Pereira Anna L, Vasconcelos Mayron A, Andrade Alexandre L, Martins Israel M, Holanda Alda K M, Gondim Ana C S, Penha Dayana P S, Bruno Katherine L, Silva Francisco O N, Teixeira Edson H
Laboratório Integrado de Biomoléculas, Departamento de Patologia E Medicina Legal, Universidade Federal Do Ceará, CEP, 60430-270, Fortaleza - CE, Brasil.
Universidade Do Estado de Minas Gerais, Unidade Divinópolis, Divinópolis, MG, 35501-179, Brasil.
Curr Microbiol. 2023 Mar 10;80(4):133. doi: 10.1007/s00284-023-03232-0.
Health care-associated infections (HAIs) contribute to a significant rate of morbidity, mortality, and financial burden on health systems. These infections are caused by multidrug-resistant bacteria that produce biofilm as the main virulence factor. This study aimed to evaluate the effect of the copper-based metallic compounds [Cu(phen)(pz)NO]Cl (I), [Cu(bpy)(pz)(NO)]Cl (II), and [Cu(phen)(INA)NO]Cl (III), where phen = phenanthroline, bpy = bipyridine, pz = pyrazinamide, and INA = isonicotinic acid, against planktonic cells and biofilms formation of Staphylococcus aureus, Staphylococcus epidermidis, and Escherichia coli. The susceptibility of the microorganisms was evaluated by minimum inhibitory concentration (MIC), minimum bacterial concentration (MBC), and time-kill curve assay on planktonic cells. The biofilm formation was evaluated by biomass quantification through staining with crystal violet (CV), colony-forming units (CFUs) quantification, and biofilm metabolic activity determination by XTT assay. The compounds showed bacteriostatic and bactericidal activity on all microorganisms analyzed. Regarding the antibiofilm activity, all metallic compounds were able to reduce significantly the biofilm biomass, colony-forming units, and the metabolic activity of remaining cells, varying the efficient concentration according to the strain analyzed. Interestingly, compounds (I), (II) and (III) did not exhibit DNA degradation activity even with up to 100 µM of these metal complexes. On the other hand, complexes (I) and (III) showed a remarkable capacity to cleave DNA upon addition of glutathione, a reducing agent (Cu/Cu) that leads to reactive oxygen species (ROS) formation. The results presented in this study showed promising antimicrobial and antibiofilm effects.
医疗保健相关感染(HAIs)给卫生系统带来了很高的发病率、死亡率和经济负担。这些感染是由产生生物膜作为主要毒力因子的多重耐药细菌引起的。本研究旨在评估铜基金属化合物[Cu(phen)(pz)NO]Cl(I)、[Cu(bpy)(pz)(NO)]Cl(II)和[Cu(phen)(INA)NO]Cl(III)的效果,其中phen = 邻菲罗啉,bpy = 联吡啶,pz = 吡嗪酰胺,INA = 异烟酸,它们对金黄色葡萄球菌、表皮葡萄球菌和大肠杆菌的浮游细胞及生物膜形成的影响。通过最小抑菌浓度(MIC)、最小杀菌浓度(MBC)和浮游细胞的时间杀菌曲线分析来评估微生物的敏感性。通过用结晶紫(CV)染色进行生物量定量、菌落形成单位(CFUs)定量以及用XTT分析测定生物膜代谢活性来评估生物膜形成。这些化合物对所有分析的微生物均表现出抑菌和杀菌活性。关于抗生物膜活性,所有金属化合物都能够显著降低生物膜生物量、菌落形成单位以及剩余细胞的代谢活性,根据所分析的菌株不同,有效浓度也有所变化。有趣的是,即使使用高达100 μM的这些金属配合物,化合物(I)、(II)和(III)也未表现出DNA降解活性。另一方面,配合物(I)和(III)在添加谷胱甘肽(一种导致活性氧(ROS)形成的还原剂(Cu/Cu))后显示出显著的切割DNA的能力。本研究呈现的结果显示出有前景的抗菌和抗生物膜效果。