Prevention and Treatment of Virulent Bacterial Biofilms with an Enzymatic Nitric Oxide-Releasing Dressing

被引:43
作者
Sulemankhil, Imran [1 ]
Ganopolsky, Jorge Gabriel [2 ]
Dieni, Christopher Anthony [2 ]
Dan, Andrei Florin [1 ]
Jones, Mitchell Lawrence [1 ,2 ]
Prakash, Satya [1 ]
机构
[1] McGill Univ, Fac Med, Dept Biomed Engn, Montreal, PQ, Canada
[2] Micropharma Ltd, Montreal, PQ, Canada
关键词
RESISTANT STAPHYLOCOCCUS-AUREUS; PSEUDOMONAS-AERUGINOSA BIOFILMS; CATHETER-RELATED INFECTIONS; ANTIMICROBIAL ACTIVITY; ANTIBIOTIC-RESISTANCE; SILICA NANOPARTICLES; HYDROGEN-PEROXIDE; IN-VITRO; SKIN; EFFICACY;
D O I
10.1128/AAC.01173-12
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The use of percutaneous medical devices often results in nosocomial infections. Attachment of microorganisms to the surfaces of these medical devices triggers biofilm formation, which presents significant complications to the health of a patient and may lead to septicemia, thromboembolism, or endocarditis if not correctly treated. Although several antimicrobials are commonly used for prevention of biofilm formation, they have limited efficacy against formed biofilms. In this study, we report the use of an enzymatic, gaseous nitric oxide (gNO)-releasing dressing for the prevention and treatment of Acinetobacter baumannii, methicillin-resistant Staphylococcus aureus, and Pseudomonas aeruginosa biofilms. Results show that the bactericidal activity against biofilms of the test strains was dependent on time and rate of gNO release from the dressing. Following 6 h of treatment, gNO-releasing dressings significantly inhibited the growth of test strains relative to vehicle control dressings, demonstrating eradication of bacterial concentrations of up to 10(5) CFU/cm(2). Complete cell death was observed for both prevention of biofilm formation and treatment of 24-h-grown biofilms after 6 h of treatment with the gNO-releasing dressings. Further, gNO-releasing dressings were more efficient against formed biofilms than other antimicrobial agents currently used. These results demonstrate that the gNO-releasing dressing can produce sufficient levels of gNO over a therapeutically relevant duration for maximal bactericidal effects against virulent bacterial strains known to cause nosocomial infections.
引用
收藏
页码:6095 / 6103
页数:9
相关论文
共 51 条
[1]  
Anstead Gregory M., 2007, V391, P227
[2]   A case of anaphylaxis to chlorhexidine during digital rectal examination [J].
Bae, Yun-Jeong ;
Park, Chan Sun ;
Lee, Jae Keun ;
Jeong, Eunheui ;
Kim, Tae-Bum ;
Cho, You Sook ;
Moon, Hee-Bom .
JOURNAL OF KOREAN MEDICAL SCIENCE, 2008, 23 (03) :526-528
[3]   Dilute povidone-iodine solutions inhibit human skin fibroblast growth [J].
Balin, AK ;
Pratt, L .
DERMATOLOGIC SURGERY, 2002, 28 (03) :210-214
[4]   Involvement of nitric oxide in biofilm dispersal of Pseudomonas aeruginosa [J].
Barraud, Nicolas ;
Hassett, Daniel J. ;
Hwang, Sung-Hei ;
Rice, Scott A. ;
Kjelleberg, Staffan ;
Webb, Jeremy S. .
JOURNAL OF BACTERIOLOGY, 2006, 188 (21) :7344-7353
[5]   Nitric oxide-mediated dispersal in single- and multi-species biofilms of clinically and industrially relevant microorganisms [J].
Barraud, Nicolas ;
Storey, Michael V. ;
Moore, Zoe P. ;
Webb, Jeremy S. ;
Rice, Scott A. ;
Kjelleberg, Staffan .
MICROBIAL BIOTECHNOLOGY, 2009, 2 (03) :370-378
[6]   Metabolic Differentiation in Biofilms as Indicated by Carbon Dioxide Production Rates [J].
Bester, Elanna ;
Kroukamp, Otini ;
Wolfaardt, Gideon M. ;
Boonzaaier, Leandro ;
Liss, Steven N. .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2010, 76 (04) :1189-1197
[7]   Catheter-related infections:: diagnosis and intravascular treatment [J].
Bouza, E ;
Burillo, A ;
Muñoz, P .
CLINICAL MICROBIOLOGY AND INFECTION, 2002, 8 (05) :265-274
[8]   A dose-response study of antibiotic resistance in Pseudomonas aeruginosa biofilms [J].
Brooun, A ;
Liu, SH ;
Lewis, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (03) :640-646
[9]   Nitric oxide function in the skin [J].
Cals-Grierson, MM ;
Ormerod, AD .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2004, 10 (04) :179-193
[10]   Nitric oxide release: Part II. Therapeutic applications [J].
Carpenter, Alexis W. ;
Schoenfisch, Mark H. .
CHEMICAL SOCIETY REVIEWS, 2012, 41 (10) :3742-3752