[In silico Screening of Flavones and its Derivatives as Potential Inhibitors of Quorum-Sensing Regulator LasR of Pseudomonas aeruginosa]
- PMID: 32163399
- DOI: 10.31857/S0026898420010024
[In silico Screening of Flavones and its Derivatives as Potential Inhibitors of Quorum-Sensing Regulator LasR of Pseudomonas aeruginosa]
Abstract
Antibiotic resistance is a global problem nowadays and in 2017 the World Health Organization published the list of bacteria for which treatment are urgently needed, where Pseudomonas aeruginosa is of critical priority. Current therapies lack efficacy because this organism creates biofilms conferring increased resistance to antibiotics and host immune responses. The strategy is to "not kill, but disarm" the pathogen and resistance will be developed slowly. It has been shown that LasI/LasR system is the main component of the quorum sensing system in P. aeruginosa. LasR is activated by the interaction with its native autoinducer. A lot flavones and their derivatives are used as antibacterial drug compounds. The purpose is to search compounds that will inhibit LasR. This leads to the inhibition of the synthesis of virulence factors thus the bacteria will be vulnerable and not virulent. We performed virtual screening using AutoDock Vina, rDock, LeDock for obtaining consensus predictions. The results of virtual screening suggest benzamides which are synthetical derivatives of flavones as potential inhibitors of transcriptional regulator LasR. These are consistent with recently published experimental data, which demonstrate the high antibacterial activity of benzamides. The compounds interact with the ligand binding domain of LasR with higher binding affinity than with DNA binding domain. Among the selected compounds, by conformational analysis, it was found that there are compounds that bind to the same amino acids of ligand binding domain as the native autoinducer. This could indicate the possibility of competitive interaction of these compounds. A number of compounds that bind to other conservative amino acids ligand binding domain have also been discovered, which will be of interest for further study. Selected compounds meet the criteria necessary for their consideration as drugs and can serve as a basis for conducting further in vitro/in vivo experiments. It could be used for the development of modern anti-infective therapy based on the quorum sensing system of P. aeruginosa.
Keywords: LasR; Pseudomonas aeruginosa; antibiotic resistance; benzamide; flavone; molecular docking; quorum sensing; virtual screening.
Similar articles
-
Structure based virtual screening for identification of potential quorum sensing inhibitors against LasR master regulator in Pseudomonas aeruginosa.Microb Pathog. 2017 Jun;107:136-143. doi: 10.1016/j.micpath.2017.03.026. Epub 2017 Mar 27. Microb Pathog. 2017. PMID: 28351711
-
Virtual screening and biological evaluation of biofilm inhibitors on dual targets in quorum sensing system.Future Med Chem. 2017 Nov;9(17):1983-1994. doi: 10.4155/fmc-2017-0127. Epub 2017 Oct 27. Future Med Chem. 2017. PMID: 29076756
-
Characterization of natural product inhibitors of quorum sensing reveals competitive inhibition of Pseudomonas aeruginosa RhlR by ortho-vanillin.Microbiol Spectr. 2024 Sep 3;12(9):e0068124. doi: 10.1128/spectrum.00681-24. Epub 2024 Jul 24. Microbiol Spectr. 2024. PMID: 39046261 Free PMC article.
-
Pseudomonas aeruginosa quorum sensing modulates immune responses: An updated review article.Immunol Lett. 2017 Oct;190:1-6. doi: 10.1016/j.imlet.2017.07.002. Epub 2017 Jul 8. Immunol Lett. 2017. PMID: 28698104 Review.
-
Anti-PqsR compounds as next-generation antibacterial agents against Pseudomonas aeruginosa: A review.Eur J Med Chem. 2019 Jun 15;172:26-35. doi: 10.1016/j.ejmech.2019.03.049. Epub 2019 Mar 25. Eur J Med Chem. 2019. PMID: 30939351 Review.
Cited by
-
Acetylation of CspC Controls the Las Quorum-Sensing System through Translational Regulation of rsaL in Pseudomonas aeruginosa.mBio. 2022 Jun 28;13(3):e0054722. doi: 10.1128/mbio.00547-22. Epub 2022 Apr 25. mBio. 2022. PMID: 35467416 Free PMC article.
-
Identification of anti-pathogenic activity among in silico predicted small-molecule inhibitors of Pseudomonas aeruginosa LasR or nitric oxide reductase (NOR).Drug Target Insights. 2023 Sep 28;17:101-109. doi: 10.33393/dti.2023.2638. eCollection 2023 Jan-Dec. Drug Target Insights. 2023. PMID: 37811195 Free PMC article.
-
Identification of the Pseudomonas aeruginosa AgtR-CspC-RsaL pathway that controls Las quorum sensing in response to metabolic perturbation and Staphylococcus aureus.PLoS Pathog. 2025 Apr 8;21(4):e1013054. doi: 10.1371/journal.ppat.1013054. eCollection 2025 Apr. PLoS Pathog. 2025. PMID: 40198682 Free PMC article.
-
Discovery of genistein derivatives as potential SARS-CoV-2 main protease inhibitors by virtual screening, molecular dynamics simulations and ADMET analysis.Front Pharmacol. 2022 Aug 25;13:961154. doi: 10.3389/fphar.2022.961154. eCollection 2022. Front Pharmacol. 2022. PMID: 36091808 Free PMC article.
-
Drug Repurposing Targeting Pseudomonas aeruginosa MvfR Using Docking, Virtual Screening, Molecular Dynamics, and Free-Energy Calculations.Antibiotics (Basel). 2022 Jan 31;11(2):185. doi: 10.3390/antibiotics11020185. Antibiotics (Basel). 2022. PMID: 35203788 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources