TIR domain containing protein from Brucella melitensis

描述（由申请人提供）：布鲁氏菌是一种高度传染性的细胞内病原体，广泛存在于哺乳动物中，可引起流产、不孕和波状热。与其他细胞内病原体不同，布鲁氏菌不编码经典的毒力因子。然而，宿主细胞的慢性细胞内持久性表明，布鲁氏菌效应物可能与未识别的真核靶标相互作用，以改变细菌生存的细胞环境。关于布鲁氏菌蛋白有助于细菌毒力的信息很少，这表明迫切需要探索布鲁氏菌发病机制。本研究旨在描述一种新发现的布鲁氏菌蛋白的作用，该蛋白被称为TcpB，由BMEI1674编码，包含一个TIR结构域，并模仿toll样受体接头蛋白TIRAP的特性。TcpB有效阻断TLR2和TLR4介导的NF-？B激活并在细菌的毒力中起重要作用。我们的研究表明TcpB与磷脂酰肌醇（PtDIns）相互作用，并与质膜和细胞骨架网络共定位。我们假设TcpB- ptdins相互作用为TcpB提供了TLR特异性，但TcpB的bb环基序介导的TcpB-微管相互作用的意义尚不清楚。TcpB介导NF-?的确切机制B抑制尚不清楚，也没有关于布鲁氏菌分泌TcpB和TcpB从含布鲁氏菌液泡中逃逸的信息。根据我们的初步研究，TcpB除了抑制先天免疫应答外，还发挥着更广泛的作用。因此，本提案将详细描述TcpB，以揭示作用机制和细菌分泌。本建议的具体目标是：

DESCRIPTION (provided by applicant): Brucellae are highly infectious intracellular pathogens found in a wide range of mammals causing abortion, infertility and undulant fever. Unlike other intracellular pathogens, Brucella spp. do not encode classical virulent factors. However, chronic intracellular persistence in host cells indicates Brucella effectors likely interact with unidentified eukaryotic targets to modify the cellular environment for bacterial survival. Minimal information is available on Brucella proteins that contribute to bacterial virulence indicating an immediate need to explore the mechanisms of Brucella pathogenesis. This proposal aims to characterize the contribution of a newly identified Brucella protein, termed TcpB encoded by BMEI1674 that contains a TIR domain and mimics properties of the Toll-like receptor adaptor protein TIRAP. TcpB efficiently blocks TLR2 and TLR4 mediated NF-?B activation and plays a significant role in the virulence of the bacterium. Our studies indicated that TcpB interacts with phosphatidylinositols (PtDIns) and co-localizes with the plasma membrane and cytoskeleton network. We hypothesize that TcpB-PtDIns interaction provides TLR specificity for TcpB, but the significance of TcpB-microtubule interaction, mediated by the BB-loop motif of TcpB is unknown. The exact mechanism of TcpB mediated NF-?B suppression is not yet understood, and no information is available on the secretion of TcpB by Brucella and the escape of TcpB from Brucella containing vacuoles. Based on our preliminary studies, TcpB plays a broader role in addition to the suppression of innate immune response. Therefore the present proposal will characterize TcpB in detail to unravel the mechanisms of action and bacterial secretion. The specific aims of the present proposal are: Aim 1. To explore the detailed mechanism of TcpB mediated NF-?B suppression. Large-scale yeast-two hybrid screening will analyze TcpB interaction with unidentified mammalian proteins. Positive interactions will be confirmed by co-immunuprecipitation and co-sub-cellular localization experiments. Aim 2. To analyze the secretion of TcpB by Brucella melitensis and membrane penetration of TcpB. Secretion of TcpB by Brucella.melitensis will be analyzed in culture medium as well as in host cells. Western analysis of concentrated culture supernatant will be performed to test the secretion of TcpB. To analyze the secretion of TcpB inside the cells, a peptide tag-based (GSK-tag) reporter system over expressing TcpB-GSK will be used. To analyze the cell permeability purified TcpB protein will be incubated with mammalian cells and intracellular localized TcpB will be determined by western blotting. A cytokine ELISA will confirm that TcpB can enter host cells as well as demonstrate the suppression of cytokine by intracellular TcpB protein. Aim 3: To analyze the effect of TcpB on tubulin polymerization and TcpB mediated activation of small GTPases. To analyze the effect of TcpB on kinetics of tubulin assembly, fluorescent-based tubulin polymerization assays will be performed in the presence of purified TcpB or peptide harboring the BB-loop motif of TcpB that mediates microtubule interaction. The role of intact microtubules for TcpB mediated NF-?B suppression will be analyzed by reporter assays in the presence of the microtubule destabilizing agent nocodazole. To investigate the TcpB mediated activation of small GTPases, GTPase pull-down assays will be performed with the cell lysate transfected with TcpB. Phagocytosis assays will be performed to address whether TcpB mediated membrane ruffles and lamellipodia protrusions enhances phagocytosis. Our Preliminary Studies have identified a B. melitensis TIR domain containing protein, termed TcpB that possesses the ability to alter signaling events in host cells and disrupt innate immune mechanisms. Critical information gained from these specific aims will begin to bridge the gap between what we know about B. melitensis virulence and how virulence is regulated. PUBLIC HEALTH RELEVANCE: Our proposal will determine the effect of a TIR domain containing protein of Brucella melitensis that suppresses NF?B signaling as well as hijack the signaling pathway of Toll-Like Receptor proteins that possess an extracellular leucine-rich domain and a cytoplasmic domain referred to as Toll/IL-1R domain or TIR domain. Brucella spp. encode a TIR domain-containing protein (27 kDa) that can suppress the innate immune responses allowing the bacterium to successfully establish an intracellular niche. We are confident of achieving our project goals based on preliminary data that demonstrate our ability in each specific aim. We will first explore the detailed mechanism of TcpB mediated NF-?B suppression. This aim will identify the various host proteins that TcpB engages. Second, we will analyze the secretion of TcpB by Brucella melitensis and membrane penetration of TcpB. This aim will link the mechanism of TcpB transport from the bacterium to the internal environment of the cell. Third, we will analyze the effect of TcpB on tubulin polymerization and TcpB mediated activation of small GTPases. This aim will identify how TcpB disrupts cell architecture and potentially alters additional host signaling processes. We are confident of achieving these goals based on preliminary data that demonstrate our ability in each specific aim. The Problem: B. melitensis, a Gram-negative facultative intracellular bacterium, induces chronic infectious disease in humans and domestic animals. While an initial framework of several B. melitensis virulence traits has been documented, little is known about the mechanisms used by Brucella virulence associated proteins that permit an intracellular lifestyle. Now, we have preliminary data supporting a role for the Brucella protein TcpB to disrupt the very early steps of host cell response to this pathogen by disrupting the initial signaling events of innate immunity. Thus, pathogenic intracellular Brucella utilize a number of mechanisms to evade macrophage killing. Unfortunately, little is known regarding how any of these Brucella proteins function mechanistically to hijack host intracellular defenses. The Product: Our Preliminary Studies have identified a B. melitensis TIR domain containing protein, termed TcpB that possesses the ability to alter signaling events in host cells and disrupt innate immune mechanisms. Critical information gained from these specific aims will begin to bridge the gap between what we know about B. melitensis virulence and how virulence is regulated.