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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...

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Autores principales: Gonzales-Siles, Lucia, Karlsson, Roger, Kenny, Diarmuid, Karlsson, Anders, Sjöling, Åsa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
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.
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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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