Discovery of potent inhibitors targeting Vibrio harveyi LuxR through shape and e-pharmacophore based virtual screening and its biological evaluation. (February 2017)

• Record Type: Journal Article
• Authors: Rajamanikandan, Sundaraj; Jeyakanthan, Jeyaraman; Srinivasan, Pappu
• Is Part Of: Microbial pathogenesis. Volume 103(2017)
• Page Start: 40
• Page End: 56
• Publication Date: 2017-02
• Subjects: Vibrio harveyi -- Quorum sensing -- e-Pharmacophore -- Shape based virtual screening -- In vitro assays; Pathogenic microorganisms -- Periodicals; Pathology, Molecular -- Periodicals; Communicable Diseases -- microbiology -- Periodicals; Communicable Diseases -- parasitology -- Periodicals; Micro-organismes pathogènes -- Périodiques; Pathologie moléculaire -- Périodiques; Electronic journals; 616.9041
• DOI: 10.1016/j.micpath.2016.12.003
• Languages: English
• ISSNs: 0882-4010

Abstract

Abstract: Quorum sensing is widely recognized as an efficient mechanism in the regulation and production of several virulence factors, biofilm formation and stress responses. For this reason, quorum sensing circuit is emerging as a novel drug target for the development of anti-infective. Recently, cinnamaldehyde derivatives have been found to interfere with master quorum sensing transcriptional regulator and thereby decreasing the DNA binding ability of LuxR. However, the exact mode of cinnamaldehyde binding with LuxR and receptor interaction still remains inconclusive. In the current study, combined method of molecular docking and molecular dynamics simulations were performed to investigate the binding mode, dynamic and energy aspects of cinnamaldehyde derivatives into the binding site of LuxR. Based on the experimental and computational evidences, LuxR-3, 4-dichloro-cinnamaldehyde complex was chosen for the development of e-pharmacophore model. Further, shape and e-pharmacophore based virtual screening were performed against ChemBridge database to find potent and suitable ligands for LuxR. By comparing the results of shape and e-pharmacophore based virtual screening; best 9 hit molecules were selected for further studies including ADMET prediction, molecular dynamics simulations and Prime MM-GBSA calculations. From the 9 hit molecules, the top most compound 3-(2, 4-dichlorophenyl)-1-(1H-pyrrol-2-yl)-2-propen-1-one (ChemBridge-7364106) was selected for in vitro assays using Vibrio harveyi . The result revealed that ChemBridge-7364106 significantly reduced the bioluminescence production in a dose dependent manner. In addition, ChemBridge-7364106 showed a significant inhibition in biofilm formation and motility in V. harveyi . The results from the study suggest that ChemBridge-7364106 could serve as an anti-quorum sensing molecule for V. harveyi . Graphical abstract: Highlights: e-Pharmacophore model was developed using LuxR-3, 4-dichloro-cinnamaldehyde complex. e-Pharmacophore- and shape-based virtual screening was carried out with ChemBridge database. Top 9 hits molecules were selected based on binding interaction, high docking score and ADMET prediction. The top most retrieved hit is biological evaluated and it showed anti-quorum sensing activity against Vibrio harveyi .