Small molecule inhibitors of Candida albicans biofilm formation

白色念珠菌生物膜形成的小分子抑制剂

• 批准号: 7455135
• 负责人: Jose L. Lopez-Ribot
• 金额: $ 16.97万
• 依托单位: UNIVERSITY OF TEXAS SAN ANTONIO
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-07-01 至 2010-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7455135
• 关键词: Acquired Immunodeficiency Syndrome; Address; Affect; Antibiotics; Antifungal Agents; Automation; Biological; Biological Assay; Biological Phenomena; Candida albicans; Candidiasis; Cells; Clinical; Complex; Defect; Development; Direct Costs; Dose; Drug Kinetics; Economics; Frequencies; Fungal Drug Resistance; Health; Health Care Costs; Hospitals; Host Defense; Human; Immune; Infection; Invaded; Laboratories; Length of Stay; Libraries; Microbial Biofilms; Microscopy; Modeling; Morbidity - disease rate; Nosocomial Infections; Organ; Organism; Patients; Phase; Phenotype; Preventive; Process; Public Health; Rate; Role; Screening procedure; Seeds; Severities; Site; Staging; Steroid therapy; Structure; Surface; Techniques; Testing; Tissue Transplantation; Tissues; analog; base; cancer therapy; candida biofilm; drug development; high throughput screening; inhibitor/antagonist; mortality; novel strategies; prevent; research study; response; small molecule; trait

DESCRIPTION (provided by applicant): Candidiasis represents now the fourth most frequent nosocomial infection in the US and worldwide and C. albicans remains the most frequent causative agent of candidiasis. Unfortunately these infections are associated with unacceptably high morbidity and mortality rates. A variety of manifestations of candidiasis are associated with biofilm formation on the surface of different types of surfaces. Biofilm formation carries important consequences since sessile cells in biofilms display phenotypic traits that are dramatically different from their planktonic counterparts, such as increased resistance to antifungal agents and protection from host defenses. Once established, biofilms have the potential to initiate or prolong infections by providing a safe reservoir from which organisms can invade local tissue, seed new infection sites, or resist eradication efforts. The net effect is that Candida biofilms adversely impact the health of these patients, with increasing frequency and severity, and with soaring economic sequelae. Therefore, the main objective of the proposed studies is to devise novel strategies to prevent C. albicans biofilm formation. To this end we will: i) use a phenotype-based approach based on the high throughput screening for small molecule compounds which inhibit C. albicans biofilm formation, and ii) characterize the biofilm-inhibitory effects of selected bioactive molecules identified as "hits" and "leads" during the initial screens. These assays take advantage of a simple, rapid, robust, accurate and highly reproducible microtiter-based model for the formation of Candida biofilms developed in this laboratory that is ideally suited for automation and high throughput applications. Small-molecule-based approaches provide powerful means to address experimentally challenging and complex biological phenomena, such as biofilm formation, while simultaneously identifying new potential targets for drug development. to public health: Biofilm formation has severe consequences for human health. The main idea behind this study is that by eliminating the ability of C. albicans to form biofilms, a substantial reduction in morbidity, mortality and extended hospital stay can be achieved while simultaneously reducing healthcare costs.

描述（由申请人提供）：念珠菌病现在是美国和全世界第四大最常见的医院感染，白色念珠菌仍然是念珠菌病最常见的病原体。不幸的是，这些感染伴随着令人无法接受的高发病率和死亡率。念珠菌病的多种表现与不同类型表面的生物膜形成有关。生物膜的形成具有重要的意义，因为生物膜中的无根细胞表现出与浮游细胞截然不同的表型特征，例如对抗真菌剂的抵抗力增强和对宿主防御的保护。一旦建立，生物膜有可能通过提供一个安全的储存库来启动或延长感染，生物体可以从该储存库侵入局部组织，播种新的感染位点，或抵抗根除努力。最终的结果是，念珠菌生物膜对这些患者的健康产生了不利的影响，其频率和严重程度都在增加，经济后遗症也在飙升。因此，提出的研究的主要目的是设计新的策略来防止白色念珠菌生物膜的形成。为此，我们将：i)使用基于表型的方法，基于高通量筛选抑制白色念珠菌生物膜形成的小分子化合物，ii)表征在初始筛选中被确定为“命中”和“先导”的选定生物活性分子的生物膜抑制作用。这些检测利用了一个简单、快速、稳健、准确和高度可重复的基于微滴的假丝酵母生物膜形成模型，该模型是本实验室开发的，非常适合自动化和高通量应用。基于小分子的方法提供了强大的手段来解决实验上具有挑战性和复杂的生物现象，如生物膜的形成，同时确定药物开发的新潜在靶点。对公众健康：生物膜的形成对人体健康有严重后果。这项研究背后的主要思想是，通过消除白色念珠菌形成生物膜的能力，可以大幅降低发病率、死亡率和延长住院时间，同时降低医疗成本。

项目成果

Addition of DNase improves the in vitro activity of antifungal drugs against Candida albicans biofilms.

• DOI: 10.1111/j.1439-0507.2011.02047.x
• 发表时间: 2012-01
• 期刊: Mycoses
• 影响因子: 4.9
• 作者: Martins M;Henriques M;Lopez-Ribot JL;Oliveira R
• 通讯作者: Oliveira R

A 96 well microtiter plate-based method for monitoring formation and antifungal susceptibility testing of Candida albicans biofilms.

• DOI: 10.3791/2287
• 发表时间: 2010-10-21
• 期刊: Journal of visualized experiments : JoVE
• 作者: Pierce, Christopher G;Uppuluri, Priya;Lopez-Ribot, Jose L
• 通讯作者: Lopez-Ribot, Jose L

Candida albicans biofilm chip (CaBChip) for high-throughput antifungal drug screening.

用于高通量抗真菌药物筛选的白色念珠菌生物膜芯片（CaBChip）。

• DOI: 10.3791/3845
• 发表时间: 2012
• 期刊: Journal of visualized experiments : JoVE
• 作者: Srinivasan,Anand;Lopez-Ribot,JoseL;Ramasubramanian,AnandK
• 通讯作者: Ramasubramanian,AnandK

Presence of extracellular DNA in the Candida albicans biofilm matrix and its contribution to biofilms.

• DOI: 10.1007/s11046-009-9264-y
• 发表时间: 2010-05
• 期刊: MYCOPATHOLOGIA
• 影响因子: 5.5
• 作者: Martins, Margarida;Uppuluri, Priya;Thomas, Derek P.;Cleary, Ian A.;Henriques, Mariana;Lopez-Ribot, Jose L.;Oliveira, Rosario
• 通讯作者: Oliveira, Rosario

An easy and economical in vitro method for the formation of Candida albicans biofilms under continuous conditions of flow.

• DOI: 10.4161/viru.1.6.13186
• 发表时间: 2010-11
• 期刊: Virulence
• 影响因子: 5.2
• 作者: Priya Uppuluri;J. Lopez-Ribot