卢苏特罗博帕格与氨基糖苷类药物联用作为抗耐万古霉素肠球菌的再利用药物

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL ACS Infectious Diseases Pub Date : 2024-04-03 DOI:10.1021/acsinfecdis.3c00737
Pengfei She, Linhui Li, Yifan Yang, Linying Zhou, Guanqing Huang, Dan Xiao and Yong Wu*, 
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引用次数: 0

摘要

由于抗生素的广泛滥用,肠球菌的耐药性不断增加。然而,抗生素发现的速度赶不上细菌耐药性产生的速度。因此,药物再利用是一种解决危机的建议策略。Lusutrombopag(LP)已被美国食品和药物管理局批准为血小板生成素受体激动剂。这项研究表明,LP 在体外对耐万古霉素肠球菌具有显著的抗菌活性,而且很少出现耐药性。此外,LP 与妥布霉素联用,在体外和体内对肠球菌具有协同抗菌作用。使用 LP 时,在体外和体内均未发现可检测到的毒性。机理研究表明,质子动力被破坏可能是 LP 具有抗菌活性的原因。总之,这些研究结果表明,LP 具有之前未被证实的潜力,可作为抗菌剂用于肠球菌引起的难治性感染。
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Lusutrombopag as a Repurposing Drug in Combination with Aminoglycosides against Vancomycin-Resistant Enterococcus

Due to the widespread abuse of antibiotics, drug resistance in Enterococcus has been increasing. However, the speed of antibiotic discovery cannot keep pace with the acquisition of bacterial resistance. Thus, drug repurposing is a proposed strategy to solve the crises. Lusutrombopag (LP) has been approved as a thrombopoietin receptor agonist by the Food and Drug Administration. This study demonstrated that LP exhibited significant antimicrobial activities against vancomycin-resistant Enterococcus in vitro with rare resistance occurrence. Further, LP combined with tobramycin exhibited synergistic antimicrobial effects in vitro and in vivo against Enterococcus. No in vitro or in vivo detectable toxicity was observed when using LP. Mechanism studies indicated that the disrupted proton motive force may account for LP’s antimicrobial activity. In summary, these results demonstrate that LP has the previously undocumented potential to serve as an antibacterial agent against refractory infections caused by Enterococcus.

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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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