{"title":"Cryptococcus neoformans Biofilm Formation and Quantification","authors":"Oscar Romero, Davier Gutierrez-Gongora, Jennifer Geddes-McAlister","doi":"10.1002/cpz1.70133","DOIUrl":null,"url":null,"abstract":"<p><i>Cryptococcus neoformans</i> is an opportunistic fungal pathogen that heads the Fungal Priority Pathogen List published by the World Health Organization (WHO) in 2022. This pathogen is a primary cause of death for immunocompromised individuals (e.g., those with HIV/AIDS, the elderly, immunotherapy recipients), causing approximately 118,000 deaths yearly worldwide. <i>C. neoformans</i> relies on virulence factors that include a polysaccharide capsule, melanin, extracellular enzymes, and thermotolerance to initiate and sustain host infection. Additionally, similar to other fungal pathogens (e.g., <i>Candida albicans</i>), <i>C. neoformans</i> may develop a biofilm organization linked to more persistent cryptococcal infections. Cryptococcal biofilms are highlighted in cases of cryptococcal meningitis, in which biofilm-like structures form that are highly resistant to host immune response and to antifungal therapies. In this regard, fungal biofilm formation has become an important area of study as a means to improve our understanding of the mechanisms regulating biofilm formation and infection and to advance the discovery of antibiofilm therapeutics. To assess biofilm properties and compare across treatments, quantification and evaluation of cell viability are important. Herein, we describe a standardized method to establish a cryptococcal biofilm and quantify total biomass and cell viability. © 2025 The Author(s). <i>Current Protocols</i> published by Wiley Periodicals LLC.</p><p><b>Basic Protocol 1</b>: Culturing and biofilm formation</p><p><b>Basic Protocol 2</b>: Biofilm quantification</p><p><b>Alternate Protocol</b>: Biofilm viability assay</p>","PeriodicalId":93970,"journal":{"name":"Current protocols","volume":"5 4","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cpz1.70133","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current protocols","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpz1.70133","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Cryptococcus neoformans is an opportunistic fungal pathogen that heads the Fungal Priority Pathogen List published by the World Health Organization (WHO) in 2022. This pathogen is a primary cause of death for immunocompromised individuals (e.g., those with HIV/AIDS, the elderly, immunotherapy recipients), causing approximately 118,000 deaths yearly worldwide. C. neoformans relies on virulence factors that include a polysaccharide capsule, melanin, extracellular enzymes, and thermotolerance to initiate and sustain host infection. Additionally, similar to other fungal pathogens (e.g., Candida albicans), C. neoformans may develop a biofilm organization linked to more persistent cryptococcal infections. Cryptococcal biofilms are highlighted in cases of cryptococcal meningitis, in which biofilm-like structures form that are highly resistant to host immune response and to antifungal therapies. In this regard, fungal biofilm formation has become an important area of study as a means to improve our understanding of the mechanisms regulating biofilm formation and infection and to advance the discovery of antibiofilm therapeutics. To assess biofilm properties and compare across treatments, quantification and evaluation of cell viability are important. Herein, we describe a standardized method to establish a cryptococcal biofilm and quantify total biomass and cell viability. © 2025 The Author(s). Current Protocols published by Wiley Periodicals LLC.
Basic Protocol 1: Culturing and biofilm formation
Basic Protocol 2: Biofilm quantification
Alternate Protocol: Biofilm viability assay
新型隐球菌生物膜的形成与定量
新型隐球菌是一种机会性真菌病原体,在世界卫生组织(世卫组织)2022年公布的真菌优先病原体清单中名列前茅。这种病原体是免疫功能低下者(例如艾滋病毒/艾滋病患者、老年人、免疫疗法接受者)的主要死亡原因,每年在全世界造成约118 000人死亡。新生C.依赖毒力因子,包括多糖胶囊、黑色素、细胞外酶和耐热性来启动和维持宿主感染。此外,与其他真菌病原体(如白色念珠菌)类似,新生假丝酵母菌可能形成与更持久的隐球菌感染相关的生物膜组织。隐球菌生物膜在隐球菌性脑膜炎病例中得到强调,其中形成的生物膜样结构对宿主免疫反应和抗真菌治疗具有高度抗性。在这方面,真菌生物膜的形成已经成为一个重要的研究领域,它可以提高我们对生物膜形成和感染的调节机制的理解,并促进抗生素治疗的发现。为了评估生物膜的特性和比较不同处理,细胞活力的量化和评估是很重要的。在这里,我们描述了一种标准化的方法来建立隐球菌生物膜和量化总生物量和细胞活力。©2025作者。当前方案由Wiley期刊有限公司出版。基本方案1:培养和生物膜形成;基本方案2:生物膜定量;备选方案:生物膜活力测定
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