Wagner Victoria E, Bushnell Daniel, Passador Luciano, Brooks Andrew I, Iglewski Barbara H
Department of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry, New York 14642, USA.
J Bacteriol. 2003 Apr;185(7):2080-95. doi: 10.1128/JB.185.7.2080-2095.2003.
Bacterial communication via quorum sensing (QS) has been reported to be important in the production of virulence factors, antibiotic sensitivity, and biofilm development. Two QS systems, known as the las and rhl systems, have been identified previously in the opportunistic pathogen Pseudomonas aeruginosa. High-density oligonucleotide microarrays for the P. aeruginosa PAO1 genome were used to investigate global gene expression patterns modulated by QS regulons. In the initial experiments we focused on identifying las and/or rhl QS-regulated genes using a QS signal generation-deficient mutant (PAO-JP2) that was cultured with and without added exogenous autoinducers [N-(3-oxododecanoyl) homoserine lactone and N-butyryl homoserine lactone]. Conservatively, 616 genes showed statistically significant differential expression (P </= 0.05) in response to the exogenous autoinducers and were classified as QS regulated. A total of 244 genes were identified as being QS regulated at the mid-logarithmic phase, and 450 genes were identified as being QS regulated at the early stationary phase. Most of the previously reported QS-promoted genes were confirmed, and a large number of additional QS-promoted genes were identified. Importantly, 222 genes were identified as being QS repressed. Environmental factors, such as medium composition and oxygen availability, eliminated detection of transcripts of many genes that were identified as being QS regulated.
据报道,细菌通过群体感应(QS)进行的通讯在毒力因子产生、抗生素敏感性和生物膜形成方面具有重要作用。先前已在机会致病菌铜绿假单胞菌中鉴定出两种QS系统,即las和rhl系统。利用针对铜绿假单胞菌PAO1基因组的高密度寡核苷酸微阵列来研究由QS调控子调节的全局基因表达模式。在最初的实验中,我们聚焦于使用一种QS信号产生缺陷型突变体(PAO-JP2)来鉴定las和/或rhl QS调控的基因,该突变体在添加和不添加外源自诱导物[N-(3-氧代十二烷酰)高丝氨酸内酯和N-丁酰高丝氨酸内酯]的情况下进行培养。保守估计,有616个基因对外源自诱导物产生了具有统计学显著差异的表达(P≤0.05),并被归类为受QS调控。共有244个基因在对数中期被鉴定为受QS调控,450个基因在稳定早期被鉴定为受QS调控。大多数先前报道的QS促进基因得到了证实,并且还鉴定出了大量额外的QS促进基因。重要的是,有222个基因被鉴定为受QS抑制。环境因素,如培养基成分和氧气供应,消除了许多被鉴定为受QS调控的基因转录本的检测。