Bacterial and fungal biofilm infections

被引:327
作者
Lynch, A. Simon [1 ]
Robertson, Gregory T. [1 ]
机构
[1] Cumbre Pharmaceut Inc, Dallas, TX 75235 USA
来源
ANNUAL REVIEW OF MEDICINE | 2008年 / 59卷
关键词
antibiotic; indwelling medical device; antibiotic tolerance; persistent infection; staphylococcal infections; antibiotic resistance;
D O I
10.1146/annurev.med.59.110106.132000
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Biofilms are communal structures of microorganisms encased in an exopolymeric coat that form on both natural and abiotic surfaces and have been associated with a variety of persistent infections that respond poorly to conventional antibiotic chemotherapy. Biofilm infections of certain indwelling medical devices by common pathogens such as staphylococci are not only associated with increased morbidity and mortality but are also significant contributors to the emergence and dissemination of antibiotic resistance traits in the nosocomial setting. Current treatment paradigms for biofilm-associated infections of semipermanent indwelling devices typically involve surgical replacement of the device combined with long-term antibiotic therapy and incur high health care costs. This review summarizes the existing data relating to the nature, prevalence, and treatment of biofilm-associated infections and highlights experimental approaches and therapies that are being pursued toward more effective treatments.
引用
收藏
页码:415 / 428
页数:14
相关论文
共 83 条
[1]   Intracellular bacterial biofilm-like pods in urinary tract infections [J].
Anderson, GG ;
Palermo, JJ ;
Schilling, JD ;
Roth, R ;
Heuser, J ;
Hultgren, SJ .
SCIENCE, 2003, 301 (5629) :105-107
[2]  
ANDERSON JM, 2000, BIOMATERIALS FACTORS, P89
[3]   Development and characterization of an in vivo central venous catheter Candida albicans biofilm model [J].
Andes, D ;
Nett, J ;
Oschel, P ;
Albrecht, R ;
Marchillo, K ;
Pitula, A .
INFECTION AND IMMUNITY, 2004, 72 (10) :6023-6031
[4]   RNAIII-inhibiting-peptide-loaded in vivo Polymethylmethacrylate prevents in vivo Staphylococcus aureus biofilm formation [J].
Anguita-Alonso, Paloma ;
Giacometti, Andrea ;
Cirioni, Oscar ;
Ghiselli, Roberto ;
Orlando, Fiorenza ;
Saba, Vittorio ;
Scalise, Giorgio ;
Sevo, Milica ;
Tuzova, Marina ;
Patel, Robin ;
Balaban, Naomi .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (07) :2594-2596
[5]  
ANTONIOS V, 2006, TREATMENT PROTOCOLS, P449
[6]   IN-VIVO VERIFICATION OF IN-VITRO MODEL OF ANTIBIOTIC-TREATMENT OF DEVICE-RELATED INFECTION [J].
BLASER, J ;
VERGERES, P ;
WIDMER, AF ;
ZIMMERLI, W .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (05) :1134-1139
[7]   Comparative assessment of antibiotic susceptibility of coagulase-negative staphylococci in biofilm versus planktonic culture as assessed by bacterial enumeration or rapid XTT colorimetry [J].
Cerca, N ;
Martins, S ;
Cerca, F ;
Jefferson, KK ;
Pier, GB ;
Oliveira, R ;
Azeredo, J .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2005, 56 (02) :331-336
[8]  
Chandra J, 2004, MICROBIAL BIOFILMS, P30
[9]   Enhanced post-stationary-phase survival of a clinical thymidine-dependent small-colony variant of Staphylococcus aureus results from lack of a functional tricarboxylic acid cycle [J].
Chatterjee, Indranil ;
Herrmann, Mathias ;
Proctor, Richard A. ;
Peters, Georg ;
Kahl, Barbara C. .
JOURNAL OF BACTERIOLOGY, 2007, 189 (07) :2936-2940
[10]   New rifamycins for the treatment of bacterial infections [J].
Combrink, Keith D. ;
Lynch, A. Simon .
EXPERT OPINION ON THERAPEUTIC PATENTS, 2007, 17 (05) :475-485