4.6 Article

Attenuation of Pseudomonas aeruginosa Virulence by Pomegranate Peel Extract

Journal

MICROORGANISMS
Volume 10, Issue 12, Pages -

Publisher

MDPI
DOI: 10.3390/microorganisms10122500

Keywords

anti-biofilm; Pseudomonas aeruginosa; pomegranate; virulence; autoinducers; phenolic compounds

Categories

Funding

  1. Progetto BOOM-2020: Micro-UNIMORE of INCOS COSMECEUTICA INDUSTRIALE, Funo di Argelato, Bologna, Italy

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In this study, the effects of pomegranate peel extract on Pseudomonas aeruginosa growth and biofilm formation were evaluated. The results showed that pomegranate peel extract can attenuate P. aeruginosa virulence by impairing bacterial growth, biofilm production, and autoinducer release. Furthermore, specific phenolic compounds in the pomegranate peel extract were consumed during incubation with bacterial cells.
Pseudomonas aeruginosa is an opportunistic pathogen often responsible for biofilm-associated infections. The high adhesion of bacterial cells onto biotic/abiotic surfaces is followed by production of an extracellular polysaccharidic matrix and formation of a sessile community (the biofilm) by the release of specific quorum-sensing molecules, named autoinducers (AI). When the concentrations of AI reach a threshold level, they induce the expression of many virulence genes, including those involved in biofilm formation, motility, pyoverdine and pyocyanin release. P. aeruginosa embedded into biofilm becomes resistant to both conventional drugs and the host's immune response. Accordingly, biofilm-associated infections are a major clinical problem underlining the need for new antimicrobial therapies. In this study, we evaluated the effects of pomegranate peel extract (PomeGr) in vitro on P. aeruginosa growth and biofilm formation; moreover, the release of four AI was assessed. The phenolic profile of PomeGr, exposed or not to bacteria, was determined by high-performance liquid chromatography coupled to electrospray ionization mass spectrometry (HPLC-ESI-MS) analysis. We found that bacterial growth, biofilm production and AI release were impaired upon PomeGr treatment. In addition, the PomeGr phenolic content was also markedly hampered following incubation with bacterial cells. In particular, punicalagin, punicalin, pedunculagin, granatin, di-(HHDP-galloyl-hexoside) pentoside and their isomers were highly consumed. Overall, these results provide novel insights on the ability of PomeGr to attenuate P. aeruginosa virulence; moreover, the AI impairment and the observed consumption of specific phenolic compounds may offer new tools in designing innovative therapeutic approaches against bacterial infections.

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