Bacterial Invasion and Trafficking within the Bladder

膀胱内的细菌入侵和贩运

• 批准号: 8461904
• 负责人: MATTHEW A MULVEY
• 金额: $ 35.02万
• 依托单位: UNIVERSITY OF UTAH
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-05-01 至 2016-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8461904
• 关键词: Actins; Acute; Adaptor Signaling Protein; Adhesives; Affect; Antibiotic Therapy; Bacteria; Bacterial Adhesins; Binding; Biological Assay; Biological Models; Bladder; Cell Culture Techniques; Cells; Chronic; Clathrin; Clathrin Adaptors; Co-Immunoprecipitations; Communicable Diseases; Complex; DNA Sequence Rearrangement; Data; Development; Epithelial Cells; Event; Family member; Gene Silencing; Growth Factor; Host Defense; Infection; Integration Host Factors; Integrins; Invaded; Kinesin; Knockout Mice; Life; Link; Mediating; Medical Economics; Microbial Biofilms; Microtubules; Motor; Mus; Nature; Organelles; Pathogenesis; Pilum; Process; Proteomics; Recurrence; Research; Rho-associated kinase; Role; Signal Transduction; Site; Testing; Therapeutic; Tissues; Urinary tract; Urinary tract infection; Uropathogenic E. coli; Work; base; cellular imaging; defined contribution; improved; in vivo; inhibitor/antagonist; insight; particle; pathogen; prevent; public health relevance; receptor; rho GTP-Binding Proteins; small molecule; trafficking; uptake

DESCRIPTION (provided by applicant): Strains of uropathogenic Escherichia coli (UPEC) are the principal causative agents of urinary tract infections (UTIs), which continuously rank among the most common of infectious diseases. UPEC can invade host bladder epithelial cells and subsequently multiply, forming large intracellular inclusions that resemble biofilms. Alternately, intracellular UPEC can persist at low levels in a more quiescent, non-replicating state that may serve as a reservoir for chronic and recurrent acute UTIs. Mounting evidence indicates that UPEC entry into host cells and tissues within the urinary tract promotes bacterial persistence in the face of both innate and adaptive host defenses, as well as antibiotic treatments. Virtually all UPEC isolates encode filamentous adhesive organelles called type 1 pili. We have found that the type 1 pilus adhesin FimH can engage host 1321 integrin receptors in a non-canonical fashion and thereby activate signaling cascades that result in the actin-dependent internalization of UPEC. Our preliminary data indicate that FimH-mediated bacterial invasion of host cells is dependent upon crosstalk between the actin and microtubule cytoskeletal networks, although the nature of this crosstalk remains undefined. The entry process also requires input from clathrin and distinct clathrin-associated adaptor proteins. Clathrin is best characterized for its role in the uptake of small molecules such as growth factors, but its ability to promote internalization of much larger particles like UPEC and other invasive pathogens has only recently been appreciated and remains poorly understood. The primary objectives of this application are to define the host factors that mediate UPEC invasion of bladder epithelial cells, with a focus on the functional roles of microtubule-actin crosstalk and clathrin. The impact that host cell invasion has on the establishment and persistence of UPEC within the host will also be assessed. It is hoped that the proposed work will provide a more complete understanding of the pathogenesis of acute, recurrent, and chronic UTIs, ultimately facilitating the development of improved therapeutics for treating and preventing these exceptionally common infections.

描述(申请人提供)：尿路致病性大肠杆菌(UPEC)菌株是尿路感染(UTIs)的主要病原体，尿路感染一直是最常见的传染病之一。UPEC可以侵袭宿主膀胱上皮细胞，随后增殖，形成类似生物膜的大型细胞内包涵体。或者，细胞内UPEC可以维持在较低的水平，处于更静止、非复制的状态，这可能是慢性和复发性急性尿路感染的储备库。越来越多的证据表明，UPEC进入尿路内的宿主细胞和组织可以促进细菌在面对固有和适应性宿主防御以及抗生素治疗时的持久性。几乎所有的UPEC分离株都编码丝状粘附性细胞器，称为1型菌毛。我们已经发现，1型粘附素FimH可以非规范的方式与宿主1321整合素受体结合，从而激活信号级联，导致肌动蛋白依赖的UPEC内化。我们的初步数据表明，FimH介导的细菌对宿主细胞的入侵依赖于肌动蛋白和微管细胞骨架网络之间的串扰，尽管这种串扰的性质仍然不确定。进入过程还需要网状蛋白和不同的网状蛋白相关的接头蛋白的输入。笼状蛋白最具特点的是它在吸收生长因子等小分子方面的作用，但它促进UPEC和其他侵袭性病原体等大得多的颗粒内化的能力直到最近才被认识到，而且仍然知之甚少。本应用的主要目的是确定介导UPEC对膀胱上皮细胞侵袭的宿主因素，重点是微管-肌动蛋白串扰和网状蛋白的功能作用。还将评估宿主细胞入侵对宿主内UPEC的建立和持久性的影响。希望拟议的工作将对急性、复发和慢性尿路感染的发病机制提供更全面的了解，最终促进改进的治疗方法的发展，以治疗和预防这些异常常见的感染。