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新型隐球菌生物膜的形成与定量分析

Cryptococcus neoformans Biofilm Formation and Quantification.

作者信息

Romero Oscar, Gutierrez-Gongora Davier, Geddes-McAlister Jennifer

机构信息

Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada.

出版信息

Curr Protoc. 2025 Apr;5(4):e70133. doi: 10.1002/cpz1.70133.

DOI:10.1002/cpz1.70133
PMID:40279259
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12026377/
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.

摘要

新型隐球菌是一种机会性真菌病原体,在世界卫生组织(WHO)2022年发布的真菌重点病原体名单中位居榜首。这种病原体是免疫功能低下个体(如艾滋病病毒/艾滋病患者、老年人、接受免疫治疗者)死亡的主要原因,在全球范围内每年导致约11.8万人死亡。新型隐球菌依靠包括多糖荚膜、黑色素、细胞外酶和耐热性等毒力因子来引发和维持宿主感染。此外,与其他真菌病原体(如白色念珠菌)类似,新型隐球菌可能形成与更持久的隐球菌感染相关的生物膜结构。在新型隐球菌脑膜炎病例中,生物膜样结构的形成对宿主免疫反应和抗真菌治疗具有高度抗性,这突出了隐球菌生物膜的问题。在这方面,真菌生物膜的形成已成为一个重要的研究领域,作为一种手段来增进我们对调节生物膜形成和感染机制的理解,并推动抗生物膜疗法的发现。为了评估生物膜特性并比较不同处理方法,细胞活力的定量和评估很重要。在此,我们描述一种标准化方法来建立新型隐球菌生物膜并量化总生物量和细胞活力。© 2025作者。由Wiley Periodicals LLC出版的《当前方案》。基本方案1:培养和生物膜形成 基本方案2:生物膜定量 替代方案:生物膜活力测定

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0549/12026377/4dcb509280b0/CPZ1-5-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0549/12026377/477a37fdcb84/CPZ1-5-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0549/12026377/4dcb509280b0/CPZ1-5-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0549/12026377/477a37fdcb84/CPZ1-5-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0549/12026377/4dcb509280b0/CPZ1-5-0-g002.jpg

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本文引用的文献

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Global incidence and mortality of severe fungal disease.全球严重真菌感染的发病率和死亡率。
Lancet Infect Dis. 2024 Jul;24(7):e428-e438. doi: 10.1016/S1473-3099(23)00692-8. Epub 2024 Jan 12.
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Assessing the Putative Anticryptococcal Properties of Crude and Clarified Extracts from Mollusks.
评估贝类粗提物和澄清提取物的抗隐球菌特性。
J Vis Exp. 2022 Dec 2(190). doi: 10.3791/64540.
4
Cerebral Cryptococcomas: A Systematic Scoping Review of Available Evidence to Facilitate Diagnosis and Treatment.脑隐球菌瘤:促进诊断与治疗的现有证据的系统综述
Pathogens. 2022 Feb 3;11(2):205. doi: 10.3390/pathogens11020205.
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Combatting the evolution of antifungal resistance in Cryptococcus neoformans.抗新型隐球菌真菌感染的耐药性演变。
Mol Microbiol. 2020 Nov;114(5):721-734. doi: 10.1111/mmi.14565. Epub 2020 Jul 22.
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Basic principles of the virulence of .的毒力的基本原则。
Virulence. 2019 Dec;10(1):490-501. doi: 10.1080/21505594.2019.1614383.
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The Crucial Role of Biofilms in Cryptococcus neoformans Survival within Macrophages and Colonization of the Central Nervous System.生物膜在新型隐球菌于巨噬细胞内存活及中枢神经系统定植中的关键作用
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