Department of Microbiology, Basic Medical Sciences Block-I, South Campus, Panjab University, Chandigarh 160014, India.
Department of Microbiology, Basic Medical Sciences Block-I, South Campus, Panjab University, Chandigarh 160014, India.
Int J Antimicrob Agents. 2015 Apr;45(4):359-67. doi: 10.1016/j.ijantimicag.2014.11.008. Epub 2014 Dec 16.
Biofilm formation is becoming a predominant feature in nosocomial infections. Since biofilms are increasingly resistant to antibiotics, making monotherapy ineffective, combination therapy appears to be relevant for their eradication. This study assessed the potential of azithromycin (AZM) and ciprofloxacin (CIP) alone and in combination in vitro and in a mouse model of urinary tract infection (UTI) induced with biofilm cells of Pseudomonas aeruginosa. In vitro antibacterial and antibiofilm activities of antibiotics alone and in combination were assessed using the fractional inhibitory concentration index (FICI), time-kill analysis and confocal laser scanning microscopy (CLSM). In vivo efficacy was evaluated in a UTI model by quantitation of bacterial burden in kidney and bladder tissue, renal histopathology, pathology index factors (MDA and NO), and pro-inflammatory (MIP-2 and IL-6) and anti-inflammatory (IL-10) cytokines. MICs of AZM and CIP for strain PAO1 were 256 and 0.5 μg/mL, respectively; MBECs were 4096 and 1024 μg/mL. Synergistic interaction was observed between AZM and CIP both against planktonic and biofilm bacteria (FICI<0.5). The combination was also able to inhibit biofilm formation (at MIC levels) as observed with CLSM. Oral therapy with AZM (500 mg/kg) and CIP (30 mg/kg) combination in mice for 4 days showed accelerated clearance of bacteria from kidney and bladder tissue, improved renal histopathology, decreased levels of MDA and NO, significant decline in MIP-2 and IL-6, and increased IL-10 in the kidney (P<0.0001). We conclude that AZM+CIP therapy holds promise against biofilm-associated UTIs as it confers antibacterial, immunomodulatory and anti-inflammatory effects.
生物膜的形成正成为医院感染的主要特征。由于生物膜对抗生素的耐药性逐渐增强,使单药治疗无效,联合治疗似乎对其清除具有相关性。本研究评估了阿奇霉素(AZM)和环丙沙星(CIP)单独和联合在体外和生物膜诱导的铜绿假单胞菌尿路感染(UTI)小鼠模型中的潜力。使用部分抑菌浓度指数(FICI)、时间杀伤分析和共聚焦激光扫描显微镜(CLSM)评估抗生素单独和联合的体外抗菌和抗生物膜活性。通过定量肾脏和膀胱组织中的细菌负荷、肾脏组织病理学、病理指数因子(MDA 和 NO)以及促炎(MIP-2 和 IL-6)和抗炎(IL-10)细胞因子,在 UTI 模型中评估体内疗效。菌株 PAO1 的 AZM 和 CIP 的 MIC 分别为 256 和 0.5μg/ml;MBEC 分别为 4096 和 1024μg/ml。AZM 和 CIP 对浮游和生物膜细菌均表现出协同作用(FICI<0.5)。在 CLSM 观察到的情况下,联合用药还能够抑制生物膜的形成(在 MIC 水平)。在小鼠中用 AZM(500mg/kg)和 CIP(30mg/kg)联合口服治疗 4 天,可加速从肾脏和膀胱组织中清除细菌,改善肾脏组织病理学,降低 MDA 和 NO 水平,显著降低 MIP-2 和 IL-6,并增加肾脏中的 IL-10(P<0.0001)。我们得出结论,AZM+CIP 治疗对生物膜相关 UTI 有希望,因为它具有抗菌、免疫调节和抗炎作用。