اثر ضدمیکروبی عصاره آبی جاشیر بر برخی از گونه‌های قارچی بیماری‌زا و برهمکنش آن با آنتی-بیوتیک نیستاتین

نویسندگان
1 دانشجوی کارشناسی ارشد، گروه علوم و مهندسی صنایع غذایی، دانشکده علوم دامی و صنایع غذایی، دانشگاه علوم کشاورزی و منابع طبیعی خوزستان، ملاثانی، ایران
2 دانشیار، گروه علوم و مهندسی صنایع غذایی، دانشکده علوم دامی و صنایع غذایی، دانشگاه علوم کشاورزی و منابع طبیعی خوزستان، ملاثانی، ایران
3 استاد، گروه علوم و مهندسی صنایع غذایی، دانشکده علوم دامی و صنایع غذایی، دانشگاه علوم کشاورزی و منابع طبیعی خوزستان، ملاثانی، ایران
4 دکتری گروه علوم و مهندسی صنایع غذایی، دانشکده کشاورزی، دانشگاه فردوسی مشهد، مشهد، ایران
چکیده
جاشیر گیاهی است که در طب سنتی به دلیل خواص درمانی آن مورد استفاده قرار می‌گرفته است. مطالعه حاضر به منظور بررسی اثر ضد قارچی عصاره آبی جاشیر بر روی آلترناریا آلترناتا، آلترناریا سولانی، ساکارومایسس سرویزیه و فوزاریوم سولانی انجام شد. روش‌های ضد قارچی مورد استفاده عبارت بودند از دیسک دیفیوژن آگار، چاهک آگار، حداقل غلظت مهارکنندگی (MIC) و حداقل غلظت قارچ‌کشی (MFC). غلظت عصاره مورد استفاده در این مطالعه 20، 40، 60 و 80 میلی‌گرم در میلی‌لیتر بود. این مطالعه نشان داد که اثر ضد قارچی وابسته به غلظت عصاره است و با غلظت افزایش می‌یابد. ساکارومایسس سرویزیه حساس‌ترین گونه به عصاره و فوزاریوم سولانی مقاوم‌ترین گونه بود. در 80 میلی‌گرم بر میلی‌لیتر عصاره، قطر بازداری برای ساکارومایسس سرویزیه به ترتیب 90/11 میلی‌متر و 13 میلی‌متر در روش دیسک دیفیوژن آگار و چاهک آگار بود. قطرهای بازداری مربوطه برای فوزاریوم سولانی به ترتیب 60/9 میلی‌متر و 20/10 میلی‌متر بود. در حالت ترکیبی (برهمکنش) عصاره آبی جاشیر با آنتی­بیوتیک نیستاتین برای تمامی سویه­های قارچی حالت هم­افزایی مشاهده شد. مقادیر MIC و MFC برای ساکارومایسس سرویزیه به ترتیب 32 و 128 میلی‌گرم بر میلی‌لیتر بود. نتایج MIC و MFC برای فوزاریوم سولانی به ترتیب 256 و > 512 میلی‌گرم در میلی‌لیتر بود. نتایج این مطالعه نشان داد که عصاره آبی جاشیر می‌تواند به عنوان یک عامل ضد قارچ طبیعی برای مهار رشد قارچ‌های بیماری‌زا در میوه‌ها و سبزیجات تازه مورد استفاده قرار گیرد.
کلیدواژه‌ها

موضوعات


عنوان مقاله English

Antimicrobial effect of Prangos ferulacea aqueous extract on some pathogenic fungal species and its interaction with nystatin antibiotic

نویسندگان English

Shahab Jalil Sarghaleh 1
Behrooz Alizadeh Behbahani 2
Mohammad Hojjati 3
Alireza Vasiee 4
Mohammad Noshad 2
1 MSc student, Department of Food Science and Technology, Faculty of Animal Science and Food Technology, Agricultural Sciences and Natural Resources University of Khuzestan, Mollasani, Iran
2 Associate Professor, Department of Food Science and Technology, Faculty of Animal Science and Food Technology, Agricultural Sciences and Natural Resources University of Khuzestan, Mollasani, Iran.
3 Professor, Department of Food Science and Technology, Faculty of Animal Science and Food Technology, Agricultural Sciences and Natural Resources University of Khuzestan, Mollasani, Iran.
4 PhD, Department of Food Science and Technology, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, Iran.
چکیده English

