4.7 Article

Antimicrobial and Antiviral Compounds of Phlomis viscosa Poiret

Journal

BIOMEDICINES
Volume 11, Issue 2, Pages -

Publisher

MDPI
DOI: 10.3390/biomedicines11020441

Keywords

Phlomis viscosa; antimicrobial compounds; antiviral compounds; flavonoids; drug-resistant microorganisms; biofilm formation

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This study identified compounds with antimicrobial and antiviral properties in Phlomis viscosa. Gas chromatography/mass spectrometry analysis was used to identify volatile compounds, while high-performance liquid chromatography, liquid chromatography-electrospray ionization-mass spectrometry, and matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry were applied for nonvolatile components. Quercetin 3-O-rutinoside, quercetin 3-O-arabinoside, and hesperidin showed significant antimicrobial activity against various bacteria, including drug-resistant strains, and also demonstrated antiviral activity against varicella zoster virus and herpes simplex virus 1.
Phlomis viscosa Poiret (an evergreen shrub) represents a valuable source of medicinal compounds. In this study, we discovered compounds with antimicrobial and antiviral properties. The aim of this study was to identify compounds of P. viscosa and estimate the antimicrobial and antiviral activity of its phytochemicals. The volatile compounds were identified using gas chromatography/mass spectrometry (GC/MS) analysis. For the identification of nonvolatile components of the extracts, high-performance liquid chromatography (HPLC), liquid chromatography-electrospray ionization-mass spectrometry (LC-ESI-MS) and matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry (MALDI-TOF-MS) were applied. Quercetin 3-O-rutinoside and hesperidin caused a significant decrease in the bacterial concentration of Agrobacterium tumefaciens, Xylella fastidiosa and Pseudomonas syringae (p < 0.001). The growth of drug-resistant microorganisms (Escherichia coli, Klebsiella pneumoniae, Acinetobacter baumannii, Serratia marcescens and Salmonella enteritidis) was inhibited by quercetin 3-O-rutinoside, quercetin 3-O-arabinoside and hesperidin. In addition, these compounds demonstrated antiquorum-sensing properties. Diosmin, hesperidin and quercetin 3-O-arabinoside significantly inhibited varicella zoster virus (VZV) (p < 0.001). Quercetin 3-O-rutinoside and quercetin 3-O-arabinoside were effective against herpes simplex virus 1 (HSV-1), including mutant strains.

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