Robbe-Saule Véronique, Jaumouillé Valentin, Prévost Marie-Christine, Guadagnini Stéphanie, Talhouarne Christelle, Mathout Hayette, Kolb Annie, Norel Françoise
Institut Pasteur, Unité des Régulations Transcriptionnelles, URA-CNRS 2172, 25 rue du Docteur Roux, 75724 Paris Cedex 15, France.
J Bacteriol. 2006 Jun;188(11):3983-94. doi: 10.1128/JB.00033-06.
In Salmonella enterica serovar Typhimurium, the stationary-phase sigma factor sigma(S) (RpoS) is required for virulence, stress resistance, biofilm formation, and development of the rdar morphotype. This morphotype is a multicellular behavior characterized by expression of the adhesive extracellular matrix components cellulose and curli fimbriae. The Crl protein of Escherichia coli interacts with sigma(S) and activates expression of sigma(S)-regulated genes, such as the csgBAC operon encoding the subunit of the curli proteins, by an unknown mechanism. Here, we showed using in vivo and in vitro experiments that the Crl protein of Salmonella serovar Typhimurium is required for development of a typical rdar morphotype and for maximal expression of the csgD, csgB, adrA, and bcsA genes, which are involved in curli and cellulose biosynthesis. In vitro transcription assays and potassium permanganate reactivity experiments with purified His(6)-Crl showed that Crl directly activated sigma(S)-dependent transcription initiation at the csgD and adrA promoters. We observed no effect of Crl on sigma(70)-dependent transcription. Crl protein levels increased during the late exponential and stationary growth phases in Luria-Beratani medium without NaCl at 28 degrees C. We obtained complementation of the crl mutation by increasing sigma(S) levels. This suggests that Crl has a major physiological impact at low concentrations of sigma(S).
在肠炎沙门氏菌鼠伤寒血清型中,稳定期σ因子σ(S)(RpoS)对于毒力、应激抗性、生物膜形成以及rdar形态型的发育是必需的。这种形态型是一种多细胞行为,其特征在于表达粘性细胞外基质成分纤维素和卷曲菌毛。大肠杆菌的Crl蛋白与σ(S)相互作用,并通过未知机制激活σ(S)调控基因的表达,例如编码卷曲蛋白亚基的csgBAC操纵子。在这里,我们通过体内和体外实验表明,鼠伤寒血清型沙门氏菌的Crl蛋白对于典型rdar形态型的发育以及参与卷曲菌毛和纤维素生物合成的csgD、csgB、adrA和bcsA基因的最大表达是必需的。用纯化的His(6)-Crl进行的体外转录测定和高锰酸钾反应性实验表明,Crl直接激活csgD和adrA启动子处的σ(S)依赖性转录起始。我们观察到Crl对σ(70)依赖性转录没有影响。在28℃不含NaCl的Luria-Beratani培养基中,指数生长后期和稳定期生长阶段Crl蛋白水平增加。我们通过提高σ(S)水平获得了crl突变的互补。这表明Crl在低浓度的σ(S)时具有主要的生理影响。