Dr FADI SOUKARIEH Fadi.Soukarieh@nottingham.ac.uk
RESEARCH FELLOW
In Silico and in Vitro-Guided Identification of Inhibitors of Alkylquinolone-Dependent Quorum Sensing in Pseudomonas aeruginosa
Soukarieh, Fadi; Vico Oton, Eduard; Dubern, Jean-Fr�d�ric; Gomes, Janice; Halliday, Nigel; de Pilar Crespo, Maria; Ram�rez-Prada, Jonathan; Insuasty, Braulio; Abonia, Rodrigo; Quiroga, Jairo; Heeb, Stephan; Williams, Paul; Stocks, Michael; C�mara, Miguel
Authors
Eduard Vico Oton
Dr JEAN DUBERN JEAN.DUBERN@NOTTINGHAM.AC.UK
SENIOR RESEARCH FELLOW
Janice Gomes
Nigel Halliday
Maria de Pilar Crespo
Jonathan Ram�rez-Prada
Braulio Insuasty
Rodrigo Abonia
Jairo Quiroga
Dr STEPHAN HEEB stephan.heeb@nottingham.ac.uk
ASSISTANT PROFESSOR
Professor PAUL WILLIAMS PAUL.WILLIAMS@NOTTINGHAM.AC.UK
PROFESSOR OF MOLECULAR MICROBIOLOGY
Professor MICHAEL STOCKS MICHAEL.STOCKS@NOTTINGHAM.AC.UK
PROFESSOR OF MEDICINAL CHEMISTRY AND DRUG DISCOVERY
Professor MIGUEL CAMARA MIGUEL.CAMARA@NOTTINGHAM.AC.UK
PROFESSOR OF MOLECULAR MICROBIOLOGY
Abstract
Pseudomonas aeruginosa is a major opportunistic pathogen in cystic fibrosis, wound and nosocomial infections, posing a serious burden to public health, due to its antibiotic resistance. The P. aeruginosa Pseudomonas Quinolone System (pqs) quorum sensing system, driven by the activation of the transcriptional regulator, PqsR (MvfR) by alkylquinolone (AQ) signal molecules, is a key player in the regulation of virulence and a potential target for the development of novel antibacterial agents. In this study, we performed in silico docking analysis, coupled with screening using a P. aeruginosa mCTX::PpqsA-lux chromosomal promoter fusion, to identify a series of new PqsR antagonists. The hit compounds inhibited pyocyanin and alkylquinolone signal molecule production in P. aeruginosa PAO1-L and PA14 strains. The inhibitor Ia, which showed the highest activity in PA14, reduced biofilmformation in PAO1-L and PA14, increasing their sensitivity to tobramycin. Furthermore, the hepatic and plasma stabilities for these compounds were determined in both rat and human in vitro microsomal assays, to gain a further understanding of their therapeutic potential. This work has uncovered a new class of P. aeruginosa PqsR antagonists with potential for hit to lead optimisation in the search for quorum sensing inhibitors for future anti-infective drug discovery programs.
Citation
Soukarieh, F., Vico Oton, E., Dubern, J.-F., Gomes, J., Halliday, N., de Pilar Crespo, M., Ramírez-Prada, J., Insuasty, B., Abonia, R., Quiroga, J., Heeb, S., Williams, P., Stocks, M., & Cámara, M. (2018). In Silico and in Vitro-Guided Identification of Inhibitors of Alkylquinolone-Dependent Quorum Sensing in Pseudomonas aeruginosa. Molecules, 23(2), 1-15. https://doi.org/10.3390/molecules23020257
Journal Article Type | Article |
---|---|
Acceptance Date | Jan 20, 2018 |
Online Publication Date | Jan 28, 2018 |
Publication Date | Jan 28, 2018 |
Deposit Date | Jan 29, 2018 |
Publicly Available Date | Jan 29, 2018 |
Journal | Molecules |
Electronic ISSN | 1420-3049 |
Publisher | MDPI |
Peer Reviewed | Peer Reviewed |
Volume | 23 |
Issue | 2 |
Article Number | 257 |
Pages | 1-15 |
DOI | https://doi.org/10.3390/molecules23020257 |
Keywords | Pseudomonas aeruginosa; PqsR; MvfR; Pseudomonas quinolone signal (PQS); alkylquinolone; quorum sensing inhibition |
Public URL | https://nottingham-repository.worktribe.com/output/907371 |
Publisher URL | http://www.mdpi.com/1420-3049/23/2/257 |
Contract Date | Jan 29, 2018 |
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Copyright Statement
Copyright information regarding this work can be found at the following address: http://creativecommons.org/licenses/by/4.0
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