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桑枝黄酮通过抑制李斯特菌溶血素 O 减轻毒力和。

Acacetin Alleviates Virulence Both and via the Inhibition of Listeriolysin O.

机构信息

Key Laboratory of Zoonosis Research, Ministry of Education, Institute of Zoonosis, College of Veterinary Medicine, Jilin University, Changchun, China.

Laigang Hospital Affiliated to Shandong First Medical University, Jinan, China.

出版信息

Foodborne Pathog Dis. 2022 Feb;19(2):115-125. doi: 10.1089/fpd.2021.0021. Epub 2021 Nov 22.

Abstract

is a ubiquitous Gram-positive foodborne pathogen that is responsible for listeriosis in both humans and several animal species. The bacterium secretes a pore-forming cholesterol-dependent cytolysin, listeriolysin O (LLO), a major virulence factor involved in the activation of cellular processes. The ability of LLO to lyse erythrocytes is a measure of LLO activity. We used hemolytic activity assay to screen the LLO inhibitors. Acacetin was found to be an LLO inhibitor, which is a di-hydroxy and mono-methoxy flavone present in various plants, including , , and . As the features of acacetin are of low toxicity and have less acquired resistance, it comes to a hotspot in drug development. In our study, we report that acacetin antagonized the hemolytic activity of culture supernatants and purified LLO by directly interfering with the formation of oligomers without inhibiting the bacterial growth and the expression of LLO. Acacetin also relieved the injury of alveolar epithelial cells by inhibiting LLO activity. Further, acacetin significantly promoted the clearance of and alleviated the histopathological damage, thereby raising survival rate, which conferred mice with effective protection against infection. Using molecular docking and dynamics simulation, we further proved the mechanism of acacetin antagonizing LLO pore-forming activity by direct binding to the second membrane-inserting helix bundle (HB2) of LLO domain 3. These data suggested that acacetin recedes the virulence of both and , and this study provided a promising candidate and potential alternative for the prevention and treatment of infections.

摘要

李斯特菌是一种普遍存在的革兰氏阳性食源性病原体,可引起人类和多种动物物种的李斯特菌病。该细菌分泌一种形成孔的胆固醇依赖性细胞溶素,即李斯特菌溶素 O(LLO),这是一种主要的毒力因子,参与细胞过程的激活。LLO 裂解红细胞的能力是衡量其活性的一个指标。我们使用溶血活性测定法筛选 LLO 抑制剂。发现黄芩素是一种 LLO 抑制剂,它是一种存在于多种植物中的二羟基和单甲氧基黄酮,包括黄芩、菊花和艾草。由于黄芩素的特点是低毒性和较少获得性耐药性,因此成为药物开发的热点。在我们的研究中,我们报告说黄芩素通过直接干扰寡聚体的形成来拮抗培养上清液和纯化的 LLO 的溶血活性,而不抑制细菌生长和 LLO 的表达。黄芩素还通过抑制 LLO 活性来减轻肺泡上皮细胞的损伤。此外,黄芩素显著促进了 的清除,并缓解了组织病理学损伤,从而提高了存活率,使小鼠对 感染有效保护。通过分子对接和动力学模拟,我们进一步证明了黄芩素通过直接结合 LLO 结构域 3 的第二个膜插入螺旋束(HB2)拮抗 LLO 孔形成活性的机制。这些数据表明,黄芩素降低了 和 的毒力,该研究为预防和治疗李斯特菌感染提供了一种有前景的候选药物和潜在的替代药物。

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