Basset Alan, Herd Muriel, Daly Raecliffe, Dove Simon L, Malley Richard
Division of Infectious Diseases, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Division of Infectious Diseases, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA
J Bacteriol. 2017 Jul 11;199(15). doi: 10.1128/JB.00078-17. Print 2017 Aug 1.
In , the type 1 pilus is involved in many steps of pathogenesis, including adherence to epithelial cells, mediation of inflammation, escape from macrophages, and the formation of biofilms. The type 1 pilus genes are expressed in a bistable fashion with cells switching between "on" and "off" expression states. Bistable expression of these genes is due to their control by RlrA, a positive regulator subject to control by a positive-feedback loop. The type 1 pilus genes are also thought to be negatively regulated by a large number of repressors. Here we show that expression of the type 1 pilus genes is thermosensitive and switched off at growth temperatures below 31°C. We also report that the on expression state of the type 1 pilus genes is highly stable, a phenomenon which we show likely contributed to the erroneous identification of many proteins as negative regulators of these genes. Finally, we exploited the effect of low temperature on pilus gene expression to help identify SP_1523, an Snf2-type protein, as a novel negative regulator of the pilus genes. Our findings establish that the type 1 pilus genes are thermoregulated and are repressed by a member of the Snf2 protein family. They also refute the notion that these genes are controlled by 8 previously described negative regulators. is the leading cause of death from respiratory infections in children. Many bacterial factors contribute to pneumococcal virulence and nasopharyngeal colonization. The type 1 pneumococcal pilus plays an important role in mouse models and in epithelial adherence and is expressed in a bistable fashion. Here we show that the "on" state is highly stable, which may explain the prior misidentification of negative regulators of pilus expression. We also show that expression of pilus genes is thermosensitive: virtually no expression can be detected at temperatures found in the anterior nares of humans. We took advantage of this property to identify a negative regulator of pilus expression, a member of a family of proteins widely conserved across Gram-positive bacteria.
在[具体情况未提及]中,1型菌毛参与了发病机制的多个步骤,包括黏附上皮细胞、介导炎症、逃避巨噬细胞以及生物膜形成。1型菌毛基因以双稳态方式表达,细胞在“开启”和“关闭”表达状态之间切换。这些基因的双稳态表达是由于它们受RlrA控制,RlrA是一种受正反馈回路调控的正调控因子。1型菌毛基因也被认为受到大量阻遏物的负调控。在此我们表明,1型菌毛基因的表达是温度敏感的,在低于31°C的生长温度下会关闭。我们还报告称,1型菌毛基因的开启表达状态高度稳定,我们发现这一现象可能导致许多蛋白质被错误鉴定为这些基因的负调控因子。最后,我们利用低温对菌毛基因表达的影响,帮助鉴定出一种Snf2型蛋白SP_1523作为菌毛基因的新型负调控因子。我们的研究结果表明,1型菌毛基因受到温度调节,并被Snf2蛋白家族的一个成员所抑制。它们还反驳了这些基因受8个先前描述的负调控因子控制的观点。[具体疾病未提及]是儿童呼吸道感染致死的主要原因。许多细菌因素导致肺炎球菌的毒力和鼻咽部定植。1型肺炎球菌菌毛在小鼠模型以及上皮黏附中发挥重要作用,并以双稳态方式表达。在此我们表明,“开启”状态高度稳定,这可能解释了先前对菌毛表达负调控因子的错误鉴定。我们还表明,菌毛基因的表达是温度敏感的:在人类前鼻孔的温度下几乎检测不到表达。我们利用这一特性鉴定出一种菌毛表达的负调控因子,它是革兰氏阳性菌中广泛保守的一个蛋白质家族的成员。