Department of Microbiology, Shahr-e-Qods Branch, Islamic Azad University, Tehran, Iran.
Department of Molecular Biology, Pasteur Institute of Iran, Tehran, Iran.
J Basic Microbiol. 2022 Oct;62(10):1229-1240. doi: 10.1002/jobm.202200156. Epub 2022 Jun 21.
Peptide IDR1018 and chitosan nanoparticles (CNs) showed antimicrobial and anti-biofilm activity against bacteria. In this study, the antimicrobial effects of peptide IDR1018 and CNs were evaluated on 50 clinical isolates of uropathogenic Escherichia coli (UPEC) resistant to ciprofloxacin. Ion gelation method was applied for CNs synthesis. Scanning electron microscope (SEM) and dynamic light scattering (DLS) were utilized to evaluate the nanoparticles. Antimicrobial and synergistic activity of peptide IDR1018 and CNs with ciprofloxacin were evaluated by microtiter broth dilution method. The checkerboard test was used to investigate the antimicrobial effects of IDR1018 and CNS in combination with ciprofloxacin. Anti-biofilm effect of ciprofloxacin, peptide IDR1018, and CNs was evaluated using crystal violet method. Fourteen (28%), 21 (42%), and 15 (30%) of clinical isolates produced strong, moderate, and weak biofilm, respectively. The CNs were spherical and uniform under electron microscopy with an average diameter of 246 nm. The minimum inhibitory concentration (MIC) values were 16-128, 20-40, and 375-750 (µg/ml) for ciprofloxacin, peptide IDR1018, and CNs, respectively. Fractional inhibitory concentration (FIC) analysis indicated a synergistic effect of ciprofloxacin in combination with peptide IDR1018, but in combination with CNs, this antibiotic showed an additive effect. Our results revealed that peptide IDR1018 and CNs have antimicrobial properties on UPEC isolates. Biofilm inhibition and biofilm eradication of clinical isolate were shown by peptide IDR1018 and CNs in a concentration-dependent manner. The antimicrobial agents alone and in combination decreased the number of viable bacteria in the biofilms. Therefore, these components seem to be a treating approach against biofilm-forming UPEC isolates.
肽 IDR1018 和壳聚糖纳米粒子 (CNs) 对耐环丙沙星的尿路致病性大肠杆菌 (UPEC) 临床分离株具有抗菌和抗生物膜活性。在这项研究中,评估了肽 IDR1018 和 CNs 对 50 株耐环丙沙星的尿路致病性大肠杆菌 (UPEC) 临床分离株的抗菌作用。离子凝胶法用于合成 CNs。扫描电子显微镜 (SEM) 和动态光散射 (DLS) 用于评估纳米粒子。微量肉汤稀释法评估肽 IDR1018 和 CNs 与环丙沙星的协同抗菌活性。棋盘试验用于研究 IDR1018 和 CNS 与环丙沙星联合的抗菌作用。结晶紫法评估环丙沙星、肽 IDR1018 和 CNs 的抗生物膜作用。14 株(28%)、21 株(42%)和 15 株(30%)临床分离株分别产生强、中、弱生物膜。电镜下 CNs 呈球形且均匀,平均直径为 246nm。环丙沙星、肽 IDR1018 和 CNs 的最低抑菌浓度 (MIC) 值分别为 16-128、20-40 和 375-750(µg/ml)。分数抑菌浓度(FIC)分析表明,环丙沙星与肽 IDR1018 联合具有协同作用,但与 CNs 联合具有相加作用。我们的结果表明,肽 IDR1018 和 CNs 对 UPEC 分离株具有抗菌特性。肽 IDR1018 和 CNs 以浓度依赖的方式抑制临床分离株的生物膜形成和生物膜清除。单独和联合使用抗菌剂可减少生物膜中活菌数量。因此,这些成分似乎是治疗生物膜形成的 UPEC 分离株的一种方法。