Prangos ferulacea is a plant that has been used in traditional medicine for its therapeutic properties. The present study was conducted to investigate the antifungal effect of P. ferulacea aqueous extract on Alternaria alternata, Alternaria solani, Saccharomyces cerevisiae, and Fusarium solani. The antifungal methods used were disc diffusion agar, well diffusion agar, minimum inhibitory concentration (MIC), and minimum fungicidal concentration (MFC). The extract concentrations used in the study were 20, 40, 60, and 80 mg/mL. The study found that the antifungal effect was concentration-dependent and increased with concentration. S. cerevisiae was the most sensitive species to the extract while F. solani was the most resistant. At 80 mg/mL, the inhibition zones for S. cerevisiae were found to be 11.90 mm and 13.00 mm in disc diffusion agar and well diffusion agar methods, respectively. The corresponding zones were 9.60 mm and 10.20 mm for F. solani, respectively. In the combined mode (interaction) of P. ferulacea aqueous extract with nystatin antibiotic, synergistic mode was observed for all fungal strains. The MIC and MFC values for S. cerevisiae were 32 and 128 mg/mL, respectively. The MIC and MFC results for F. solani were found to 256 and > 512 mg/mL, respectively. The results of this study showed that P. ferulacea aqueous extract could be used as a natural antifungal agent to inhibit the growth of pathogenic fungi on fresh fruits and vegetables.

