Karlsson Sture, Dupuy Bruno, Mukherjee Kakoli, Norin Elisabeth, Burman Lars G, Akerlund Thomas
Department of Molecular Epidemiology and Biotechnology, Swedish Institute for Infectious Disease Control, S-171 82 Solna, Sweden.
Infect Immun. 2003 Apr;71(4):1784-93. doi: 10.1128/IAI.71.4.1784-1793.2003.
Growth temperature was found to control the expression of toxins A and B in Clostridium difficile VPI 10463, with a maximum at 37 degrees C and low levels at 22 and 42 degrees C in both peptone yeast (PY) and defined media. The up-regulation of toxin A and B mRNA and protein levels upon temperature upshift from 22 to 37 degrees C followed the same kinetics, showing that temperature control occurred at the level of transcription. Experiments with Clostridium perfringens using gusA as a reporter gene demonstrated that both toxin gene promoters were temperature controlled and that their high activity at 37 degrees C was dependent on the alternative sigma factor TcdD. Furthermore, tcdD was found to be autoinduced at 37 degrees C. Glucose down-regulated all these responses in the C. perfringens constructs, similar to its impact on toxin production in C. difficile PY broth cultures. C. difficile proteins induced at 37 degrees C and thus coregulated with the toxins by temperature were demonstrated by two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis and identified as enzymes involved in butyric acid production and as electron carriers in oxidation-reduction reactions. The regulation of toxin production in C. difficile by temperature is a novel finding apparently reflecting an adaptation of the expression of its virulence to mammalian hosts.
研究发现,生长温度可控制艰难梭菌VPI 10463中A毒素和B毒素的表达,在蛋白胨酵母(PY)培养基和限定培养基中,37℃时毒素表达量最高,22℃和42℃时表达量较低。当温度从22℃升至37℃时,毒素A和B的mRNA及蛋白水平上调,呈现相同的动力学变化,表明温度调控发生在转录水平。以产气荚膜梭菌为实验对象,使用gusA作为报告基因的实验表明,两种毒素基因启动子均受温度控制,且它们在37℃时的高活性依赖于替代σ因子TcdD。此外,发现tcdD在37℃时可自我诱导。葡萄糖可下调产气荚膜梭菌构建体中的所有这些反应,这与其对艰难梭菌PY肉汤培养物中毒素产生的影响类似。通过二维十二烷基硫酸钠-聚丙烯酰胺凝胶电泳证明,在37℃诱导产生并因此与毒素受温度共同调控的艰难梭菌蛋白,被鉴定为参与丁酸生成的酶以及氧化还原反应中的电子载体。艰难梭菌毒素产生受温度调控是一项新发现,显然反映了其毒力表达对哺乳动物宿主的适应性。