Inhibition of quorum sensing in Pseudomonas aeruginosa biofilm bacteria by a halogenated furanone compound

被引:746
作者
Hentzer, M
Riedel, K
Rasmussen, TB
Heydorn, A
Andersen, JB
Parsek, MR
Rice, SA
Eberl, L
Molin, S
Hoiby, N
Kjelleberg, S
Givskov, M [1 ]
机构
[1] Tech Univ Denmark, BioCtr DTU, Dept Mol Microbiol, DK-2800 Lyngby, Denmark
[2] Tech Univ Munich, Lehrstuhl Mikrobiol, D-85350 Freising Weihenstephan, Germany
[3] Northwestern Univ, Dept Civil Engn, Inst Technol, Evanston, IL 60208 USA
[4] Univ New S Wales, Sch Microbiol & Immunol, Sydney, NSW 2052, Australia
[5] Univ Copenhagen Hosp, Rigshosp, Dept Clin Microbiol, DK-2100 Copenhagen, Denmark
来源
MICROBIOLOGY-SGM | 2002年 / 148卷
关键词
biofilms; quorum sensing inhibitors; green-fluorescent protein;
D O I
10.1099/00221287-148-1-87
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Novel molecular tools have been constructed which allow for in situ detection of N-acyl homoserine lactone (AHL)-mediated quorum sensing in Pseudomonas aeruginosa biofilms. The reporter responds to AHL activation of LasR lay expression of an unstable version of the green-fluorescent protein (Gfp). Gfp-based reporter technology has been applied for non-destructive, single-cell-level detection of quorum sensing in laboratory-based P. aeruginosa biofilms. It is reported that a synthetic halogenated furanone compound, which is a derivative of the secondary metabolites produced by the Australian macroalga Delisea pulchra, is capable of interfering with AHL-mediated quorum sensing in P. aeruginosa. It is demonstrated that the furanone compound specifically represses expression of a PlasB-gfp reporter fusion without affecting growth or protein synthesis. In addition, it reduces the production of important virulence factors, indicating a general effect on target genes of the las quorum sensing circuit. The furanone was applied to P. aeruginosa biofilms established in biofilm flow chambers. The Gfp-based analysis reveals that the compound penetrates microcolonies and blocks cell signalling and quorum sensing in most biofilm cells. The compound did not affect initial attachment to the abiotic substratum. It does, however, affect the architecture of the biofilm and enhances the process of bacterial detachment, leading to a loss of bacterial biomass from the substratum.
引用
收藏
页码:87 / 102
页数:16
相关论文
共 90 条
[1]   Vfr controls quorum sensing in Pseudomonas aeruginosa [J].
Albus, AM ;
Pesci, EC ;
RunyenJanecky, LJ ;
West, SEH ;
Iglewski, BH .
JOURNAL OF BACTERIOLOGY, 1997, 179 (12) :3928-3935
[2]  
Andersen JB, 1998, APPL ENVIRON MICROB, V64, P2240
[3]   gfp-based N-acyl homoserine-lactone sensor systems for detection of bacterial communication [J].
Andersen, JB ;
Heydorn, A ;
Hentzer, M ;
Eberl, L ;
Geisenberger, O ;
Christensen, BB ;
Molin, S ;
Givskov, M .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (02) :575-585
[4]   A second operator is involved in Pseudomonas aeruginosa elastase (lasB) activation [J].
Anderson, RM ;
Zimprich, CA ;
Rust, L .
JOURNAL OF BACTERIOLOGY, 1999, 181 (20) :6264-6270
[5]   GENETIC AND BIOCHEMICAL-PROPERTIES OF AN EXTRACELLULAR NEUTRAL METALLOPROTEASE FROM STAPHYLOCOCCUS-HYICUS SUBSP HYICUS [J].
AYORA, S ;
GOTZ, F .
MOLECULAR & GENERAL GENETICS, 1994, 242 (04) :421-430
[7]   MOLECULAR CHARACTERIZATION AND NUCLEOTIDE-SEQUENCE OF THE PSEUDOMONAS-AERUGINOSA ELASTASE STRUCTURAL GENE [J].
BEVER, RA ;
IGLEWSKI, BH .
JOURNAL OF BACTERIOLOGY, 1988, 170 (09) :4309-4314
[8]   Green fluorescent protein as a marker for Pseudomonas spp. [J].
Bloemberg, GV ;
OToole, GA ;
Lugtenberg, BJJ ;
Kolter, R .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (11) :4543-4551
[9]   SYNTHESIS OF MULTIPLE EXOPRODUCTS IN PSEUDOMONAS-AERUGINOSA IS UNDER THE CONTROL OF RHLR-RHLI, ANOTHER SET OF REGULATORS IN STRAIN PAO1 WITH HOMOLOGY TO THE AUTOINDUCER-RESPONSIVE LUXR-LUXI FAMILY [J].
BRINT, JM ;
OHMAN, DE .
JOURNAL OF BACTERIOLOGY, 1995, 177 (24) :7155-7163
[10]   ZINC AND IRON REGULATE TRANSLATION OF THE GENE ENCODING PSEUDOMONAS-AERUGINOSA ELASTASE [J].
BRUMLIK, MJ ;
STOREY, DG .
MOLECULAR MICROBIOLOGY, 1992, 6 (03) :337-344