Production of acyl-homoserine lactone quorum-sensing signals by gram-negative plant-associated bacteria.

Many gram-negative bacteria regulate expression of specialized gene sets in response to population density. This regulatory mechanism, called autoinduction or quorum-sensing, is based on the production by the bacteria of a small, diffusible signal molecule called the autoinducer. In the most well-studied systems the autoinducers are N-acylated derivatives of L-homoserine lactone (acyl-HSL). Signal specificity is conferred by the length, and the nature of the substitution at C-3, of the acyl side-chain. We evaluated four acyl-HSL bioreporters, based on tra of Agrobacterium tumefaciens, lux of Vibrio fischeri, las of Pseudomonas aeruginosa, and pigment production by Chromobacterium violaceum, for their ability to detect sets of 3-oxo acyl-HSLs, 3-hydroxy acyl-HSLs, and alkanoyl-HSLs with chain lengths ranging from C4 to C12. The traG::lacZ fusion reporter from the A. tumefaciens Ti plasmid was the single most sensitive and versatile detector of the four. Using this reporter, we screened 106 isolates representing seven genera of bacteria that associate with plants. Most of the Agrobacterium, Rhizobium, and Pantoea isolates and about half of the Erwinia and Pseudomonas isolates gave positive reactions. Only a few isolates of Xanthomonas produced a detectable signal. We characterized the acyl-HSLs produced by a subset of the isolates by thin-layer chromatography. Among the pseudomonads and erwinias, most produced a single dominant activity chromatographing with the properties of N-(3-oxo-hexanoyl)-L-HSL. However, a few of the erwinias, and the P. fluorescens and Ralstonia solanacearum isolates, produced quite different signals, including 3-hydroxy forms, as well as active compounds that chromatographed with properties unlike any of our standards. The few positive xanthomonas, and almost all of the agrobacteria, produced small amounts of a compound with the chromatographic properties of N-(3-oxo-octanoyl)-L-HSL. Members of the genus Rhizobium showed the greatest diversity, with some producing as few as one and others producing as many as seven detectable signals. Several isolates produced extremely nonpolar compounds indicative of very long acyl side-chains. Production of these compounds suggests that quorum-sensing is common as a gene regulatory mechanism among gram-negative plant-associated bacteria.

[1]  L. Thomashow,et al.  Role of a phenazine antibiotic from Pseudomonas fluorescens in biological control of Gaeumannomyces graminis var. tritici , 1988, Journal of bacteriology.

[2]  K. Nealson,et al.  Cellular Control of the Synthesis and Activity of the Bacterial Luminescent System , 1970, Journal of bacteriology.

[3]  J. Kijne,et al.  Bacteriocin small of Rhizobium leguminosarum belongs to the class of N-acyl-L-homoserine lactone molecules, known as autoinducers and as quorum sensing co-transcription factors , 1996, Journal of bacteriology.

[4]  E. Greenberg,et al.  Census and consensus in bacterial ecosystems: the LuxR-LuxI family of quorum-sensing transcriptional regulators. , 1996, Annual review of microbiology.

[5]  King Eo,et al.  Two simple media for the demonstration of pyocyanin and fluorescin. , 1954 .

[6]  D. Wood,et al.  Phenazine antibiotic biosynthesis in Pseudomonas aureofaciens 30-84 is regulated by PhzR in response to cell density , 1994, Journal of bacteriology.

[7]  M. Schell,et al.  Identification of 3‐hydroxypalmitic acid methyl ester as a novel autoregulator controlling virulence in Ralstonia solanacearum , 1997, Molecular microbiology.

[8]  M. Schell,et al.  A two-component system in Ralstonia (Pseudomonas) solanacearum modulates production of PhcA-regulated virulence factors in response to 3-hydroxypalmitic acid methyl ester , 1997, Journal of bacteriology.

[9]  G L Kenyon,et al.  Structural identification of autoinducer of Photobacterium fischeri luciferase. , 1981, Biochemistry.

[10]  J H Lamb,et al.  Quorum sensing and Chromobacterium violaceum: exploitation of violacein production and inhibition for the detection of N-acylhomoserine lactones. , 1997, Microbiology.

[11]  Margret I. Moré,et al.  Enzymatic Synthesis of a Quorum-Sensing Autoinducer Through Use of Defined Substrates , 1996, Science.

[12]  M. Chilton,et al.  Agrobacterium tumefaciens DNA and PS8 bacteriophage DNA not detected in crown gall tumors. , 1974, Proceedings of the National Academy of Sciences of the United States of America.

[13]  E. Greenberg,et al.  Cell-to-cell signaling in the symbiotic nitrogen-fixing bacterium Rhizobium leguminosarum: autoinduction of a stationary phase and rhizosphere-expressed genes , 1996, Journal of bacteriology.

[14]  M. Chilton,et al.  Plasmid required for virulence of Agrobacterium tumefaciens , 1975, Journal of bacteriology.

[15]  Z. Bánfalvi,et al.  Localization of symbiotic mutations in Rhizobium meliloti , 1983, Journal of bacteriology.

[16]  M. Schell,et al.  Hierarchical autoinduction in Ralstonia solanacearum: control of acyl-homoserine lactone production by a novel autoregulatory system responsive to 3-hydroxypalmitic acid methyl ester , 1997, Journal of bacteriology.

[17]  E. Greenberg,et al.  Structure of the autoinducer required for expression of Pseudomonas aeruginosa virulence genes. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[18]  A. Poplawsky,et al.  pigB determines a diffusible factor needed for extracellular polysaccharide slime and xanthomonadin production in Xanthomonas campestris pv. campestris , 1997, Journal of bacteriology.

