The Efficacy of Plant Extracts Against Key Food-Borne Pathogens: A Mechanistic, Applications, and Advances
Abstract
1. Introduction
2. Methodology
3. Bioactive Compounds and Extraction Characteristics
3.1. Clove (Syzygium aromaticum)
3.2. Pomegranate (Punica granatum L.)
3.3. Cranberry (Vaccinium macrocarpon) Pomace Extract
3.4. Garlic (Allium sativum)
3.5. Cinnamon (Cinnamomum zeylanicum)
4. Antibacterial Potential of Herbal Extracts
4.1. Clove (Syzygium aromaticum)
4.2. Pomegranate (Punica granatum)
4.3. Cranberry (Vaccinium macrocarpon)
4.4. Garlic (Allium sativum)
4.5. Cinnamon Oil (Cinnamomum zeylanicum)
| Plant | Extraction Method | Food-Relevant Antimicrobial Findings | Ref. |
|---|---|---|---|
| Clove | Hydrodistillation, ethanol extraction | MIC: 0.21–1.67 μL/mL; reduced bacterial counts in model food systems | [30,40] |
| Pomegranate | Ethanolic peel extraction | Reduced Salmonella contamination; effective meat decontamination | [50,51] |
| Cranberry | Acidified ethanol extraction | Inhibited ESBL-E. coli virulence; reduced S. aureus in cooked meat | [39,51,52] |
| Garlic | Steam distillation (oil) | Garlic oil more effective than powder against H. pylori | [62] |
| Cinnamon | Steam distillation | Reduced L. monocytogenes by ~2 log CFU/g in meat systems | [64] |
4.6. Practical Relevance and Integrated Antimicrobial Mechanisms
5. Antioxidant Potential of Herbal Extract
6. Applications
6.1. Gastrointestinal Infectious Diarrheal Disorders
6.2. Gastrointestinal Infectious Ulcer Disorders
6.3. Food Preservation
6.4. Safety and Regulatory Considerations
7. Conclusions
8. Challenges and Future Perspectives in the Application of Plant Extracts in the Food Industry
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- Mortazavi, N.; Aliakbarlu, J.; Imani, M. The Antibacterial Effects of Engineered Salmonella Phage PVP-SE1 Endolysin on the Planktonic Cells and Biofilms of Food-Borne Pathogens and Its Antibacterial Activity in Milk. Food Biosci. 2025, 71, 107274. [Google Scholar] [CrossRef]
- Pires, S.M.; Devleesschauwer, B. Estimates of Global Disease Burden Associated with Foodborne Pathogens. In Foodborne Infections and Intoxications; Elsevier: Amsterdam, The Netherlands, 2021; pp. 3–17. ISBN 978-0-12-819519-2. [Google Scholar]
- Lake, I.R.; Barker, G.C. Climate Change, Foodborne Pathogens and Illness in Higher-Income Countries. Curr. Environ. Health Rep. 2018, 5, 187–196. [Google Scholar] [CrossRef]
- Hamaideh, S.; Olaimat, A.; Al-Holy, M.; Ababneh, A.; Shahbaz, H.; Abughoush, M.; Al-Nabulsi, A.; Osaili, T.; Ayyash, M.; Holley, R. The Influence of Technological Shifts in the Food Chain on the Emergence of Foodborne Pathogens: An Overview. Appl. Microbiol. 2024, 4, 594–606. [Google Scholar] [CrossRef]
- Al-Seghayer, M.S.; Al-Sarraj, F.M. The Outbreak of Foodborne Disease by Pathogenic Enterobacteriaceae Antimicrobial Resistance—A Review. Asian Food Sci. J. 2021, 20, 91–99. [Google Scholar] [CrossRef]
- Adley, C.C.; Ryan, M.P. The Nature and Extent of Foodborne Disease. In Antimicrobial Food Packaging; Elsevier: Amsterdam, The Netherlands, 2025; pp. 3–14. ISBN 978-0-323-90747-7. [Google Scholar]
- Todd, E.C.D. Foodborne Disease in the Middle East. In Water, Energy & Food Sustainability in the Middle East; Murad, S., Baydoun, E., Daghir, N., Eds.; Springer International Publishing: Cham, Switzerland, 2017; pp. 389–440. ISBN 978-3-319-48919-3. [Google Scholar]
