Mihu Mircea Radu, Cabral Vitor, Pattabhi Rodney, Tar Moses T, Davies Kelvin P, Friedman Adam J, Martinez Luis R, Nosanchuk Joshua D
Department of Medicine, Division of Critical Care, St. Anthony Hospital, Oklahoma City, Oklahoma, USA.
Department of Medicine, Division of Infectious Diseases, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, New York, USA.
Antimicrob Agents Chemother. 2016 Dec 27;61(1). doi: 10.1128/AAC.02020-16. Print 2017 Jan.
Staphylococcus aureus is frequently isolated in the setting of infections of indwelling medical devices, which are mediated by the microbe's ability to form biofilms on a variety of surfaces. Biofilm-embedded bacteria are more resistant to antimicrobial agents than their planktonic counterparts and often cause chronic infections and sepsis, particularly in patients with prolonged hospitalizations. In this study, we demonstrate that sustained nitric oxide-releasing nanoparticles (NO-np) interfere with S. aureus adhesion and prevent biofilm formation on a rat central venous catheter (CVC) model of infection. Confocal and scanning electron microscopy showed that NO-np-treated staphylococcal biofilms displayed considerably reduced thicknesses and bacterial numbers compared to those of control biofilms in vitro and in vivo, respectively. Although both phenotypes, planktonic and biofilm-associated staphylococci, of multiple clinical strains were susceptible to NO-np, bacteria within biofilms were more resistant to killing than their planktonic counterparts. Furthermore, chitosan, a biopolymer found in the exoskeleton of crustaceans and structurally integrated into the nanoparticles, seems to add considerable antimicrobial activity to the technology. Our findings suggest promising development and translational potential of NO-np for use as a prophylactic or therapeutic against bacterial biofilms on CVCs and other medical devices.
金黄色葡萄球菌经常在留置医疗设备感染的情况下被分离出来,这是由该微生物在各种表面形成生物膜的能力介导的。与浮游菌相比,生物膜包裹的细菌对抗菌剂更具抗性,并且常常导致慢性感染和败血症,尤其是在住院时间延长的患者中。在本研究中,我们证明持续释放一氧化氮的纳米颗粒(NO-np)会干扰金黄色葡萄球菌的黏附,并在大鼠中心静脉导管(CVC)感染模型上防止生物膜形成。共聚焦显微镜和扫描电子显微镜显示,与体外和体内的对照生物膜相比,经NO-np处理的葡萄球菌生物膜的厚度和细菌数量分别显著降低。尽管多种临床菌株的浮游菌和生物膜相关葡萄球菌这两种表型均对NO-np敏感,但生物膜内的细菌比浮游菌更难被杀死。此外,壳聚糖是一种存在于甲壳类动物外骨骼中的生物聚合物,在结构上整合到纳米颗粒中,似乎为该技术增添了相当大的抗菌活性。我们的研究结果表明,NO-np作为预防或治疗CVC和其他医疗设备上细菌生物膜的药物具有良好的开发和转化潜力。