可可豆精油的活性成分萜烯-4-醇减轻耐多药金黄色葡萄球菌和肺炎克雷伯菌的生物膜形成能力

Pub Date : 2022-09-03 DOI:10.1080/22311866.2022.2154264
Priya Cheruvanachari, Subhaswaraj Pattnaik, M. Mishra, P. Pragyandipta, P. Naik
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引用次数: 3

摘要

摘要微生物对传统抗生素耐药性发生率的增加促使科学界寻找替代治疗方案。在这种情况下,减缓生物膜的形成被认为是可行的替代方案。由于植物衍生的精油是具有广泛药理价值的生物活性植物化学物质的丰富遗产,在本研究中,对从大熊猫雄花中提取的Kewda精油(KEO)的生物活性成分对金黄色葡萄球菌和肺炎克雷伯菌及其参考菌株MTCC-740和MTCC-109的抗菌和抗菌膜活性进行了评价。萜烯-4-醇对金黄色葡萄球菌和肺炎克雷伯菌的最小抑制浓度(MIC)分别为50和25mM。在MIC水平下,萜烯-4-醇对参考菌株MTCC-740和MTCC-109均表现出抗菌活性,其区域分别为16和14mm。在用亚MIC的萜烯-4-醇处理时,观察到胞外多糖(EPS)产量的显著降低,这从刚果红琼脂(CRA)的定性测定中是明显的。此外,对EPS产量的减少进行了量化,对金黄色葡萄球菌的减少为67.51±1.29%。光和荧光显微镜分析也证实了萜烯-4-醇的抗生物膜潜力,因为观察到生物膜形成的厚度显著减少。计算机研究深入了解了萜烯-4-醇在与生物膜形成和耐药性相关的靶蛋白结合中的作用。因此,萜烯-4-醇可以被认为是对抗生物膜相关慢性感染和耐药性的假定候选药物。图形摘要
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Terpinen-4-ol, An Active Constituent of Kewda Essential Oil, Mitigates Biofilm Forming Ability of Multidrug Resistant Staphylococcus aureus and Klebsiella pneumoniae
Abstract The increased incidence of microbial resistance to traditional antibiotics has urged the scientific community to look for alternative therapeutic regimens. In this context, mitigation of biofilm formation is considered as viable alternative. Since, plant derived essential oils are rich heritage of bioactive phytochemicals with widespread pharmacological values, in the present study Terpinen-4-ol, bioactive constituent of Kewda essential oil (KEO) extracted from Pandanus odorifer male flower was evaluated for its antimicrobial and antibiofilm activities against Staphylococcus aureus and Klebsiella pneumoniae and their reference strains, MTCC-740 and MTCC-109. The minimum inhibitory concentration (MIC) of Terpinen-4-ol against S. aureus and K. pneumoniae was 50 and 25 mM, respectively. At MIC level, Terpinen-4-ol exhibited antibacterial activities against both the reference strains i.e. MTCC-740 and MTCC-109 with a zone of 16 and 14 mm, respectively. On treatment with sub-MIC of Terpinen-4-ol, a significant reduction in exopolysaccharides (EPS) production was observed as evident from qualitative Congo red agar (CRA) assay. Further, the reduction in EPS production was quantified with a reduction of 67.51±1.29% against S. aureus. The light and fluorescence microscopic analysis also corroborated the antibiofilm potential of Terpinen-4-ol as a significant reduction in the thickness of biofilm formation was observed. In silico studies provided an insight into the action of Terpinen-4-ol in binding to target proteins associated with biofilm formation and drug resistance. Thus, Terpinen-4-ol could be considered as putative drug candidate in the fight against biofilm associated chronic infections and drug resistance. GRAPHICAL ABSTRACT
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