Al-2-Dependent Quorum Sensing in the Gram-Positive Bacterium Streptococcus pyogen

革兰氏阳性菌化脓性链球菌中 Al-2 依赖性群体感应

• 批准号: 7404446
• 负责人: MICHAEL J FEDERLE
• 金额: $ 1.13万
• 依托单位: PRINCETON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-04-15 至 2008-05-15
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7404446
• 关键词: Bacteria; Behavior; Binding; Biochemical; Cell Communication; Cell Fractionation; Cell Signaling Process; Cell physiology; Cells; Chemicals; Cysteine Protease; Detection; Development; Endopeptidases; Fluorescence-Activated Cell Sorting; Gene Targeting; Genes; Genetic; Goals; Gram-Positive Bacteria; Green Fluorescent Proteins; Hemolysin; Libraries; Monitor; Mutagenesis; Peptide Hydrolases; Population Density; Production; Proteins; Radiolabeled; Research; Role; Signal Transduction; Signaling Molecule; Streptococcus; Streptococcus pyogenes; Structure; Virulence; X-Ray Crystallography; antimicrobial; novel; pathogen; promoter; quorum sensing; radiotracer; receptor; tool

DESCRIPTION (provided by applicant): Quorum sensing is a cell-cell communication process by which bacteria regulate behaviors as a function of cell population density. Quorum sensing involves the production, secretion, and detection of signal molecules termed autoinducers. While most autoinducers are highly specific for the species of bacteria that produces them, one autoinducer, termed AI-2, is produced and detected by many species, and functions as an interspecies signaling molecule. AI-2 is known to regulate numerous functions in Gram-positive bacteria, but in these cases, the AI-2 signaling cascade has not been investigated. The research in this proposal aims to define the role of AI-2 and the AI-2 signal transduction cascade in the Gram-positive pathogen Streptococcus pyogenes. To achieve these goals, I will develop genetic tools and use them to identify and characterize the S. pyogenes AI-2 quorum sensing signal transduction circuit, identify quorum sensing target genes, and determine the chemical moiety that functions as the S. pyogenes AI-2 signal. It has been a long-standing goal in the quorum sensing field to control bacterial virulence by manipulating cell-cell communication. Results from this research will contribute to the development of such novel antimicrobial therapies. The specific aims are: (1) Identify the luxS/AI-2 quorum sensing signal transduction circuit. AI-2 controls production of SLS (hemolysin) and SpeB (cysteine protease) which are required for S. pyogenes virulence. Transposon mutageneses, followed by screens for altered production of hemolysin and protease will be used to identify genes required for AI-2 detection and signal transduction. (2) Identify genes regulated by AI-2. A library of random S. pyogenes promoters fused to a gfp gene, optimized for Gram-positive bacteria, will be constructed and introduced into a luxS S. pyogenes strain. Altered GFP production will be monitored by fluorescence activated cell sorting (FACS) following exogenous addition of synthetically prepared AI-2. This screen should identify AI-2-activated and AI-2-repressed genes. (3) Determine the structure of the S. pyogenes AI-2 receptor and AI-2 molecule. A biochemical approach complementary to that in aim 1 will employ radiolabeled AI-2 and cell fractionation to identify the S. pyogenes Al-2 receptor. The gene encoding the receptor will be cloned and the protein expressed and purified. X-ray crystallography will be used to determine the structure of all or a portion of the receptor with and without bound AI-2.

描述（由申请人提供）：群体感应是一种细胞-细胞通信过程，细菌通过该过程调节作为细胞群体密度的函数的行为。群体感应包括产生、分泌和检测称为自身诱导物的信号分子。虽然大多数自诱导物对产生它们的细菌物种具有高度特异性，但一种称为AI-2的自诱导物由许多物种产生和检测，并作为种间信号分子发挥作用。已知AI-2调节革兰氏阳性细菌中的许多功能，但在这些情况下，AI-2信号级联尚未被研究。本研究旨在明确AI-2在革兰氏阳性病原体化脓性链球菌中的作用以及AI-2信号转导级联。为了实现这些目标，我将开发遗传工具，并使用它们来识别和表征S。化脓性链球菌AI-2群体感应信号转导通路，鉴定群体感应靶基因，并确定作为S.化脓性链球菌AI-2信号。通过调控细胞间的通讯来控制细菌的毒力是群体感应领域的一个长期目标。这项研究的结果将有助于这种新型抗菌疗法的发展。具体目的是：（1）确定luxS/AI-2群体感应信号转导通路。AI-2控制S.化脓菌毒力转座子诱变，然后筛选溶血素和蛋白酶的产生改变，将用于鉴定AI-2检测和信号转导所需的基因。(2)识别AI-2调控的基因。随机S.将构建与gfp基因融合的化脓性链球菌启动子，并将其导入luxS S。化脓性链球菌在外源性添加合成制备的AI-2后，通过荧光激活细胞分选（FACS）监测改变的GFP产生。这个屏幕应该确定AI-2激活和AI-2抑制基因。(3)确定了S.化脓性链球菌AI-2受体和AI-2分子。与目标1互补的生物化学方法将采用放射性标记的AI-2和细胞分级分离来鉴定S。化脓性链球菌Al-2受体将克隆编码受体的基因，并表达和纯化蛋白质。X射线晶体学将用于确定具有和不具有结合的AI-2的受体的全部或一部分的结构。