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

被引:0
|
作者
Varney, Adam M. [1 ,2 ]
Smitten, Kirsty L. [3 ,4 ]
Southam, Hannah M. [4 ]
Fairbanks, Simon D. [3 ]
Robertson, Craig C. [3 ]
Thomas, Jim A. [3 ]
McLean, Samantha [1 ]
机构
[1] Nottingham Trent Univ, Sch Sci & Technol, Nottingham NG11 8NS, England
[2] Med Technol Innovat Facil MTIF, Nottingham NG11 8NS, England
[3] Univ Sheffield, Dept Chem, Sheffield S3 7HF, England
[4] Univ Sheffield, Sch Biosci, Sheffield S10 2TN, England
来源
ACS INFECTIOUS DISEASES | 2024年 / 10卷 / 09期
关键词
AMR; ruthenium; combinatorial therapy; ESKAPE; Galleria; DRUG DISCOVERY; RESISTANCE; ANTIBIOTICS; MECHANISMS; ECONOMICS; PIPELINE; TARGETS; FUTURE;
D O I
10.1021/acsinfecdis.4c00447
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The crystal structure of a previously reported antimicrobial Ru-II 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 Ru-II-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 Ru-II 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.
引用
收藏
页码:3346 / 3357
页数:12
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