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So different and still so similar: The plant compound rosmarinic acid mimics bacterial homoserine lactone quorum sensing signals
Apart from inter-bacteria communication quorum sensing (QS) mechanisms also enable inter-domain interactions. To interfere with bacterial QS, plants were found to secrete compounds; most of which of unknown identity. We have identified the plant compound rosmarinic acid (RA) to modulate Pseudomonas...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857781/ https://www.ncbi.nlm.nih.gov/pubmed/27195067 http://dx.doi.org/10.1080/19420889.2016.1156832 |
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author | Corral-Lugo, Andrés Daddaoua, Abdelali Ortega, Alvaro Espinosa-Urgel, Manuel Krell, Tino |
author_facet | Corral-Lugo, Andrés Daddaoua, Abdelali Ortega, Alvaro Espinosa-Urgel, Manuel Krell, Tino |
author_sort | Corral-Lugo, Andrés |
collection | PubMed |
description | Apart from inter-bacteria communication quorum sensing (QS) mechanisms also enable inter-domain interactions. To interfere with bacterial QS, plants were found to secrete compounds; most of which of unknown identity. We have identified the plant compound rosmarinic acid (RA) to modulate Pseudomonas aeruginosa QS by binding to the RhlR QS regulator. RA was found to be a homoserine-lactone (HSL) mimic that caused agonistic effects on transcription, resulting ultimately in a stimulation of several RhlR controlled phenotypes like virulence factor synthesis or biofilm formation. Our study was initiated by in silico screening of an RhlR model with compound libraries, demonstrating that this approach is suitable to tackle a major bottleneck in signal transduction research, which is the identification of sensor protein ligands. Previous work has shown that plant compounds interfere with the function of orphan QS regulators. Our study demonstrates that this has not necessarily to be the case since RhlR forms a functional pair with the RhlI synthase. A wide range of structurally dissimilar compounds have been found to mimic HSLs suggesting that this class of QS regulators is characterized by a significant plasticity in the recognition of effector molecules. Further research will show to what extent RA impacts on QS mechanisms of other bacteria. |
format | Online Article Text |
id | pubmed-4857781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-48577812016-05-18 So different and still so similar: The plant compound rosmarinic acid mimics bacterial homoserine lactone quorum sensing signals Corral-Lugo, Andrés Daddaoua, Abdelali Ortega, Alvaro Espinosa-Urgel, Manuel Krell, Tino Commun Integr Biol Article Addendum Apart from inter-bacteria communication quorum sensing (QS) mechanisms also enable inter-domain interactions. To interfere with bacterial QS, plants were found to secrete compounds; most of which of unknown identity. We have identified the plant compound rosmarinic acid (RA) to modulate Pseudomonas aeruginosa QS by binding to the RhlR QS regulator. RA was found to be a homoserine-lactone (HSL) mimic that caused agonistic effects on transcription, resulting ultimately in a stimulation of several RhlR controlled phenotypes like virulence factor synthesis or biofilm formation. Our study was initiated by in silico screening of an RhlR model with compound libraries, demonstrating that this approach is suitable to tackle a major bottleneck in signal transduction research, which is the identification of sensor protein ligands. Previous work has shown that plant compounds interfere with the function of orphan QS regulators. Our study demonstrates that this has not necessarily to be the case since RhlR forms a functional pair with the RhlI synthase. A wide range of structurally dissimilar compounds have been found to mimic HSLs suggesting that this class of QS regulators is characterized by a significant plasticity in the recognition of effector molecules. Further research will show to what extent RA impacts on QS mechanisms of other bacteria. Taylor & Francis 2016-04-14 /pmc/articles/PMC4857781/ /pubmed/27195067 http://dx.doi.org/10.1080/19420889.2016.1156832 Text en © 2016 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License http://creativecommons.org/licenses/by-nc/3.0/, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Article Addendum Corral-Lugo, Andrés Daddaoua, Abdelali Ortega, Alvaro Espinosa-Urgel, Manuel Krell, Tino So different and still so similar: The plant compound rosmarinic acid mimics bacterial homoserine lactone quorum sensing signals |
title | So different and still so similar: The plant compound rosmarinic acid mimics bacterial homoserine lactone quorum sensing signals |
title_full | So different and still so similar: The plant compound rosmarinic acid mimics bacterial homoserine lactone quorum sensing signals |
title_fullStr | So different and still so similar: The plant compound rosmarinic acid mimics bacterial homoserine lactone quorum sensing signals |
title_full_unstemmed | So different and still so similar: The plant compound rosmarinic acid mimics bacterial homoserine lactone quorum sensing signals |
title_short | So different and still so similar: The plant compound rosmarinic acid mimics bacterial homoserine lactone quorum sensing signals |
title_sort | so different and still so similar: the plant compound rosmarinic acid mimics bacterial homoserine lactone quorum sensing signals |
topic | Article Addendum |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857781/ https://www.ncbi.nlm.nih.gov/pubmed/27195067 http://dx.doi.org/10.1080/19420889.2016.1156832 |
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