Stopping bacterial adhesion: A novel approach to treating infections

被引:81
作者
Bavington, C
Page, C
机构
[1] Sackler Inst Pulm Pharmacol, London SE1 1UL, England
[2] GlycoMar Ltd, European Ctr Marine Biotechnol, Dunstaffnage Marine Lab, Oban, Argyll, Scotland
关键词
bacterial adhesion; biofilm; carbohydrates;
D O I
10.1159/000086243
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Adhesion and colonization are prerequisites for the establishment of bacterial pathogenesis. The prevention of adhesion is an attractive target for the development of new therapies in the prevention of infection. Bacteria have developed a multiplicity of adhesion mechanisms commonly targeting surface carbohydrate structures, but our ability to rationally design effective antiadhesives is critically affected by the limitations of our knowledge of the human 'glycome' and of the bacterial function in relation to it. The potential for the future development of carbohydrate-based antiadhesives has been demonstrated by a significant number of in vitro and in vivo studies. Such therapies will be particularly relevant for infections of mucosal surfaces where topical application or delivery is possible. Copyright (C) 2005 S. Karger AG, Basel.
引用
收藏
页码:335 / 344
页数:10
相关论文
共 159 条
[1]   Role of lipopolysaccharides in the adhesion, retention, and transport of Escherichia coli JM109 [J].
Abu-Lail, NI ;
Camesano, TA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2003, 37 (10) :2173-2183
[2]   In vitro binding of Helicobacter pylori to monohexosylceramides [J].
Abul-Milh, M ;
Foster, DB ;
Lingwood, CA .
GLYCOCONJUGATE JOURNAL, 2001, 18 (03) :253-260
[3]   The lactosylceramide binding specificity of Helicobacter pylori [J].
Ångström, J ;
Teneberg, S ;
Milh, MA ;
Larsson, T ;
Leonardsson, I ;
Olsson, BM ;
Halvarsson, MÖ ;
Danielsson, D ;
Näslund, I ;
Ljungh, Å ;
Wadström, T ;
Karlsson, KA .
GLYCOBIOLOGY, 1998, 8 (04) :297-309
[4]   Lectins as defence molecules in vertebrates and invertebrates [J].
Arason, GJ .
FISH & SHELLFISH IMMUNOLOGY, 1996, 6 (04) :277-289
[5]   Isolation of conjunctival mucin and differential interaction with Pseudomonas aeruginosa strains of varied pathogenic potential [J].
Aristoteli, LP ;
Bojarski, B ;
Willcox, MDP .
EXPERIMENTAL EYE RESEARCH, 2003, 77 (06) :699-710
[6]   Analysis of the interaction of Aeromonas caviae, A-hydrophila and A-sobria with mucins [J].
Ascencio, F ;
Martinez-Arias, W ;
Romero, MJ ;
Wadström, T .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 1998, 20 (03) :219-229
[7]   Synthetic oligosaccharides as heparin-mimetics displaying anticoagulant properties [J].
Avci, FY ;
Karst, NA ;
Linhardt, RJ .
CURRENT PHARMACEUTICAL DESIGN, 2003, 9 (28) :2323-2335
[8]   Pseudomonas aeruginosa outer membrane protein F is an adhesin in bacterial binding to lung epithelial cells in culture [J].
Azghani, AO ;
Idell, S ;
Bains, M ;
Hancock, REW .
MICROBIAL PATHOGENESIS, 2002, 33 (03) :109-114
[9]   A BETA-LINKED MANNAN INHIBITS ADHERENCE OF PSEUDOMONAS-AERUGINOSA TO HUMAN LUNG EPITHELIAL-CELLS [J].
AZGHANI, AO ;
WILLIAMS, I ;
HOLIDAY, DB ;
JOHNSON, AR .
GLYCOBIOLOGY, 1995, 5 (01) :39-44
[10]   Inhibition by dextran of Pseudomonas aeruginosa adherence to epithelial cells [J].
Barghouthi, S ;
Guerdoud, LM ;
Speert, DP .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 154 (06) :1788-1793