Schellackia ptyodactyli sp. n. is described from the fan-footed gecko Ptyodactylus hasselquistii (Donndorf) found the lower Jordan Valley, Cis-Jordan. Endogenous development was studied in geckoes necropsied 7-11 days after being inoculated with blood containing sporozoites from naturally infected geckoes of the same species. Merogony and gamogony/oogony stages, as well as sporozoites, are described by light and electron microscopy. Merogony stages, microgamonts and sporozoites conformed in fine structure to that of other eimerian coccidia. whereas wall forming bodies of the macrogamonts showed some divergence from the general pattern characteristic of eimerians and Schellackia cf. agamae. Merogony stages occurred simultaneously with gamonts and sporozoites. In the blood, sporozoites entered leucocytes, thrombocytes and erythrocytes. Parasitaemia persisted for up to 2 years in some naturally infected geckoes in captivity.
Spermiogenesis and the spermatozoon were studied in the digenean Mesocoelium monas Rudolphi, 1819 (from the toad Bufo sp. in Gabon). An ultrastructural study revealed that spermiogenesis follows the usual pattern found in digeneans, i.e. proximo-distal fusion of axonemes with a median cytoplasmic process followed by elongation. The spermatozoon has two fully incorporated axonemes with the 9 +“1” trepaxonematan pattem. Indirect immunofluorescence localization of tubulin and fluorescent labelling of the nucleus were used to obtain additional information on the structure of the spermatozoon. It was thus shown that one of the axonemes is slightly shorter than the other (190 versus 220 pm) and that the filiform nucleus (65 pm in length) is located at the distal extremity of the spermatozoon (220 pm in length). Various monoclonal and polyclonal antibodies, specific to alpha, beta, acetylated-alpha, or general tubulin, were used and produced similar labelling.
The ultrastructural cytology and reproduction of Amphiacantha longa Caullery et Mesnil, 1914 is described. Mcrogonial reproduction was not observed. The sporogony follows two lines: free disporoblastic. and enveloped, polysporoblastic, involving sporoblast mother cells. The enveloped sporogony is endogenous in spore sacs of sporont origin, daughter cells are formed by vacuolation. Probably all stages have coupled nuclei. Both free and enveloped spores are equipped with an extrusion apparatus composed of a flat polar sac, a straight polar filament of manubrium type, and a posterior globular appendix. Manubrium and appendix are enclosed in a membraneous coat. Circular elements of coat material occur in the proximity of the extrusion apparatus. The membraneous coat and the surface layer of the manubrium penetrate the polar sac. The extrusion apparatus is located at the wide pole of the spore, the nuclei at the narrower pole. Hosts are gregarines of the genus Lecudina Mingazzini, living in the gut of the polychaete Lumbrinereis fragilis (O. F. Muller). The cytology and reproduction are discussed and compared to other genera of metchnikovellideans, to the chytridiopsid genera, and to microsporidia expressing the typical cytology for the group. Metchnikovellideans and chytridiopsids exhibit cytological and reproductive similarities. The species is redescribed, the diagnosis of the genus Amphiacantha Caullery et Mesnil, 1914 is emended, and the new family Amphiacanthidae, comprising the genera Amphiacantha and Amphiamblys Caullery et Mesnil, 1914, is established.
The anterior jejunum from common vole naturally infected with Giardia microti (Kofoid et Christiansen, 1915) was examined by ТЕМ and compared with the anterior jejunum from control (metronidazole-treated, Giardia-free) common voles (Pallas, 1778). Giardia microti infection resulted in significant diffuse shortening of microvilli and significant greater microvillous diameters. In addition, deformations of the microvilli were observed at the margin of the ventral disc. The microvilli attached to the lateral crest of the ventral disc were vesiculated with a disorganised filamentous core and contained whorled structures resembling “myelin-like figures”. The findings are discussed in context of the Giardia-epithelial cell interaction.
The ultrastructure and histochemistry of the tegument and penetration glands of adult Amphilina foliacea from the body cavity and the tissues of the internal organs of Acipenser ruthenus and A. stellatus were studied. New data on the localization in the tissue, development and in encapsulation of the adult A. foliacea mostly in the liver of A. ruthenus were obtained. The well developed penetration glands are necessary for penetration into the tissue and for migration of A. foliacea into the body cavity of the hosts. The tegument of the adult A. foliacea is a syncytium with cytons deeply embedded into the parenchyma. The secretory activity of the tegument of worms has a protective function against the immune system of the host. Our results give further information about the phylogeny of Amphilinidea and confirm the view of the close phylogenetic relationship of Amphilinidea and Cestoidea.
