Therapeutic potential of biofilm-dispersing enzymes

被引:162
作者
Kaplan, Jeffrey B. [1 ]
机构
[1] Univ Med & Dent New Jersey, New Jersey Dent Sch, Dept Oral Biol, Newark, NJ 07103 USA
关键词
Biofilm; Dispersin B; Device infection; DNase I; Extracellular DNA; PNAG; ACETYLGLUCOSAMINE SURFACE POLYSACCHARIDE; STAPHYLOCOCCUS-EPIDERMIDIS; PSEUDOMONAS-AERUGINOSA; EXTRACELLULAR DNA; ACTINOBACILLUS-ACTINOMYCETEMCOMITANS; STREPTOCOCCUS-PNEUMONIAE; INTERCELLULAR ADHESIN; MATRIX; RELEASE; DETACHMENT;
D O I
10.1177/039139880903200903
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Surface-attached colonies of bacteria known as biofilms play a major role in the pathogenesis of medical device infections. Biofilm colonies are notorious for their resistance to antibiotics and host defenses, which makes most device infections difficult or impossible to eradicate. Bacterial cells in a biofilm are held together by an extracellular polymeric matrix that is synthesized by the bacteria themselves. Enzymes that degrade biofilm matrix polymers have been shown to inhibit biofilm formation, detach established biofilm colonies, and render biofilm cells sensitive to killing by antimicrobial agents. This review discusses the potential use of biofilm matrix-degrading enzymes as anti-biofilm agents for the treatment and prevention of device infections. Two enzymes, deoxyribonuclease I and the glycoside hydrolase dispersin B, will be reviewed in detail. In vitro and in vivo studies demonstrating the anti-biofilm activities of these two enzymes will be summarized, and the therapeutic potential and possible drawbacks of using these enzymes as clinical agents will be discussed. (Int J Artif Organs 2009; 32: 545-54)
引用
收藏
页码:545 / 554
页数:10
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