Abstract
Seasonal variations in the ex vivo phagocytic function of blood cells from tench, including ingestion capacity of inert particles and its destruction (microbicide capacity) assessed by measurement of superoxide anion production, were studied. Tench were maintained under natural conditions throughout the year, and the different assays of samples taken during each season were initially performed in vitro at 22°C and the results compared. Subsequently, assays were performed at the same temperature as that of the water ponds in which the fish were kept (“seasonal temperature”: 12°C in winter, 22°C in spring and autumn and 30°C in summer) and the results compared seasonally. The results at 22°C showed that phagocytic capacity was greatest in spring and summer and lowest in winter. However, when phagocytic capacity was measured at seasonal temperature, highest values appeared in winter and lowest in summer and autumn. Nitroblue tetrazolium reduction by tench phagocytes after phagocytosing latex beads demonstrated a similar seasonal behaviour at both 22°C in each season and at seasonal temperature. The highest values appeared in summer, which suggests a better microbicide capacity in this season. The results obtained in this study suggest that for a correct interpretation of ex vivo phagocytic capacity of fish through the year it is necessary to use the same assay temperature as that of the water in which the fish is kept.
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Abbreviations
- MS222:
-
tricaine methanesulphonate
- PBS:
-
phosphate-buffered saline
- NBT:
-
nitroblue tetrazolium
- PEI:
-
phagocytic efficiency index
- PP:
-
percent phagocytosis
References
Angelidis P, Baudin-Laurencin F (1988) Effects of temperature on chemiluminescence of phagocytes from sea bass, Dicentrarchus labrax L. J Fish Dis 11: 281–288
Ainsworth AJ, Dexiang C, Waterstrat PR, Greenway T (1991) Effect of temperature on the immune system of channel catfish (Ictalurus punctatus) I. Leucocyte distribution and phagocyte function in the anterior kidney at 10°C. Comp Biochem Physiol 100A: 907–912
Avtalion RR (1981) Environmental control of the immune response in fish. CRC Crit Rev. Environ Control 11: 163–188
Bodammer JE (1986) Ultrastructural observations on peritoneal exudate cells from the striped bass. Vet Immunol Immunopathol 12: 127–140
Collazos ME, Ortega F, Barriga C (1994) Effect of temperature on the immune system of a cyprinid fish (Tinca tinca, L). Blood phagocyte function at low temperature. Fish Shelfish Immunol 4: 231–238
De la Fuente M (1985) Changes in the macrophage funtion with aging. Comp Biochem Physiol 81: 955–938
Finco-Kent D, Thune RL (1987) Phagocytosis by catfish neutrophils. J Fish Biol 31: 41–49
Fujii T (1981) Antibody-enhanced phagocytosis of lamprey polymorphonuclear leucocytes against sheep erythrocytes. Cell Tissue Res 219: 41–51
Jørgensen J, Robertsen B, Engstad R (1991) Phagocytosis of yeat glucan particles by Atlantic salmon macrophages. Dev Comp Immunol 15 [Suppl 1]: S85
MacArthur JI, Fletcher TC (1985) Phagocytosis in fish. In: Manning MJ, Tatner MF (eds) Fish immunology. Academic Press, New York, pp 29–46
MacArthur JI, Fletcher TC, Pirie BJS, Davison RJL, Thomson AW (1984) Peritoneal inflammatory cells in plaice, Pleuronectes platessa L.: effects of stress and endotoxin. J Fish Biol 25: 69–81
MacArthur JI, Fletcher TC, Thomson AW (1983) Distribution of radiolabeled erythrocytes and the effect of temperature on clearance in the plaice (Pleuronectes platessa L). J Reticuloendothel Soc 34: 13–21
