Department of Microbiology and Immunobiology, Harvard Medical School, Boston, Massachusetts, United States of America.
PLoS Pathog. 2011 Aug;7(8):e1002153. doi: 10.1371/journal.ppat.1002153. Epub 2011 Aug 4.
Facultative bacterial pathogens must adapt to multiple stimuli to persist in the environment or establish infection within a host. Temperature is often utilized as a signal to control expression of virulence genes necessary for infection or genes required for persistence in the environment. However, very little is known about the molecular mechanisms that allow bacteria to adapt and respond to temperature fluctuations. Listeria monocytogenes (Lm) is a food-borne, facultative intracellular pathogen that uses flagellar motility to survive in the extracellular environment and to enhance initial invasion of host cells during infection. Upon entering the host, Lm represses transcription of flagellar motility genes in response to mammalian physiological temperature (37°C) with a concomitant temperature-dependent up-regulation of virulence genes. We previously determined that down-regulation of flagellar motility is required for virulence and is governed by the reciprocal activities of the MogR transcriptional repressor and the bifunctional flagellar anti-repressor/glycosyltransferase, GmaR. In this study, we determined that GmaR is also a protein thermometer that controls temperature-dependent transcription of flagellar motility genes. Two-hybrid and gel mobility shift analyses indicated that the interaction between MogR and GmaR is temperature sensitive. Using circular dichroism and limited proteolysis, we determined that GmaR undergoes a temperature-dependent conformational change as temperature is elevated. Quantitative analysis of GmaR in Lm revealed that GmaR is degraded in the absence of MogR and at 37°C (when the MogR:GmaR complex is less stable). Since MogR represses transcription of all flagellar motility genes, including transcription of gmaR, changes in the stability of the MogR:GmaR anti-repression complex, due to conformational changes in GmaR, mediates repression or de-repression of flagellar motility genes in Lm. Thus, GmaR functions as a thermo-sensing anti-repressor that incorporates temperature signals into transcriptional control of flagellar motility. To our knowledge, this is the first example of a protein thermometer that functions as an anti-repressor to control a developmental process in bacteria.
兼性细菌病原体必须适应多种刺激才能在环境中生存或在宿主中建立感染。温度通常被用作控制感染所需的毒力基因或在环境中生存所需基因表达的信号。然而,对于细菌如何适应和响应温度波动的分子机制知之甚少。李斯特菌(Lm)是一种食源性病原体,是一种兼性细胞内病原体,它利用鞭毛运动在细胞外环境中生存,并在感染过程中增强对宿主细胞的初始入侵。进入宿主后,Lm 会响应哺乳动物生理温度(37°C)抑制鞭毛运动基因的转录,同时伴随温度依赖性的毒力基因上调。我们之前确定,鞭毛运动的下调对于毒力是必需的,并且由 MogR 转录抑制剂和双功能鞭毛反抑制剂/糖基转移酶 GmaR 的相互作用来调节。在这项研究中,我们确定 GmaR 也是一种蛋白质温度计,可控制鞭毛运动基因的温度依赖性转录。双杂交和凝胶迁移率改变分析表明 MogR 和 GmaR 之间的相互作用对温度敏感。使用圆二色性和有限蛋白酶解,我们确定 GmaR 随着温度升高发生温度依赖性构象变化。Lm 中 GmaR 的定量分析表明,在没有 MogR 和在 37°C 时(当 MogR:GmaR 复合物不太稳定时),GmaR 会被降解。由于 MogR 抑制所有鞭毛运动基因的转录,包括 gmaR 的转录,因此 GmaR 构象变化导致 MogR:GmaR 反抑制复合物稳定性的变化,介导 Lm 中鞭毛运动基因的抑制或去抑制。因此,GmaR 作为一种温度感应反抑制剂发挥作用,将温度信号纳入鞭毛运动的转录控制中。据我们所知,这是第一个作为反抑制剂发挥作用的蛋白质温度计的例子,可控制细菌中的发育过程。