对一种单核钌复合物的体外和体内研究表明,它是一种在生理条件下高效、速效、广谱的抗菌剂。

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2024-09-13 Epub Date: 2024-08-06 DOI:10.1021/acsinfecdis.4c00447
Adam M Varney, Kirsty L Smitten, Hannah M Southam, Simon D Fairbanks, Craig C Robertson, Jim A Thomas, Samantha McLean
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引用次数: 0

摘要

本文展示了以前报道过的一种针对细菌 DNA 的抗菌 RuII 复合物的晶体结构。在模拟尿液和血浆的培养基中,利用导致导尿管相关性尿路感染(CA)的革兰氏阴性细菌临床分离物进行的研究表明,在所有测试条件下都能保持良好的抗菌活性。用一系列金黄色葡萄球菌临床分离菌株进行的实验表明,与之前报道的大多数基于 RuII 的抗菌剂不同,该化合物即使在 MRSA 菌株中也能保持强效活性。此外,利用处于指数生长早期和不同 pH 值条件下的细菌进行的实验表明,该化合物在一系列与临床环境相关的条件下也能保持其活性。与传统抗生素或之前报道过的类似二核 RuII 复合物共同处理的组合研究表明,这种化合物没有拮抗作用。事实上,尽管所有组合都显示出明显的相加抗菌活性,但在一种情况下,这种效果接近于协同作用。研究发现,对感染了 ESKAPE 病原体鲍曼不动杆菌耐多药菌株的 Galleria Mellonella 模型生物,在单剂量使用铅复合物后 48 小时内就能成功治疗并完全清除病菌,而且对宿主没有任何可检测到的有害影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In Vitro and In Vivo Studies on a Mononuclear Ruthenium Complex Reveals It is a Highly Effective, Fast-Acting, Broad-Spectrum Antimicrobial in Physiologically Relevant Conditions.

In Vitro and In Vivo Studies on a Mononuclear Ruthenium Complex Reveals It is a Highly Effective, Fast-Acting, Broad-Spectrum Antimicrobial in Physiologically Relevant Conditions.

The crystal structure of a previously reported antimicrobial RuII complex that targets bacterial DNA is presented. Studies utilizing clinical isolates of Gram-negative bacteria that cause catheter-associated urinary tract infection, (CA)UTI, in media that model urine and plasma reveal that good antimicrobial activity is maintained in all conditions tested. Experiments with a series of Staphylococcus aureus clinical isolates show that, unlike the majority of previously reported RuII-based antimicrobial leads, the compound retains its potent activity even in MRSA strains. Furthermore, experiments using bacteria in early exponential growth and at different pHs reveal that the compound also retains its activity across a range of conditions that are relevant to those encountered in clinical settings. Combinatorial studies involving cotreatment with conventional antibiotics or a previously reported analogous dinuclear RuII complex showed no antagonistic effects. In fact, although all combinations show distinct additive antibacterial activity, in one case, this effect approaches synergy. It was found that the Galleria Mellonella model organism infected with a multidrug resistant strain of the ESKAPE pathogen Acinetobacter baumannii could be successfully treated and totally cleared within 48 h after a single dose of the lead complex with no detectable deleterious effect to the host.

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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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