- Mafe, A.N.; Büsselberg, D. Impact of Metabolites from Foodborne Pathogens on Cancer. Foods 2024, 13, 3886. [Google Scholar] [CrossRef]
- Jha, N.K.; Arfin, S.; Jha, S.K.; Kar, R.; Dey, A.; Gundamaraju, R.; Ashraf, G.M.; Gupta, P.K.; Dhanasekaran, S.; Abomughaid, M.M.; et al. Re-Establishing the Comprehension of Phytomedicine and Nanomedicine in Inflammation-Mediated Cancer Signaling. Semin. Cancer Biol. 2022, 86, 1086–1104. [Google Scholar] [CrossRef]
- Rahman, M.d.M.; Islam, M.d.R.; Shohag, S.; Ahasan, M.d.T.; Sarkar, N.; Khan, H.; Hasan, A.M.; Cavalu, S.; Rauf, A. Microbiome in Cancer: Role in Carcinogenesis and Impact in Therapeutic Strategies. Biomed. Pharmacother. 2022, 149, 112898. [Google Scholar] [CrossRef]
- Zhang, Y.; Chen, R.; Zhang, D.; Qi, S.; Liu, Y. Metabolite Interactions between Host and Microbiota during Health and Disease: Which Feeds the Other? Biomed. Pharmacother. 2023, 160, 114295. [Google Scholar] [CrossRef]
- Awad, D.A.; Masoud, H.A.; Hamad, A. Climate Changes and Food-Borne Pathogens: The Impact on Human Health and Mitigation Strategy. Clim. Change 2024, 177, 92. [Google Scholar] [CrossRef]
- Singh, B.K.; Delgado-Baquerizo, M.; Egidi, E.; Guirado, E.; Leach, J.E.; Liu, H.; Trivedi, P. Climate Change Impacts on Plant Pathogens, Food Security and Paths Forward. Nat. Rev. Microbiol. 2023, 21, 640–656. [Google Scholar] [CrossRef]
- Abukhattab, S.; Taweel, H.; Awad, A.; Crump, L.; Vonaesch, P.; Zinsstag, J.; Hattendorf, J.; Abu-Rmeileh, N.M.E. Systematic Review and Meta-Analysis of Integrated Studies on Salmonella and Campylobacter Prevalence, Serovar, and Phenotyping and Genetic of Antimicrobial Resistance in the Middle East—A One Health Perspective. Antibiotics 2022, 11, 536. [Google Scholar] [CrossRef]
- Alsayeqh, A.F.; Baz, A.H.A.; Darwish, W.S. Antimicrobial-Resistant Foodborne Pathogens in the Middle East: A Systematic Review. Environ. Sci. Pollut. Res. 2021, 28, 68111–68133. [Google Scholar] [CrossRef]
- Escher, N.A.; Muhummed, A.M.; Hattendorf, J.; Vonaesch, P.; Zinsstag, J. Systematic Review and Meta-analysis of Integrated Studies on Antimicrobial Resistance Genes in Africa—A One Health Perspective. Trop. Med. Int. Health 2021, 26, 1153–1163. [Google Scholar] [CrossRef]
- Rakholiya, K.D.; Kaneria, M.J.; Chanda, S.V. Medicinal Plants as Alternative Sources of Therapeutics against Multidrug-Resistant Pathogenic Microorganisms Based on Their Antimicrobial Potential and Synergistic Properties. In Fighting Multidrug Resistance with Herbal Extracts, Essential Oils and Their Components; Elsevier: Amsterdam, The Netherlands, 2013; pp. 165–179. ISBN 978-0-12-398539-2. [Google Scholar]
- Weerakkody, N.S.; Caffin, N.; Turner, M.S.; Dykes, G.A. In Vitro Antimicrobial Activity of Less-Utilized Spice and Herb Extracts against Selected Food-Borne Bacteria. Food Control 2010, 21, 1408–1414. [Google Scholar] [CrossRef]
- Abdelmontaleb, H.S.; Abdelmeged, D.A.; Hamdy, S.M.; Hammam, M.G.; Ebid, W.M.A. Exploring the Potential of Using Pomegranate and Mango Peel Powders as Natural Food Additives Targeting Safety of White Soft Cheese. Int. J. Food Microbiol. 2025, 434, 111158. [Google Scholar] [CrossRef] [PubMed]
- Chan, C.-L.; Gan, R.-Y.; Shah, N.P.; Corke, H. Polyphenols from Selected Dietary Spices and Medicinal Herbs Differentially Affect Common Food-Borne Pathogenic Bacteria and Lactic Acid Bacteria. Food Control 2018, 92, 437–443. [Google Scholar] [CrossRef]
