In silico and in vitro-guided identification of inhibitors of alkylquinolone-dependent quorum sensing in pseudomonas aeruginosa

dc.contributor.authorSoukarieh, Fadi
dc.contributor.authorOton, Eduard Vico
dc.contributor.authorDubern, Jean Frédéric
dc.contributor.authorGomes, Janice
dc.contributor.authorHalliday, Nigel M.
dc.contributor.authorde Pilar Crespo, Maria
dc.contributor.authorRamírez-Prada, Jonathan
dc.contributor.authorInsuasty O, Braulio
dc.contributor.authorAbonía, Rodrigo
dc.contributor.authorQuiroga, Jairo
dc.contributor.authorHeeb, Stephan
dc.contributor.authorWilliams, Paul M.
dc.contributor.authorStocks, Michael John
dc.contributor.authorCámara, Miguel Ángel
dc.date.accessioned2019-07-09T20:35:24Z
dc.date.available2019-07-09T20:35:24Z
dc.date.issued2018-01-28
dc.description.abstractPseudomonas 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. © 2018 by the authors.en_US
dc.identifier.issn14203049
dc.identifier.urihttps://repositorio.usc.edu.co/handle/20.500.12421/320
dc.language.isoenen_US
dc.publisherMDPI AGen_US
dc.subjectAlkylquinoloneen_US
dc.subjectMvfRen_US
dc.subjectPqsRen_US
dc.subjectPseudomonas aeruginosaen_US
dc.subjectPseudomonas quinolone signal (PQS)en_US
dc.subjectQuorum sensing inhibition.en_US
dc.subjectantiinfective agenten_US
dc.subjectTranscription Factorsen_US
dc.subjectIofilmen_US
dc.subjectDrug effecten_US
dc.subjectGeneticsen_US
dc.subjectPhysiologyen_US
dc.subjectBiofilmsen_US
dc.subjectMolecular Docking Simulationen_US
dc.subjectQuinolonesen_US
dc.titleIn silico and in vitro-guided identification of inhibitors of alkylquinolone-dependent quorum sensing in pseudomonas aeruginosaen_US
dc.typeArticleen_US

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