Methodological aspects of assessing phagocytosis of Vibrio anguillarum by leucocytes of gilthead seabream (Sparus aurata L.) by flow cytometry and electron microscopy (original) (raw)

Abstract

In this paper we optimize a flow cytometric method for evaluating the phagocytic activity of leucocytes in gilthead seabream (Sparus aurata L.) and characterize the phagocytic cells observed. Optimal conditions were established for the fluorescein-labelling and analysis of the bacterium Vibrio anguillarum by flow cytometry. Head-kidney leucocytes were incubated with the heat-killed fluorescein isothiocyanate (FITC)-labelled bacteria for different periods, during which the kinetics of phagocytosis was studied. Attached and interiorized bacteria were distinguished. Although phagocytic ability reached a maximum after 60 min, phagocytic capacity reached its maximum at 20 min. The amount of ingested bacteria per phagocyte was estimated from the mean fluorescence of the leucocytes. Cytochalasin B or colchicine was used to inhibit phagocytosis. Monocyte-macrophages and acidophilic granulocytes showed phagocytic activity as demonstrated by transmission electron microscopy. In conclusion, the technique presented allows the screening of thousands of cells, and individual cell evaluation, by quantifying interiorized particles in fish phagocytes. Our ultrastructural results demonstrate that V. anguillarum is actively phagocytized by seabream macrophages and acidophilic granulocytes.

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Authors and Affiliations

  1. Department of Cell Biology, Faculty of Biology, University of Murcia, E-30100 Murcia, Spain Tel.: 34–68–307100; Fax: 34–68–363963; e-mail: meseguer@fcu.um.es, , , , , , ES
    M. A. Esteban, V. Mulero, J. Muñoz & J. Meseguer

Authors

  1. M. A. Esteban
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  2. V. Mulero
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  3. J. Muñoz
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  4. J. Meseguer
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Received: 21 July 1997 / Accepted: 7 January 1998

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Esteban, M., Mulero, V., Muñoz, J. et al. Methodological aspects of assessing phagocytosis of Vibrio anguillarum by leucocytes of gilthead seabream (Sparus aurata L.) by flow cytometry and electron microscopy.Cell Tissue Res 293, 133–141 (1998). https://doi.org/10.1007/s004410051105

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