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Decoding the genetic and functional diversity of the DSF quorum-sensing system in Stenotrophomonas maltophilia

Stenotrophomonas maltophilia uses the Diffusible Signal Factor (DSF) quorum sensing (QS) system to mediate intra- and inter-specific signaling and regulate virulence-related processes. The components of this system are encoded by the rpf cluster, with genes rpfF and rpfC encoding for the DSF synthas...

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Autores principales: Huedo, Pol, Yero, Daniel, Martinez-Servat, Sònia, Ruyra, Àngels, Roher, Nerea, Daura, Xavier, Gibert, Isidre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517397/
https://www.ncbi.nlm.nih.gov/pubmed/26284046
http://dx.doi.org/10.3389/fmicb.2015.00761
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author Huedo, Pol
Yero, Daniel
Martinez-Servat, Sònia
Ruyra, Àngels
Roher, Nerea
Daura, Xavier
Gibert, Isidre
author_facet Huedo, Pol
Yero, Daniel
Martinez-Servat, Sònia
Ruyra, Àngels
Roher, Nerea
Daura, Xavier
Gibert, Isidre
author_sort Huedo, Pol
collection PubMed
description Stenotrophomonas maltophilia uses the Diffusible Signal Factor (DSF) quorum sensing (QS) system to mediate intra- and inter-specific signaling and regulate virulence-related processes. The components of this system are encoded by the rpf cluster, with genes rpfF and rpfC encoding for the DSF synthase RpfF and sensor RpfC, respectively. Recently, we have shown that there exist two variants of the rpf cluster (rpf-1 and rpf-2), distinguishing two groups of S. maltophilia strains. Surprisingly, only rpf-1 strains produce detectable DSF, correlating with their ability to control biofilm formation, swarming motility and virulence. The evolutive advantage of acquiring two different rpf clusters, the phylogenetic time point and mechanism of this acquisition and the conditions that activate DSF production in rpf-2 strains, are however not known. Examination of this cluster in various species suggests that its variability originated most probably by genetic exchange between rhizosphere bacteria. We propose that rpf-2 variant strains make use of a strategy recently termed as “social cheating.” Analysis of cellular and extracellular fatty acids (FAs) of strains E77 (rpf-1) and M30 (rpf-2) suggests that their RpfFs have also a thioesterase activity that facilitates the release of unspecific FAs to the medium in addition to DSF. Production of DSF in rpf-1 strains appears in fact to be modulated by some of these extracellular FAs in addition to other factors such as temperature and nutrients, while in rpf-2 strains DSF biosynthesis is derepressed only upon detection of DSF itself, suggesting that they require cohabitation with DSF-producer bacteria to activate their DSF regulatory machinery. Finally, we show that the mixed rpf-1/rpf-2 population presents synergism in DSF production and virulence capacity in an in vivo infection model. Recovery and quantification of DSF from co-infected animals correlates with the observed mortality rate.
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spelling pubmed-45173972015-08-17 Decoding the genetic and functional diversity of the DSF quorum-sensing system in Stenotrophomonas maltophilia Huedo, Pol Yero, Daniel Martinez-Servat, Sònia Ruyra, Àngels Roher, Nerea Daura, Xavier Gibert, Isidre Front Microbiol Public Health Stenotrophomonas maltophilia uses the Diffusible Signal Factor (DSF) quorum sensing (QS) system to mediate intra- and inter-specific signaling and regulate virulence-related processes. The components of this system are encoded by the rpf cluster, with genes rpfF and rpfC encoding for the DSF synthase RpfF and sensor RpfC, respectively. Recently, we have shown that there exist two variants of the rpf cluster (rpf-1 and rpf-2), distinguishing two groups of S. maltophilia strains. Surprisingly, only rpf-1 strains produce detectable DSF, correlating with their ability to control biofilm formation, swarming motility and virulence. The evolutive advantage of acquiring two different rpf clusters, the phylogenetic time point and mechanism of this acquisition and the conditions that activate DSF production in rpf-2 strains, are however not known. Examination of this cluster in various species suggests that its variability originated most probably by genetic exchange between rhizosphere bacteria. We propose that rpf-2 variant strains make use of a strategy recently termed as “social cheating.” Analysis of cellular and extracellular fatty acids (FAs) of strains E77 (rpf-1) and M30 (rpf-2) suggests that their RpfFs have also a thioesterase activity that facilitates the release of unspecific FAs to the medium in addition to DSF. Production of DSF in rpf-1 strains appears in fact to be modulated by some of these extracellular FAs in addition to other factors such as temperature and nutrients, while in rpf-2 strains DSF biosynthesis is derepressed only upon detection of DSF itself, suggesting that they require cohabitation with DSF-producer bacteria to activate their DSF regulatory machinery. Finally, we show that the mixed rpf-1/rpf-2 population presents synergism in DSF production and virulence capacity in an in vivo infection model. Recovery and quantification of DSF from co-infected animals correlates with the observed mortality rate. Frontiers Media S.A. 2015-07-28 /pmc/articles/PMC4517397/ /pubmed/26284046 http://dx.doi.org/10.3389/fmicb.2015.00761 Text en Copyright © 2015 Huedo, Yero, Martinez-Servat, Ruyra, Roher, Daura and Gibert. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Public Health
Huedo, Pol
Yero, Daniel
Martinez-Servat, Sònia
Ruyra, Àngels
Roher, Nerea
Daura, Xavier
Gibert, Isidre
Decoding the genetic and functional diversity of the DSF quorum-sensing system in Stenotrophomonas maltophilia
title Decoding the genetic and functional diversity of the DSF quorum-sensing system in Stenotrophomonas maltophilia
title_full Decoding the genetic and functional diversity of the DSF quorum-sensing system in Stenotrophomonas maltophilia
title_fullStr Decoding the genetic and functional diversity of the DSF quorum-sensing system in Stenotrophomonas maltophilia
title_full_unstemmed Decoding the genetic and functional diversity of the DSF quorum-sensing system in Stenotrophomonas maltophilia
title_short Decoding the genetic and functional diversity of the DSF quorum-sensing system in Stenotrophomonas maltophilia
title_sort decoding the genetic and functional diversity of the dsf quorum-sensing system in stenotrophomonas maltophilia
topic Public Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517397/
https://www.ncbi.nlm.nih.gov/pubmed/26284046
http://dx.doi.org/10.3389/fmicb.2015.00761
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