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A comparative study of in‐vitro and in‐silico anti‐candidal activity and GC–MS profiles of snow mountain garlic vs. normal garlic

机译:雪山大蒜与普通大蒜的体外和计算机抗念珠菌活性和GC-MS曲线的比较研究

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Abstract Aim The study aimed to profile the volatile phytocomposition of snow mountain garlic (SMG) compared to normal garlic and investigate the anti‐Candida efficacy against clinically relevant multi‐drug resistant isolates of Candida species. Methods and Results Herein, SMG has shown significantly superior fungicidal power at 2x‐MIC dose against C. albicans and C. glabrata in killing kinetic evaluation unlike the fungistatic effect of normal garlic. GC–MS headspace‐based profiling of SMG showed 5 unique volatile compounds and a 5‐fold higher content of saponins than normal garlic. In an in‐silico analysis, cholesta‐4,6‐dien‐3‐ol,(3‐beta) was uniquely identified in SMG as a potential inhibitor with high binding affinity to the active site of exo‐1,3‐betaglucan synthase, an established anti‐candida drug target crucial for the biofilm matrix formation, thus suggesting a plausible anti‐Candida mechanism. Conclusion The in‐vitro and in‐silico studies have demonstrated the Candida‐cidal and anti‐biofilm activities of SMG, distinguishing it from the Candida‐static efficacy of normal garlic. Significance and Impact of the study This is the first report that identifies several phytochemical signatures of SMG along with a potential anti‐Candida compound, that is cholesta‐4,6‐dien‐3‐ol,(3‐beta)‐, which appears worthy of detailed studies in the future to explore the utility of SMG as a fungal phytotherapy agent, especially against drug‐resistant Candida sp.
机译:摘要 目的 分析雪山大蒜(SMG)与普通大蒜相比的挥发性植物组成,并探讨其对临床相关念珠菌属多重耐药菌株的抗念珠菌疗效。方法和结果 在此,与普通大蒜的抑菌作用不同,SMG 在 2x-MIC 剂量下显示出对白色念珠菌和光滑梭菌的杀灭力显着优于白色念珠菌和光滑念珠菌。基于GC-MS顶空的SMG分析显示,SMG含有5种独特的挥发性化合物,皂苷含量是普通大蒜的5倍。在计算机分析中,胆甾醇-4,6-二烯-3-醇(3-β)在SMG中被唯一鉴定为一种潜在的抑制剂,与外-1,3-β-葡聚糖合酶的活性位点具有高结合亲和力,外-1,3-β-葡聚糖合酶是一种已建立的抗念珠菌药物靶标,对生物膜基质的形成至关重要,从而表明了一种合理的抗念珠菌机制。结论 体外和计算机研究证实了SMG的念珠菌杀灭活性和抗生物膜活性,使其与普通大蒜的念珠菌静态功效区分开来。研究的意义和影响 这是第一份确定 SMG 的几种植物化学特征以及潜在的抗念珠菌化合物的报告,即胆甾烷-4,6-二烯-3-醇,(3-β)-,这似乎值得在未来进行详细研究,以探索 SMG 作为真菌植物治疗剂的效用,特别是针对耐药念珠菌属。

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