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艰难梭菌毒素A和B及其σ因子TcdD的表达受温度控制。

Expression of Clostridium difficile toxins A and B and their sigma factor TcdD is controlled by temperature.

作者信息

Karlsson Sture, Dupuy Bruno, Mukherjee Kakoli, Norin Elisabeth, Burman Lars G, Akerlund Thomas

机构信息

Department of Molecular Epidemiology and Biotechnology, Swedish Institute for Infectious Disease Control, S-171 82 Solna, Sweden.

出版信息

Infect Immun. 2003 Apr;71(4):1784-93. doi: 10.1128/IAI.71.4.1784-1793.2003.

Abstract

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.

摘要

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。

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