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FlpS, the FNR-Like Protein of Streptococcus suis Is an Essential, Oxygen-Sensing Activator of the Arginine Deiminase System
Streptococcus (S.) suis is a zoonotic pathogen causing septicemia and meningitis in pigs and humans. During infection S. suis must metabolically adapt to extremely diverse environments of the host. CcpA and the FNR family of bacterial transcriptional regulators are important for metabolic gene regul...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039431/ https://www.ncbi.nlm.nih.gov/pubmed/27455333 http://dx.doi.org/10.3390/pathogens5030051 |
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author | Willenborg, Jörg Koczula, Anna Fulde, Marcus de Greeff, Astrid Beineke, Andreas Eisenreich, Wolfgang Huber, Claudia Seitz, Maren Valentin-Weigand, Peter Goethe, Ralph |
author_facet | Willenborg, Jörg Koczula, Anna Fulde, Marcus de Greeff, Astrid Beineke, Andreas Eisenreich, Wolfgang Huber, Claudia Seitz, Maren Valentin-Weigand, Peter Goethe, Ralph |
author_sort | Willenborg, Jörg |
collection | PubMed |
description | Streptococcus (S.) suis is a zoonotic pathogen causing septicemia and meningitis in pigs and humans. During infection S. suis must metabolically adapt to extremely diverse environments of the host. CcpA and the FNR family of bacterial transcriptional regulators are important for metabolic gene regulation in various bacteria. The role of CcpA in S. suis is well defined, but the function of the FNR-like protein of S. suis, FlpS, is yet unknown. Transcriptome analyses of wild-type S. suis and a flpS mutant strain suggested that FlpS is involved in the regulation of the central carbon, arginine degradation and nucleotide metabolism. However, isotopologue profiling revealed no substantial changes in the core carbon and amino acid de novo biosynthesis. FlpS was essential for the induction of the arcABC operon of the arginine degrading pathway under aerobic and anaerobic conditions. The arcABC-inducing activity of FlpS could be associated with the level of free oxygen in the culture medium. FlpS was necessary for arcABC-dependent intracellular bacterial survival but redundant in a mice infection model. Based on these results, we propose that the core function of S. suis FlpS is the oxygen-dependent activation of the arginine deiminase system. |
format | Online Article Text |
id | pubmed-5039431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-50394312016-10-04 FlpS, the FNR-Like Protein of Streptococcus suis Is an Essential, Oxygen-Sensing Activator of the Arginine Deiminase System Willenborg, Jörg Koczula, Anna Fulde, Marcus de Greeff, Astrid Beineke, Andreas Eisenreich, Wolfgang Huber, Claudia Seitz, Maren Valentin-Weigand, Peter Goethe, Ralph Pathogens Article Streptococcus (S.) suis is a zoonotic pathogen causing septicemia and meningitis in pigs and humans. During infection S. suis must metabolically adapt to extremely diverse environments of the host. CcpA and the FNR family of bacterial transcriptional regulators are important for metabolic gene regulation in various bacteria. The role of CcpA in S. suis is well defined, but the function of the FNR-like protein of S. suis, FlpS, is yet unknown. Transcriptome analyses of wild-type S. suis and a flpS mutant strain suggested that FlpS is involved in the regulation of the central carbon, arginine degradation and nucleotide metabolism. However, isotopologue profiling revealed no substantial changes in the core carbon and amino acid de novo biosynthesis. FlpS was essential for the induction of the arcABC operon of the arginine degrading pathway under aerobic and anaerobic conditions. The arcABC-inducing activity of FlpS could be associated with the level of free oxygen in the culture medium. FlpS was necessary for arcABC-dependent intracellular bacterial survival but redundant in a mice infection model. Based on these results, we propose that the core function of S. suis FlpS is the oxygen-dependent activation of the arginine deiminase system. MDPI 2016-07-21 /pmc/articles/PMC5039431/ /pubmed/27455333 http://dx.doi.org/10.3390/pathogens5030051 Text en © 2016 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 Willenborg, Jörg Koczula, Anna Fulde, Marcus de Greeff, Astrid Beineke, Andreas Eisenreich, Wolfgang Huber, Claudia Seitz, Maren Valentin-Weigand, Peter Goethe, Ralph FlpS, the FNR-Like Protein of Streptococcus suis Is an Essential, Oxygen-Sensing Activator of the Arginine Deiminase System |
title | FlpS, the FNR-Like Protein of Streptococcus suis Is an Essential, Oxygen-Sensing Activator of the Arginine Deiminase System |
title_full | FlpS, the FNR-Like Protein of Streptococcus suis Is an Essential, Oxygen-Sensing Activator of the Arginine Deiminase System |
title_fullStr | FlpS, the FNR-Like Protein of Streptococcus suis Is an Essential, Oxygen-Sensing Activator of the Arginine Deiminase System |
title_full_unstemmed | FlpS, the FNR-Like Protein of Streptococcus suis Is an Essential, Oxygen-Sensing Activator of the Arginine Deiminase System |
title_short | FlpS, the FNR-Like Protein of Streptococcus suis Is an Essential, Oxygen-Sensing Activator of the Arginine Deiminase System |
title_sort | flps, the fnr-like protein of streptococcus suis is an essential, oxygen-sensing activator of the arginine deiminase system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039431/ https://www.ncbi.nlm.nih.gov/pubmed/27455333 http://dx.doi.org/10.3390/pathogens5030051 |
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