The oogonia and oocytes in the ovaries of Toxocara canis are joined to a cytoplasmic process called the rachis. The rachis is a muchbranched cytoplasmic mass without cell components in the germinal zone. At the end of the germinal zone and in the growth zone the cytoplasmic mass is formed into a central axial cylinder, containing small dense granules, lipid drops and glycogen. Throughout the growth zone shell granules similar to those present in the oocytes are also present in the rachis. Anterior to the opening of the ovaries into the oviduct the rachis disappears. The ovarian wall is composed of epithelial cells, adjoining the basal lamina. They are characterized by the presence of large numbers of mitochondria, especially in the germinal zone. The epithelial cells in the growth zone also contain rough endoplasmic reticulum, ribosomes and bundles of microfibrils. A dense tubular material occurs between the basal membrane of the epithelial cells and the basal lamina as well as in the wall intercellular spaces in the ovarian growth zone. Multivesicular labyrinthlike formations can also be observed in the epithelial intercellular spaces in the central portion of the T. canis ovary.
The fine structure of the oviduct, oviduct-uterine junction and uterus of the nematode Toxocara canis (Werner, 1782) is described. Columnar-type epithelioid cells with numerous microvilli at the apical membrane border the oviduct lumen. Many electron dense secretory products are present in these cells. The cells lining the oviduct-uterine junction have no microvilli. They are coated with an electron-dense layer and contain numerous membrane-bound dense material containing bodies. Externally, the cells are surrounded by a basal lamina and muscle cells. The epithelial cells lining the greater part of the paired uteri appear to be rather flat. The oocytes inside the oviduct are covered with a dense thick plasma membrane and contain lipid droplets, dense granules and glycogen. The morphology of the oocytes before the fertilization inside the oviduct-uterine junction resembles that of the oocyte in the oviduct. After the fertilization the egg shell formation takes place. The egg shell of T.canis is composed of four layers: uterine, vitelline, middle chitinous and inner layer. The differences between the fine structure of the egg shell of T. canis and other related nematodes are discussed.
Results of a study on trypanorhynch ccstodes of fishes from Indonesian coastal waters are presented. A new species, Dasyrhynchus thomasi sp. n., is described, and five species are recorded which all represent new locality records: Tentacularia coryphaenae Bose, 1797; Nyhelinia africana Dollfus, 1960; Nybelinia scoliodoni (Vijayalakshmi, Vijayalakshmi et Gangadharam, 1996); Sphyriocephalus dollfusi Bussieras et Aldrin, 1968; and Otobothrium penetrans Linton, 1907, Their known ranges of distribution are extended to the East-Indian Ocean. Scanning and transmission electron microscopy was used to clarify details of the tentacular armature and surface morphology of T. coryphaenae, D. thomasi and O. penetrans. In T. coryphaenae, hook-like microtriches along the bothridial tegument are embedded in the distal cytoplasm, sometimes showing a split base. The solid tentacular hooks are embedded into a fibrillar, highly ordered tentacular wall. D. thomasi is distinguished by its characteristically shaped bothridia and a triple chainette with winged hooks on the external surface of the tentacle. Tufts of microtrichcs with ciliated sensory receptors arc regularly arranged on the bothridial surface of O. penetrans. They show similarities to sensory receptors reported from other trypanorhynch cestodes. Otobothrium pephrikos Dollfus, 1969 is considered a junior synonym for O. penetrans, and the variability of the scolex within trypanorhynch cestodes is emphasised.
The ultrastructure of the endogenous stages - merozoites, microgamonts, macrogamonts and oocysts, of Sarcocystis muriviperae from the snakes Vipera palaestinae and Coluber jugularis is described. Snakes were infected via white mice fed on sporocysts obtained from naturally infected snakes of the same species. Snakes examined 4 days post-infection contained only young and premature gamonts. Infection in snakes sacrificed on day 7 post-infection consisted predominantly of mature microgamonts and macrogamonts; snakes examined on day 10 post-infection revealed only oocysts. The fine structure of the endogenous stages from the two snakes, including size and contents of the wall-forming bodies, was identical, confirming their suggested conspecificity. Observed endogenous stages also conformed in their major details with the same developmental stages of other Sarcocystis species studied from other snakes and mammalian definitive hosts and from in vitro culture. However, they differed from the latter in size and contents of the wall-forming bodies. The observed fertilization process was reminiscent of that described earlier in S. bovicanis.
Subepidermal glands of the body of Troglocaridicola sp. (from the cavemicolous shrimp Troglocaris sp. in eastern Italy) were observed by transmission electron microscopy. The reservoir and duct of the glands arc lined with longitudinal microlubulcs. Membrane-bound granules inside the gland show a distinctive pattern: they contain fibres, 18 nm in diameter, regularly arranged in bundles with a 5 nm space between libres. From a survey of the available literature on glands of Platyhelminthes, it is concluded that this structure is known only in this species. Glands with regularly arranged 18 nm fibres, if characteristic for the Scutariellidae, could be considered an autapomorphy of this family, distinguishing it from other members of the Temnocephalida.