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Surface sensing triggers a broad‐spectrum antimicrobial response in Pseudomonas aeruginosa

Interspecies bacterial competition may occur via cell‐associated or secreted determinants and is key to successful niche colonization. We previously evolved Pseudomonas aeruginosa in the presence of Staphylococcus aureus and identified mutations in the Wsp surface‐sensing signalling system. Surprisi...

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Autores principales: Gdaniec, Bartosz Gerard, Allard, Pierre‐Marie, Queiroz, Emerson Ferreira, Wolfender, Jean‐Luc, van Delden, Christian, Köhler, Thilo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496599/
https://www.ncbi.nlm.nih.gov/pubmed/32573899
http://dx.doi.org/10.1111/1462-2920.15139
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author Gdaniec, Bartosz Gerard
Allard, Pierre‐Marie
Queiroz, Emerson Ferreira
Wolfender, Jean‐Luc
van Delden, Christian
Köhler, Thilo
author_facet Gdaniec, Bartosz Gerard
Allard, Pierre‐Marie
Queiroz, Emerson Ferreira
Wolfender, Jean‐Luc
van Delden, Christian
Köhler, Thilo
author_sort Gdaniec, Bartosz Gerard
collection PubMed
description Interspecies bacterial competition may occur via cell‐associated or secreted determinants and is key to successful niche colonization. We previously evolved Pseudomonas aeruginosa in the presence of Staphylococcus aureus and identified mutations in the Wsp surface‐sensing signalling system. Surprisingly, a ΔwspF mutant, characterized by increased c‐di‐GMP levels and biofilm formation capacity, showed potent killing activity towards S. aureus in its culture supernatant. Here, we used an unbiased metabolomic analysis of culture supernatants to identify rhamnolipids, alkyl quinoline N‐oxides and two siderophores as members of four chemical clusters, which were more abundant in the ΔwspF mutant supernatants. Killing activities were quorum‐sensing controlled but independent of c‐di‐GMP levels. Based on the metabolomic analysis, we formulated a synthetic cocktail of four compounds, showing broad‐spectrum anti‐bacterial killing, including both Gram‐positive and Gram‐negative bacteria. The combination of quorum‐sensing‐controlled killing and Wsp‐system mediated biofilm formation endows P. aeruginosa with capacities essential for niche establishment and host colonization.
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spelling pubmed-74965992020-09-25 Surface sensing triggers a broad‐spectrum antimicrobial response in Pseudomonas aeruginosa Gdaniec, Bartosz Gerard Allard, Pierre‐Marie Queiroz, Emerson Ferreira Wolfender, Jean‐Luc van Delden, Christian Köhler, Thilo Environ Microbiol Research Articles Interspecies bacterial competition may occur via cell‐associated or secreted determinants and is key to successful niche colonization. We previously evolved Pseudomonas aeruginosa in the presence of Staphylococcus aureus and identified mutations in the Wsp surface‐sensing signalling system. Surprisingly, a ΔwspF mutant, characterized by increased c‐di‐GMP levels and biofilm formation capacity, showed potent killing activity towards S. aureus in its culture supernatant. Here, we used an unbiased metabolomic analysis of culture supernatants to identify rhamnolipids, alkyl quinoline N‐oxides and two siderophores as members of four chemical clusters, which were more abundant in the ΔwspF mutant supernatants. Killing activities were quorum‐sensing controlled but independent of c‐di‐GMP levels. Based on the metabolomic analysis, we formulated a synthetic cocktail of four compounds, showing broad‐spectrum anti‐bacterial killing, including both Gram‐positive and Gram‐negative bacteria. The combination of quorum‐sensing‐controlled killing and Wsp‐system mediated biofilm formation endows P. aeruginosa with capacities essential for niche establishment and host colonization. John Wiley & Sons, Inc. 2020-07-10 2020-08 /pmc/articles/PMC7496599/ /pubmed/32573899 http://dx.doi.org/10.1111/1462-2920.15139 Text en © 2020 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Gdaniec, Bartosz Gerard
Allard, Pierre‐Marie
Queiroz, Emerson Ferreira
Wolfender, Jean‐Luc
van Delden, Christian
Köhler, Thilo
Surface sensing triggers a broad‐spectrum antimicrobial response in Pseudomonas aeruginosa
title Surface sensing triggers a broad‐spectrum antimicrobial response in Pseudomonas aeruginosa
title_full Surface sensing triggers a broad‐spectrum antimicrobial response in Pseudomonas aeruginosa
title_fullStr Surface sensing triggers a broad‐spectrum antimicrobial response in Pseudomonas aeruginosa
title_full_unstemmed Surface sensing triggers a broad‐spectrum antimicrobial response in Pseudomonas aeruginosa
title_short Surface sensing triggers a broad‐spectrum antimicrobial response in Pseudomonas aeruginosa
title_sort surface sensing triggers a broad‐spectrum antimicrobial response in pseudomonas aeruginosa
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496599/
https://www.ncbi.nlm.nih.gov/pubmed/32573899
http://dx.doi.org/10.1111/1462-2920.15139
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