Notes: SYNOPSIS. Trichodina urinicola was found in newts, Triturus cristatus and T. taeniatus, in three localities in Czechoslovakia. The ciliate populations showed important differences on the basis of which they were separated as three new forms of this species: T. urinicola f. typica, T. urinicola f. bohemica, both from Triturus cristatus, and T. urinicola f. taeniatus from Triturus taeniatus. The great variability of trichodinids is evident from the literature as well as from our own observations, so that these new forms are to be regarded as provisional ones until it is possible to decide on the basis of a large number of observations the extent of specificity and variation of individual endozoic species of Trichodina. A detailed description of these forms is given as well as a comparison with the known species of trichodinids inhabiting the urinary tract of amphibians. A brief comment on the present taxonomy of the Urceolaridae in general is outlined.The need for a uniform description of these ciliates is emphasized; in connection with this, the taxonomic value of individual body characters is discussed. Special attention is paid to the adhesive disk of Trichodina, the structure of which is of greatest importance in the taxonomy of this group. On the basis of Dogel's and Fauré-Fremiet's descriptive methods employed in study of trichodinids, a proposal of a uniform description of Trichodina is made which involves all the important features of these protozoa.

Notes: . The first ultrastructural study of the actinosporean genus Triactinomyxon was carried out on Triactinomyxon legeri from the intestinal epithelium of Tubifex tubifex. The developmental cycle starts with bi- and uninucleate cells. We propose that these cells may be an early proliferative phase of the cycle and may unite to give rise to the four-cell stage, initiating pansporoblast formation. Valvogenic cells transform in the long stylus and anchor-like projections of the spore. In the capsulogenic cells, the primordium of the polar capsules originates as a simple, dense, club-shaped structure not observed in other actinosporeans. In all other respects, actinosporean ultrastructure follows more or less similar patterns. Comparison of actinosporean and myxosporean species gives evidence of considerable structural similarity, exemplified in both classes by the occurrence of cell junctions in their multicellular spores, identical polar capsules and their morphogenesis, cell-in-cell condition, pansporoblast formation, and presence of dense bodies (sporoplasmosomes) primarily in the sporoplasm. This unity of patterns speaks in favor of the postulated actinosporean-myxosporean transformation, which warrants further study.

Notes: . Ultrastructural studies on Eimeria (syn. Epieimeria) anguillae (Apicomplexa), parasite of the digestive tract of the eel, have shown that the development of this parasite takes place completely within the host cell. Merogony and gamogony are intracellular but in the epicytoplasmic position. Sporogony is also located within the epithelial cells, which agrees with assignment of this coccidian in the family Eimeriidae. However, depending on the intensity of infection and the physiopathological reaction of the host, the gamont may behave in two ways. 1) In massive infections, gamogony stages cause a genuine destruction of intestinal epithelium. Large numbers of gamonts form nodules and parts of the seriously destroyed epithelium peel off and are released into the lumen of the gut and quickly discharged into the outer environment. This discharged epithelium envelops cells containing immature oocysts that then sporulate outside the host. 2) In light infections, the host cells, which are necrotic due to the presence of a zygote, are pushed between the surrounding intact cells towards the base of the epithelium. Closely above its basal lamella, the oocyst then undergoes sporulation. These results show no taxonomically important biological features (e.g. special mode of implantation to the host cell or active movement of the zygote). Because the morphological characteristics of Epieimeria do not differ significantly from Eimeria, we propose to suppress the genus Epieimeria Dyková and Lom, 1981, and relegate its species into the genus Eimeria.