- Luo, P.; Feng, X.; Liu, S.; Jiang, Y. Traditional Uses, Phytochemistry, Pharmacology and Toxicology of Ruta graveolens L.: A Critical Review and Future Perspectives. Drug Des. Dev. Ther. 2024, 18, 6459–6485. [Google Scholar] [CrossRef]
- Almasri, R.S.; Bedir, A.S.; Al Raish, S.M. Comprehensive Ethnopharmacological Analysis of Medicinal Plants in the UAE: Lawsonia inermis, Nigella sativa, Ziziphus spina-christi, Allium cepa, Allium sativum, Cymbopogon schoenanthus, Matricaria aurea, Phoenix dactylifera, Portulaca oleracea, Reichardia tingitana, Salvadora persica, Solanum lycopersicum, Trigonella foenum-graecum, Withania somnifera, and Ziziphus lotus. Nutrients 2025, 17, 411. [Google Scholar] [CrossRef]
- Elnady, R.E.; Abdon, M.S.; Shaheen, H.R.; Eladawy, R.M.; Azar, Y.O.; Al Raish, S.M. The Future of Alopecia Treatment: Plant Extracts, Nanocarriers, and 3D Bioprinting in Focus. Pharmaceutics 2025, 17, 584. [Google Scholar] [CrossRef]
- Al Raish, S.M.; Almasri, R.S.; Bedir, A.S. Ancient Remedies, Modern Medicine: A Review of Antidiabetic, Cardioprotective, and Antimicrobial Activities of Date Palm (Phoenix dactylifera), Tomato (Solanum lycopersicum), Fenugreek (Trigonella foenum-graecum), and Ashwagandha (Withania somnifera). Biology 2025, 14, 695. [Google Scholar] [CrossRef]
- Shokr, M.M.; Eladawy, R.M.; Azar, Y.O.; Al Raish, S.M. Probiotics and the Gut–Brain Axis: Emerging Therapeutic Strategies for Epilepsy and Depression Comorbidity. Foods 2025, 14, 2926. [Google Scholar] [CrossRef]
- Bedir, A.S.; Almasri, R.S.; Azar, Y.O.; Elnady, R.E.; Al Raish, S.M. Exploring the Therapeutic Potential of Allium Cepa and Allium Sativum Extracts: Current Strategies, Emerging Applications, and Sustainability Utilization. Biology 2025, 14, 1088. [Google Scholar] [CrossRef]
- Abdul Aziz, A.H.; Rizkiyah, D.N.; Qomariyah, L.; Irianto, I.; Che Yunus, M.A.; Putra, N.R. Unlocking the Full Potential of Clove (Syzygium Aromaticum) Spice: An Overview of Extraction Techniques, Bioactivity, and Future Opportunities in the Food and Beverage Industry. Processes 2023, 11, 2453. [Google Scholar] [CrossRef]
- Al Raish, S.M.; Almasri, R.S.; Bedir, A.S.; Elkahwagy, A.A. Phytochemical Composition, Bioactive Compounds, and Antidiabetic Potential of Four Medicinal Plants Native to the UAE: Capparis spinosa, Citrullus colocynthis, Morus alba, and Rhazya stricta. Biology 2025, 14, 1146. [Google Scholar] [CrossRef] [PubMed]
- Bedir, A.S.; Almasri, R.S.; Al Raish, S.M. Therapeutic Efficacy of Nigella Sativa and Ziziphus Lotus: Sustainable Strategies for Diabetes, Antimicrobial Resistance, and Health Treatment. Front. Nutr. 2025, 12, 1592423. [Google Scholar] [CrossRef]
- Gengatharan, A.; Rahim, M.H.A. The Application of Clove Extracts as a Potential Functional Component in Active Food Packaging Materials and Model Food Systems: A Mini-Review. Appl. Food Res. 2023, 3, 100283. [Google Scholar] [CrossRef]
- Idowu, S.; Adekoya, A.E.; Igiehon, O.O.; Idowu, A.T. Clove (Syzygium aromaticum) Spices: A Review on Their Bioactivities, Current Use, and Potential Application in Dairy Products. Food Meas. 2021, 15, 3419–3435. [Google Scholar] [CrossRef]
- El-Maati, M.F.A.; Mahgoub, S.A.; Labib, S.M.; Al-Gaby, A.M.A.; Ramadan, M.F. Phenolic Extracts of Clove (Syzygium aromaticum) with Novel Antioxidant and Antibacterial Activities. Eur. J. Integr. Med. 2016, 8, 494–504. [Google Scholar] [CrossRef]
