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ORIGINAL RESEARCH article

Front. Nutr.

Sec. Nutrition and Food Science Technology

Volume 12 - 2025 | doi: 10.3389/fnut.2025.1694017

This article is part of the Research TopicMicrobial Food Safety at the Nutrition Interface: Impacts on Public Health Outcomes, Risk Communication, and Food System ResilienceView all articles

Antibacterial properties of Solenostemma argel (Del.) Hayne Against Salmonella Strains from Chicken Meat: Integrated GC–MS Phytochemical Profiling and Molecular Docking Analysis

Provisionally accepted
Abdulrahman  AlhudhaibiAbdulrahman Alhudhaibi1*Mahmoud  DahabMahmoud Dahab2Hajo  IdrissHajo Idriss1Megren  Faisal AlmoteriMegren Faisal Almoteri3Prof.Dr. Emad  M AbdallahProf.Dr. Emad M Abdallah4*
  • 1Imam Muhammad Ibn Saud Islamic University, Riyadh, Saudi Arabia
  • 2Universiti Malaya, Federal Territory of Kuala Lumpur, Malaysia
  • 3King Saud Hospital, Unayzah, Saudi Arabia
  • 4Qassim University College of Science, Buraydah, Saudi Arabia

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

Background: Salmonella enterica is a leading cause of foodborne illness worldwide and poultry products, particularly chicken meat and there is growing interest in using plant extracts to protect chicken meat from Salmonella contamination during refrigeration. Solenostemma argel is a medicinal plant traditionally used to treat gastrointestinal disorders and quantitative data on its activity against Salmonella enterica are limited. Methods: Methanolic leaf extract was profiled by GC–MS to document major phytochemical classes. Antibacterial activity against clinical/retail S. enterica isolates was evaluated by disc diffusion and broth microdilution to determine inhibition zones, minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC). A panel of GC–MS–identified constituents was subjected to in silico computational study based on oral-toxicity prediction and molecular docking against modelled outer-membrane proteins implicated in LPS assembly and membrane integrity (OmpV, LptE) to prioritize plausible membrane-active leads. Results: The methanolic extract displayed modest inhibition in disc-diffusion assays (mean inhibition zones were 7.8–9.7 mm). All S. enterica isolates shared a uniform MIC of 12.5 mg/mL; MBCs were strain-dependent (25 mg/mL for one isolate; 100 mg/mL for two isolates), yielding MBC/MIC ratios of 2–8 and indicating primarily bacteriostatic activity for some strains. GC–MS profiling revealed several volatile and semi-volatile metabolites of potential biological interest. However, it is important to note that some peaks, such as 1,3-dioxane and 2-[2-[2-(2-acetyloxyethoxy)ethoxy]ethoxy]ethanol, may represent laboratory-derived contaminants rather than genuine plant metabolites, emphasizing the need for rigorous contamination controls and complementary analytical approaches in future work. In silico docking prioritized a steroidal candidate (Estra-1,3,5(10)-trien-17β-ol) with the highest predicted affinities to OmpV (−7.9 kcal·mol⁻¹) and LptE (−6.7 kcal·mol⁻¹). Toxicity predictions suggested low oral toxicity for the majority of screened constituents. Conclusion: The methanolic leaf extract of Solenostemma argel exhibited moderate to weak in vitro anti-Salmonella activity, supported by computational docking results, and provide a foundation for further isolation, purification, and characterization of its active constituents.

Keywords: secondary metabolites, Antibacterial activity, Plants, Natural Products, computationalbiology, food-safety, Poultry

Received: 27 Aug 2025; Accepted: 14 Oct 2025.

Copyright: © 2025 Alhudhaibi, Dahab, Idriss, Almoteri and Abdallah. 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:
Abdulrahman Alhudhaibi, amalhudhaibi@imamu.edu.sa
Prof.Dr. Emad M Abdallah, 140208@qu.edu.sa

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