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February 12, 2026PLoS ONE0 citationsOpen Access

Antibiofilm and antibacterial activity of maslinic acid against Vancomycin-Resistant Enterococci (VRE)

SASomaia M. AbdelmegeedMMMohamed Gamal MohamedMSMohamed N. Seleem

Key Points

  • This research aims to evaluate the antibiofilm and antibacterial properties of maslinic acid against vancomycin-resistant Enterococcus (VRE).
  • Initial screening identified the potency of maslinic acid with minimum inhibitory concentrations (MICs) between 4 to 8 µg/mL.
  • Time-kill assays were conducted to compare maslinic acid's bacteriostatic activity with linezolid.
  • Cytotoxicity and hemolysis assays assessed the safety of maslinic acid in mammalian cells.
  • Biofilm disruption was measured, and the efficacy of maslinic acid was tested in a Caenorhabditis elegans infection model.
  • Maslinic acid demonstrated potent antibacterial activity against 13 clinical enterococcal isolates.
  • It effectively disrupted established Enterococcus faecalis biofilms by approximately 50%.
  • In the Caenorhabditis elegans model, maslinic acid reduced bacterial burden by 80%, outperforming linezolid.

Abstract

The emergence of vancomycin-resistant Enterococcus (VRE) has posed a significant global health threat, especially in healthcare settings where treatment options are increasingly limited due to rising antibiotic resistance. Maslinic acid, a naturally occurring pentacyclic triterpene found in olives, is known for its diverse biological activities, including anti-inflammatory, anticancer, antioxidant, and antimicrobial effects. In this study, we investigated the antibacterial and antibiofilm potential of maslinic acid against VRE. Initial screening identified maslinic acid as a potent hit, with minimum inhibitory concentrations (MICs) ranging from 4 to 8 µg/mL across 13 clinical enterococcal isolates, including multidrug-resistant strains. Time-kill assays demonstrated bacteriostatic activity comparable to linezolid, while cytotoxicity and hemolysis assays confirmed its safety in mammalian cells. Furthermore, maslinic acid disrupted established Enterococcus faecalis biofilms by approximately 50%, whereas linezolid was not effective against biofilms. Notably, maslinic acid significantly reduced bacterial burden in a Caenorhabditis elegans infection model by 80%, outperforming linezolid. These findings highlight maslinic acid as a promising candidate for the development of new therapies targeting VRE, with the added advantage of antibiofilm activity and a favorable safety profile.

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Cite This Study

Abdelmegeed et al. (2026) studied this question.

synapsesocial.com/papers/698d6d9f5be6419ac0d52a8bhttps://doi.org/10.1371/journal.pone.0342234
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