- Ju, J.; Xu, X.; Xie, Y.; Guo, Y.; Cheng, Y.; Qian, H.; Yao, W. Inhibitory Effects of Cinnamon and Clove Essential Oils on Mold Growth on Baked Foods. Food Chem. 2018, 240, 850–855. [Google Scholar] [CrossRef]
- Hateet, R.; Hachim, A.; Shawi, H. Biological Activity of Eugenol Acetate as Antibacterial and Antioxidant Agent, Isolation from Myrtus communis L. Essential Oil. Int. J. Bioeng. Biotechnol. 2016, 1, 6–11. [Google Scholar]
- Pichette, A.; Larouche, P.; Lebrun, M.; Legault, J. Composition and Antibacterial Activity of Abies balsamea Essential Oil. Phytother. Res. 2006, 20, 371–373. [Google Scholar] [CrossRef] [PubMed]
- Melgarejo-Sánchez, P.; Núñez-Gómez, D.; Martínez-Nicolás, J.J.; Hernández, F.; Legua, P.; Melgarejo, P. Pomegranate Variety and Pomegranate Plant Part, Relevance from Bioactive Point of View: A Review. Bioresour. Bioprocess. 2021, 8, 2. [Google Scholar] [CrossRef]
- Moradi, M.-T.; Karimi, A.; Shahrani, M.; Hashemi, L.; Ghaffari-Goosheh, M.-S. Anti-Influenza Virus Activity and Phenolic Content of Pomegranate (Punica granatum L.) Peel Extract and Fractions. Avicenna J. Med. Biotechnol. 2019, 11, 285–291. [Google Scholar]
- Nazeam, J.A.; AL-Shareef, W.A.; Helmy, M.W.; El-Haddad, A.E. Bioassay-Guided Isolation of Potential Bioactive Constituents from Pomegranate Agrifood by-Product. Food Chem. 2020, 326, 126993. [Google Scholar] [CrossRef]
- Sun, S.; Huang, S.; Shi, Y.; Shao, Y.; Qiu, J.; Sedjoah, R.-C.A.-A.; Yan, Z.; Ding, L.; Zou, D.; Xin, Z. Extraction, Isolation, Characterization and Antimicrobial Activities of Non-Extractable Polyphenols from Pomegranate Peel. Food Chem. 2021, 351, 129232. [Google Scholar] [CrossRef] [PubMed]
- Pacheco-Quito, E.-M.; Avila-Cunalata, D.; Cuenca-León, K. Cariostatic Agents: From Silver Diamine Fluoride to Emerging Bioactive Compounds. Clin. Cosmet. Investig. Dent. 2025, 17, 237–257. [Google Scholar] [CrossRef]
- Gong, S.; Fei, P.; Sun, Q.; Guo, L.; Jiang, L.; Duo, K.; Bi, X.; Yun, X. Action Mode of Cranberry Anthocyanin on Physiological and Morphological Properties of Staphylococcus aureus and Its Application in Cooked Meat. Food Microbiol. 2021, 94, 103632. [Google Scholar] [CrossRef]
- Côté, J.; Caillet, S.; Doyon, G.; Dussault, D.; Sylvain, J.-F.; Lacroix, M. Antimicrobial Effect of Cranberry Juice and Extracts. Food Control 2011, 22, 1413–1418. [Google Scholar] [CrossRef]
- Samarasinghe, S.; Reid, R.; Al-Bayati, M. The Anti-Virulence Effect of Cranberry Active Compound Proanthocyanins (PACs) on Expression of Genes in the Third-Generation Cephalosporin-Resistant Escherichia coli CTX-M-15 Associated with Urinary Tract Infection. Antimicrob. Resist. Infect. Control 2019, 8, 181. [Google Scholar] [CrossRef] [PubMed]
- Das, G.; Gonçalves, S.; Basilio Heredia, J.; Romano, A.; Jiménez-Ortega, L.A.; Gutiérrez-Grijalva, E.P.; Shin, H.S.; Patra, J.K. Cardiovascular Protective Effect of Cinnamon and Its Major Bioactive Constituents: An Update. J. Funct. Foods 2022, 97, 105045. [Google Scholar] [CrossRef]
- Miron, T.; Rabinkov, A.; Mirelman, D.; Wilchek, M.; Weiner, L. The Mode of Action of Allicin: Its Ready Permeability through Phospholipid Membranes May Contribute to Its Biological Activity. Biochim. Biophys. Acta (BBA)-Biomembr. 2000, 1463, 20–30. [Google Scholar] [CrossRef]