Notes: Heavy infections with enigmatic mobile organisms have recently been found in the blood of carp (Cyprinus carpio) in Central Europe. The organisms measure up to 15 μm, are variable in shape, and exhibit an unceasing twitching or dancing movement. Their developmental cycle starts with a primary cell enclosing a secondary cell. The former grows while the latter produces inside itself by a series of binary fissions and internal cleavages up to eight secondary cells, each of which encloses an inner (tertiary) cell of its own. In addition, up to four tiny cells with compact nuclei (“residual bodies”) also result from divisions of the secondary cells. Primary cells containing the products of the division of secondary cells finally disintegrate, releasing the secondary cells, which in their turn become new primary cells and repeat the cycle all over again. The structure and behavior of these organisms were so incompatible with existing ideas on myxosporean development that their myxosporean affinity was at first unrecognized. The final proof of their identity–appearance of myxosporean spores in sterile, experimentally infected hosts–is still to be presented. The interpretation of the myxosporean features of their life cycle (i.e., [1] the pericyte nature of the primary cell, [2] proliferation by disintegration of the pseudoplasmodial primary cell, [3] no rigidly fixed pattern in vegetative development), their ultrastructure (i.e., [1] characteristic bundles of microtubules and numerous free ribosomes in secondary cells, [2] lack of centrioles, [3] membranes enclosing the secondary cells within the primary cells), and facts on their epizootiology (i.e., [1] no success at transmission via leeches, [2] the occurrence of these organisms along with Sphaerospora renicola Dykova and Lom) suggest that they are stages of S. renicola from the kidney of carp. Similar mobile organisms were found in the blood of fry of two other fishes (Gobio gobi and Tinca tinca) which are also hosts for a Sphaerospora that infects the kidney. This suggests that these organisms represent an early phase in the developmental cycle in the genus Sphaerospora. The existence of cells enveloped one within the other (secondary and tertiary cells) in the developmental cycle, a characteristic myxosporean feature itself, is an intriguing parallel to similarly enclosed cells in sporogenesis of Paramyxea (Ascetospora).

Notes: Abstract Freshwater fish in Czechoslovakia were examined for species of the genus Sphaerospora Thélohan, 1892 and for myxosporean life cycle stages in the blood. In addition to perch infected with S. pectinacea Bocharova & Donets, 1974, renal tubules of seven host species harboured thus far unidentified Sphaerospora species. A new species, S. gobionis sp.nov. is described from renal tubules of Gobio gobio. In populations of Gobio gobio, Tinea tinea and Rutilus rutilus harbouring infections with different Sphaerospora species, organisms identified as mobile myxosporean life cycle stages were detected in the blood, where they undergo a proliferative cycle. These organisms were reminiscent of stages in the blood of common carp fingerlings, supposedly identical with Sphaerospora renicola Dyková & Lorn. It is possible that the blood stages found in the three cyprinid hosts represent stages of the life cycle of their respective Sphaerospora species. If this is correct, further studies may show if the presence of proliferative stages in the bloodstream is a character distinctive of the genus Sphaerospora.

Notes: Abstract. Eimeria branchiphila sp. nov. is described from the roach, Rutilus rutilus L., collected in Bulgaria. Sporulated oocysts were found in gill secondary lamellae and less frequently were associated with melano-macrophage centres in the spleen and in kidney interstitial tissue. In the gills, parasite cells identified as zygotes and sporulation stages were also encountered. This unusual site of sporulation represents a mechanism of sporocyst dispersal previously not recorded in fish coccidia.

Notes: Abstract. Histopathological studies on natural and experimental infections of nineteen microsporidian species from fishes distinguished two types of tissue reactions.The first type is characteristic of infections with xenoma-inducing microsporidian species and comprises three successive stages: a weakly reactive stage, a productive stage with the formation of granulomas and a stage of granuloma involution. Following the first stage, tissue reactions are directed towards the isolation of the parasite and result in its complete elimination and host tissue repair. The extent of pathological changes probably depends on the number of parasite cells which initiated the infection.The second type is represented by Pleistophora species infecting muscles or oocytes. Host tissue reaction is surprisingly slight during the schizogony and sporogony and does not tend to isolate the invaded muscle fibres. A slight lymphocytic infiltration of myosepta indicates the first stage of tissue reaction. The tissue reaction only reaches the productive stage when mature spores completely fill the contents of the infected muscle fibre. A thick wall of fibroblasts may be formed to demarcate the parasite mass as soon as it undergoes necrotic changes. The extent of pathological changes probably depends on the ability of early developmental stages of the parasite to spread the infection within the host.In both types of tissue reaction, the spores are destroyed by complete digestion within host phagocytic cells.

