Two-Component System Response Regulators of Salmonella enterica Serovar Typhi during Host Cell Interactions Murret-Labarthe, Claudie Kerhoas, Maud Dufresne, Karine Daigle, France Microorganisms Article In order to survive external stresses, bacteria need to adapt quickly to changes in their environment. One adaptive mechanism is to coordinate and alter their gene expression by using two-component systems (TCS). TCS are composed of a sensor kinase that activates a transcriptional response regulator by phosphorylation. TCS are involved in motility, virulence, nutrient acquisition, and envelope stress in many bacteria. The pathogenic bacteria Salmonella enterica serovar Typhi (S. Typhi) possess 30 TCSs, is specific to humans, and causes typhoid fever. Here, we have individually deleted each of the 30 response regulators. We have determined their role during interaction with host cells (epithelial cells and macrophages). Deletion of most of the systems (24 out of 30) resulted in a significant change during infection. We have identified 32 new phenotypes associated with TCS of S. Typhi. Some previously known phenotypes associated with TCSs in Salmonella were also confirmed. We have also uncovered phenotypic divergence between Salmonella serovars, as distinct phenotypes between S. Typhi and S. Typhimurium were identified for cpxR. This finding highlights the importance of specifically studying S. Typhi to understand its pathogenesis mechanisms and to develop strategies to potentially reduce typhoid infections. MDPI 2020-05-13 /pmc/articles/PMC7285189/ /pubmed/32413972 http://dx.doi.org/10.3390/microorganisms8050722 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Murret-Labarthe, Claudie
Kerhoas, Maud
Dufresne, Karine
Daigle, France
New Roles for Two-Component System Response Regulators of Salmonella enterica Serovar Typhi during Host Cell Interactions
title New Roles for Two-Component System Response Regulators of Salmonella enterica Serovar Typhi during Host Cell Interactions
title_full New Roles for Two-Component System Response Regulators of Salmonella enterica Serovar Typhi during Host Cell Interactions
title_fullStr New Roles for Two-Component System Response Regulators of Salmonella enterica Serovar Typhi during Host Cell Interactions
title_full_unstemmed New Roles for Two-Component System Response Regulators of Salmonella enterica Serovar Typhi during Host Cell Interactions
title_short New Roles for Two-Component System Response Regulators of Salmonella enterica Serovar Typhi during Host Cell Interactions
title_sort new roles for two-component system response regulators of salmonella enterica serovar typhi during host cell interactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7285189/
https://www.ncbi.nlm.nih.gov/pubmed/32413972
http://dx.doi.org/10.3390/microorganisms8050722
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