异硫氰酸烯丙酯通过靶向白色念珠菌的信号转导途径、麦角固醇生物合成和细胞周期发挥抗真菌活性。

Shivani Balasaheb Patil, Ashwini Khanderao Jadhav, Rakesh Kumar Sharma, Sargun Tushar Basrani, Tanjila Chandsaheb Gavandi, Sayali Ashok Chougule, Shivanand Ramappa Yankanchi, Sankunny Mohan Karuppayil
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引用次数: 0

摘要

背景和目的:近年来,白色念珠菌被列入因耐药性而构成威胁的感染名单,这促使研究人员寻找最先进、最有效的抗真菌药物。为此,本研究调查了异硫氰酸烯丙酯(AITC)对白色念珠菌的可能作用模式:本研究通过浮游生物检测、芽管抑制检测、粘附和生物膜形成检测来检查生长和毒力因子。此外,还进行了麦角甾醇测定、活性氧产生分析、细胞周期分析和实时聚合酶链反应定量分析,目的是找出其作用模式。在一项体内研究中,使用了一种生物医学模式生物(如家蚕)来证明 AITC 对白僵菌感染的抗感染能力:结果:0.125 毫克/毫升的异硫氰酸烯丙酯可完全抑制白僵菌麦角固醇的生物合成。异硫氰酸烯丙酯能在白僵菌的浮游细胞和生物膜细胞中产生活性氧。在 0.125 毫克/毫升的浓度下,AITC 可使细胞停滞在细胞周期的 G2/M 阶段,这可能会诱导白僵菌凋亡。实时聚合酶链反应定量分析发现,在 0.125 毫克/毫升浓度下,AITC 通过下调 PDE2、CEK1 和 TEC1,使其分别变化 2.54 倍、1.91 倍和 1.04 倍,上调 MIG1、NRG1 和 TUP1,使其分别变化 9.22 倍、3.35 倍和 7.80 倍,从而抑制芽管形成等毒力因子。体内研究表明,AITC 处理可成功保护蚕免受白僵菌感染,并通过防止白僵菌在体内定殖提高蚕的存活率:体外和体内研究表明,AITC 可以作为治疗白僵菌感染的一种替代疗法。
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Antifungal activity of Allyl isothiocyanate by targeting signal transduction pathway, ergosterol biosynthesis, and cell cycle in Candida albicans.

Background and purpose: In recent years, the inclusion of Candida albicans on the list of infections that pose a threat due to drug resistance has urged researchers to look into cutting-edge and effective antifungal medications. In this regard, the current study investigated the probable mode of action of allyl isothiocyanate (AITC) against Candida albicans.

Materials and methods: In this study, planktonic assay, germ tube inhibition assay, adhesion, and biofilm formation assay were performed to check the growth and virulence factors. Furthermore, ergosterol assay, reactive oxygen production analysis, cell cycle analysis, and quantitative real-time polymerase chain reaction analysis were performed with the aim of finding the mode of action. A biomedical model organism, like a silkworm, was used in an in vivo study to demonstrate AITC anti-infective ability against C. albicans infection.

Results: Allyl isothiocyanate completely inhibited ergosterol biosynthesis in C. albicans at 0.125 mg/ml. Allyl isothiocyanate produces reactive oxygen species in both planktonic and biofilm cells of C. albicans. At 0.125 mg/ml concentration, AITC arrested cells at the G2/M phase of the cell cycle, which may induce apoptosis in C. albicans. In quantitative real-time polymerase chain reaction analysis, it was found that AITC inhibited virulence factors, like germ tube formation, at 0.125 mg/ml concentration by downregulation of PDE2, CEK1, TEC1 by 2.54-, 1.91-, and 1.04-fold change, respectively, and upregulation of MIG1, NRG1, and TUP1 by 9.22-, 3.35-, and 7.80-fold change, respectively. The in vivo study showed that AITC treatment successfully protected silkworms against C. albicans infections and increased their survival rate by preventing internal colonization by C. albicans.

Conclusion: In vitro and in vivo studies revealed that AITC can be an alternative therapeutic option for the treatment of C. albicans infection.

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来源期刊
Current Medical Mycology
Current Medical Mycology Medicine-Infectious Diseases
CiteScore
2.10
自引率
0.00%
发文量
16
审稿时长
4 weeks
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