TY - JOUR
T1 - Piceatannol
T2 - a renaissance in antibacterial innovation unveiling synergistic potency and virulence disruption against serious pathogens
AU - Koshak, Abdulrahman E.
AU - Elfaky, Mahmoud A.
AU - Albadawi, Dina A.I.
AU - Abdallah, Hossam M.
AU - Mohamed, Gamal A.
AU - Ibrahim, Sabrin R.M.
AU - Alzain, Abdulrahim A.
AU - Khafagy, El Sayed
AU - Elsayed, Eslam M.
AU - Hegazy, Wael A.H.
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature Switzerland AG 2024.
PY - 2025/2
Y1 - 2025/2
N2 - In the relentless battle against multi-drug resistant Gram-negative bacteria, piceatannol emerges as a beacon of hope, showcasing unparalleled antibacterial efficacy and a unique ability to disrupt virulence factors. Our study illuminates the multifaceted prowess of piceatannol against prominent pathogens—Proteus mirabilis, Pseudomonas aeruginosa, Acinetobacter baumannii, and Klebsiella pneumoniae. Notably, piceatannol demonstrated a remarkable ability to inhibit biofilm formation, reduce bacterial mobility, and diminish extracellular enzyme synthesis. Mechanistic insights into piceatannol’s activity unraveled its impact on membrane potential, proton motive force, and ATP production. Furthermore, our study delved into piceatannol's anti-quorum sensing (QS) activity, showcasing its potential to downregulate QS-encoding genes and affirming its affinity to critical QS receptors through molecular docking. Crucially, piceatannol exhibited a low propensity for resistance development, positioning it as a promising candidate for combating antibiotic-resistant strains. Its mild effect on red blood cells (RBCs) suggests safety even at higher concentrations, reinforcing its potential translational value. In an in vivo setting, piceatannol demonstrated protective capabilities, significantly reducing pathogenesis in mice infected with P. aeruginosa and P. mirabilis. This comprehensive analysis positions piceatannol as a renaissance in antibacterial innovation, offering a versatile and effective strategy to confront the evolving challenges posed by resilient Gram-negative pathogens.
AB - In the relentless battle against multi-drug resistant Gram-negative bacteria, piceatannol emerges as a beacon of hope, showcasing unparalleled antibacterial efficacy and a unique ability to disrupt virulence factors. Our study illuminates the multifaceted prowess of piceatannol against prominent pathogens—Proteus mirabilis, Pseudomonas aeruginosa, Acinetobacter baumannii, and Klebsiella pneumoniae. Notably, piceatannol demonstrated a remarkable ability to inhibit biofilm formation, reduce bacterial mobility, and diminish extracellular enzyme synthesis. Mechanistic insights into piceatannol’s activity unraveled its impact on membrane potential, proton motive force, and ATP production. Furthermore, our study delved into piceatannol's anti-quorum sensing (QS) activity, showcasing its potential to downregulate QS-encoding genes and affirming its affinity to critical QS receptors through molecular docking. Crucially, piceatannol exhibited a low propensity for resistance development, positioning it as a promising candidate for combating antibiotic-resistant strains. Its mild effect on red blood cells (RBCs) suggests safety even at higher concentrations, reinforcing its potential translational value. In an in vivo setting, piceatannol demonstrated protective capabilities, significantly reducing pathogenesis in mice infected with P. aeruginosa and P. mirabilis. This comprehensive analysis positions piceatannol as a renaissance in antibacterial innovation, offering a versatile and effective strategy to confront the evolving challenges posed by resilient Gram-negative pathogens.
KW - Anti-virulence
KW - Antibacterial
KW - Drug discovery
KW - Gram-negative bacteria
KW - Industrial development
KW - Piceatannol
KW - Quorum sensing
UR - http://www.scopus.com/inward/record.url?scp=85193480023&partnerID=8YFLogxK
U2 - 10.1007/s10123-024-00532-8
DO - 10.1007/s10123-024-00532-8
M3 - Article
C2 - 38767683
AN - SCOPUS:85193480023
SN - 1139-6709
VL - 28
SP - 213
EP - 225
JO - International Microbiology
JF - International Microbiology
IS - 2
ER -