Department of microbiology, Tagore medical college and hospital, Melakottaiyur Street, 600127 Rathinamangalam, Chennai, Tamil Nadu, India.
Department of microbiology, Saveetha medical college, 602105 Thandalam, Chennai, India.
J Mycol Med. 2018 Mar;28(1):193-200. doi: 10.1016/j.mycmed.2017.07.010. Epub 2017 Aug 21.
Candida species is the fourth common cause of blood stream infections all over the world which is life threatening. Invasive candidiasis leads to increased mortality and morbidity especially in immunosuppressed. The antifungal resistance pattern in high-risk patients is major concern.
The present study was to access the anticandidal activity of leaves, bark and seeds of Cassia fistula against fluconazole resistant Candida species, C. albicans, C. glabrata, C. krusei, C. tropicalis, C. kefyr and C. parapsilosis isolated from HIV patients. The predominant phytochemical component responsible for fungicidal activity was to be accessed.
Ethanol, chloroform, petroleum ether and aqueous extracts of leaves, bark and seeds of C. fistula linn. was evaluated against Microbial type culture collection (MTCC) Candida strains and 21 fluconazole resistant clinical isolates. Antifungal activity was evaluated by agar diffusion and broth dilution techniques. The active phytochemical component present in the ethanol extract of seeds was accessed by high performance thin layer chromatography. The docking study was done with lanosterol 14-alpha demethylase, the azole drug target with the predominant phytochemical from the extract having antifungal activity.
All the extracts of C. fistula showed excellent anticandidal activity. Ethanol extract of C. fistula seed exhibited the most inhibitory activity. C. krusei and C. parapsilosis were the most inhibited and C. kefyr was the least inhibited species. The predominant phytochemical active component of the ethanol extract of seed was gallic acid. Gallic acid showed excellent binding with lanosterol 14-alpha demethylase.
The present study reports the antifungal activity of various extracts of Cassia fistula for the first time against fluconazole resistant Candida isolates. We can conclude that the polyphenolic compound gallic acid is a potent natural antifungal agent. Further research is needed to assess the pharmacokinetic property.
念珠菌属是全球第四大常见的血流感染病原体,具有生命威胁性。侵袭性念珠菌病会导致死亡率和发病率增加,尤其是在免疫抑制患者中。高危患者的抗真菌耐药模式是主要关注点。
本研究旨在评估金腰子叶、皮和种子的抗真菌活性,以对抗分离自 HIV 患者的氟康唑耐药念珠菌属,包括白色念珠菌、光滑念珠菌、克柔念珠菌、热带念珠菌、近平滑念珠菌和季也蒙念珠菌。评估负责杀菌活性的主要植物化学成分。
评估金腰子叶、皮和种子的乙醇、氯仿、石油醚和水提取物对微生物类型培养物收集(MTCC)念珠菌株和 21 株氟康唑耐药临床分离株的抗真菌活性。通过琼脂扩散和肉汤稀释技术评估抗真菌活性。通过高效薄层色谱法评估种子乙醇提取物中存在的活性植物化学成分。用唑类药物靶标羊毛甾醇 14-α 去甲基酶对接提取物中具有抗真菌活性的主要植物化学成分。
金腰子的所有提取物均显示出优异的抗真菌活性。金腰子种子的乙醇提取物表现出最强的抑制活性。克柔念珠菌和近平滑念珠菌的抑制作用最强,而季也蒙念珠菌的抑制作用最弱。种子乙醇提取物的主要活性植物化学成分是没食子酸。没食子酸与羊毛甾醇 14-α 去甲基酶表现出良好的结合。
本研究首次报道了金腰子各种提取物对氟康唑耐药念珠菌属的抗真菌活性。我们可以得出结论,多酚类化合物没食子酸是一种有效的天然抗真菌剂。需要进一步研究来评估其药代动力学特性。