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将离子载体 PBT2 再利用治疗耐多药淋病奈瑟菌感染。

Repurposing the Ionophore, PBT2, for Treatment of Multidrug-Resistant Neisseria gonorrhoeae Infections.

机构信息

Institute for Glycomics, Griffith Universitygrid.1022.1, Gold Coast Campus, Queensland, Australia.

The Center for Microbial Pathogenesis, The Abigail Wexner Research Institute at Nationwide Children's Hospital and The Department of Pediatrics, The Ohio State University, Ohio, USA.

出版信息

Antimicrob Agents Chemother. 2022 Sep 20;66(9):e0231821. doi: 10.1128/aac.02318-21. Epub 2022 Aug 18.

DOI:10.1128/aac.02318-21
PMID:35980187
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9487457/
Abstract

Multidrug-resistant (MDR) N. gonorrhoeae is a current public health threat. New therapies are urgently needed. PBT2 is an ionophore that disrupts metal homeostasis. PBT2 administered with zinc is shown to reverse resistance to antibiotics in several bacterial pathogens. Here we show that both N. meningitidis and MDR N. gonorrhoeae are sensitive to killing by PBT2 alone. PBT2 is, thus, a candidate therapeutic for MDR N. gonorrhoeae infections.

摘要

耐多药(MDR)淋病奈瑟菌是当前的公共卫生威胁。迫切需要新的治疗方法。PBT2 是一种离子载体,可破坏金属动态平衡。研究表明,PBT2 与锌联合使用可逆转几种细菌病原体对抗生素的耐药性。本文显示,脑膜炎奈瑟球菌和耐多药淋病奈瑟菌均对 PBT2 的单独杀伤作用敏感。因此,PBT2 是治疗耐多药淋病奈瑟菌感染的候选药物。

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本文引用的文献

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J Antimicrob Chemother. 2021 Oct 11;76(11):2850-2853. doi: 10.1093/jac/dkab291.
2
Copper(II) Binding to PBT2 Differs from That of Other 8-Hydroxyquinoline Chelators: Implications for the Treatment of Neurodegenerative Protein Misfolding Diseases.铜(II)与 PBT2 的结合不同于其他 8-羟基喹啉螯合剂:对神经退行性蛋白错误折叠疾病治疗的启示。
Inorg Chem. 2020 Dec 7;59(23):17519-17534. doi: 10.1021/acs.inorgchem.0c02754. Epub 2020 Nov 23.
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Repurposing a neurodegenerative disease drug to treat Gram-negative antibiotic-resistant bacterial sepsis.将一种神经退行性疾病药物重新用于治疗革兰氏阴性抗生素耐药性细菌性败血症。
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Detection of Ciprofloxacin-Resistant, β-Lactamase-Producing Neisseria meningitidis Serogroup Y Isolates - United States, 2019-2020.检测对环丙沙星耐药、产β-内酰胺酶的脑膜炎奈瑟菌血清群 Y 分离株 - 美国,2019-2020 年。
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