Metastable Iron Sulfides Gram-Dependently Counteract Resistant Gardnerella Vaginalis for Bacterial Vaginosis Treatment

被引:32
作者
Fang, Ling [1 ,2 ,3 ]
Ma, Ruonan [1 ,2 ]
Gao, Xuejiao J. [4 ]
Chen, Lei [1 ]
Liu, Yuan [5 ]
Huo, Yanwu [6 ]
Wei, Taotao [6 ]
Wang, Xiaonan [1 ]
Wang, Qian [1 ]
Wang, Haojue [3 ]
Cui, Chengjun [3 ]
Shi, Qifeng [3 ]
Jiang, Jing [1 ]
Gao, Lizeng [1 ,2 ,5 ]
机构
[1] Chinese Acad Sci, Inst Biophys, CAS Engn Lab Nanozyme, Beijing 100101, Peoples R China
[2] Yangzhou Univ, Inst Translat Med, Dept Pharmacol, Sch Med, Yangzhou 225009, Jiangsu, Peoples R China
[3] Xishan Peoples Hosp Wuxi City, Wuxi 214105, Jiangsu, Peoples R China
[4] Jiangxi Normal Univ, Coll Chem & Chem Engn, Nanchang 330022, Jiangxi, Peoples R China
[5] Zhengzhou Univ, Joint Lab Nanozymes Zhengzhou Univ Acad Med Sci, Zhengzhou 450052, Henan, Peoples R China
[6] Chinese Acad Sci, Inst Biophys, Natl Lab Biomacromol, Beijing 100101, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
bacterial vaginosis; Gram-dependent; metastable iron sulfide; polysulfide species; resistant Gardnerella vaginalis; CRYSTAL-STRUCTURE REFINEMENT; PHOSPHOTRANSFERASE SYSTEM; SILVER NANOPARTICLES; PATHOGENESIS; VAGINOLYSIN; CHEMISTRY; OXIDE;
D O I
10.1002/advs.202104341
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bacterial vaginosis (BV) is the most common vaginal infection found in women in the world. Due to increasing drug-resistance of virulent pathogen such as Gardnerella vaginalis (G. vaginalis), more than half of BV patients suffer recurrence after antibotics treatment. Here, metastable iron sulfides (mFeS) act in a Gram-dependent manner to kill bacteria, with the ability to counteract resistant G. vaginalis for BV treatment. With screening of iron sulfide minerals, metastable Fe3S4 shows suppressive effect on bacterial growth with an order: Gram-variable G. vaginalis >Gram-negative bacteria>> Gram-positive bacteria. Further studies on mechanism of action (MoA) discover that the polysulfide species released from Fe3S4 selectively permeate bacteria with thin wall and subsequently interrupt energy metabolism by inhibiting glucokinase in glycolysis, and is further synergized by simultaneously released ferrous iron that induces bactericidal damage. Such multiple MoAs enable Fe3S4 to counteract G. vaginalis strains with metronidazole-resistance and persisters in biofilm or intracellular vacuole, without developing new drug resistance and killing probiotic bacteria. The Fe3S4 regimens successfully ameliorate BV with resistant G. vaginalis in mouse models and eliminate pathogens from patients suffering BV. Collectively, mFeS represent an antibacterial alternative with distinct MoA able to treat challenged BV and improve women health.
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页数:18
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