Schurr M J, Yu H, Boucher J C, Hibler N S, Deretic V
Department of Microbiology, University of Texas Health Science Center, San Antonio 78284-7758, USA.
J Bacteriol. 1995 Oct;177(19):5670-9. doi: 10.1128/jb.177.19.5670-5679.1995.
Overproduction of the exopolysaccharide alginate causes mucoid colony morphology in Pseudomonas aeruginosa and is considered a major virulence determinant expressed by this organism during chronic respiratory infections in cystic fibrosis. One of the principal regulatory elements governing conversion to mucoidy in P. aeruginosa is AlgU, an alternative sigma factor which is 66% identical to and functionally interchangeable with sigma E from Escherichia coli and Salmonella typhimurium. sigma E has been implicated in the expression of systems enhancing bacterial resistance to environmental stress. In this study, we report that the gene encoding AlgU is transcribed in wild-type nonmucoid P. aeruginosa from multiple promoters (P1 through P5) that fall into three categories: (i) the P1 and P3 promoters, which display strong similarity to the -35 and -10 canonical sequences of sigma E promoters and were found to be absolutely dependent on AlgU; (ii) the P2 promoter, which was less active in algU mutants, but transcription of which was not completely abrogated in algU::Tcr cells; and (iii) the transcripts corresponding to P4 and P5, which were not affected by inactivation of algU. Introduction of E. coli rpoE (encoding sigma E) or algU into P. aeruginosa algU::Tcr strains restored P1 and P3 transcription and brought the P2 signal back to the wild-type level. The AlgU-dependent promoters P1 and P3 were inducible by heat shock in wild-type nonmucoid P. aeruginosa PAO1. At the protein level, induction of AlgU synthesis under conditions of extreme heat shock was detected by metabolic labeling of newly synthesized proteins, two-dimensional gel analysis, and reaction with polyclonal antibodies raised against an AlgU peptide. Another AlgU-dependent promoter, the proximal promoter of algR, was also found to be induced by heat shock. Under conditions of high osmolarity, growth at elevated temperature induced alginate synthesis in the wild-type nonmucoid P. aeruginosa PAO1. Cumulatively, these results suggest that algU itself is subject to complex regulation and is inducible by extreme heat shock, that the alginate system is a subset of the stress-responsive elements controlled by AlgU, and that AlgU and, by extension, its homologs in other organisms (e.g., sigma E in S. typhimurium) may play a role in bacterial virulence and adjustments to adverse growth conditions.
胞外多糖藻酸盐的过量产生会导致铜绿假单胞菌形成黏液样菌落形态,并且被认为是该菌在囊性纤维化患者慢性呼吸道感染期间表达的一种主要毒力决定因素。在铜绿假单胞菌中,控制向黏液样转变的主要调控元件之一是AlgU,它是一种替代σ因子,与大肠杆菌和鼠伤寒沙门氏菌的σE有66%的同源性且功能可互换。σE与增强细菌对环境应激抵抗力的系统表达有关。在本研究中,我们报道编码AlgU的基因在野生型非黏液样铜绿假单胞菌中由多个启动子(P1至P5)转录,这些启动子可分为三类:(i)P1和P3启动子,它们与σE启动子的-35和-10标准序列高度相似,并且发现完全依赖于AlgU;(ii)P2启动子,在algU突变体中活性较低,但在algU::Tcr细胞中其转录并未完全消除;(iii)与P4和P5对应的转录本,不受algU失活的影响。将大肠杆菌的rpoE(编码σE)或algU导入铜绿假单胞菌algU::Tcr菌株可恢复P1和P3转录,并使P2信号恢复到野生型水平。野生型非黏液样铜绿假单胞菌PAO1中,AlgU依赖的启动子P1和P3可被热休克诱导。在蛋白质水平上,通过对新合成蛋白质进行代谢标记、二维凝胶分析以及与针对AlgU肽产生的多克隆抗体反应,检测到在极端热休克条件下AlgU合成的诱导。另一个AlgU依赖的启动子algR的近端启动子也被发现可被热休克诱导。在高渗透压条件下,野生型非黏液样铜绿假单胞菌PAO1在高温下生长会诱导藻酸盐合成。综合这些结果表明,algU本身受到复杂调控且可被极端热休克诱导,藻酸盐系统是由AlgU控制的应激反应元件的一个子集,并且AlgU以及由此延伸的其他生物体中的同源物(如鼠伤寒沙门氏菌中的σE)可能在细菌毒力和对不利生长条件的适应中发挥作用。