Studies on the Pseudomonas aeruginosa cell-to-cell signal PQS

铜绿假单胞菌细胞间信号PQS的研究

• 批准号: 7348539
• 负责人: EVERETT C PESCI
• 金额: $ 32.18万
• 依托单位: EAST CAROLINA UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-12-01 至 2012-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7348539
• 关键词: Address; Age; Animals; Antibiotic Resistance; Antibiotics; Arylformamidase; Bacteria; Binding; Biochemical; Biological Assay; Caenorhabditis elegans; Cell Communication; Cells; Characteristics; Charcoal; Chronic; Complex; DNA; Data; Development; Dextrans; Electrophoretic Mobility Shift Assay; Environment; Future; Gel; Gene Cluster; Gene Expression; Gene Expression Profiling; Gene Structure; Genes; Goals; Human; Infection; Insecta; Kinetics; Kynurenine; Learning; Link; Lung; Maps; Methods; Modeling; Mutation; Nosocomial Infections; Organism; Pathway interactions; Plants; Polymerase Chain Reaction; Primer Extension; Production; Property; Proteins; Pseudomonas; Pseudomonas aeruginosa; Quinolones; Range; Regulation; Reporter; Research; Resistance development; Respiratory physiology; Role; Signal Transduction; Site; System; Testing; Therapeutic Intervention; Time; Virulence; analog; antimicrobial; cystic fibrosis patients; dextran; enzyme substrate; inhibitor/antagonist; interest; mutant; novel; pathogen; research study

DESCRIPTION (provided by applicant): Pseudomonas aeruginosa is responsible for approximately 10% of the hospital-acquired infections in the U.S., and causes a chronic, debilitating lung infection in most cystic fibrosis patients. Adding to the significance of these infections is the fact that this organism is capable of rapidly developing resistance to many antibiotics, which significantly limits treatment options. While the need for novel antimicrobial treatments has been pressing for years, the development of useful new antibiotics has been difficult. One promising line of research has centered on the cell-to-cell signaling systems used by bacteria to control many functions, including virulence. P. aeruginosa uses three different intercellular signaling systems to coordinate gene expression and the topic of this proposal is the signal 2-heptyl-3-hydroxy-4-quinolone [referred to as the Pseudomonas Quinolone Signal (PQS)]. PQS is required for virulence in plants, insects, and animals and is produced in the lungs of cystic fibrosis patients who are infected by P. aeruginosa. Our plan is to complete experiments that will help us to better understand the significance of PQS in P. aeruginosa cell-to-cell signaling and virulence. We propose focused experiments that will address how PQS activates genes, and the mechanisms behind its synthesis. The long term goal of this research is to develop methods that interfere with PQS signaling. We believe that the PQS signaling system and the components required for its proper function will provide targets at which to aim future therapeutic interventions that will decrease P. aeruginosa virulence.

描述（由申请人提供）：铜绿假单胞菌是美国约10%的医院获得性感染的原因，并在大多数囊性纤维化患者中引起慢性、使人衰弱的肺部感染。增加这些感染的重要性是，这种生物体能够迅速对许多抗生素产生耐药性，这大大限制了治疗选择。虽然对新型抗菌治疗的需求多年来一直很迫切，但开发有用的新抗生素一直很困难。一个有希望的研究方向集中在细菌用来控制包括毒力在内的许多功能的细胞间信号系统上。铜绿假单胞菌使用三种不同的细胞间信号传导系统来协调基因表达，本提案的主题是信号2-庚基-3-羟基-4-喹诺酮[称为假单胞菌喹诺酮信号（PQS）]。PQS是植物、昆虫和动物中的毒力所必需的，并且在被铜绿假单胞菌感染的囊性纤维化患者的肺中产生。我们的计划是完成实验，这将有助于我们更好地了解PQS在铜绿假单胞菌细胞间信号传导和毒力中的意义。我们提出了重点实验，将解决如何PQS激活基因，其合成背后的机制。这项研究的长期目标是开发干扰PQS信号传导的方法。我们相信，PQS信号系统及其正常功能所需的组分将为未来降低铜绿假单胞菌毒力的治疗干预提供目标。