ORIGINAL RESEARCH article

Front. Cell. Infect. Microbiol.

Sec. Antibiotic Resistance and New Antimicrobial drugs

Volume 15 - 2025 | doi: 10.3389/fcimb.2025.1604507

This article is part of the Research TopicAdvances in New Combinational Therapies for Treatment of MDR PathogensView all 7 articles

Eco-Friendly Silver Nanoparticles from Garlic: A Novel Therapeutic Approach for Treating Escherichia fergusonii Wound Infections

Provisionally accepted
  • 1University of Almaarefa, Riyadh, Saudi Arabia
  • 2Zagazig University, Zagazig, Al Sharqia, Egypt
  • 3Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia
  • 4Port Said University, Port Said, Egypt

The final, formatted version of the article will be published soon.

Complicated wound infections pose a significant challenge to patient recovery and healthcare systems, particularly due to the emergence of less common but highly resistant multidrug-resistant (MDR) pathogens that undermine the efficacy of conventional antibiotic therapies. This growing threat highlights the urgent need for innovative antimicrobial approaches. In this study, we synthesized eco-friendly silver nanoparticles (AgNPs) using garlic extract to combat complicated wound infections caused by a typical MDR pathogens.Genetic sequencing of 16S rRNA gene, aligned with phenotypic identification methods, confirmed that Escherichia fergusonii (E. fergusonii) as a significant a typical pathogen responsible for complicated wound infections, with a prevalence rate of 24% (12 out of 50 cases). Antimicrobial susceptibility testing revealed that all identified E. fergusonii strains exhibited MDR patterns. Garlic extract, analyzed using GC-MS and UPLC-ESI-MS/MS, identified sulfur-containing bioactive compounds such as allyl methyl trisulfide, dimethyl trisulfide, and allicin, which facilitated the biosynthesis of AgNPs. Stable, spherical AgNPs (15-20 nm) with strong antimicrobial properties were confirmed under optimal conditions (10 mL garlic extract, 40°C, pH 8.0). Their properties were validated using UV-Vis spectroscopy, XRD, and TEM. Antibacterial assays of AgNPs showed mean inhibition zones of 28±0.5 mm and MIC values of 100 µg/mL. TEM analysis revealed that AgNPs compromised bacterial membrane integrity, leading to structural damage, increased permeability, and leakage of intracellular contents. Simultaneously, they induced a concentration-dependent depletion of intracellular glutathione (GSH) in E. fergusonii, suggesting that both membrane disruption and oxidative stress synergistically contribute to bacterial cell lysis and death. A strong synergistic interaction was observed between AgNPs, used at a safe concentration below 50 µM as confirmed by cytotoxicity assays, and antibiotics such as ciprofloxacin, as evidenced by a fractional inhibitory concentration (FIC) index of 0.37. Time-kill assays demonstrated rapid 3 bacterial eradication when AgNPs were combined with antibiotics such as ciprofloxacin. These findings underscore the promise of garlic-derived silver nanoparticles (AgNPs) as a fast-acting, eco-friendly option for treating complex wound infections caused by atypical multidrugresistant (MDR) pathogens.

Keywords: wound infections, MDR, AgNPs, Garlic extract, E. fergusonii, TEM Abbreviations: MDR: multidrug-resistant, AgNPs: silver nanoparticles, E. fergusonii: Escherichia fergusonii

Received: 02 Apr 2025; Accepted: 02 Jun 2025.

Copyright: © 2025 Abdelkhalig, Gamal, Ghaly, Alharbi, Alharbi, Bendary and Abousaty. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Nada Alharbi, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia
Mahmoud Mohammed Bendary, Port Said University, Port Said, Egypt

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