Department of Microbiology and Immunology, Institute of Biosciences of Botucatu (IBB), São Paulo State University (UNESP), Botucatu, Brazil.
Department of Chemistry and Biochemistry, Institute of Biosciences of Botucatu (IBB), São Paulo State University (UNESP), Botucatu, Brazil.
Microb Drug Resist. 2020 Mar;26(3):179-189. doi: 10.1089/mdr.2019.0038. Epub 2019 Jun 25.
We investigated the responses and mechanisms of action of methicillin-resistant (MRSA) metabolism when exposed under sublethal concentrations of the synergistic antibacterial combination of nisin + oxacillin (¼ of maximum sublethal concentration) and sublethal concentrations of oxacillin only and nisin only. A total of 135 proteins were identified, showing an alteration in the expression of 85 proteins when treatment was compared with untreated bacteria (control). When the bacteria were treated using the combination, there was an increase in the expression of proteins related to resistance (., beta-lactamase) and also in the ones involved in protein synthesis, and there was a decrease in the expression of proteins related to stress and alterations in proteins related to bacterial energy metabolism. Bacterial oxidative stress showed that the combination was able to induce oxidative stress ( < 0.05) and increase enzyme activities and lipid hydroperoxide levels compared with individual treatments. The analysis of cell ultrastructure showed damage in MRSA, especially on the bacterial wall and the plasma membrane, with cell lysis and death. Thus, the changes caused by these treatments affected different proteins related to the bacterial biological processes and signaling pathways such as cell division, structure, stress, regulation, bacterial resistance, protein synthesis, gene expression, energetic metabolism, and virulence. It was observed that synergism among antimicrobials has high potential in therapeutic use and may reduce the required amounts of antibacterial substances in addition to being effective on different targets in bacterial cells.
我们研究了耐甲氧西林金黄色葡萄球菌(MRSA)在亚致死浓度的协同抗菌组合(即乳链菌肽+苯唑西林的四分之一最大亚致死浓度)和亚致死浓度的苯唑西林和乳链菌肽单独作用下的反应和作用机制。共鉴定出 135 种蛋白质,与未经处理的细菌(对照)相比,处理组有 85 种蛋白质的表达发生了变化。当用组合处理细菌时,与耐药相关的蛋白质(例如β-内酰胺酶)和参与蛋白质合成的蛋白质的表达增加,与应激相关的蛋白质和与细菌能量代谢相关的蛋白质的表达减少。细菌氧化应激表明,与单独处理相比,该组合能够诱导氧化应激(<0.05)并增加酶活性和脂质过氧化物水平。细胞超微结构分析显示,MRSA 受到损伤,特别是细胞壁和质膜受损,出现细胞裂解和死亡。因此,这些处理引起的变化影响了与细菌生物过程和信号通路相关的不同蛋白质,如细胞分裂、结构、应激、调节、细菌耐药性、蛋白质合成、基因表达、能量代谢和毒力。观察到抗菌药物之间的协同作用具有很高的治疗应用潜力,除了对细菌细胞中的不同靶点有效外,还可能减少抗菌物质的所需用量。