Sustained Nitric Oxide-Releasing Nanoparticles Induce Cell Death in Candida albicans Yeast and Hyphal Cells, Preventing Biofilm Formation In Vitro and in a Rodent Central Venous Catheter Model

被引:39
作者
Ahmadi, Mohammed S. [1 ]
Lee, Hiu Ham [1 ]
Sanchez, David A. [2 ]
Friedman, Adam J. [3 ]
Tar, Moses T. [4 ]
Davies, Kelvin P. [4 ]
Nosanchuk, Joshua D. [5 ,6 ]
Martinez, Luis R. [1 ]
机构
[1] New York Inst Technol, NYIT Coll Osteopath Med, Dept Biomed Sci, Old Westbury, NY 11568 USA
[2] Howard Univ, Coll Med, Washington, DC USA
[3] George Washington Univ, Sch Med & Hlth Sci, Dept Dermatol, Washington, DC 20052 USA
[4] Albert Einstein Coll Med, Dept Urol, Bronx, NY 10467 USA
[5] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Div Infect Dis, Bronx, NY 10467 USA
[6] Albert Einstein Coll Med, Dept Microbiol & Immunol, Bronx, NY 10467 USA
关键词
CRITICALLY-ILL PATIENTS; PERSISTER CELLS; INFECTIONS; RESISTANCE; DELIVERY; EFFICACY; PATHOGEN; SUSCEPTIBILITY; MORTALITY; PLATFORM;
D O I
10.1128/AAC.02659-15
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Candida albicans is a leading nosocomial pathogen. Today, candidal biofilms are a significant cause of catheter infections, and such infections are becoming increasingly responsible for the failure of medical-implanted devices. C. albicans forms biofilms in which fungal cells are encased in an autoproduced extracellular polysaccharide matrix. Consequently, the enclosed fungi are protected from antimicrobial agents and host cells, providing a unique niche conducive to robust microbial growth and a harbor for recurring infections. Here we demonstrate that a recently developed platform comprised of nanoparticles that release therapeutic levels of nitric oxide (NO-np) inhibits candidal biofilm formation, destroys the extracellular polysaccharide matrices of mature fungal biofilms, and hinders biofilm development on surface biomaterials such as the lumen of catheters. We found NO-np to decrease both the metabolic activity of biofilms and the cell viability of C. albicans in vitro and in vivo. Furthermore, flow cytometric analysis found NO-np to induce apoptosis in biofilm yeast cells in vitro. Moreover, NO-np behave synergistically when used in combination with established antifungal drug therapies. Here we propose NO-np as a novel treatment modality, especially in combination with standard antifungals, for the prevention and/or remediation of fungal biofilms on central venous catheters and other medical devices.
引用
收藏
页码:2185 / 2194
页数:10
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