- Liaqat, A.; Zahoor, T.; Atif Randhawa, M.; Shahid, M. Characterization and Antimicrobial Potential of Bioactive Components of Sonicated Extract from Garlic (Allium sativum) against Foodborne Pathogens. J. Food Process Preserv. 2019, 43, e13936. [Google Scholar] [CrossRef]
- Bhatwalkar, S.B.; Mondal, R.; Krishna, S.B.N.; Adam, J.K.; Govender, P.; Anupam, R. Antibacterial Properties of Organosulfur Compounds of Garlic (Allium sativum). Front. Microbiol. 2021, 12, 613077. [Google Scholar] [CrossRef]
- Jain, M.; Patil, N.; Mohammed, A.; Hamzah, Z. Valorization of Garlic (Allium sativum L.) Byproducts: Bioactive Compounds, Biological Properties, and Applications. J. Food Sci. 2025, 90, e70152. [Google Scholar] [CrossRef]
- Cao, W.; Li, L.; Wang, J.; Guo, W.; Chen, W.; Pan, L.; Li, D. Effects of Black Garlic Polyphenols on the Physicochemical Characteristics, Antioxidant Activity, and Sensory Evaluation of Yogurt. Gels 2025, 11, 561. [Google Scholar] [CrossRef] [PubMed]
- Ramachandran, E.; Dhanapal, S.; Gopika, U.G.; Ariyamuthu, R. From Spice to Mind: How Cinnamon Supports Women’s Mental Health. J. Ayurveda Holist. Med. 2025, 13, 94–104. [Google Scholar] [CrossRef]
- Almatroodi, S.A.; Alsahli, M.A.; Almatroudi, A.; Anwar, S.; Verma, A.K.; Dev, K.; Rahmani, A.H. Cinnamon and Its Active Compounds: A Potential Candidate in Disease and Tumour Management through Modulating Various Genes Activity. Gene Rep. 2020, 21, 100966. [Google Scholar] [CrossRef]
- Khan, K.; Al-Khalaifah, H.; Ahmad, N.; Khan, M.T.; Alonaizan, R.; Khan, R.U.; Naz, S.; Abudabos, A.; Alhidary, I.A. Dietary Supplementation of Cinnamon and Turmeric Powder Enhances Growth Performance, Nutrient Digestibility, Immune Response, and Renal Function in Broiler Chickens. Poult. Sci. 2025, 104, 105556. [Google Scholar] [CrossRef]
- Aguilar-Zarate, P.; Wong-Paz, J.E.; Buenrostro-Figueroa, J.J.; Ascacio, J.A.; Contreras-Esquivel, J.C.; Aguilar, C.N. Ellagitannins: Bioavailability, Purification and Biotechnological Degradation. Mini Rev. Med. Chem. 2018, 18, 1244–1252. [Google Scholar] [CrossRef]
- Jeyakumar, G.E.; Lawrence, R. Mechanisms of Bactericidal Action of Eugenol against Escherichia coli. J. Herbal. Med. 2021, 26, 100406. [Google Scholar] [CrossRef]
- Ramadan, M.F. (Ed.) Clove (Syzygium aromaticum): Chemistry, Functionality and Applications; Academic Press: London, UK; San Diego, CA, USA; Cambridge, MA, USA; Kidlington, UK, 2022; ISBN 978-0-323-85177-0. [Google Scholar]
- Howell, A.B.; D’Souza, D.H. The Pomegranate: Effects on Bacteria and Viruses That Influence Human Health. Evid.-Based Complement. Altern. Med. 2013, 2013, 606212. [Google Scholar] [CrossRef]
- Pérez, C.; Anesini, C. In Vitro Antibacterial Activity of Argentine Folk Medicinal Plants against Salmonella typhi. J. Ethnopharmacol. 1994, 44, 41–46. [Google Scholar] [CrossRef] [PubMed]
- Kon, K.V.; Rai, M.K. Plant Essential Oils and Their Constituents in Coping with Multidrug-Resistant Bacteria. Expert. Rev. Anti-Infect. Ther. 2012, 10, 775–790. [Google Scholar] [CrossRef] [PubMed]
- Salim, A.; Deiana, P.; Fancello, F.; Molinu, M.G.; Santona, M.; Zara, S. Antimicrobial and Antibiofilm Activities of Pomegranate Peel Phenolic Compounds: Varietal Screening through a Multivariate Approach. J. Bioresour. Bioprod. 2023, 8, 146–161. [Google Scholar] [CrossRef]
