The Dual Role of the Medicinal Mushroom Fomitopsis pinicola in Inhibiting Biofilm and Reducing Antibiotic Resistance of Methicillin-Resistant Staphylococcus aureus

IF 3.5 2区 农林科学 Q2 FOOD SCIENCE & TECHNOLOGY
Başar Karaca, Noah Kyalo Kilonzo, Şilan Korkmaz, Okan Onar, Özlem Yıldırım, Arzu Çöleri Cihan
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Abstract

This study investigates the antimicrobial, antibiofilm, and anti-quorum sensing activity of Fomitopsis pinicola against methicillin-resistant Staphylococcus aureus (MRSA) strains and its potential to improve the efficacy of conventional antibiotics and exert selective cytotoxic effects on cancer cells. Ethanolic extracts of F. pinicola were analyzed for antibacterial activity by MIC and time-kill assays. Synergistic interactions with antibiotics were quantified using checkerboard assays. Antibiofilm activity was analyzed on polystyrene and stainless-steel surfaces. Anti-quorum sensing activity was determined by the inhibition of violacein in Chromobacterium violaceum. Efflux pump inhibition was assessed by the accumulation of the ethidium bromide. The down-regulation of virulence genes (agrA, hla) was measured by qRT-PCR (quantitative real-time reverse-transcription PCR). FT-IR (Fourier transform infrared spectroscopy) spectroscopy characterized the bioactive compounds, and the cytotoxicity assays on HT-29 colon cancer and Vero cells evaluated selective toxicity. The extract showed strong antibacterial effects with a MIC of 312.5 μg/mL and concentration-dependent bactericidal activity. Synergistic interactions with antibiotics led to FIC indices ≤ 0.5. The extract significantly inhibited biofilm formation and eradicated already formed biofilms. Sub-MIC concentrations reduced quorum sensing by 85.01%, inhibited efflux pump activity, and down-regulated virulence-associated genes. FT-IR analysis confirmed the presence of triterpenoids and terpenoids. The extract displayed selective cytotoxicity on HT-29 cancer cells, showing strong inhibition, while normal Vero cells were spared. These results emphasize the potential of F. pinicola as a robust candidate for antimicrobial therapeutics, especially against biofilm-associated and multidrug-resistant pathogens, as well as a selective anticancer agent.

药用菌平灰拟南芥在抑制耐甲氧西林金黄色葡萄球菌生物膜和降低耐药性中的双重作用
本研究探讨了平孔拟南芥对耐甲氧西林金黄色葡萄球菌(MRSA)的抑菌活性、抗生物膜活性和抗群体感应活性,以及其提高常规抗生素疗效和对癌细胞施加选择性细胞毒作用的潜力。采用MIC法和时效法对皮尼屈菌乙醇提取物的抑菌活性进行了分析。与抗生素的协同相互作用采用棋盘法定量。分析了其在聚苯乙烯和不锈钢表面的抗菌活性。通过对堇菜色素的抑制,测定了其抗群体感应活性。通过溴化乙锭的积累来评估外排泵的抑制作用。采用qRT-PCR (quantitative real-time reverse-transcription PCR)检测毒力基因(agrA、hla)的下调情况。傅里叶变换红外光谱(FT-IR)表征了生物活性化合物,并对HT-29结肠癌和Vero细胞进行了细胞毒性试验,评估了选择性毒性。该提取物具有较强的抑菌作用,MIC为312.5 μg/mL,且具有浓度依赖性。与抗生素协同作用导致FIC指数≤0.5。提取物能显著抑制生物膜的形成,并能清除已形成的生物膜。亚mic浓度降低了85.01%的群体感应,抑制了外排泵的活性,并下调了毒力相关基因。FT-IR分析证实了三萜和萜类化合物的存在。提取物对HT-29癌细胞表现出选择性的细胞毒性,表现出较强的抑制作用,而对正常的Vero细胞则没有作用。这些结果强调了pinicola作为抗微生物治疗药物的强大候选药物的潜力,特别是针对生物膜相关和多重耐药病原体,以及选择性抗癌药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Food Science & Nutrition
Food Science & Nutrition Agricultural and Biological Sciences-Food Science
CiteScore
7.40
自引率
5.10%
发文量
434
审稿时长
24 weeks
期刊介绍: Food Science & Nutrition is the peer-reviewed journal for rapid dissemination of research in all areas of food science and nutrition. The Journal will consider submissions of quality papers describing the results of fundamental and applied research related to all aspects of human food and nutrition, as well as interdisciplinary research that spans these two fields.
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