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The role of the two-component systems Cpx and Arc in protein alterations upon gentamicin treatment in Escherichia coli
BACKGROUND: The aminoglycoside antibiotic gentamicin was supposed to induce a crosstalk between the Cpx- and the Arc-two-component systems (TCS). Here, we investigated the physical interaction of the respective TCS components and compared the results with their respective gene expression and protein...
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/PMC5604497/ https://www.ncbi.nlm.nih.gov/pubmed/28923010 http://dx.doi.org/10.1186/s12866-017-1100-9 |
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author | Ćudić, Emina Surmann, Kristin Panasia, Gianna Hammer, Elke Hunke, Sabine |
author_facet | Ćudić, Emina Surmann, Kristin Panasia, Gianna Hammer, Elke Hunke, Sabine |
author_sort | Ćudić, Emina |
collection | PubMed |
description | BACKGROUND: The aminoglycoside antibiotic gentamicin was supposed to induce a crosstalk between the Cpx- and the Arc-two-component systems (TCS). Here, we investigated the physical interaction of the respective TCS components and compared the results with their respective gene expression and protein abundance. The findings were interpreted in relation to the global proteome profile upon gentamicin treatment. RESULTS: We observed specific interaction between CpxA and ArcA upon treatment with the aminoglycoside gentamicin using Membrane-Strep-tagged protein interaction experiments (mSPINE). This interaction was neither accompanied by detectable phosphorylation of ArcA nor by activation of the Arc system via CpxA. Furthermore, no changes in absolute amounts of the Cpx- and Arc-TCS could be determined with the sensitive single reaction monitoring (SRM) in presence of gentamicin. Nevertheless, upon applying shotgun mass spectrometry analysis after treatment with gentamicin, we observed a reduction of ArcA ~ P-dependent protein synthesis and a significant Cpx-dependent alteration in the global proteome profile of E. coli. CONCLUSIONS: This study points to the importance of the Cpx-TCS within the complex regulatory network in the E. coli response to aminoglycoside-caused stress. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-017-1100-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5604497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56044972017-09-20 The role of the two-component systems Cpx and Arc in protein alterations upon gentamicin treatment in Escherichia coli Ćudić, Emina Surmann, Kristin Panasia, Gianna Hammer, Elke Hunke, Sabine BMC Microbiol Research Article BACKGROUND: The aminoglycoside antibiotic gentamicin was supposed to induce a crosstalk between the Cpx- and the Arc-two-component systems (TCS). Here, we investigated the physical interaction of the respective TCS components and compared the results with their respective gene expression and protein abundance. The findings were interpreted in relation to the global proteome profile upon gentamicin treatment. RESULTS: We observed specific interaction between CpxA and ArcA upon treatment with the aminoglycoside gentamicin using Membrane-Strep-tagged protein interaction experiments (mSPINE). This interaction was neither accompanied by detectable phosphorylation of ArcA nor by activation of the Arc system via CpxA. Furthermore, no changes in absolute amounts of the Cpx- and Arc-TCS could be determined with the sensitive single reaction monitoring (SRM) in presence of gentamicin. Nevertheless, upon applying shotgun mass spectrometry analysis after treatment with gentamicin, we observed a reduction of ArcA ~ P-dependent protein synthesis and a significant Cpx-dependent alteration in the global proteome profile of E. coli. CONCLUSIONS: This study points to the importance of the Cpx-TCS within the complex regulatory network in the E. coli response to aminoglycoside-caused stress. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-017-1100-9) contains supplementary material, which is available to authorized users. BioMed Central 2017-09-18 /pmc/articles/PMC5604497/ /pubmed/28923010 http://dx.doi.org/10.1186/s12866-017-1100-9 Text en © The Author(s). 2017 Open Access This 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 Ćudić, Emina Surmann, Kristin Panasia, Gianna Hammer, Elke Hunke, Sabine The role of the two-component systems Cpx and Arc in protein alterations upon gentamicin treatment in Escherichia coli |
title | The role of the two-component systems Cpx and Arc in protein alterations upon gentamicin treatment in Escherichia coli |
title_full | The role of the two-component systems Cpx and Arc in protein alterations upon gentamicin treatment in Escherichia coli |
title_fullStr | The role of the two-component systems Cpx and Arc in protein alterations upon gentamicin treatment in Escherichia coli |
title_full_unstemmed | The role of the two-component systems Cpx and Arc in protein alterations upon gentamicin treatment in Escherichia coli |
title_short | The role of the two-component systems Cpx and Arc in protein alterations upon gentamicin treatment in Escherichia coli |
title_sort | role of the two-component systems cpx and arc in protein alterations upon gentamicin treatment in escherichia coli |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5604497/ https://www.ncbi.nlm.nih.gov/pubmed/28923010 http://dx.doi.org/10.1186/s12866-017-1100-9 |
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