[19]  P. Murphy,et al.  Agrobacterium conjugation and gene regulation by N-acyl-L-homoserine lactones , 1993, Nature.

[20]  B. Iglewski,et al.  Roles of Pseudomonas aeruginosa las and rhl quorum-sensing systems in control of elastase and rhamnolipid biosynthesis genes , 1997, Journal of bacteriology.

[21]  J. Reiser,et al.  Autoinducer-mediated regulation of rhamnolipid biosurfactant synthesis in Pseudomonas aeruginosa. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[22]  S. Farrand,et al.  The tra region of the nopaline-type Ti plasmid is a chimera with elements related to the transfer systems of RSF1010, RP4, and F , 1996, Journal of bacteriology.

[23]  P. Dunlap,et al.  Multiple N-acyl-L-homoserine lactone autoinducers of luminescence in the marine symbiotic bacterium Vibrio fischeri , 1994, Journal of bacteriology.

[24]  E. Greenberg,et al.  A quorum-sensing system in the free-living photosynthetic bacterium Rhodobacter sphaeroides , 1997, Journal of bacteriology.

[25]  H. Vogel,et al.  Acetylornithinase of Escherichia coli: partial purification and some properties. , 1956, The Journal of biological chemistry.

[26]  J. M. Dow,et al.  A novel regulatory system required for pathogenicity of Xanthomonas campestris is mediated by a small diffusible signal molecule , 1997, Molecular microbiology.

[27]  P. Li,et al.  TraI, a LuxI homologue, is responsible for production of conjugation factor, the Ti plasmid N-acylhomoserine lactone autoinducer. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[28]  S. Molin,et al.  Involvement of N‐acyl‐l‐homoserine lactone autoinducers in controlling the multicellular behaviour of Serratia liquefaciens , 1996, Molecular microbiology.

[29]  D. Roop,et al.  Four new derivatives of the broad-host-range cloning vector pBBR1MCS, carrying different antibiotic-resistance cassettes. , 1995, Gene.

[30]  M. Gambello,et al.  Expression of Pseudomonas aeruginosa virulence genes requires cell-to-cell communication. , 1993, Science.

[31]  J. Cui,et al.  Purification, characterization and biological role of a pheromone produced byXanthomonas campestrispv.campestris , 1997 .

[32]  P. Reeves,et al.  The lux autoinducer regulates the production of exoenzyme virulence determinants in Erwinia carotovora and Pseudomonas aeruginosa. , 1993, The EMBO journal.

[33]  S. Farrand,et al.  Capsular polysaccharide biosynthesis and pathogenicity in Erwinia stewartii require induction by an N-acylhomoserine lactone autoinducer , 1995, Journal of bacteriology.

[34]  E. Greenberg,et al.  Quorum sensing in bacteria: the LuxR-LuxI family of cell density-responsive transcriptional regulators , 1994, Journal of bacteriology.

[35]  K. Tanaka,et al.  A hierarchical quorum‐sensing cascade in Pseudomonas aeruginosa links the transcriptional activators LasR and RhIR (VsmR) to expression of the stationary‐phase sigma factor RpoS , 1996, Molecular microbiology.

[36]  K. Rinehart,et al.  Detecting and characterizing N-acyl-homoserine lactone signal molecules by thin-layer chromatography. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[37]  W. Fuqua,et al.  A LuxR-LuxI type regulatory system activates Agrobacterium Ti plasmid conjugal transfer in the presence of a plant tumor metabolite , 1994, Journal of bacteriology.

[38]  P. Dunlap,et al.  Cell density-dependent modulation of the Vibrio fischeri luminescence system in the absence of autoinducer and LuxR protein , 1992, Journal of bacteriology.

[39]  A. Boronin,et al.  A Seven-Gene Locus for Synthesis of Phenazine-1-Carboxylic Acid by Pseudomonas fluorescens2-79 , 1998, Journal of bacteriology.

[40]  M. Pirhonen,et al.  A small diffusible signal molecule is responsible for the global control of virulence and exoenzyme production in the plant pathogen Erwinia carotovora. , 1993, The EMBO journal.

[41]  J. Michiels,et al.  luxI- and luxR-Homologous Genes of Rhizobium etli CNPAF512 Contribute to Synthesis of Autoinducer Molecules and Nodulation of Phaseolus vulgaris , 1998, Journal of bacteriology.

[42]  J. M. Dow,et al.  Synthesis of Extracellular Polysaccharide, Extracellular Enzymes, and Xanthomonadin in Xanthomonas campestris: Evidence for the Involvement of Two Intercellular Regulatory Signals , 1998 .

[43]  M. Cámara,et al.  Characterisation of the yenI/yenR locus from Yersinia enterocolitica mediating the synthesis of two N‐acylhomoserine lactone signal molecules , 1995, Molecular microbiology.

[44]  G. Salmond,et al.  Multiple N-acyl-L-homoserine lactone signal molecules regulate production of virulence determinants and secondary metabolites in Pseudomonas aeruginosa. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[45]  Stephen K. Farrand,et al.  Conjugation factor of Agrobacterium tumefaciens regulates Ti plasmid transfer by autoinduction , 1993, Nature.

[46]  M K Winson,et al.  Quorum sensing in Aeromonas hydrophila and Aeromonas salmonicida: identification of the LuxRI homologs AhyRI and AsaRI and their cognate N-acylhomoserine lactone signal molecules , 1997, Journal of bacteriology.