Antimicrobial and Antiviral Compounds of Phlomis viscosa Poiret.

Autor: Yarmolinsky L; Eastern R&D Center, Kiryat Arba 9010000, Israel., Nakonechny F; Department of Chemical Engineering, Ariel University, Ariel 4070000, Israel., Budovsky A; Research & Development Authority, Barzilai University Medical Center, Ashkelon 7830604, Israel., Zeigerman H; Institute of Biochemistry, Food Science and Nutrition, The Robert H. Smith Faculty of Agriculture, Food and Environment, Hebrew University of Jerusalem, Rehovot 7610001, Israel., Khalfin B; Eastern R&D Center, Kiryat Arba 9010000, Israel.; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva 8410501, Israel., Sharon E; Institute for Personalized and Translational Medicine, Ariel University, Ariel 4070000, Israel., Yarmolinsky L; Arnie Miller Laboratories, Beer-Sheva 8430713, Israel., Ben-Shabat S; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva 8410501, Israel., Nisnevitch M; Department of Chemical Engineering, Ariel University, Ariel 4070000, Israel.
Jazyk: angličtina
Zdroj: Biomedicines [Biomedicines] 2023 Feb 02; Vol. 11 (2). Date of Electronic Publication: 2023 Feb 02.
DOI: 10.3390/biomedicines11020441
Abstrakt: 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.
Databáze: MEDLINE