Cerqueira Melo Rita de Cássia, Martins Aline Andrade, Melo Andressa Leite Ferraz, Vicente Jean Carlos Pael, Sturaro Mariana Carvalho, Arantes Julia Pimentel, Rossato Luana, de Souza Gleyce Hellen de Almeida, Simionatto Simone
Health Sciences Research Laboratory, Federal University of Grande Dourados (UFGD), Dourados 79804970, Mato Grosso do Sul, Brazil.
Antibiotics (Basel). 2024 Aug 1;13(8):723. doi: 10.3390/antibiotics13080723.
Antimicrobial resistance (AMR) has emerged as a significant threat to public health, particularly in infections caused by critically important Gram-negative bacteria. The development of novel antibiotics has its limitations, and therefore it is crucial to explore alternative strategies to effectively combat infections with resistant pathogens. In this context, the present study investigated the antibacterial potency of 560 compounds against the multidrug-resistant (MDR) strains of and . The evaluated compounds were selected from the Pandemic Response Box (PRB) and COVID Box (CB) and subjected to assays to determine the inhibitory concentration (IC), minimum bactericidal concentration (MBC), and biofilm formation. Further, the effects of these compounds on membrane integrity were assessed through protein quantification. Several of the evaluated compounds, including fusidic acid, MMV1580853, and MMV1634399, exhibited a significant reduction in biofilm formation and growth in . Trimethoprim exhibited potential against . The IC values of the compounds indicated significant microbial growth inhibition at various concentrations. These findings underscore the potency of the existing antibiotics and novel compounds in combating the MDR strains of bacteria. The importance of reconsidering the known antibiotics and utilizing drug repositioning strategies to address the increasing risk of AMR is highlighted.
抗菌药物耐药性(AMR)已成为对公共卫生的重大威胁,尤其是在由至关重要的革兰氏阴性菌引起的感染中。新型抗生素的开发存在局限性,因此探索替代策略以有效对抗耐药病原体感染至关重要。在此背景下,本研究调查了560种化合物对[具体细菌名称1]和[具体细菌名称2]的多药耐药(MDR)菌株的抗菌效力。评估的化合物选自大流行应对盒(PRB)和新冠盒(CB),并进行测定以确定抑制浓度(IC)、最低杀菌浓度(MBC)和生物膜形成情况。此外,通过蛋白质定量评估这些化合物对膜完整性的影响。包括夫西地酸、MMV1580853和MMV1634399在内的几种评估化合物在[具体细菌名称1]中生物膜形成和生长显著减少。甲氧苄啶对[具体细菌名称2]表现出潜在活性。化合物的IC值表明在不同浓度下对微生物生长有显著抑制作用。这些发现强调了现有抗生素和新型化合物对抗细菌MDR菌株的效力。突出了重新考虑已知抗生素并利用药物重新定位策略来应对日益增加的AMR风险的重要性。