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丁香酚对人体真菌病原体的抗真菌机制研究。

Investigation of Antifungal Mechanisms of Thymol in the Human Fungal Pathogen, .

机构信息

Radiation Research Division, Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, Jeongeup-si 56212, Jeollabuk-do, Korea.

Department of Radiation Science and Technology, University of Science and Technology, Daejeon 34113, Yuseong-gu, Korea.

出版信息

Molecules. 2021 Jun 7;26(11):3476. doi: 10.3390/molecules26113476.

Abstract

Due to lifespan extension and changes in global climate, the increase in mycoses caused by primary and opportunistic fungal pathogens is now a global concern. Despite increasing attention, limited options are available for the treatment of systematic and invasive mycoses, owing to the evolutionary similarity between humans and fungi. Although plants produce a diversity of chemicals to protect themselves from pathogens, the molecular targets and modes of action of these plant-derived chemicals have not been well characterized. Using a reverse genetics approach, the present study revealed that thymol, a monoterpene alcohol from L., (Lamiaceae), exhibits antifungal activity against by regulating multiple signaling pathways including calcineurin, unfolded protein response, and HOG (high-osmolarity glycerol) MAPK (mitogen-activated protein kinase) pathways. Thymol treatment reduced the intracellular concentration of Ca by controlling the expression levels of calcium transporter genes in a calcineurin-dependent manner. We demonstrated that thymol decreased -glycosylation by regulating the expression levels of genes involved in glycan-mediated post-translational modifications. Furthermore, thymol treatment reduced endogenous ergosterol content by decreasing the expression of ergosterol biosynthesis genes in a HOG MAPK pathway-dependent manner. Collectively, this study sheds light on the antifungal mechanisms of thymol against .

摘要

由于寿命延长和全球气候的变化,原发性和机会性真菌病原体引起的真菌感染的增加现在是一个全球性的关注问题。尽管越来越受到关注,但由于人类和真菌之间存在进化上的相似性,系统性和侵袭性真菌感染的治疗选择仍然有限。尽管植物产生了多种化学物质来保护自己免受病原体的侵害,但这些植物衍生化学物质的分子靶标和作用方式尚未得到很好的描述。本研究采用反向遗传学方法,发现来自唇形科的百里香中的单萜醇百里香酚对 具有抗真菌活性,其通过调节多个信号通路,包括钙调神经磷酸酶、未折叠蛋白反应和 HOG(高渗透压甘油)MAPK(丝裂原激活蛋白激酶)通路。百里香酚通过控制钙转运基因的表达水平,以钙调神经磷酸酶依赖性方式降低细胞内 Ca 的浓度。我们证明,百里香酚通过调节糖基化介导的翻译后修饰相关基因的表达水平来降低 -糖基化。此外,百里香酚通过 HOG MAPK 通路依赖性方式降低甾醇生物合成基因的表达,从而减少内源性麦角固醇的含量。总的来说,这项研究揭示了百里香酚对 的抗真菌机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3715/8201179/75eb4fa67b4f/molecules-26-03476-g001.jpg

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