Notes: Abstract. Studies on an experimental infection of the stickleback (Gasterosteus aculeatus L.) with the microsporidian Glugea anomala conducted until day 126 post infection confirmed that xenoparasitic formations typical of the intracellular development of this microsporidian were responsible for a marked tissue reaction in the host. After a single oral infection, xenoparasitic formations developed in the subepithelial connective tissue of the glandular part of the stomach. The course of xenoma development was asynchronous. Up to the ‘cyst’ stage (xenomas filled with mature spores), their growth and development caused a pressure atrophy in the surrounding tissue. Later, the response to the presence of the xenoparasitic formation was the development of a granulomatous inflammatory reaction. Locally, the host responded to the infection by phagocytosis of mature spores by locally derived macrophages. In massive infections, changes occurred in the subepithelial connective tissue of the glandular part of the stomach (often the complete disappearance of tubular glands), which may result in a permanent influence on the function of this organ.

Notes: SYNOPSIS. Brooklynella hostilis is a new genus and new species of highly lethal Chilodonella-like parasite in the gills of marine fishes. It differs from other dysteriid ciliates by a combination of these features: 1) posterior-ventral adhesive apparatus consisting of a single glandular organelle that lacks a distinct discharging canal or podite; 2) the kinetosomes cover the entire ventral surface, except the left posterior portion of the body; the outer right kinety is divided into 2 segments; the middle postoral kinetyues as a row of kinetosomes without cilia around the glandular organelle; 3) there are never more than 9 nematodesmata; and 4), there are numerous small micronuclei. The lesions caused by the infection vary from a mild inflammatory reaction to extreme tissue damage resulting in severe hemorrhages, desquamation, and fusion of the gill lamellae.

Notes: SYNOPSIS. Morphogenesis, and the cortical structures of Brooklynella hostilis, a cyrtophorine gymnostome ciliate ectoparasitic on marine fishes, were studied from protargol silver-impregnated preparations and with the aid of electron microscopy. The pattern of morphogenesis of Brooklynella is close to that found in less differentiated species of the families Chlamydodontidae (e.g., in the genus Trithigmostoma) and Dysteriidae (e.g., in the genus Hartmanula). The full number of kineties in the opisthe is restored after division from a segment of the left one of the 3 kinetics producing the oral rows. The oral rows consist of a double row of kinetosomes arranged in a zig-zag pattern; only the outer row is ciliated, the inner one being barren. However, the positions of the postciliary and transverse fibers indicate that the oral rows are not homologs of an undulating membrane but are akin to a membranelle.In association with the ventral somatic kinetosomes there are 4 postciliary fibers; a rather aberrant, transversally oriented kinetodesma; 2 microtubular, transverse fibers plus a transverse fibrousspur; and one to several ribbons of subkinetal microtubular fibers. Not directly associated with the kinetosomes are fibrous strands running subpellicularly between the kinetosomes and also deep into the cytoplasm. The cortical structures of Brooklynella are compared with those of some other groups of ciliates of about the same phylogenetic level in which the subkinetal microtubules can also be found– rhynchodine, suctorian, and chonotrich ciliates.The nasse consists of 6–8 nematodesmata not closely associated with the microtubular cytopharyngeal tube. The former have a distinctly developed densely fibrous capitulum containing barren kinetosomes which originally produced the nematodesma during stomatogenesis; the capitulum is connected by a fibrous link to the microtubular shaft. Extending from the oral rows to the capitula are fibrous structures strongly reminiscent of filamentous reticulum in hymenostome and peritrich ciliates.The structure of the posterio-ventral glandular organelle is also described and discussed.