Selective Agents to Block Virulence in Gram-negative Pathogens

阻断革兰氏阴性病原体毒力的选择性药物

• 批准号: 8452688
• 负责人: ROBERT MARTIN BLUMENTHAL
• 金额: $ 21.26万
• 依托单位: UNIVERSITY OF TOLEDO
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-05-01 至 2015-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8452688
• 关键词: Adopted; Affect; Anabolism; Anti-Bacterial Agents; Antibiotic Resistance; Antibiotics; Bacterial Antibiotic Resistance; Bacterial Infections; Bioinformatics; Cause of Death; Cessation of life; Complement; Developed Countries; Development; Disease; Effectiveness; Enzymatic Biochemistry; Enzymes; Genes; Goals; Gram-Negative Bacteria; Growth; Health Care Costs; Human; Infection; Infectious Agent; Lead; Libraries; Ligase; Measures; Metabolic Pathway; Metabolism; Methionine; Methods; Microbial Biofilms; Molecular Target; Morbidity - disease rate; Natural Immunity; Organism; Orthologous Gene; Pathogenesis; Pharmaceutical Preparations; Phase; Positioning Attribute; Production; Property; Reporter Genes; Research; Resistance; Signal Pathway; Signal Transduction; Testing; Therapeutic Intervention; Validation; Viola; Virulence; Virulence Factors; Wages; War; Work; analog; bacterial resistance; design; experience; high throughput screening; inhibitor/antagonist; innovation; killings; meetings; methyl group; microbial; mortality; pathogen; pathogenic bacteria; pressure; prevent; programs; promoter; quorum sensing; response; screening; selective prevention; weapons

DESCRIPTION (provided by applicant): The spectacular rise of bacterial antibiotic resistance is a serious problem, particularly among Gram-negative pathogens, increasing morbidity, mortality and healthcare costs. Despite over a century of intense effort focused on killing pathogenic bacteria, these organisms have developed and shared increasingly inventive ways to overcome the best drugs we have been able to produce. There is growing evidence that a different approach, aimed at inhibiting virulence without inhibiting growth per se, can prevent or cure disease without inevitably leading to resistance. Our long term goal is to develop approaches that will selectively prevent the onset of virulence in bacterial pathogens. Our objective for this application is to develop selective inhibitors that block virulence and inhibit biofilm formation in Gram-negative human pathogens without otherwise interfering with their growth. Our central hypothesis is that biosynthesis of the quorum sensing (QS) molecules that trigger a virulence response can be selectively inhibited, without affecting the essential aspects of bacterial metabolism, by altering the common precursor for these QS molecules. Because these organisms will remain viable, but functionally avirulent, there will be much weaker selective pressure for resistance to QS inhibition. We plan to accomplish our project goals through the following complementary initial specific aims: (1) design and test alternative substrates and inhibitors for target enzymes that selectively block the production of QS molecules; and (2) use a new screening method to identify QS inhibitors on a broader scale. Once these aims have been achieved we will move to Phase II of this project, which involves: (1) focusing our quorum sensing inhibitor development towards specific pathogenic species; and (2) testing the ability of these inhibitors to synergistically increase the effectiveness of currently used antibiotics. The contribution of our proposed research will be the development of an approach that leads to new drugs while minimizing selection for bacterial resistance. This work is significant because it is designed to validate an alternative approach that does not rely on microbial death to overcome bacterial infections.

描述（由申请人提供）：细菌抗生素耐药性的急剧上升是一个严重的问题，特别是在革兰氏阴性病原体中，增加了发病率、死亡率和医疗保健成本。尽管世纪以来人们一直在努力杀死致病菌，但这些生物体已经开发并分享了越来越多的创造性方法，以克服我们能够生产的最好的药物。越来越多的证据表明，一种不同的方法，旨在抑制毒力而不抑制生长本身，可以预防或治愈疾病，而不会不可避免地导致耐药性。我们的长期目标是开发选择性预防细菌病原体毒力发作的方法。本申请的目的是开发选择性抑制剂，其阻断革兰氏阴性人类病原体中的毒力并抑制生物膜形成，而不干扰其生长。我们的中心假设是，生物合成的群体感应（QS）分子，触发毒力反应，可以选择性地抑制，而不影响细菌代谢的基本方面，通过改变这些QS分子的共同前体。由于这些微生物将保持活力，但功能上无毒，因此对QS抑制的抗性的选择压力要弱得多。我们计划通过以下互补的初始具体目标来实现我们的项目目标：（1）设计和测试选择性阻断QS分子产生的靶酶的替代底物和抑制剂;（2）使用新的筛选方法在更广泛的范围内识别QS抑制剂。一旦这些目标实现，我们将进入该项目的第二阶段，其中包括：（1）将我们的群体感应抑制剂开发集中在特定的致病物种上;（2）测试这些抑制剂协同提高目前使用的抗生素有效性的能力。我们提出的研究的贡献将是开发一种方法，导致新的药物，同时尽量减少细菌耐药性的选择。这项工作意义重大，因为它旨在验证一种不依赖微生物死亡来克服细菌感染的替代方法。