This study reports light and electron microscopical aspects of a myxosporean found in the gills of the freshwater teleost Astyanax keithi Géry, Planquete & Le Bail, 1996 (family Characidae), collected from the estuarine region of the Amazon River, near Belém, Brazil. The prevalence of infection was 23%. In interlamellar spaces of the gills, ellipsoidal whitish cyst-like plasmodia structures were present, which contained spores. The spores had a spermatozoa-like appearance (47.8 ± 0.71 µm in total length) with a fusiform body (15.2 ± 0.77 µm in length, 5.7 ± 0.71 µm in width and 4.2 ± 0.31 µm in thickness), and each of the 2 valves presented a tapering tail (32.6 ± 1.11 µm in length). The valves surrounded a binucleate sporoplasm cell and 2 polar capsules (5.0 ± 0.13 µm in length, 1.5 ± 0.07 µm in width) that contained 8 to 9 coils of the polar filament. In the sporoplasm, several unique sporoplasmosomes were visible. A synoptic table of spore measurements of known Brazilian Henneguya species is presented. The spores differed from those of previously described species. Based on spore morphology, it is concluded that this species belongs to the family Myxobolidae, genus Henneguya, and that it constitutes a new species: H. astyanax n. sp. KEY WORDS: Ultrastructure · Henneguya · Myxozoa · Parasite · Teleost
Resale or republication not permitted without written consent of the publisherDis Aquat Org 53: [55][56][57][58][59][60] 2003 Henneguya astyanax n. sp., found in the gills of the Amazonian teleost fish Astyanax keithi (fam. Characidae).
MATERIALS AND METHODSA total of 30 specimens of the teleost fish Astynax keithi Géry, Planquete & Le Bail, 1996 (fam. Characidae), known by the Brazilian common name 'piaba transparente', were obtained from the estuarine region of the Amazon River (01°11' 30'' S, 47°18' 54'' W) near Belém, Brazil.Fragments of gill filaments, containing some cystlike plasmodia, were teased apart to release spores, which were observed by Nomarski differential interference contrast optics (DIC), for measurement and description.For transmission electron microscopy (TEM), isolated spores and fragments of cysts were fixed in 3% glutaraldehyde in 0.2 M sodium cacodylate buffer (pH 7.2) for 5 h at 4°C, washed overnight in the same buffer at 4°C, and postfixed in 2% OsO 4 buffered with the same solution for 4 h at the same temperature. Following ethanol-series and propylene oxide dehydration, samples were embedded in Epon. Semithin sections were stained with methylene blue-Azur II. Ultrathin sections were cut with a diamond knife, contrasted with uranyl acetate and lead citrate, and observed in a JEOL 100CXII TEM at 60 kV.
RESULTSThe parasites appeared as ellipsoidal whitish cystlike structures (~250 µm in size), located on the gills (Fig. 1) and composed of a mass of spores, each 47.8 µm in total length, possessing 2 refractile bodies (polar capsules). According to these criteria, the parasite belongs to the phylum Myxozoa (Lom & Noble 1984).The spores are spindle-shaped with 2 asymmetrical v...