TY - JOUR
T1 - Multimodal Inhibition of Pectobacterium brasiliense Virulence by the Citrus Flavanone Naringenin
AU - Pun, Manoj
AU - Galsurker, Ortal
AU - Khazanov, Netaly
AU - Charkowski, Amy
AU - Yelin, Shani
AU - Kerem, Zohar
AU - Weitman, Michal
AU - Senderowitz, Hanoch
AU - Yedidia, Iris
N1 - Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society
PY - 2025/8/20
Y1 - 2025/8/20
N2 - Naringenin, a flavanone from citrus, was studied for its ability to reduce virulence in Pectobacterium, a phytopathogen causing soft rot disease in crop plants. Naringenin downregulated quorum sensing (QS) and suppressed critical virulence determinants in Pectobacterium brasiliense Pb1692, including plant cell wall-degrading enzymes, bacterial motility, and biofilm formation, consequently reducing disease symptoms in two host plants. Molecular docking simulations revealed a plausible binding mode for naringenin within the QS protein ExpI, which were maintained during microsecond-long Molecular Dynamics simulations. These simulations provided atomic-scale insight into specific interactions and estimated binding free energies, supporting naringenin’s QS inhibition mode of action. In contrast, S-adenosyl methionine, the natural ligand of ExpI, was unable to maintain a stable binding mode in the ExpI site during simulations. Beyond QS disruption, naringenin induced reactive oxygen species accumulation and compromised DNA repair, indicating a multimodal mechanism of action. Despite these promising findings, naringenin’s limited aqueous solubility challenges practical applications.
AB - Naringenin, a flavanone from citrus, was studied for its ability to reduce virulence in Pectobacterium, a phytopathogen causing soft rot disease in crop plants. Naringenin downregulated quorum sensing (QS) and suppressed critical virulence determinants in Pectobacterium brasiliense Pb1692, including plant cell wall-degrading enzymes, bacterial motility, and biofilm formation, consequently reducing disease symptoms in two host plants. Molecular docking simulations revealed a plausible binding mode for naringenin within the QS protein ExpI, which were maintained during microsecond-long Molecular Dynamics simulations. These simulations provided atomic-scale insight into specific interactions and estimated binding free energies, supporting naringenin’s QS inhibition mode of action. In contrast, S-adenosyl methionine, the natural ligand of ExpI, was unable to maintain a stable binding mode in the ExpI site during simulations. Beyond QS disruption, naringenin induced reactive oxygen species accumulation and compromised DNA repair, indicating a multimodal mechanism of action. Despite these promising findings, naringenin’s limited aqueous solubility challenges practical applications.
KW - Pectobacterium brasiliense
KW - ROS
KW - molecular docking
KW - molecular dynamics
KW - naringenin
KW - quorum sensing inhibitor
UR - https://www.scopus.com/pages/publications/105013814161
U2 - 10.1021/acs.jafc.5c04312
DO - 10.1021/acs.jafc.5c04312
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C2 - 40767039
AN - SCOPUS:105013814161
SN - 0021-8561
VL - 73
SP - 20792
EP - 20809
JO - Journal of Agricultural and Food Chemistry
JF - Journal of Agricultural and Food Chemistry
IS - 33
ER -