Flow cytometry and FACS applied to filamentous fungi

被引:54
作者
Bleichrodt, Robert-Jan [1 ]
Read, Nick D. [1 ]
机构
[1] Univ Manchester, Div Infect Immun & Resp Med, Manchester Fungal Infect Grp, CTF Bldg,46 Grafton St, Manchester M13 9NT, Lancs, England
关键词
FACS; Filamentous fungi; Flow cytometry; Fluorescence; Microcolony; Single cell; ASPERGILLUS-FUMIGATUS; GENOME SIZE; ANTIFUNGAL ACTIVITY; GLOMUS-INTRARADICES; BUDDING YEAST; ESSENTIAL OIL; CELL-WALL; IN-VITRO; BINDING; PROTEIN;
D O I
10.1016/j.fbr.2018.06.001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Flow cytometry is an automated, laser-or impedance-based, high throughput method that allows very rapid analysis of multiple chemical and physical characteristics of single cells within a cell population. It is an extremely powerful technology that has been used for over four decades with filamentous fungi. Although single cells within a cell population are normally analysed rapidly on a cell-by-cell basis using the technique, flow cytometry can also be used to analyse cell (e.g. spore) aggregates or entire microcolonies. Living or fixed cells can be stained with a wide range of fluorescent reporters to label different cell components or measure different physiological processes. Flow cytometry is also suited for measurements of cell size, interaction, aggregation or shape using non-labelled cells by means of analysing their light scattering characteristics. Fluorescence-activated cell sorting (FAGS) is a specialized form of flow cytometry that provides a method for sorting a heterogeneous mixture of cells into two or more containers based upon the fluorescence and/or light scattering properties of each cell. The major advantage of analysing cells by flow cytometry over microscopy is the speed of analysis: thousands of cells can be analysed per second or sorted in minutes. Drawbacks of flow cytometry are that specific cells cannot be followed in time and normally spatial information relating to individual cells is lacking. A big advantage over microscopy is when using FACS, cells with desired characteristics can be sorted for downstream experimentation (e.g. for growth, infection, enzyme production, gene expression assays or 'omits' approaches). In this review, we explain the basic concepts of flow cytometry and FACS, define its advantages and disadvantages in comparison with microscopy, and describe the wide range of applications in which these powerful technologies have been used with filamentous fungi. (C) 2018 Published by Elsevier Ltd on behalf of British Mycological Society.
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页码:1 / 15
页数:15
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