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金诺芬增强厄他培南对耐碳青霉烯类大肠埃希菌的抗菌作用。

Auranofin enhances the antibacterial effects of ertapenem against carbapenem-resistant Escherichia coli.

机构信息

Department of Biomedical Laboratory Science, College of Medical Sciences, Soonchunhyang University, Asan, Chungnam 31538, Republic of Korea.

Department of Biomedical Laboratory Science, College of Medical Sciences, Soonchunhyang University, Asan, Chungnam 31538, Republic of Korea; Department of Medical Sciences, Graduate School, Soonchunhyang University, Asan, Chungnam 31538, Republic of Korea.

出版信息

Diagn Microbiol Infect Dis. 2024 Sep;110(1):116413. doi: 10.1016/j.diagmicrobio.2024.116413. Epub 2024 Jun 22.

Abstract

The prevalence of carbapenem-resistant Escherichia coli (CREC) is increasing worldwide, and infections caused by CREC are associated with substantial morbidity and mortality rates. It is within this context that combination therapy has been reported as an effective strategy for treating resistant bacteria. Auranofin was approved by the FDA for treating rheumatoid arthritis. We confirmed that auranofin restored the susceptibility of ertapenem to CREC through synergy checkerboard and time-kill analyses. We also demonstrated that sub-MIC levels of auranofin significantly inhibited the expression of carbapenemase (bla) and efflux pump (acrA, acrD, and tolC) genes. The combination of auranofin and ertapenem suppressed the expression levels of motility (motA and flhD) genes, decreasing motility, which is a known pathogenic factor in CREC. Taken together, our results indicate that auranofin exerted a synergistic effect with ertapenem by suppressing the expression of carbapenemase and efflux pump genes and reducing the motility and virulence factors against CREC.

摘要

碳青霉烯类耐药大肠杆菌(CREC)的流行率在全球范围内呈上升趋势,由 CREC 引起的感染与较高的发病率和死亡率相关。正是在这种情况下,联合治疗被报道为治疗耐药菌的有效策略。金诺芬已被 FDA 批准用于治疗类风湿性关节炎。我们通过协同棋盘和时间杀伤分析证实,金诺芬通过协同作用恢复了厄他培南对 CREC 的敏感性。我们还表明,亚 MIC 水平的金诺芬可显著抑制碳青霉烯酶(bla)和外排泵(acrA、acrD 和 tolC)基因的表达。金诺芬和厄他培南的联合使用抑制了运动性(motA 和 flhD)基因的表达水平,降低了运动性,这是 CREC 中已知的致病因素。综上所述,我们的研究结果表明,金诺芬通过抑制碳青霉烯酶和外排泵基因的表达以及降低运动性和毒力因子对 CREC 的作用,与厄他培南发挥协同作用。

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