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Proteomic analysis of enterotoxigenic Escherichia coli (ETEC) in neutral and alkaline conditions
BACKGROUND: Enterotoxigenic Escherichia coli (ETEC) is a major cause of diarrhea in children and travelers to endemic areas. Secretion of the heat labile AB(5) toxin (LT) is induced by alkaline conditions. In this study, we determined the surface proteome of ETEC exposed to alkaline conditions (pH 9...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5219706/ https://www.ncbi.nlm.nih.gov/pubmed/28061865 http://dx.doi.org/10.1186/s12866-016-0914-1 |
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author | Gonzales-Siles, Lucia Karlsson, Roger Kenny, Diarmuid Karlsson, Anders Sjöling, Åsa |
author_facet | Gonzales-Siles, Lucia Karlsson, Roger Kenny, Diarmuid Karlsson, Anders Sjöling, Åsa |
author_sort | Gonzales-Siles, Lucia |
collection | PubMed |
description | BACKGROUND: Enterotoxigenic Escherichia coli (ETEC) is a major cause of diarrhea in children and travelers to endemic areas. Secretion of the heat labile AB(5) toxin (LT) is induced by alkaline conditions. In this study, we determined the surface proteome of ETEC exposed to alkaline conditions (pH 9) as compared to neutral conditions (pH 7) using a LPI Hexalane FlowCell combined with quantitative proteomics. Relative quantitation with isobaric labeling (TMT) was used to compare peptide abundance and their corresponding proteins in multiple samples at MS/MS level. For protein identification and quantification samples were analyzed using either a 1D-LCMS or a 2D-LCMS approach. RESULTS: Strong up-regulation of the ATP synthase operon encoding F1Fo ATP synthase and down-regulation of proton pumping proteins NuoF, NuoG, Ndh and WrbA were detected among proteins involved in regulating the proton and electron transport under alkaline conditions. Reduced expression of proteins involved in osmotic stress was found at alkaline conditions while the Sec-dependent transport over the inner membrane and outer membrane protein proteins such as OmpA and the β-Barrel Assembly Machinery (BAM) complex were up-regulated. CONCLUSIONS: ETEC exposed to alkaline environments express a specific proteome profile characterized by up-regulation of membrane proteins and secretion of LT toxin. Alkaline microenvironments have been reported close to the intestinal epithelium and the alkaline proteome may hence represent a better view of ETEC during infection. |
format | Online Article Text |
id | pubmed-5219706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-52197062017-01-11 Proteomic analysis of enterotoxigenic Escherichia coli (ETEC) in neutral and alkaline conditions Gonzales-Siles, Lucia Karlsson, Roger Kenny, Diarmuid Karlsson, Anders Sjöling, Åsa BMC Microbiol Research Article BACKGROUND: Enterotoxigenic Escherichia coli (ETEC) is a major cause of diarrhea in children and travelers to endemic areas. Secretion of the heat labile AB(5) toxin (LT) is induced by alkaline conditions. In this study, we determined the surface proteome of ETEC exposed to alkaline conditions (pH 9) as compared to neutral conditions (pH 7) using a LPI Hexalane FlowCell combined with quantitative proteomics. Relative quantitation with isobaric labeling (TMT) was used to compare peptide abundance and their corresponding proteins in multiple samples at MS/MS level. For protein identification and quantification samples were analyzed using either a 1D-LCMS or a 2D-LCMS approach. RESULTS: Strong up-regulation of the ATP synthase operon encoding F1Fo ATP synthase and down-regulation of proton pumping proteins NuoF, NuoG, Ndh and WrbA were detected among proteins involved in regulating the proton and electron transport under alkaline conditions. Reduced expression of proteins involved in osmotic stress was found at alkaline conditions while the Sec-dependent transport over the inner membrane and outer membrane protein proteins such as OmpA and the β-Barrel Assembly Machinery (BAM) complex were up-regulated. CONCLUSIONS: ETEC exposed to alkaline environments express a specific proteome profile characterized by up-regulation of membrane proteins and secretion of LT toxin. Alkaline microenvironments have been reported close to the intestinal epithelium and the alkaline proteome may hence represent a better view of ETEC during infection. BioMed Central 2017-01-07 /pmc/articles/PMC5219706/ /pubmed/28061865 http://dx.doi.org/10.1186/s12866-016-0914-1 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Gonzales-Siles, Lucia Karlsson, Roger Kenny, Diarmuid Karlsson, Anders Sjöling, Åsa Proteomic analysis of enterotoxigenic Escherichia coli (ETEC) in neutral and alkaline conditions |
title | Proteomic analysis of enterotoxigenic Escherichia coli (ETEC) in neutral and alkaline conditions |
title_full | Proteomic analysis of enterotoxigenic Escherichia coli (ETEC) in neutral and alkaline conditions |
title_fullStr | Proteomic analysis of enterotoxigenic Escherichia coli (ETEC) in neutral and alkaline conditions |
title_full_unstemmed | Proteomic analysis of enterotoxigenic Escherichia coli (ETEC) in neutral and alkaline conditions |
title_short | Proteomic analysis of enterotoxigenic Escherichia coli (ETEC) in neutral and alkaline conditions |
title_sort | proteomic analysis of enterotoxigenic escherichia coli (etec) in neutral and alkaline conditions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5219706/ https://www.ncbi.nlm.nih.gov/pubmed/28061865 http://dx.doi.org/10.1186/s12866-016-0914-1 |
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