School of Science and Technology, Nottingham Trent University, Clifton Lane, Nottingham NG11 8NS, U.K.
Medical Technologies Innovation Facility (MTIF), Clifton Lane, Nottingham NG11 8NS, U.K.
ACS Infect Dis. 2024 Sep 13;10(9):3346-3357. doi: 10.1021/acsinfecdis.4c00447. Epub 2024 Aug 6.
The crystal structure of a previously reported antimicrobial Ru 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 clinical isolates show that, unlike the majority of previously reported Ru-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 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 model organism infected with a multidrug resistant strain of the ESKAPE pathogen 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.
呈现了先前报道的一种靶向细菌 DNA 的抗菌 Ru 配合物的晶体结构。在模拟尿液和血浆的培养基中利用引起导管相关尿路感染(CAUTI)的革兰氏阴性临床分离菌进行的研究表明,在所有测试条件下都保持了良好的抗菌活性。对一系列临床分离株的实验表明,与大多数先前报道的基于 Ru 的抗菌先导化合物不同,该化合物即使在 MRSA 菌株中也保持其强大的活性。此外,使用处于早期指数生长期和不同 pH 值的细菌进行的实验表明,该化合物在与临床环境中遇到的相关条件范围内也保持其活性。涉及与常规抗生素或先前报道的类似双核 Ru 配合物联合治疗的组合研究没有显示拮抗作用。事实上,尽管所有组合都表现出明显的相加抗菌活性,但在一种情况下,这种效应接近协同作用。研究发现,受多药耐药 ESKAPE 病原体感染的模式生物在单次给予先导配合物后 48 小时内可以成功治疗并完全清除,对宿主没有可检测到的有害影响。