Flow cytometry and FACS applied to filamentous fungi

被引:46
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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共 104 条
  • [1] Role of Trehalose Biosynthesis in Aspergillus fumigatus Development, Stress Response, and Virulence
    Al-Bader, Nadia
    Vanier, Ghyslaine
    Liu, Hong
    Gravelat, Fabrice N.
    Urb, Mirjam
    Hoareau, Christopher M. -Q.
    Campoli, Paolo
    Chabot, Josee
    Filler, Scott G.
    Sheppard, Donald C.
    [J]. INFECTION AND IMMUNITY, 2010, 78 (07) : 3007 - 3018
  • [2] QUANTITATIVE FLOW-CYTOMETRY - ANALYSIS OF PROTEIN DISTRIBUTIONS IN BUDDING YEAST - A MINIREVIEW
    ALBERGHINA, L
    PORRO, D
    [J]. YEAST, 1993, 9 (08) : 815 - 823
  • [3] Genome size variation in the pine fusiform rust pathogen Cronartium quercuum f.sp. fusiforme as determined by flow cytometry
    Anderson, Claire L.
    Kubisiak, Thomas L.
    Nelson, C. Dana
    Smith, Jason A.
    Davis, John M.
    [J]. MYCOLOGIA, 2010, 102 (06) : 1295 - 1302
  • [4] Weakening and delayed mortality of Fusarium oxysporum by heat treatment:: Flow cytometry and growth studies
    Assaraf, MP
    Ginzburg, C
    Katan, J
    [J]. PHYTOPATHOLOGY, 2002, 92 (09) : 956 - 963
  • [5] Conidial viability assay for rapid susceptibility testing of Aspergillus species
    Balajee, SA
    Marr, KA
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (08) : 2741 - 2745
  • [6] Determination of Mycotoxin Production of Fusarium Species in Genetically Modified Maize Varieties by Quantitative Flow Immunocytometry
    Banati, Hajnalka
    Darvas, Bela
    Feher-Toth, Szilvia
    Czeh, Arpad
    Szekacs, Andras
    [J]. TOXINS, 2017, 9 (02):
  • [7] High-throughput screening of filamentous fungi using nanoliter-range droplet-based microfluidics
    Beneyton, Thomas
    Wijaya, I. Putu Mahendra
    Postros, Prexilia
    Najah, Majdi
    Leblond, Pascal
    Couvent, Angelique
    Mayot, Estelle
    Griffiths, Andrew D.
    Drevelle, Antoine
    [J]. SCIENTIFIC REPORTS, 2016, 6
  • [8] F-Actin Dynamics in Neurospora crassa
    Berepiki, Adokiye
    Lichius, Alexander
    Shoji, Jun-Ya
    Tilsner, Jens
    Read, Nick D.
    [J]. EUKARYOTIC CELL, 2010, 9 (04) : 547 - 557
  • [9] USE OF FLOW-CYTOMETRY IN INDUSTRIAL MICROBIOLOGY FOR STRAIN IMPROVEMENT PROGRAMS
    BETZ, JW
    ARETZ, W
    HARTEL, W
    [J]. CYTOMETRY, 1984, 5 (02): : 145 - 150
  • [10] High-throughput FACS-based mutant screen identifies a gain-of-function allele of the Fusarium graminearum adenylyl cyclase causing deoxynivalenol over-production
    Blum, Ailisa
    Benfield, Aurelie H.
    Stiller, Jiri
    Kazan, Kemal
    Batley, Jacqueline
    Gardiner, Donald M.
    [J]. FUNGAL GENETICS AND BIOLOGY, 2016, 90 : 1 - 11