Limonene inhibits Candida albicans growth by inducing apoptosis

白色念珠菌 生物膜 柠檬烯 细胞周期 白色体 形态发生 微生物学 细胞凋亡 氧化应激 生物 细胞生物学 DNA损伤 化学 生物化学 精油 植物 DNA 细菌 遗传学 基因
作者
Archana Thakre,Gajanan Zore,Santosh Kodgire,Rubina Kazi,Shradha V. Mulange,Rajendra Patil,Amruta Shelar,B. Santhakumari,Mahesh J. Kulkarni,Kiran R. Kharat,Sankunny Mohan Karuppayil
出处
期刊:Medical Mycology [Oxford University Press]
被引量:70
标识
DOI:10.1093/mmy/myx074
摘要

Anti-Candida potential of limonene was evaluated against planktonic growth, biofilm (adhesion, development and maturation) and morphogenesis of Candida albicans in this study. Limonene is a major constituent of citrus oil and most frequently used terpene in food and beverage industry due to its pleasant fragrance, nontoxic, and is generally recognized as safe (GRAS) flavoring agent as well as treatment option in many gastrointestinal diseases.Limonene exhibited excellent anti-Candida activity and was equally effective against planktonic growth of C. albicans isolates differentially susceptible to FLC (N = 35). Limonene inhibited morphogenesis significantly at low concentration. However, it showed stage dependent activity against biofilm formation, that is, it was more effective against adhesion followed by development and maturation. Limonene also exhibited excellent synergy with FLC against planktonic and biofilm growth. SWATH-MS analysis led to identification of limonene responsive proteins that provided molecular insight of its anti-Candida activity. Proteomic analysis revealed upregulation of proteins involved in cell wall glucan synthesis (Kre6); oxidative stress (Rhr2, Adh7 and Ebp1); DNA damage stress (Mbf1 and Npl3); nucleolar stress (Rpl11, Rpl7, Rpl29, Rpl15) and down regulation of cytoskeleton organization (Crn1, Pin3, Cct8, Rbl2), and so forth, in response to limonene. Limonene mediated down regulation of Tps3 indicates activation of caspase (CaMca1) and induction of apoptosis in C. albicans. These results suggest that limonene inhibits C. albicans growth by cell wall/membrane damage induced oxidative stress that leads to DNA damage resulting into modulation of cell cycle and induction of apoptosis through nucleolar stress and metacaspase dependent pathway.

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