Location and morphological identification of Myxosporida and evaluation of the effect of freezing and Giemsa staining on the spore length

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Veröffentlicht: Nov 17, 2017
DOI: https://doi.org/10.12681/jhvms.14913
K. GATZIA (Κ. ΓΚΑΤΖΙΑ)
Laboratory of Ichthyology and Aquatic Animal Health, Faculty of Veterinary Medicine, University of Thessaly
E. TZIRONI (Ε. ΤΖΙΡΩΝΗ)
Laboratory of Ichthyology and Aquatic Animal Health, Faculty of Veterinary Medicine, University of Thessaly
K. BITCHAVA (Κ. ΜΠΙΤΧΑΒΑ)
Laboratory of Ichthyology and Aquatic Animal Health, Faculty of Veterinary Medicine, University of Thessaly
F. ATHANASSOPOULOU (Φ. ΑΘΑΝΑΣΟΠΟΥΛΟΥ)
Laboratory of Ichthyology and Aquatic Animal Health, Faculty of Veterinary Medicine, University of Thessaly
Abstract

Enteromyxum leei, Ceratomyxa spp., Polysporoplasma spans are myxosporea usually found in cultured Mediterranean marine fish. The present study refers to the evaluation of the seasonality and prevalence caused by myxosporea infections in cultured sharpsnout seabream (Puntazzo puntazzo C.) and gilthead seabream {Spams aurata L.). The main target organ of all infected fish was the intestine and some-times the gallbladder and the kidney were also target organs. The highest prevalence was observed during summer in cultured sharpsnout seabream. P. sparis has been observed in gilthhead seabream, which proved to be the main host of this parasite, but it was also observed in cultured sharpsnout seabream. The main target organ in all infected fish was the kidney. The highest prevalence was observed during summer in cultured gilthead seabream. Mature spores of Ceratomyxa diplodae were observed in sharpsnout seabream. The main target organ of the parasite in cultured fish was the gallbladder. The morphology and size observations of myxosporeans mentioned above were also studied. Freezing in -20 °C (for 1 and 6 months) and the effect of Giemsa staining in myxosporean mature spore's size were evaluated. According to the results, 6 months freezing and Giemsa staining reduced significantly the size of mature spores. Finally, the protocol for Giemsa staining for the three different myxosporea species, usually found in cultured mediterranean marine fish, was standardized. Fresh smears were stained by Giemsa, according to protocol used for fresh smears. For E. leei the best results were obtained after immersing the smears in the stain for 20 min, for C diplodae after immersing the smears in the stain for 30 min and for P. sparis after immersing the smears in the stain for 24 min.

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