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A Bacterial Quorum Sensing Molecule Elicits a General Stress Response in Saccharomyces cerevisiae

Bacteria assess their population density through a chemical communication mechanism termed quorum sensing, in order to coordinate group behavior. Most research on quorum sensing has focused primarily on its role as an intraspecies chemical signaling mechanism that enables the regulation of certain p...

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Autores principales: Delago, Antonia, Gregor, Rachel, Dubinsky, Luba, Dandela, Rambabu, Hendler, Adi, Krief, Pnina, Rayo, Josep, Aharoni, Amir, Meijler, Michael M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8481950/
https://www.ncbi.nlm.nih.gov/pubmed/34603220
http://dx.doi.org/10.3389/fmicb.2021.632658
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author Delago, Antonia
Gregor, Rachel
Dubinsky, Luba
Dandela, Rambabu
Hendler, Adi
Krief, Pnina
Rayo, Josep
Aharoni, Amir
Meijler, Michael M.
author_facet Delago, Antonia
Gregor, Rachel
Dubinsky, Luba
Dandela, Rambabu
Hendler, Adi
Krief, Pnina
Rayo, Josep
Aharoni, Amir
Meijler, Michael M.
author_sort Delago, Antonia
collection PubMed
description Bacteria assess their population density through a chemical communication mechanism termed quorum sensing, in order to coordinate group behavior. Most research on quorum sensing has focused primarily on its role as an intraspecies chemical signaling mechanism that enables the regulation of certain phenotypes through targeted gene expression. However, in recent years several seminal studies have revealed important phenomena in which quorum sensing molecules appear to serve additional roles as interspecies signals that may regulate microbial ecology. In this study, we asked whether the budding yeast Saccharomyces cerevisiae can sense chemical signals from prokaryotes. When exposed to a variety of quorum sensing molecules from different bacterial species and from Candida albicans we found that N-(3-oxododecanoyl)-L-homoserine lactone (C12) from the opportunistic human pathogen Pseudomonas aeruginosa induces a remarkable stress response in yeast. Microarray experiments confirmed and aided in interpreting these findings, showing a unique and specific expression pattern that differed significantly from the response to previously described stress factors. We further characterized this response and report preliminary findings on the molecular basis for the recognition of C12 by the yeast.
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spelling pubmed-84819502021-10-01 A Bacterial Quorum Sensing Molecule Elicits a General Stress Response in Saccharomyces cerevisiae Delago, Antonia Gregor, Rachel Dubinsky, Luba Dandela, Rambabu Hendler, Adi Krief, Pnina Rayo, Josep Aharoni, Amir Meijler, Michael M. Front Microbiol Microbiology Bacteria assess their population density through a chemical communication mechanism termed quorum sensing, in order to coordinate group behavior. Most research on quorum sensing has focused primarily on its role as an intraspecies chemical signaling mechanism that enables the regulation of certain phenotypes through targeted gene expression. However, in recent years several seminal studies have revealed important phenomena in which quorum sensing molecules appear to serve additional roles as interspecies signals that may regulate microbial ecology. In this study, we asked whether the budding yeast Saccharomyces cerevisiae can sense chemical signals from prokaryotes. When exposed to a variety of quorum sensing molecules from different bacterial species and from Candida albicans we found that N-(3-oxododecanoyl)-L-homoserine lactone (C12) from the opportunistic human pathogen Pseudomonas aeruginosa induces a remarkable stress response in yeast. Microarray experiments confirmed and aided in interpreting these findings, showing a unique and specific expression pattern that differed significantly from the response to previously described stress factors. We further characterized this response and report preliminary findings on the molecular basis for the recognition of C12 by the yeast. Frontiers Media S.A. 2021-09-16 /pmc/articles/PMC8481950/ /pubmed/34603220 http://dx.doi.org/10.3389/fmicb.2021.632658 Text en Copyright © 2021 Delago, Gregor, Dubinsky, Dandela, Hendler, Krief, Rayo, Aharoni and Meijler. https://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) and the copyright owner(s) 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 Microbiology
Delago, Antonia
Gregor, Rachel
Dubinsky, Luba
Dandela, Rambabu
Hendler, Adi
Krief, Pnina
Rayo, Josep
Aharoni, Amir
Meijler, Michael M.
A Bacterial Quorum Sensing Molecule Elicits a General Stress Response in Saccharomyces cerevisiae
title A Bacterial Quorum Sensing Molecule Elicits a General Stress Response in Saccharomyces cerevisiae
title_full A Bacterial Quorum Sensing Molecule Elicits a General Stress Response in Saccharomyces cerevisiae
title_fullStr A Bacterial Quorum Sensing Molecule Elicits a General Stress Response in Saccharomyces cerevisiae
title_full_unstemmed A Bacterial Quorum Sensing Molecule Elicits a General Stress Response in Saccharomyces cerevisiae
title_short A Bacterial Quorum Sensing Molecule Elicits a General Stress Response in Saccharomyces cerevisiae
title_sort bacterial quorum sensing molecule elicits a general stress response in saccharomyces cerevisiae
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8481950/
https://www.ncbi.nlm.nih.gov/pubmed/34603220
http://dx.doi.org/10.3389/fmicb.2021.632658
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