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Functional analysis of Salmonella Typhi adaptation to survival in water
Contaminated water is a major risk factor associated with the transmission of Salmonella enterica serovar Typhi (S. Typhi), the aetiological agent of human typhoid. However, little is known about how this pathogen adapts to living in the aqueous environment. We used transcriptome analysis (RNA‐seq)...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282856/ https://www.ncbi.nlm.nih.gov/pubmed/30450829 http://dx.doi.org/10.1111/1462-2920.14458 |
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author | Kingsley, Robert A. Langridge, Gemma Smith, Sarah E. Makendi, Carine Fookes, Maria Wileman, Tom M. El Ghany, Moataz Abd Keith Turner, A. Dyson, Zoe A. Sridhar, Sushmita Pickard, Derek Kay, Sally Feasey, Nicholas Wong, Vanessa Barquist, Lars Dougan, Gordon |
author_facet | Kingsley, Robert A. Langridge, Gemma Smith, Sarah E. Makendi, Carine Fookes, Maria Wileman, Tom M. El Ghany, Moataz Abd Keith Turner, A. Dyson, Zoe A. Sridhar, Sushmita Pickard, Derek Kay, Sally Feasey, Nicholas Wong, Vanessa Barquist, Lars Dougan, Gordon |
author_sort | Kingsley, Robert A. |
collection | PubMed |
description | Contaminated water is a major risk factor associated with the transmission of Salmonella enterica serovar Typhi (S. Typhi), the aetiological agent of human typhoid. However, little is known about how this pathogen adapts to living in the aqueous environment. We used transcriptome analysis (RNA‐seq) and transposon mutagenesis (TraDIS) to characterize these adaptive changes and identify multiple genes that contribute to survival. Over half of the genes in the S. Typhi genome altered expression level within the first 24 h following transfer from broth culture to water, although relatively few did so in the first 30 min. Genes linked to central metabolism, stress associated with arrested proton motive force and respiratory chain factors changed expression levels. Additionally, motility and chemotaxis genes increased expression, consistent with a scavenging lifestyle. The viaB‐associated gene tviC encoding a glcNAc epimerase that is required for Vi polysaccharide biosynthesis was, along with several other genes, shown to contribute to survival in water. Thus, we define regulatory adaptation operating in S. Typhi that facilitates survival in water. |
format | Online Article Text |
id | pubmed-6282856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62828562018-12-14 Functional analysis of Salmonella Typhi adaptation to survival in water Kingsley, Robert A. Langridge, Gemma Smith, Sarah E. Makendi, Carine Fookes, Maria Wileman, Tom M. El Ghany, Moataz Abd Keith Turner, A. Dyson, Zoe A. Sridhar, Sushmita Pickard, Derek Kay, Sally Feasey, Nicholas Wong, Vanessa Barquist, Lars Dougan, Gordon Environ Microbiol Research Articles Contaminated water is a major risk factor associated with the transmission of Salmonella enterica serovar Typhi (S. Typhi), the aetiological agent of human typhoid. However, little is known about how this pathogen adapts to living in the aqueous environment. We used transcriptome analysis (RNA‐seq) and transposon mutagenesis (TraDIS) to characterize these adaptive changes and identify multiple genes that contribute to survival. Over half of the genes in the S. Typhi genome altered expression level within the first 24 h following transfer from broth culture to water, although relatively few did so in the first 30 min. Genes linked to central metabolism, stress associated with arrested proton motive force and respiratory chain factors changed expression levels. Additionally, motility and chemotaxis genes increased expression, consistent with a scavenging lifestyle. The viaB‐associated gene tviC encoding a glcNAc epimerase that is required for Vi polysaccharide biosynthesis was, along with several other genes, shown to contribute to survival in water. Thus, we define regulatory adaptation operating in S. Typhi that facilitates survival in water. John Wiley & Sons, Inc. 2018-11-18 2018-11 /pmc/articles/PMC6282856/ /pubmed/30450829 http://dx.doi.org/10.1111/1462-2920.14458 Text en © 2018 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Kingsley, Robert A. Langridge, Gemma Smith, Sarah E. Makendi, Carine Fookes, Maria Wileman, Tom M. El Ghany, Moataz Abd Keith Turner, A. Dyson, Zoe A. Sridhar, Sushmita Pickard, Derek Kay, Sally Feasey, Nicholas Wong, Vanessa Barquist, Lars Dougan, Gordon Functional analysis of Salmonella Typhi adaptation to survival in water |
title | Functional analysis of Salmonella Typhi adaptation to survival in water |
title_full | Functional analysis of Salmonella Typhi adaptation to survival in water |
title_fullStr | Functional analysis of Salmonella Typhi adaptation to survival in water |
title_full_unstemmed | Functional analysis of Salmonella Typhi adaptation to survival in water |
title_short | Functional analysis of Salmonella Typhi adaptation to survival in water |
title_sort | functional analysis of salmonella typhi adaptation to survival in water |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282856/ https://www.ncbi.nlm.nih.gov/pubmed/30450829 http://dx.doi.org/10.1111/1462-2920.14458 |
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