- Wu, V.C.-H.; Qiu, X.; Bushway, A.; Harper, L. Antibacterial Effects of American Cranberry (Vaccinium macrocarpon) Concentrate on Foodborne Pathogens. LWT-Food Sci. Technol. 2008, 41, 1834–1841. [Google Scholar] [CrossRef]
- Tamkutė, L.; Vaicekauskaitė, R.; Gil, B.M.; Rovira Carballido, J.; Venskutonis, P.R. Black Chokeberry (Aronia melanocarpa L.) Pomace Extracts Inhibit Food Pathogenic and Spoilage Bacteria and Increase the Microbiological Safety of Pork Products. J. Food Process. Preserv. 2021, 45, e15220. [Google Scholar] [CrossRef]
- Boira, C.; Jolibois, J.; Durduret, A.; Tiguemounine, J.; Szewezyk, C.; De Tollenaere, M.; Scandolera, A.; Reynaud, R. Cranberry Oil: A Potent Natural Intimate Care Ingredient Displaying Antioxidant and Anti-Inflammatory Effects and Promoting Beneficial Vaginal Lactobacillus. Int. J. Mol. Sci. 2025, 26, 2176. [Google Scholar] [CrossRef] [PubMed]
- Alqasoumi, S. Anti-Secretagogue and Antiulcer Effects of Cinnamon Cinnamomum zeylanicum in Rats. J. Pharmacog. Phytother. 2012, 4, 53–61. [Google Scholar] [CrossRef]
- Rashid, A.; Qayum, A.; Bacha, S.A.S.; Liang, Q.; Liu, Y.; Kang, L.; Chi, Z.; Chi, R.; Han, X.; Ekumah, J.-N.; et al. Preparation and Functional Characterization of Pullulan-Sodium Alginate Composite Film Enhanced with Ultrasound-Assisted Clove Essential Oil Nanoemulsions for Effective Preservation of Cherries and Mushrooms. Food Chem. 2024, 457, 140048. [Google Scholar] [CrossRef]
- Mia, M.S.; Ara, R.; Rahman, O.; Shaha, L.C.; Galib, R.M.; Alam, M. Valorization of Fruit Peel Extracts as Natural Preservatives: Characterization and Efficacy in Preserving Chicken Meatballs. Appl. Food Res. 2025, 5, 100981. [Google Scholar] [CrossRef]
- Jany, J.F.; Nupur, A.H.; Akash, S.I.; Karmoker, P.; Mazumder, M.A.R.; Alim, M.A. Fortification of Functional Yogurt by the Phytochemicals Extracted from Pomegranate Peel. Appl. Food Res. 2024, 4, 100479. [Google Scholar] [CrossRef]
- Sallam, K.I.; Raslan, M.T.; Sabala, R.F.; Abd-Elghany, S.M.; Mahros, M.A.; Elshebrawy, H.A. Antimicrobial Effect of Garlic against Foodborne Pathogens in Ground Mutton. Food Microbiol. 2024, 120, 104462. [Google Scholar] [CrossRef] [PubMed]
- Ahmed, N.; El-Fateh, M.; Amer, M.S.; El-Shafei, R.A.; Bilal, M.; Diarra, M.S.; Zhao, X. Antioxidative and Cytoprotective Efficacy of Ethanolic Extracted Cranberry Pomace against Salmonella Enteritidis Infection in Chicken Liver Cells. Antioxidants 2023, 12, 460. [Google Scholar] [CrossRef] [PubMed]
- Gülçin, İ.; Elmastaş, M.; Aboul-Enein, H.Y. Antioxidant Activity of Clove Oil—A Powerful Antioxidant Source. Arab. J. Chem. 2012, 5, 489–499. [Google Scholar] [CrossRef]
- Côté, J.; Caillet, S.; Doyon, G.; Sylvain, J.-F.; Lacroix, M. Bioactive Compounds in Cranberries and Their Biological Properties. Crit. Rev. Food Sci. Nutr. 2010, 50, 666–679. [Google Scholar] [CrossRef]
- Błaszczyk, N.; Rosiak, A.; Kałużna-Czaplińska, J. The Potential Role of Cinnamon in Human Health. Forests 2021, 12, 648. [Google Scholar] [CrossRef]
- Sharokhi Rezaei, S.; Nouri, L.; Mazaheri, M.; Adlnasab, L. Mycotoxin Control Using Natural Solutions: Assessing Cinnamon Extract’s Impact on Aflatoxin Production. Iran. J. Chem. Chem. Eng. 2025, 44, 2339–2354. [Google Scholar] [CrossRef]
- Dong, J.; Fan, Z.; Luo, T.; Deng, C.; Zheng, X.; Cai, C.; Ou, R.; Liu, Z.; Liu, T.; Wang, Q. Dual-Mode Synergistic Antibacterial Films Based on Photothermal Effect and Controlled Release of Cinnamon Essential Oil Microcapsules for Food Packaging. Chem. Eng. J. 2025, 519, 165173. [Google Scholar] [CrossRef]
