Dawson Charlotte S, Garcia-Ceron Donovan, Rajapaksha Harinda, Faou Pierre, Bleackley Mark R, Anderson Marilyn A
Department of Biochemistry and Genetics, La Trobe Institute for Molecular Science. La Trobe University, Australia.
Department of Biochemistry, Cambridge Centre for Proteomics, Milner Therapeutics Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, Cambridge, UK.
J Extracell Vesicles. 2020 Apr 16;9(1):1750810. doi: 10.1080/20013078.2020.1750810. eCollection 2020.
Fungal extracellular vesicles (EVs) have been implicated in host-pathogen and pathogen-pathogen communication in some fungal diseases. In depth research into fungal EVs has been hindered by the lack of specific protein markers such as those found in mammalian EVs that have enabled sophisticated isolation and analysis techniques. Despite their role in fungal EV biogenesis, ESCRT proteins such as Vps23 (Tsg101) and Bro1 (ALIX) are not present as fungal EV cargo. Furthermore, tetraspanin homologs are yet to be identified in many fungi including the model yeast S. cerevisiae. We performed de novo identification of EV protein markers for the major human fungal pathogen Candida albicans with adherence to MISEV2018 guidelines. EVs were isolated by differential ultracentrifugation from DAY286, ATCC90028 and ATCC10231 yeast cells, as well as DAY286 biofilms. Whole cell lysates (WCL) were also obtained from the EV-releasing cells. Label-free quantitative proteomics was performed to determine the set of proteins consistently enriched in EVs compared to WCL. 47 proteins were consistently enriched in C. albicans EVs. We refined these to 22 putative C. albicans EV protein markers including the claudin-like Sur7 family (Pfam: PF06687) proteins Sur7 and Evp1 (orf19.6741). A complementary set of 62 EV depleted proteins was selected as potential negative markers. The marker proteins for C. albicans EVs identified in this study will be useful tools for studies on EV biogenesis and cargo loading in C. albicans and potentially other fungal species and will also assist in elucidating the role of EVs in C. albicans pathogenesis. Many of the proteins identified as putative markers are fungal specific proteins indicating that the pathways of EV biogenesis and cargo loading may be specific to fungi, and that assumptions made based on studies in mammalian cells could be misleading. A1 - ATCC10231; A9 - ATCC90028; DAY B - DAY286 biofilm; DAY Y - DAY286 yeast; EV - extracellular vesicle; Evp1 - extracellular vesicle protein 1 (orf19.6741); GO - gene ontology; Log(FC) - log(fold change); MCC - membrane compartment of Can1; MDS - multidimensional scaling; MISEV - minimal information for studies of EVs; sEVs - small EVs; SP - signal peptide; TEMs - tetraspanin enriched microdomains; TM - transmembrane; VDM - vesicle-depleted medium; WCL - whole cell lysate.
真菌细胞外囊泡(EVs)在某些真菌疾病的宿主-病原体和病原体-病原体通讯中发挥作用。由于缺乏特定的蛋白质标记物,如在哺乳动物EVs中发现的那些能够实现精密分离和分析技术的标记物,对真菌EVs的深入研究受到了阻碍。尽管ESCRT蛋白如Vps23(Tsg101)和Bro1(ALIX)在真菌EV生物发生中发挥作用,但它们并不作为真菌EV的货物存在。此外,在包括模式酵母酿酒酵母在内的许多真菌中尚未鉴定出四跨膜蛋白同源物。我们按照MISEV2018指南对主要人类真菌病原体白色念珠菌的EV蛋白标记物进行了从头鉴定。通过差速超速离心从DAY286、ATCC90028和ATCC10231酵母细胞以及DAY286生物膜中分离出EVs。还从释放EV的细胞中获得了全细胞裂解物(WCL)。进行了无标记定量蛋白质组学分析,以确定与WCL相比在EVs中持续富集的蛋白质组。47种蛋白质在白色念珠菌EVs中持续富集。我们将这些蛋白质细化为22种推定的白色念珠菌EV蛋白标记物,包括claudin样Sur7家族(Pfam:PF06687)的蛋白质Sur7和Evp1(orf19.6741)。选择了一组互补的62种EV缺失蛋白作为潜在的阴性标记物。本研究中鉴定出的白色念珠菌EV标记蛋白将成为研究白色念珠菌以及潜在其他真菌物种中EV生物发生和货物装载的有用工具,也将有助于阐明EVs在白色念珠菌致病机制中的作用。许多被鉴定为推定标记物的蛋白质是真菌特异性蛋白质,这表明EV生物发生和货物装载途径可能是真菌特有的,基于哺乳动物细胞研究做出的假设可能会产生误导。A1 - ATCC10231;A9 - ATCC90028;DAY B - DAY286生物膜;DAY Y - DAY286酵母;EV - 细胞外囊泡;Evp1 - 细胞外囊泡蛋白1(orf19.6741);GO - 基因本体;Log(FC) - 对数(倍数变化);MCC - Can1的膜区室;MDS - 多维标度法;MISEV - EVs研究的最小信息;sEVs - 小EVs;SP - 信号肽;TEMs - 富含四跨膜蛋白的微区;TM - 跨膜;VDM - 囊泡耗尽培养基;WCL - 全细胞裂解物