Scaffold of Selenium Nanovectors and Honey Phytochemicals for Inhibition of Pseudomonas aeruginosa Quorum Sensing and Biofilm Formation
Honey is an excellent source of polyphenolic compounds that are effective in attenuating quorum sensing (QS), a chemical process of cell-to-cell communication system used by the opportunistic pathogen to regulate virulence and biofilm formation. However, lower water solubility and inadequate bioavai...
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Published in | Frontiers in cellular and infection microbiology Vol. 7; p. 93 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
23.03.2017
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Subjects | |
Online Access | Get full text |
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Summary: | Honey is an excellent source of polyphenolic compounds that are effective in attenuating quorum sensing (QS), a chemical process of cell-to-cell communication system used by the opportunistic pathogen
to regulate virulence and biofilm formation. However, lower water solubility and inadequate bioavailability remains major concerns of these therapeutic polyphenols. Its therapeutic index can be improved by using nano-carrier systems to target QS signaling potently. In the present study, we fabricated a unique drug delivery system comprising selenium nanoparticles (SeNPs; non-viral vectors) and polyphenols of honey (HP) for enhancement of anti-QS activity of HP against
PAO1. The developed selenium nano-scaffold showed superior anti-QS activity, anti-biofilm efficacy, and anti-virulence potential in both
and
over its individual components, SeNPs and HP. LasR is inhibited by selenium nano-scaffold
. Using computational molecular docking studies, we have also demonstrated that the anti-virulence activity of selenium nano-scaffold is reliant on molecular binding that occurs between HP and the QS receptor LasR through hydrogen bonding and hydrophobic interactions. Our preliminary investigations with selenium-based nano-carriers hold significant promise to improve anti-virulence effectiveness of phytochemicals by enhancing effective intracellular delivery. |
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Bibliography: | Edited by: Matthew C. Wolfgang, University of North Carolina at Chapel Hill, USA These authors have contributed equally to this work. Reviewed by: Sang Sun Yoon, Yonsei University, South Korea; Vaidurya Pratap Sahi, Karlsruhe Institute of Technology, Germany |
ISSN: | 2235-2988 2235-2988 |
DOI: | 10.3389/fcimb.2017.00093 |