Candida albicans responses to antifungals and cell wall stress

白色念珠菌对抗真菌药物和细胞壁应激的反应

• 批准号: 8824827
• 负责人: CORNELIUS J CLANCY
• 金额: --
• 依托单位: VETERANS HEALTH ADMINISTRATION
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-04-01 至 2018-09-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8824827
• 关键词: 3-Dimensional; Anidulafungin; Antibiotics; Antifungal Agents; Antifungal Therapy; Area; Attenuated; Candida; Candida albicans; Candidiasis; Caspofungin; Catheters; Cell Wall; Cell membrane; Cells; Chemotherapy-Oncologic Procedure; Clinical; Diagnostic tests; Disseminated candidiasis; Drug Exposure; Employee Strikes; Environment; Enzymes; Equilibrium; Failure; Fluorescence Recovery After Photobleaching; Fluorescence Resonance Energy Transfer; Fungal Drug Resistance; Gastrointestinal Surgical Procedures; Gene Expression; Goals; Guanine; Guanine Nucleotide Exchange Factors; Health; Host Defense; Human; In Vitro; Industrial fungicide; Infection; Intra-abdominal; Intravenous; Investigation; Kidney Failure; Life; Link; MAP Kinase Gene; Methods; Micafungin; Modeling; Molecular; Molecular Profiling; Morphogenesis; Mus; Nature; Neutropenia; Output; Pathogenesis; Pathway interactions; Patients; Pattern; Phosphatidylinositols; Phosphoric Monoester Hydrolases; Phosphotransferases; Predisposition; Process; Regulation; Research; Resistance; Risk Factors; Sepsis; Series; Signal Transduction; Site; Stress; Techniques; Time; Veterans; Virulence; Virulence Factors; candidemia; cellular imaging; effective therapy; glucan synthase; immunosuppressed; improved; in vivo; innovation; insight; mortality; mouse model; mutant; novel; pathogen; public health relevance; response; transcription factor; transcriptome sequencing

Candidemia, the fourth most common bloodstream infection in the U.S., and other forms of systemic candidiasis are associated with mortality rates of 40% or more despite treatment with antifungal agents. The Candida albicans cell wall is central to the pathogenesis of candidiasis, but mechanisms that link cell wall regulation and virulence are only beginning to be understood. Recently, we demonstrated that C. albicans rapidly delocalizes phosphatidylinositol-(4,5)-bisphosphate (PI(4,5)P2) and septins as part of the natural response to the cell wall-active antifungal caspofungin. Furthermore, we identified a novel C. albicans PI(4,5)P2-septin pathway that regulates cell wall integrity and virulence among mice with candidiasis. We hypothesize that the ability to activate or down-regulate the PI(4,5)P2-septin pathway as dictated by the environment (i.e., balanced regulation) is necessary for optimal C. albicans responses to cell wall stress during drug exposure or invasive candidiasis. The objectives of this project are to prove our balanced regulation hypothesis, validate the proposed PI(4,5)P2-septin pathway, and identify its outputs. We will pursue three specific aims. The first aim is to demonstrate that balanced PI(4,5)P2 regulation correlates with protective responses to caspofungin. Dynamic PI(4,5)P2 responses will be correlated with cellular viability in PI(4,5)P2- regulatory mutants and caspofungin-susceptible and -resistant C. albicans strains. The second aim is to establish interactions between PI(4,5)P2 and other PI(4,5)P2-septin pathway components during caspofungin exposure and invasive candidiasis. Interactions will be assessed by tracking components during time-lapse live cell imaging, demonstrating physical interactions, and visualizing interactions within cells by fluorescence resonance energy transfer (FRET). PI(4,5)P2 levels in pathway mutants will be directly correlated with PKC- MAPK cell wall integrity pathway activation. The third aim is to link transcription factors to the PI(4,5)P2-septin pathway, and identify transcriptional outputs and pathway targets that contribute to caspofungin responses and pathogenesis. Transcriptional outputs will be defined during intra-abdominal candidiasis of mice by using RNA-Seq, a largely unbiased method that comprehensively quantitates gene expression. The project employs a series of innovative techniques to study a novel pathway that is relevant to antifungal drug resistance and the pathogenesis of candidiasis. Therefore, it is likely to yield clinically useful insights that would not be obtained through other studies. Our findings will be significant because they will explain how the PI(4,5)P2-septin pathway governs cell wall integrity, echinocandin susceptibility and resistance, and pathogenesis, and place the pathway within the context of other regulators of these processes. The project will open new avenues of investigation that will define, in detail, the molecular and cellular mechanisms by which the PI(4,5)P2-septin pathway contributes to diverse types of candidiasis, and the impact of cell wall regulation on interactions with the host.

念珠菌病是美国第四大最常见的血液感染，以及其他形式的系统性感染