- Jayathilake, A.L.; Jayasinghe, M.A.; Walpita, J. Development of Ginger, Turmeric Oleoresins and Pomegranate Peel Extracts Incorporated Pasteurized Milk with Pharmacologically Important Active Compounds. Appl. Food Res. 2022, 2, 100063. [Google Scholar] [CrossRef]
- Iqbal, S.; Haleem, S.; Akhtar, M.; Zia-ul-Haq, M.; Akbar, J. Efficiency of Pomegranate Peel Extracts in Stabilization of Sunflower Oil under Accelerated Conditions. Food Res. Int. 2008, 41, 194–200. [Google Scholar] [CrossRef]
- Česonienė, L.; Labokas, J.; Jasutienė, I.; Šarkinas, A.; Kaškonienė, V.; Kaškonas, P.; Kazernavičiūtė, R.; Pažereckaitė, A.; Daubaras, R. Bioactive Compounds, Antioxidant, and Antibacterial Properties of Lonicera Caerulea Berries: Evaluation of 11 Cultivars. Plants 2021, 10, 624. [Google Scholar] [CrossRef]
- Palombo, E.A. Phytochemicals from Traditional Medicinal Plants Used in the Treatment of Diarrhoea: Modes of Action and Effects on Intestinal Function. Phytother. Res. 2006, 20, 717–724. [Google Scholar] [CrossRef]
- Malviya, S.; Arvind; Jha, A.; Hettiarachchy, N. Antioxidant and Antibacterial Potential of Pomegranate Peel Extracts. J. Food Sci. Technol. 2014, 51, 4132–4137. [Google Scholar] [CrossRef]
- Park, S.-Y.; Kim, Y.D.; Kim, M.S.; Kim, K.-T.; Kim, J.Y. Cinnamon (Cinnamomum cassia) Water Extract Improves Diarrhea Symptoms by Changing the Gut Environment: A Randomized Controlled Trial. Food Funct. 2023, 14, 1520–1529. [Google Scholar] [CrossRef]
- Qnais, E.Y.; Elokda, A.S.; Abu Ghalyun, Y.Y.; Abdulla, F.A. Antidiarrheal Activity of the Aqueous Extract of Punica granatum (Pomegranate) Peels. Pharm. Biol. 2007, 45, 715–720. [Google Scholar] [CrossRef]
- Imani, G.; Khalilian, A.; Dastan, D.; Imani, B.; Mehrpooya, M. Effects of Cinnamon Extract on Complications of Treatment and Eradication of Helicobacter Pylori in Infected People. J. Herbmed. Pharmacol. 2019, 9, 55–60. [Google Scholar] [CrossRef]
- Yeomans, N.D.; Naesdal, J. Systematic Review: Ulcer Definition in NSAID Ulcer Prevention Trials. Aliment. Pharmacol. Ther. 2008, 27, 465–472. [Google Scholar] [CrossRef] [PubMed]
- Issac, A.; Gopakumar, G.; Kuttan, R.; Maliakel, B.; Krishnakumar, I.M. Safety and Anti-Ulcerogenic Activity of a Novel Polyphenol-Rich Extract of Clove Buds (Syzygium aromaticum L). Food Funct. 2015, 6, 842–852. [Google Scholar] [CrossRef] [PubMed]
- Abdel-Kawi, S.H.; Hashem, K.S.; Saad, M.K.; Fekry, G.; Abdel-Hameed, E.M.M. The Ameliorative Effects of Cinnamon Oil against Ethanol-Induced Gastric Ulcer in Rats by Regulating Oxidative Stress and Promoting Angiogenesis. J. Mol. Histol. 2022, 53, 573–587. [Google Scholar] [CrossRef]
- Alqirnawdi, M.A.A.; Khotimah, H.; Santosa, S.; Mintaroem, K. The Effect of Cinnamon to the Expression of SOD-1 and TNF-α in Indomethacin-Induced Gastric Ulcer Rat. AIP Conf. Proc. 2020, 2231, 030008. [Google Scholar] [CrossRef]
- Khan, M.K.; Hassan, S.; Imran, M.; Ahmad, M.H. Chapter 22—Extraction of Bioactive Compounds from Clove (Syzygium aromaticum). In Clove (Syzygium aromaticum): Chemistry, Functionality and Applications; Ramadan, M.F., Ed.; Academic Press: London, UK; San Diego, CA, USA; Cambridge, MA, USA; Kidlington, UK, 2022; ISBN 978-0-323-85177-0. [Google Scholar]
