天然类黄酮通过增强吞噬体酸化来对抗胞质MRSA。

IF 8.2 2区 生物学 Q1 CELL BIOLOGY
Xiaohui Si, Ruoyi Lv, Ziwen Cai, Zhigang Sun, Wenjing Zhang, Jing Wang, Xiaoye Liu
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引用次数: 0

摘要

耐多药细菌(MDR)的出现,特别是胞质耐甲氧西林金黄色葡萄球菌(MRSA)的出现正在引起大量感染,并对全球公共卫生构成紧迫威胁。抗生素耐药时代阻碍了仅针对细菌的抗生素的发展,突出了对替代治疗策略的需求。宿主作用疗法正在成为解决新型抗生素短缺和预防新型耐药细菌的主要方法。在此,我们探索了五种类黄酮的作用模式,通过宿主作用的抗菌作用来对抗胞质MRSA。体外和体内模型均显示黄酮类化合物在抗胞浆性MRSA肺部感染方面的功效。转录组学和蛋白质组学分析表明,这些类黄酮的抗菌靶点与吞噬体途径有关。机制研究进一步表明,黄酮类化合物促进溶酶体酸化,确定其为宿主作用的抗菌药物的可行靶点。这些发现表明,类黄酮治疗是一种很有前途的宿主作用治疗策略,可用于对抗胞质性MRSA感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Natural flavonoids combat cytosolic MRSA by potentiating phagosome acidification.

The emergence of multidrug-resistant bacteria (MDR), particularly in cytosolic methicillin-resistant Staphylococcus aureus (MRSA) are causing substantial infections and posing an urgent global threat to public health. The era of antibiotic resistant has hindered the development of antibiotics that solely target bacteria, highlighting the need for alternative therapeutic strategies. Host-acting therapies are emerging as a dominant approach to address the shortage of novel antibiotics and prevent novel-resistant bacteria. Herein, we explored the modes of action of five flavonoids that combat cytosolic MRSA through host-acting antibacterial effects. Both in vitro and in vivo models demonstrated the efficacy of flavonoids in combating cytosolic MRSA lung infections. Transcriptomic and proteomic analyses revealed that the antibacterial targets of these flavonoids are linked to the phagosome pathway. Mechanistic studies further showed that flavonoids enhance lysosomal acidification, identifying it as a viable target for host-acting antibacterial drugs. These findings suggest that flavonoid treatments represent a promising host-acting therapeutic strategy for combating cytosolic MRSA infections.

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来源期刊
CiteScore
11.00
自引率
0.00%
发文量
180
期刊介绍: Cell Communication and Signaling (CCS) is a peer-reviewed, open-access scientific journal that focuses on cellular signaling pathways in both normal and pathological conditions. It publishes original research, reviews, and commentaries, welcoming studies that utilize molecular, morphological, biochemical, structural, and cell biology approaches. CCS also encourages interdisciplinary work and innovative models, including in silico, in vitro, and in vivo approaches, to facilitate investigations of cell signaling pathways, networks, and behavior. Starting from January 2019, CCS is proud to announce its affiliation with the International Cell Death Society. The journal now encourages submissions covering all aspects of cell death, including apoptotic and non-apoptotic mechanisms, cell death in model systems, autophagy, clearance of dying cells, and the immunological and pathological consequences of dying cells in the tissue microenvironment.
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