• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

XF-73,一种具有快速杀菌活性的新型抗葡萄球菌膜活性剂。

XF-73, a novel antistaphylococcal membrane-active agent with rapid bactericidal activity.

作者信息

Ooi Nicola, Miller Keith, Hobbs Joanne, Rhys-Williams William, Love William, Chopra Ian

机构信息

Antimicrobial Research Centre and Institute of Molecular and Cellular Biology, University of Leeds, Leeds, UK.

出版信息

J Antimicrob Chemother. 2009 Oct;64(4):735-40. doi: 10.1093/jac/dkp299. Epub 2009 Aug 18.

DOI:10.1093/jac/dkp299
PMID:19689976
Abstract

OBJECTIVES

XF-73 is a novel porphyrin antibacterial agent previously reported to inhibit a range of gram-positive bacterial species, including Staphylococcus aureus. Its mode of action is unknown. Using S. aureus as a model organism we sought to examine the basis of its antibacterial activity.

METHODS

The effects of XF-73 on the growth and survival of S. aureus SH1000 were investigated by viable count and culture absorbance techniques. Inhibition of macromolecular synthesis and disruption of membrane integrity after exposure to XF-73 were examined by radiolabelling experiments, the BacLight fluorescent dye assay and measurement of K(+) and ATP leakage from the cell. The effect of XF-73 on a staphylococcal coupled transcription-translation system was also investigated.

RESULTS

XF-73 was rapidly bactericidal against S. aureus SH1000 and demonstrated more rapid killing kinetics than all other comparator agents when tested at an equivalent multiple (4x) of the MIC. Exposure of S. aureus to XF-73 for 10 min completely inhibited DNA, RNA and protein synthesis. XF-73 had no effect on transcription and translation in vitro. Cells exposed to XF-73 gave a positive response in the BacLight assay, which detects membrane damage. The drug also caused substantial loss of K(+) and ATP from the cell, but did not promote bacterial lysis.

CONCLUSIONS

XF-73 exhibited rapid membrane-perturbing activity, which is likely to be responsible for inhibition of macromolecular synthesis and the death of staphylococci exposed to the drug.

摘要

目的

XF - 73是一种新型卟啉类抗菌剂,此前报道其可抑制包括金黄色葡萄球菌在内的多种革兰氏阳性菌。其作用机制尚不清楚。我们以金黄色葡萄球菌作为模式生物,试图探究其抗菌活性的基础。

方法

通过活菌计数和培养物吸光度技术研究XF - 73对金黄色葡萄球菌SH1000生长和存活的影响。通过放射性标记实验、BacLight荧光染料测定以及测量细胞内钾离子(K⁺)和三磷酸腺苷(ATP)泄漏情况,检测暴露于XF - 73后大分子合成的抑制和膜完整性的破坏。还研究了XF - 73对葡萄球菌偶联转录 - 翻译系统的影响。

结果

XF - 73对金黄色葡萄球菌SH1000具有快速杀菌作用,在以最低抑菌浓度(MIC)的等效倍数(4倍)进行测试时,其杀菌动力学比所有其他对照剂都更快。将金黄色葡萄球菌暴露于XF - 73 10分钟可完全抑制DNA、RNA和蛋白质合成。XF - 73在体外对转录和翻译没有影响。暴露于XF - 73的细胞在检测膜损伤的BacLight测定中呈阳性反应。该药物还导致细胞内大量钾离子和ATP流失,但未促进细菌裂解。