- Haro-González, J.N.; Castillo-Herrera, G.A.; Martínez-Velázquez, M.; Espinosa-Andrews, H. Clove Essential Oil (Syzygium aromaticum L. Myrtaceae): Extraction, Chemical Composition, Food Applications, and Essential Bioactivity for Human Health. Molecules 2021, 26, 6387. [Google Scholar] [CrossRef]
- Severo, C.; Anjos, I.; Souza, V.G.L.; Canejo, J.P.; Bronze, M.R.; Fernando, A.L.; Coelhoso, I.; Bettencourt, A.F.; Ribeiro, I.A.C. Development of Cranberry Extract Films for the Enhancement of Food Packaging Antimicrobial Properties. Food Packag. Shelf Life 2021, 28, 100646. [Google Scholar] [CrossRef]
- Sridhar, A.; Ponnuchamy, M.; Kumar, P.S.; Kapoor, A. Food Preservation Techniques and Nanotechnology for Increased Shelf Life of Fruits, Vegetables, Beverages and Spices: A Review. Environ. Chem. Lett. 2021, 19, 1715–1735. [Google Scholar] [CrossRef]
- Kumar, S.; Singh, N.; Devi, L.S.; Kumar, S.; Kamle, M.; Kumar, P.; Mukherjee, A. Neem Oil and Its Nanoemulsion in Sustainable Food Preservation and Packaging: Current Status and Future Prospects. J. Agric. Food Res. 2022, 7, 100254. [Google Scholar] [CrossRef]
- Khalili, M.; Najafi, A.; Razavi, R. Preservative Activity of Free and Nano-Encapsulated Pomegranate Peel Extract Obtained Using Cold Plasma and Ultrasound-Assisted Method in Increasing the Shelf Life of Thigh Mutton Mince. Appl. Food Res. 2025, 5, 100668. [Google Scholar] [CrossRef]
- Dong, Y.; Zhang, J.; Xie, A.; Yue, X.; Li, M.; Zhou, Q. Garlic Peel Extract as an Antioxidant Inhibits Triple-Negative Breast Tumor Growth and Angiogenesis by Inhibiting Cyclooxygenase-2 Expression. Food Sci. Nutr. 2024, 12, 6886–6895. [Google Scholar] [CrossRef] [PubMed]

| Plant | Main Bioactive Compounds | Target Food-Borne Pathogens | Ref. |
|---|---|---|---|
| Clove (Syzygium aromaticum) | Eugenol, eugenol acetate, α-humulene, β-caryophyllene | S. aureus, E. coli, Y. enterocolitica, B. cereus, molds | [40,41,42,54,55] |
| Pomegranate (Punica granatum) | Punicalagin, ellagic acid, tannins | S. Typhi, L. monocytogenes, E. coli, S. aureus, K. pneumoniae | [50,51,52,53,56,57] |
| Cranberry (Vaccinium macrocarpon) | Proanthocyanidins (PACs), anthocyanins | ESBL-E. coli, MDR-E. coli, S. mutans, S. aureus | [39,51,52,58,59] |
| Garlic (Allium sativum) | Allicin, organosulfur compounds | H. pylori, Gram-positive and Gram-negative foodborne pathogens | [60,61,62,63] |
| Cinnamon (Cinnamomum zeylanicum) | Cinnamaldehyde, catechins, procyanidins | L. monocytogenes, E. coli, A. flavus, A. parasiticus | [64,65] |
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2026 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.
Share and Cite
Al Raish, S.M. The Efficacy of Plant Extracts Against Key Food-Borne Pathogens: A Mechanistic, Applications, and Advances. Microorganisms 2026, 14, 621. https://doi.org/10.3390/microorganisms14030621
Al Raish SM. The Efficacy of Plant Extracts Against Key Food-Borne Pathogens: A Mechanistic, Applications, and Advances. Microorganisms. 2026; 14(3):621. https://doi.org/10.3390/microorganisms14030621
Chicago/Turabian StyleAl Raish, Seham M. 2026. "The Efficacy of Plant Extracts Against Key Food-Borne Pathogens: A Mechanistic, Applications, and Advances" Microorganisms 14, no. 3: 621. https://doi.org/10.3390/microorganisms14030621
APA StyleAl Raish, S. M. (2026). The Efficacy of Plant Extracts Against Key Food-Borne Pathogens: A Mechanistic, Applications, and Advances. Microorganisms, 14(3), 621. https://doi.org/10.3390/microorganisms14030621

