Usnic acid, a natural antimicrobial agent able to inhibit bacterial biofilm formation on polymer surfaces

被引:196
作者
Francolini, I
Norris, P
Piozzi, A
Donelli, G
Stoodley, P
机构
[1] Allegheny Singer Res Inst, Ctr Genom Sci, Pittsburgh, PA 15212 USA
[2] Montana State Univ, Ctr Biofilm Engn, Bozeman, MT 59717 USA
[3] Univ Roma La Sapienza, Dept Chem, I-00185 Rome, Italy
[4] Ist Super Sanita, Dept Technol & Hlth, I-00161 Rome, Italy
关键词
D O I
10.1128/AAC.48.11.4360-4365.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In modern medicine, artificial devices are used for repair or replacement of damaged parts of the body, delivery of drugs, and monitoring the status of critically ill patients. However, artificial surfaces are often susceptible to colonization by bacteria and fungi. Once microorganisms have adhered to the surface, they can form biofilms, resulting in highly resistant local or systemic infections. At this time, the evidence suggests that (+)-usnic acid, a secondary lichen metabolite, possesses antimicrobial activity against a number of planktonic gram-positive bacteria, including Staphylococcus aureus, Enterococcus faecalis, and Enterococcus faecium. Since lichens are surface-attached communities that produce antibiotics, including usnic acid, to protect themselves from colonization by other bacteria, we hypothesized that the mode of action of usnic acid may be utilized in the control of medical biofilms. We loaded (+)-usnic acid into modified polyurethane and quantitatively assessed the capacity of (+)-usnic acid to control biofilm formation by either S. aureus or Pseudomonas aeruginosa under laminar flow conditions by using image analysis. (+)-Usnic acid-loaded polymers did not inhibit the initial attachment of S. aureus cells, but killing the attached cells resulted in the inhibition of biofilm. Interestingly, although P. aeruginosa biofilms did form on the surface of (+)-usnic acid-loaded polymer, the morphology of the biofilm was altered, possibly indicating that (+)-usnic acid interfered with signaling pathways.
引用
收藏
页码:4360 / 4365
页数:6
相关论文
共 40 条
[1]   Efficacy of silver-coating central venous catheters in reducing bacterial colonization [J].
Bach, A ;
Eberhardt, H ;
Frick, A ;
Schmidt, H ;
Böttiger, BW ;
Martin, E .
CRITICAL CARE MEDICINE, 1999, 27 (03) :515-521
[2]   Molecular characterization and action of usnic acid: a drug that inhibits proliferation of mouse polyomavirus in vitro and whose main target is RNA transcription [J].
Campanella, L ;
Delfini, M ;
Ercole, P ;
Iacoangeli, A ;
Risuleo, G .
BIOCHIMIE, 2002, 84 (04) :329-334
[3]   Bacterial biofilms: A common cause of persistent infections [J].
Costerton, JW ;
Stewart, PS ;
Greenberg, EP .
SCIENCE, 1999, 284 (5418) :1318-1322
[4]  
CRAIG WA, 1988, INFECT CONT HOSP EP, V9, P417
[5]   The involvement of cell-to-cell signals in the development of a bacterial biofilm [J].
Davies, DG ;
Parsek, MR ;
Pearson, JP ;
Iglewski, BH ;
Costerton, JW ;
Greenberg, EP .
SCIENCE, 1998, 280 (5361) :295-298
[6]   New polymer-antibiotic systems to inhibit bacterial biofilm formation: A suitable approach to prevent central venous catheter-associated infections [J].
Donelli, G ;
Francolini, I ;
Piozzi, A ;
Di Rosa, R ;
Marconi, W .
JOURNAL OF CHEMOTHERAPY, 2002, 14 (05) :501-507
[7]   Efficacy of antiadhesive, antibiotic and antiseptic coatings in preventing catheter-related infections: Review [J].
Donelli, G ;
Francolini, I .
JOURNAL OF CHEMOTHERAPY, 2001, 13 (06) :595-606
[8]   EFFECT OF GROWTH-RATE ON RESISTANCE OF GRAM-NEGATIVE BIOFILMS TO CETRIMIDE [J].
EVANS, DJ ;
ALLISON, DG ;
BROWN, MRW ;
GILBERT, P .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1990, 26 (04) :473-478
[9]   EFFICACY OF AN ATTACHABLE SUBCUTANEOUS CUFF FOR THE PREVENTION OF INTRAVASCULAR CATHETER-RELATED INFECTION - A RANDOMIZED, CONTROLLED TRIAL [J].
FLOWERS, RH ;
SCHWENZER, KJ ;
KOPEL, RF ;
FISCH, MJ ;
TUCKER, SI ;
FARR, BM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1989, 261 (06) :878-883
[10]  
GHIONE M, 1988, CHEMIOTERAPIA, V7, P302