Solubility and bioactivity of the Pseudomonas quinolone signal are increased by a Pseudomonas aeruginosa-produced surfactant

被引:69
作者
Calfee, MW [1 ]
Shelton, JG [1 ]
McCubrey, JA [1 ]
Pesci, EC [1 ]
机构
[1] E Carolina Univ, Sch Med, Dept Microbiol & Immunol, Greenville, NC 27834 USA
关键词
D O I
10.1128/IAI.73.2.878-882.2005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pseudomonas aeruginosa is a gram-negative bacterium that causes serious infections in immunocompromised individuals and cystic fibrosis patients. This opportunistic pathogen controls many of its virulence factors and cellular functions through the activity of three cell-to-cell signals, N-(3-oxododecanoyl)-L-homoserine lactone, N-butyryi-L-homoserine lactone, and the Pseudomonas quinolone signal (PQS). The activity of these signals is dependent upon their ability to dissolve in and freely diffuse through the aqueous solution in which P. aeruginosa happens to reside. Despite this, our data indicated that PQS was relatively insoluble in aqueous solutions, which led us to postulate that P. aeruginosa could be producing a PQS-solubilizing factor. In this report, we show that the P. aeruginosa-produced biosurfactant rhamnolipid greatly enhances the solubility of PQS in aqueous solutions. The enhanced solubility of PQS led to an increase in PQS bioactivity, as measured by both a gene induction assay and an apoptosis assay. This is the first demonstration of the importance of a bacterial surfactant in the solubilization and bioactivity of a cell-to-cell signal.
引用
收藏
页码:878 / 882
页数:5
相关论文
共 40 条
[1]   Rhamnolipid-induced removal of lipopolysaccharide from Pseudomonas aeruginosa:: Effect on cell surface properties and interaction with hydrophobic substrates [J].
Al-Tahhan, RA ;
Sandrin, TR ;
Bodour, AA ;
Maier, RM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (08) :3262-3268
[2]   Quinolone action against human topoisomerase IIα:: Stimulation of enzyme-mediated double-stranded DNA cleavage [J].
Bromberg, KD ;
Burgin, AB ;
Osheroff, N .
BIOCHEMISTRY, 2003, 42 (12) :3393-3398
[3]   Interference with Pseudomonas quinolone signal synthesis inhibits virulence factor expression by Pseudomonas aeruginosa [J].
Calfee, MW ;
Coleman, JP ;
Pesci, EC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (20) :11633-11637
[4]   A quorum sensing-associated virulence gene of Pseudomonas aeruginosa encodes a LysR-like transcription regulator with a unique self-regulatory mechanism [J].
Cao, H ;
Krishnan, G ;
Goumnerov, B ;
Tsongalis, J ;
Tompkins, R ;
Rahme, LG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (25) :14613-14618
[5]   A bacterial cell to cell signal in the lungs of cystic fibrosis patients [J].
Collier, DN ;
Anderson, L ;
McKnight, SL ;
Noah, TL ;
Knowles, M ;
Boucher, R ;
Schwab, U ;
Gilligan, P ;
Pesci, EC .
FEMS MICROBIOLOGY LETTERS, 2002, 215 (01) :41-46
[6]   Autolysis and autoaggregation in Pseudomonas aeruginosa colony morphology mutants [J].
D'Argenio, DA ;
Calfee, MW ;
Rainey, PB ;
Pesci, EC .
JOURNAL OF BACTERIOLOGY, 2002, 184 (23) :6481-6489
[7]   Rhamnolipid surfactant production affects biofilm architecture in Pseudomonas aeruginosa PAO1 [J].
Davey, ME ;
Caiazza, NC ;
O'Toole, GA .
JOURNAL OF BACTERIOLOGY, 2003, 185 (03) :1027-1036
[8]   GROWTH OF FACTOR-DEPENDENT HEMATOPOIETIC PRECURSOR CELL-LINES [J].
DEXTER, TM ;
GARLAND, J ;
SCOTT, D ;
SCOLNICK, E ;
METCALF, D .
JOURNAL OF EXPERIMENTAL MEDICINE, 1980, 152 (04) :1036-1047
[9]   The Pseudomonas aeruginosa quinolone signal molecule overcomes the cell density-dependency of the quorum sensing hierarchy, regulates rhl-dependent genes at the onset of stationary phase and can be produced in the absence of LasR [J].
Diggle, SP ;
Winzer, K ;
Chhabra, SR ;
Chhabra, SR ;
Worrall, KE ;
Cámara, M ;
Williams, P .
MOLECULAR MICROBIOLOGY, 2003, 50 (01) :29-43
[10]   DIVERSE PSEUDOMONAS-AERUGINOSA GENE-PRODUCTS STIMULATE RESPIRATORY EPITHELIAL-CELLS TO PRODUCE INTERLEUKIN-8 [J].
DIMANGO, E ;
ZAR, HJ ;
BRYAN, R ;
PRINCE, A .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (05) :2204-2210