A new myxosporean species, Trilosporoides platessae gen. et sp. n. (Multivalvulida), is described from the gallbladder of the plaice Pleuronectes platessa L. (Pleuronectidae) from Denmark. The myxospore of T. platessae is conical in side view, with a 24 µm long, pointed posterior projection. In apical view, the myxospore (diameter 9.4 µm) is round, trilobed and with three spherical polar capsules arranged peripherally, equidistant and opening peripherally through protruding tips. The polar capsules are of different sizes, one often larger than the others (diameter 3.3 µm vs. 2.5 µm). Apart from the long posterior projection, the myxospore of T. platessae differs from those of the three known species of Trilospora Noble, 1959 and from all genera within the order Multivalvulida Shulman, 1959 in the arrangement of the polar capsules. Trilosporoides platessae may temporarily be placed in the vicinity of the Trilosporidae.
The first ultrastructural description of Ceratomyxa tenuispora Kabata, 1960 (Myxozoa, Bivalvulida) from Madeira Island (Portugal), a parasite found in the gall bladder of the commercially important black-scabbard fish, Aphanopus carbo Lowe is presented. This parasite possesses spherical to ellipsoidal disporous trophozoites. Spores have a central crescent-shaped body averaging 11.0 µm in length, 28.5 µm in thickness and 12.1 µm in width. The valves have two long opposite lateral processes (ribbon-like structures or tails), each averaging 173 µm in length. The total thickness of the spore averages 375 µm. The spore has two sub-spherical polar capsules (∼5.2 × 4.1 µm), each with a polar filament with 7 to 8 coils. Some ultrastructural aspects of the sporogonic stages are described. The trophozoites develop without contact with epithelial cells. The cytoplasmic membrane has numerous evenly distributed external slender projections about 0.3 to 0.7 µm long. The sporogenesis produces two spores without pansporoblast formation. In the matrix of the capsular primordium, microtubules with an unusual organisation were observed. A binucleate sporoplasm that contains several sporoplasmosomes and dense bodies fills the spore cavity and extends to the tails without penetrating them.
Data on external ultrastructure of myxospores and internal ultrastructure of advanced pseudoplasmodia and myxospores of topotypic samples of Sphaerospora ranae (Morelle, 1929) from Rana dalmatina Bonaparte are provided, together with in situ hybridisation results. In both frogs examined, the infection was restricted to renal tubules and corpuscles. The infection site restriction was confirmed by light and transmission electron microscopy, as well as by in situ hybridisation. In addition, large myxospore masses measuring up to 500 μm were detected in seminal vesicles. Only late-sporogonic stages, i.e. pseudoplasmodia harbouring immature and/or mature myxospores, were observed and analysed. Scanning electron microscopy revealed that spores have smooth surface with exception of posterior valvular bulges, which possess numerous outwards opening internal canals. As revealed by both scanning and transmission electron microscopy, the canals are continuous invaginations of the outer spore surface. Myxospores of S. ranae are characterised by the presence of two uninucleate sporoplasms, bilayered polar capsules, S/H-shaped polar filaments in transversal section and multilayered polar filament eversion pole plugging complex. Ultrastructural observations are discussed in the context of available data for other species of Sphaerospora sensu stricto and apparent synchronisation of myxospore shedding with a brief aquatic breeding phase of vertebrate intermediate host is highlighted.