Olivier G, Eaton CA, Campbell N (1986) Interation between Aeromonas salmonicida and peritoneal macrophages of brook trout (Salvelinus fontinalis). Vet Immunol Immunopathol 12: 223–234
O'Neill JG (1985) An in vitro study of polymorphonuclear phagocytosis and the effect of temperature. In: Manning MJ, Tatner MF (eds) Fish immunology. Academic Press, New York, pp 47–55
Ozaki H, Ohwaki M, Fukada T (1983) Studies on lectins of amago (Oncorhynchus rhodurus) I. Amago ova lectin and its receptor on homologous macrophages. Dev Comp Immunol 7: 77–87
Parish N, Wrathmell A, Harris JE (1985) Phagocytic cells in the dogfish (Scyliorhinus canicula, L). In: Manning MJ, Tatner MF (eds) Fish immunology. Academic Press, New York, pp 71–83
Pedrera IM, Collazos ME, Ortega E, Barriga C (1992a) In vitro study of the phagocytic processes in splenic granulocytes of the tench (Tinca tinca, L). Dev Comp Immunol 16: 431–439
Pedrera IM, Rodriguez AB, Pariente JA, Collazos ME, Barriga C (1992b) Study of the non-specific immunological response of spring tench (Tinca tinca, L.). Fish Shellfish Immunol 2: 263–274
Pedrera IM, Rodriguez AB, Salido GM, Barriga C (1993) Phagocytic process of head kidney granulocytes of tench (Tinca tinca, L.). Fish Shellfish Immunol 2: 411–421
Plytycz B, Flory CM, Galvan I, Secombes CJ (1989) Leukocytes of rainbow trout (Oncorhynchus mykiss) pronephros: cell types producing superoxide anion. Dev Comp Immunol 13: 217–224
Rossi F (1986) The O 2− forming NADPH oxidase of the phagocytes: nature, mechanism of activation and function. Biochim Biophys Acta 853: 65–89.
Rowley A, Page M (1985) Ultrastructural, cytochemical and functional studies on the eosinophilic granulocytes of larval lampreys. Cell Tissue Res 240: 705–709
Scott AL, Klesius PH (1981) Chemiluminescence: a novel analysis of phagocytosis in fish. Develop Biol Standard 49: 243–254
Scott AL, Rogers WA, Klesius PH (1985) Chemiluminescence by peripheral blood phagocytes from channel catfish: function of opsonin and temperature. Dev Comp Immunol 9: 241–250
Secombes CJ (1990) Isolation of salmonid macrophages and analysis of their killing activity. In: Stolen JS et al (eds) Techniques in fish immunology. SOS Publications, New Jersey, pp 137–154
Secombes CJ, Chung S, Jeffries AH (1988) Superoxide anion production by rainbow trout macrophages detected by the reduction of ferricytochrome c. Dev Comp Immunol 12: 201–206
Secombes CJ, Fletcher TC (1992) The role of phagocytes in the protective mechanisms of fish. Annu Rev Fish Dis 2: 53–71
Siwicki AK (1989) Immunostimulating influence of levamisole on non-specific immunity in carp (Cyprinus carpio). Dev Comp Immunol 13: 87–91
Sniezko SF (1969) Cold-blooded vertebrate immunity to Metazoa. In: Jackson GJ et al (eds) Immunity to parasitic animals, Vol I. Appleton-Century Crofts, New York, pp 267–275
Sohnle PG, Chusid MJ (1983) The effect of temperature on the chemiluminescence response of neutrophils from rainbow trout and man. J Comp Pathol 93: 493–497
Thuvander A, Norrgren L, Fossum C (1987) Phagocytic cells in blood from rainbow trout, Salmo gairdneri (Richardson), characterized by flow cytometry and electron microscopy. J Fish Biol 31: 197–208
Zapata AG, Varas A, Torroba M (1992) Seasonal variations in the immune system of lower vertebrates. Immunol Today 13: 142–147
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Collazos, M.E., Barriga, C. & Ortega, E. Seasonal changes in phagocytic capacity and superoxide anion production of blood phagocytes from tench (Tinca tinca, L.). J Comp Physiol B 165, 71–76 (1995). https://doi.org/10.1007/BF00264688
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DOI: https://doi.org/10.1007/BF00264688