Pearson J P, Passador L, Iglewski B H, Greenberg E P
Department of Microbiology, University of Iowa, Iowa City 52242.
Proc Natl Acad Sci U S A. 1995 Feb 28;92(5):1490-4. doi: 10.1073/pnas.92.5.1490.
Quorum sensing systems are used by a number of Gram-negative bacterial species to regulate specific sets of genes in a cell density-dependent manner. Quorum sensing involves synthesis and detection of extracellular signals termed autoinducers. As shown in recombinant Escherichia coli, the Pseudomonas aeruginosa autoinducer (PAI) N-(3-oxododecanoyl)homoserine lactone, together with the lasR gene product, activate the P. aeruginosa lasB gene. In this study, PAI was shown to activate lasB-lacZ expression in a P. aeruginosa lasR mutant containing a plasmid with lasR under the control of the lac promoter. The concentration of PAI necessary for half-maximal activation of the lasB-lacZ fusion was approximately 1 microM, which is within the range of PAI levels found in P. aeruginosa culture fluids. The effect of PAI on a P. aeruginosa lasR mutant containing a plasmid with lasR under the control of its own promoter and containing the lasB-lacZ fusion was also tested. Although extracts of culture fluid activated the lasB promoter in this construct, concentrations of PAI as high as 10 microM did not. This indicates the presence of a second extracellular factor (factor 2) that is required for lasB activation in P. aeruginosa when lasR is controlled by its own promoter but not when lasR is controlled by a strong foreign promoter. Factor 2 was shown to be N-butyrylhomoserine lactone. Although recombinant E. coli cells containing the PAI synthase gene, lasI, produce PAI, these cells do not produce factor 2. Furthermore, a P. aeruginosa mutant that produced about 0.1% of the wild-type level of PAI made about 5% of the wild-type level of factor 2. This indicates that factor 2 synthesis results from the activity of a gene product other than PAI synthase. The role of factor 2 in virulence gene regulation remains to be determined, but this compound may affect the expression of lasR, which in turn activates transcription of numerous virulence genes in the presence of sufficient PAI. Apparently, multiple quorum sensing systems can occur and interact with each other in a single bacterial species.
群体感应系统被许多革兰氏阴性细菌用于以细胞密度依赖的方式调节特定的基因集。群体感应涉及细胞外信号(称为自诱导物)的合成与检测。如在重组大肠杆菌中所示,铜绿假单胞菌自诱导物(PAI)N-(3-氧代十二烷酰)高丝氨酸内酯与lasR基因产物一起激活铜绿假单胞菌的lasB基因。在本研究中,PAI被证明能在含有受lac启动子控制的lasR质粒的铜绿假单胞菌lasR突变体中激活lasB-lacZ表达。lasB-lacZ融合体半数最大激活所需的PAI浓度约为1 microM,这在铜绿假单胞菌培养液中发现的PAI水平范围内。还测试了PAI对含有受自身启动子控制的lasR且含有lasB-lacZ融合体的质粒的铜绿假单胞菌lasR突变体的影响。尽管培养液提取物激活了该构建体中的lasB启动子,但高达10 microM的PAI浓度却不能。这表明存在第二种细胞外因子(因子2),当lasR受自身启动子控制时,它是铜绿假单胞菌中lasB激活所必需的,但当lasR受强外源启动子控制时则不是。因子2被证明是N-丁酰高丝氨酸内酯。虽然含有PAI合成酶基因lasI的重组大肠杆菌细胞产生PAI,但这些细胞不产生因子2。此外,一个产生约0.1%野生型水平PAI的铜绿假单胞菌突变体产生了约5%野生型水平的因子2。这表明因子2的合成是由PAI合成酶以外的基因产物的活性导致的。因子2在毒力基因调控中的作用仍有待确定,但这种化合物可能影响lasR的表达,而lasR在有足够PAI存在时又会激活众多毒力基因的转录。显然,多个群体感应系统可能在单个细菌物种中出现并相互作用。