H2S production and virulence of Treponema denticola

齿垢密螺旋体的 H2S 产生和毒力

• 批准号: 6722461
• 负责人: LIANRUI CHU
• 金额: $ 20.59万
• 依托单位: UNIVERSITY OF TEXAS HLTH SCIENCE CENTER
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-09-01 至 2007-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6722461
• 关键词: Treponema; Treponema infection; affinity chromatography; bacterial proteins; clinical research; cysteine; enzyme activity; enzyme inhibitors; gene induction /repression; glutathione; high performance liquid chromatography; human subject; hydrogen sulfide; immunoelectron microscopy; laboratory mouse; laboratory rabbit; mass spectrometry; molecular cloning; nucleic acid sequence; oral bacteria; pathologic process; periodontitis; periodontium disorder; polymerase chain reaction; protein glutamine gamma glutamyltransferase; virulence; western blottings

DESCRIPTION: This application is an extension of current research examining the association between H2S production and virulence of Treponema denticola. T. denticola has been identified as an important member of a consortium of microorganisms as etiologic in the initiation and progression of periodontal diseases. In addition, the existence of volatile sulfur compounds produced at destructive sites is a characteristic feature of periodontal diseases, with H2S as a major compound in this family. Nevertheless, the metabolic pathways used to produce H2S are not well understood. Previous studies suggest that glutathione present in host cells can be a substrate for H2S production. Recently, we have shown that T. denticola has the capacity to utilize glutathione as a substrate to produce high levels of H2S. We have identified three enzymes that are required for the successful metabolism of glutathione: gamma-glutamyltransferase (GGT), cysteinylglycinase (CGase), and cystalysin. GGT converts glutathione into Cys-Gly and glutamic acid; CGase catalyze Cys-Gly to Cys and glycine; and cystalysin digests L-cysteine into H2S, ammonia, and pyruvate. We have also demonstrated that the addition of cystalysin and L-cysteine resulted in apoptosis of HGF and PDL cells and that glutathione was essential for lesion formation by T. denticola in an animal model. Based on these and other studies, three Specific Aims are proposed using biochemical, molecular genetic, and cell biologic studies to address the hypothesis that these three metabolic enzymes play a key role in T denticola pathogenesis. Specific Aim 1: To molecularly characterize the genes and proteins involved in converting glutathione to H2S. Specific Aim 2: To genetically characterize, by gene inactivation, the enzyme pathway of T. denticola that produces H2S from glutathione. Specific Aim 3: To measure the effects of the H2S/NH3 producing pathway on T. denticola virulence in vitro and in vivo. This application is designed to provide both seminal and critical information about the enzyme pathway of T. denticola to produce H2S from glutathione. The outcomes will elucidate the mechanisms of action that each member of the enzyme pathway plays in the virulence capacity of T. denticola.

描述：此应用是当前研究的扩展，该研究研究了H2S产生与treponema denticola的毒力之间的关联。在牙周疾病的启动和进展中，牙链球菌已被确定为微生物财团的重要成员。此外，在破坏性部位产生的挥发性硫化合物的存在是牙周疾病的一个特征，H2s是该家族的主要化合物。然而，用于产生H2S的代谢途径尚不清楚。先前的研究表明，存在于宿主细胞中的谷胱甘肽可能是H2S产生的底物。最近，我们已经表明，牙霉菌具有利用谷胱甘肽作为底物产生高水平H2s的能力。我们已经确定了谷胱甘肽成功代谢所需的三种酶：γ-谷氨酰转移酶（GGT），胱烷基甘油酶（CGASE）（CGASE）和Cystalysin。 GGT将谷胱甘肽转化为Cys-Gly和谷氨酸。 CGase将Cys-Gly催化为Cys和甘氨酸；囊肿蛋白将L-半胱氨酸消化成H2S，氨和丙酮酸。我们还证明，胱胱氨典蛋白酶和L-半胱氨酸的添加导致HGF和PDL细胞凋亡，并且谷胱甘肽在动物模型中对牙霉菌的病变形成至关重要。基于这些研究和其他研究，提出了三个特定目标，使用生化，分子遗传和细胞生物学研究提出，以解决这三种代谢酶在T牙本质发病机理中起关键作用的假设。具体目标1：分子表征与将谷胱甘肽转化为H2s的基因和蛋白质。特定目的2：通过基因失活而遗传表征牙霉菌的酶途径，从谷胱甘肽产生H2。具体目标3：测量H2S/NH3产生途径对体外和体内牙齿牙齿毒力的影响。该应用程序旨在提供有关牙霉菌的酶途径的精液和关键信息，以从谷胱甘肽产生H2s。结果将阐明酶途径的每个成员以牙霉菌的毒力能力发挥作用的作用机理。