کلیدواژه‌ها English

Prangos ferulacea
Aqueous extract
Pathogenic fungi
antifungal effect
Shelf-life
[1] Barzee, T. J., Cao, L., Pan, Z., & Zhang, R. (2021). Fungi for future foods. Journal of Future Foods, 1(1), 25-37.
[2] Sharma, R. L., Ahir, R. R., Yadav, S. L., Sharma, P., & Ghasolia, R. P. (2021). Effect of nutrients and plant extracts on Alternaria blight of tomato caused by Alternaria Alternata. Journal of Plant Diseases and Protection, 128(4), 951-960.
[3] Escrivá, L., Oueslati, S., Font, G., & Manyes, L. (2017). Alternaria Mycotoxins in Food and Feed: An Overview. Journal of Food Quality, 2017, 1569748.
[4] Pan, C., Yang, K., Erhunmwunsee, F., Li, Y.-X., Liu, M., Pan, S., Yang, D., Lu, G., Ma, D., & Tian, J. (2023). Inhibitory effect of cinnamaldehyde on Fusarium solani and its application in postharvest preservation of sweet potato. Food Chemistry, 408, 135213.
[5] Kebede, H., Liu, X., Jin, J., & Xing, F. (2020). Current status of major mycotoxins contamination in food and feed in Africa. Food Control, 110, 106975.
[6] Carrascal-Hernández, D. C., Flórez-López, E., Peralta-Ruiz, Y., Chaves-López, C., & Grande-Tovar, C. D. (2022). Eco-Friendly Biocontrol Strategies of Alternaria Phytopathogen Fungus: A Focus on Gene-Editing Techniques. Agriculture, 12(10).
[7] González-Estrada, R., Carvajal-Millán, E., Ragazzo-Sánchez, J., Bautista-Rosales, P., & Calderón-Santoyo, M. (2017). Control of blue mold decay on Persian lime: Application of covalently cross-linked arabinoxylans bioactive coatings with antagonistic yeast entrapped. LWT-Food Science and Technology, 85, 187-196.
[8] Behbahani, B. A., Shahidi, F., Yazdi, F. T., & Mohebbi, M. (2013). Antifungal effect of aqueous and ethanolic mangrove plant extract on pathogenic fungus" in vitro". International Journal of Agronomy and Plant Production, 4(7), 1652-1658.
[9] Rahmati-Joneidabad, M., Alizadeh Behbahani, B., & Noshad, M. (2021). Antifungal effect of Satureja khuzestanica essential oil on Aspergillus niger, Botrytis cinerea, and Rhizopus stolonifer causing strawberry’s rot and mold. Journal of food science and technology (Iran), 18(115), 171-180.
[10] Sureshjani, M. H., Yazdi, F. T., Mortazavi, S. A., Behbahani, B. A., & Shahidi, F. (2014). Antimicrobial effects of Kelussia odoratissima extracts against food borne and food spoilage bacteria" in vitro. Journal of Paramedical Sciences, 5(2), 115-120.
[11] Alizadeh Behbahani, B., Falah, F., Vasiee, A., & Tabatabaee Yazdi, F. (2021). Control of microbial growth and lipid oxidation in beef using a Lepidium perfoliatum seed mucilage edible coating incorporated with chicory essential oil. Food science & nutrition, 9(5), 2458-2467.
[12] Alizadeh Behbahani, B., & Imani Fooladi, A. A. (2018). Development of a novel edible coating made by Balangu seed mucilage and Feverfew essential oil and investigation of its effect on the shelf life of beef slices during refrigerated storage through intelligent modeling. Journal of Food Safety, 38(3), e12443.
[13] Heydari, S., Jooyandeh, H., Alizadeh Behbahani, B., & Noshad, M. (2020). The impact of Qodume Shirazi seed mucilage‐based edible coating containing lavender essential oil on the quality enhancement and shelf life improvement of fresh ostrich meat: An experimental and modeling study. Food Science & Nutrition, 8(12), 6497-6512.
[14] Falah, F., Shirani, K., Vasiee, A., Yazdi, F. T., & Behbahani, B. A. (2021). In vitro screening of phytochemicals, antioxidant, antimicrobial, and cytotoxic activity of Echinops setifer extract. Biocatalysis and Agricultural Biotechnology, 35, 102102.
[15] Yazdi, F. T., & Behbahani, B. A. (2013). Antimicrobial effect of the aqueous and ethanolic Teucrium polium L. extracts on gram positive and gram negative bacteria “in vitro”. Archives of Advances in Biosciences, 4(4), 56-62.
[16] Garavand, F., Eghbal, N., Nooshkam, M., Miraballes, I., & Jafari, S. M. (2021). Salt, spices, and seasonings formulated with nano/microencapsulated ingredients. In Application of Nano/Microencapsulated Ingredients in Food Products (pp. 435-467): Elsevier.
[17] Jalil Sarghaleh, S., Alizadeh Behbahani, B., Hojjati, M., Vasiee, A., & Noshad, M. (2023). Evaluation of the constituent compounds, antioxidant, anticancer, and antimicrobial potential of Prangos ferulacea plant extract and its effect on Listeria monocytogenes virulence gene expression. Frontiers in Microbiology, 14. doi:10.3389/fmicb.2023.1202228.
[18] Emamghoreishi, M., Taghavi, A., & Javidnia, K. (2012). The effect of aqueous and methanolic extracts of Prangos ferulacea on formalin-induced pain in mice. Journal of Jahrom University of Medical Sciences, 9(4), 2-7.
[19] Shokoohinia, Y., Sajjadi, S.-E., Gholamzadeh, S., Fattahi, A., & Behbahani, M. (2014). Antiviral and cytotoxic evaluation of coumarins from Prangos ferulacea. Pharmaceutical biology, 52(12), 1543-1549.
[20] Tabatabaei Yazdi, F., Nooshkam, M., Shahidi, F., Asadi, F., & Alizadeh-Behbahani, B. (2018). Evaluation of antimicrobial activity and antioxidant potential of chitosan Maillard-based conjugates in vitro. Applied Microbiology In Food Industries, 4(3), 1-15.
[21] Shahidi, F., Tabatabaei Yazdi, F., Nooshkam, M., Zareie, Z., & Fallah, F. (2020). Chemical modification of chitosan through non-enzymatic glycosylation reaction to improve its antimicrobial and anti-oxidative properties. Iranian Food Science and Technology Research Journal, 16(1), 117-129.
[22] Nooshkam, M., Falah, F., Zareie, Z., Tabatabaei Yazdi, F., Shahidi, F., & Mortazavi, S. A. (2019). Antioxidant potential and antimicrobial activity of chitosan–inulin conjugates obtained through the Maillard reaction. Food Science and Biotechnology, 28(6), 1861-1869.
[23] Alizadeh Behbahani, B., Noshad, M., & Falah, F. (2020). The combined effect of the combined Fennel and Clove essential oils on Staphylococcus epidermidis, Bacillus cereus, Salmonella typhi and Enterobacter aerogenes using Checkerboard assay (fractional inhibitory concentration index). Journal of food science and technology (Iran), 17(106), 75-83.
[24] Badalamenti, N., Maresca, V., Di Napoli, M., Bruno, M., Basile, A., & Zanfardino, A. (2022). Chemical Composition and Biological Activities of Prangos ferulacea Essential Oils. Molecules, 27(21), 7430.
[25] Zengin, G., Sinan, K. I., Ak, G., Mahomoodally, M. F., Paksoy, M. Y., Picot-Allain, C., . . . Custodio, L. (2020). Chemical profile, antioxidant, antimicrobial, enzyme inhibitory, and cytotoxicity of seven Apiaceae species from Turkey: A comparative study. Industrial Crops and Products, 153, 112572.
[26] Hekmat Zadeh, S. F., Gharaghani, M., Nouripour-Sisakht, S., & Razmjoue, D. (2022). Chemical composition of Prangos ferulacea (L.) Lindl., and Prangos uloptera DC. essential oils and their antifungal activities. Journal of Herbmed Pharmacology, 11(4), 585-591.
[27] Lagrouh, F., Dakka, N., & Bakri, Y. (2017). The antifungal activity of Moroccan plants and the mechanism of action of secondary metabolites from plants. Journal de Mycologie Médicale, 27(3), 303-311.