Attenuation of Pathogenicity in Candida albicans by Application of Polyphenols

M. K. Shrivash, Sonal Mishra, S. Panwar, Shabnam Sircaik, J. Pandey, K. Misra
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引用次数: 4

Abstract

Candida albicans is one of the most pathogenic and opportunistic class of fungi. Its emergence disturbs the human biome and can create serious damage in immunocompromised conditions. Hyphal growth and biofilm formation are mainly the core factors leading to progression of pathogenicity in C. albicans. The drug resistance towards azoles has created a demand of new novel pharmacologically active compounds. Although there are several pathways and factors known for causing pathogenicity there is none single connected pathway known for the whole mechanism such as SAP5, N-myrstyltransferase, Erg11 and Efg1 proteins. In the present study we have focussed on all the pathways and sorted major factors contributing in more than one pathways. The plant based polyphenols that have been studied here are non-toxic and more efficient as compared to the marketed azoles. These selected polyphenols were found to be capable of causing cell death of C. albicans up to 20% and inhibiting hyphal growth up to 90% as compared to Fluconazole. Biologically the polyphenols have been found to be more active on glyoxylate pathway.
多酚对白色念珠菌致病性的抑制作用
白色念珠菌是最具致病性和机会性的一类真菌。它的出现扰乱了人类生物群落,并可在免疫功能低下的情况下造成严重损害。菌丝生长和生物膜形成是导致白色念珠菌致病性进展的主要核心因素。对唑类药物的耐药性对新型药理活性化合物产生了需求。虽然有几种已知的致病途径和因素,但没有一个已知的完整机制的单一连接途径,如SAP5、N-myrstyltransferase、Erg11和Efg1蛋白。在目前的研究中,我们专注于所有的途径,并分类了在多个途径中起作用的主要因素。这里研究的植物多酚是无毒的,比市面上的唑类更有效。与氟康唑相比,这些选择的多酚能够引起白色念珠菌高达20%的细胞死亡,抑制菌丝生长高达90%。生物学上发现,多酚类物质在乙醛酸途径上更活跃。
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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