结论

XF - 73表现出快速的膜扰动活性,这可能是抑制大分子合成以及导致暴露于该药物的葡萄球菌死亡的原因。

相似文献

1
XF-73, a novel antistaphylococcal membrane-active agent with rapid bactericidal activity.XF-73,一种具有快速杀菌活性的新型抗葡萄球菌膜活性剂。
J Antimicrob Chemother. 2009 Oct;64(4):735-40. doi: 10.1093/jac/dkp299. Epub 2009 Aug 18.
2
In vitro activity of XF-73, a novel antibacterial agent, against antibiotic-sensitive and -resistant Gram-positive and Gram-negative bacterial species.新型抗菌药物 XF-73 对敏感和耐药的革兰阳性和革兰阴性细菌的体外活性。
Int J Antimicrob Agents. 2010 Jun;35(6):531-6. doi: 10.1016/j.ijantimicag.2010.02.008. Epub 2010 Mar 25.
3
XF-70 and XF-73, novel antibacterial agents active against slow-growing and non-dividing cultures of Staphylococcus aureus including biofilms.XF-70 和 XF-73,新型抗菌剂,对包括生物膜在内的生长缓慢和非分裂的金黄色葡萄球菌具有活性。
J Antimicrob Chemother. 2010 Jan;65(1):72-8. doi: 10.1093/jac/dkp409.
4
Extracellular and intracellular bactericidal activities of XF-70 against small-colony variant hemB mutants of meticillin-susceptible and meticillin-resistant Staphylococcus aureus.XF-70 对耐甲氧西林金黄色葡萄球菌和甲氧西林敏感金黄色葡萄球菌小菌落变异株 hemB 突变体的细胞外和细胞内杀菌活性。
Int J Antimicrob Agents. 2011 Jun;37(6):576-9. doi: 10.1016/j.ijantimicag.2011.01.015. Epub 2011 Mar 16.
5
Consequences of daptomycin-mediated membrane damage in Staphylococcus aureus.达托霉素介导的金黄色葡萄球菌膜损伤的后果。
J Antimicrob Chemother. 2008 Nov;62(5):1003-8. doi: 10.1093/jac/dkn321. Epub 2008 Jul 31.
6
Anti-staphylococcal activity and mode of action of clofazimine.氯法齐明的抗葡萄球菌活性及作用方式。
J Antimicrob Chemother. 2004 Mar;53(3):435-40. doi: 10.1093/jac/dkh114. Epub 2004 Feb 4.
7
Antibacterial activity and mode of action of tert-butylhydroquinone (TBHQ) and its oxidation product, tert-butylbenzoquinone (TBBQ).叔丁基对苯二酚(TBHQ)及其氧化产物叔丁基苯醌(TBBQ)的抗菌活性和作用模式。
J Antimicrob Chemother. 2013 Jun;68(6):1297-304. doi: 10.1093/jac/dkt030. Epub 2013 Mar 5.
8
In vitro pharmacodynamics of novel rifamycin ABI-0043 against Staphylococcus aureus.新型利福霉素ABI - 0043对金黄色葡萄球菌的体外药效学
J Antimicrob Chemother. 2008 Jul;62(1):156-60. doi: 10.1093/jac/dkn133. Epub 2008 Apr 9.
9
Comparison of assays for detection of agents causing membrane damage in Staphylococcus aureus.检测金黄色葡萄球菌中引起膜损伤的病原体的检测方法比较。
J Antimicrob Chemother. 2004 Dec;54(6):1127-9. doi: 10.1093/jac/dkh476. Epub 2004 Nov 5.
10
The silver cation (Ag+): antistaphylococcal activity, mode of action and resistance studies.银离子(Ag+):抗葡萄球菌活性、作用机制和耐药性研究。
J Antimicrob Chemother. 2013 Jan;68(1):131-8. doi: 10.1093/jac/dks372. Epub 2012 Sep 25.

引用本文的文献

1
Biofilm-Associated Candidiasis: Pathogenesis, Prevalence, Challenges and Therapeutic Options.生物膜相关性念珠菌病:发病机制、患病率、挑战与治疗选择
Pharmaceuticals (Basel). 2025 Mar 25;18(4):460. doi: 10.3390/ph18040460.
2
Antibacterials with Novel Chemical Scaffolds in Clinical Development.处于临床开发阶段的具有新型化学骨架的抗菌药物。
Drugs. 2025 Mar;85(3):293-323. doi: 10.1007/s40265-024-02137-x. Epub 2025 Jan 23.
3
A Review of Antibacterial Candidates with New Modes of Action.具有新型作用机制的抗菌候选药物综述。
ACS Infect Dis. 2024 Oct 11;10(10):3440-3474. doi: 10.1021/acsinfecdis.4c00218. Epub 2024 Jul 17.
4
Bacterial persisters: molecular mechanisms and therapeutic development.细菌持久态:分子机制与治疗开发。
Signal Transduct Target Ther. 2024 Jul 17;9(1):174. doi: 10.1038/s41392-024-01866-5.
5
Screening of the novel antimicrobial drug, XF-73, against 2,527 species clinical isolates.对新型抗菌药物 XF-73 进行了 2527 种临床分离株的筛选。
Front Cell Infect Microbiol. 2023 Oct 11;13:1264456. doi: 10.3389/fcimb.2023.1264456. eCollection 2023.
6
Biochemistry, Mechanistic Intricacies, and Therapeutic Potential of Antimicrobial Peptides: An Alternative to Traditional Antibiotics.抗菌肽的生物化学、机制复杂性和治疗潜力:传统抗生素的替代物。
Curr Med Chem. 2024;31(37):6110-6139. doi: 10.2174/0109298673268458230926105224.
7
Antimicrobial effects of XF drugs against and its biofilms.XF药物对……及其生物被膜的抗菌作用。 (原文中“against”后面缺少具体对象)
Front Fungal Biol. 2023 Aug 22;4:1225647. doi: 10.3389/ffunb.2023.1225647. eCollection 2023.
8
Staph wars: the antibiotic pipeline strikes back.葡萄球菌之战:抗生素管道奋起反击。
Microbiology (Reading). 2023 Sep;169(9). doi: 10.1099/mic.0.001387.
9
Photodynamic Antimicrobial Activity of a Novel 5,10,15,20-Tetrakis (4-Ethylphenyl) Porphyrin against Clinically Important Bacteria.新型5,10,15,20-四(4-乙基苯基)卟啉对临床重要细菌的光动力抗菌活性
Pharmaceuticals (Basel). 2023 Jul 26;16(8):1059. doi: 10.3390/ph16081059.
10
Efficacy of a Novel Antibacterial Agent Exeporfinium Chloride, (XF-73), Against Antibiotic-Resistant Bacteria in Mouse Superficial Skin Infection Models.新型抗菌剂氯化艾克泊芬(XF-73)在小鼠浅表皮肤感染模型中对抗耐药菌的疗效
Infect Drug Resist. 2023 Jul 25;16:4867-4879. doi: 10.2147/IDR.S417231. eCollection 2023.