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Ultrastructure of the oncospheral envelopes in the pseudophyllidean cestode Eubothrium salvelini [Schrank, 1790]

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Swiderski Z. , Brunanska M. , Mlocicki D. , Conn D. B.

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nr 4

EN

The aim of this study is to describe the ultrastructure of oncospheral envelopes in the pseudophyllidean cestode Eubothrium salvelini, a parasite of salmonid fishes. Our results indicate that the eggs of E. salvelini differ in their ultrastructure from those of the majority of the Pseudophyllidea. The entire embryonic development, including differentiation of the mature, infective oncosphere of E. salvelini takes place in the uterus and not in the aquatic environment, as is common for other pseudophyllideans. Egg maturation is not simultaneous; together with mature eggs containing fully differentiated oncospheres, can be found numerous small immature, nonfertilized and nonviable abortive eggs. The normally developing eggs of E. salvelini are large, oval and nonoperculated. Three envelopes surround the infective hexacanths: (1) the eggshell; (2) the outer envelope originating from macromere fusion; (3) the inner envelope formed by numerous mesomeres which usually persist in the mature eggs. Our observations confirm that both the outer and the inner envelopes of E. salvelini eggs are cellular in origin and syncytial in nature. The typical oncospheral membrane was not observed in this species. New data on the origin and ultrastructure of oncospheral envelopes may present useful criteria for phylogenetic analysis of lower cestodes. Ontogenetic characters, such as ultrastructural aspect of morphogenesis of infective larval stages, are proposed as phylogenetic indicators in studies of cestode evolution.

2

Ultrastructure of the tegument of the anoplocephalid cestode Mosgovoyia ctenoides [Railliet, 1890] Beveridge, 1978

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Mlocicki D. , Eira C. , Zebrowska J. , Miquel J. , Swiderski Z.

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nr 3

3

Ultrastructure and cytochemistry of vitellogenesis in Wenyonia virilis Woodland, 1923 [Cestoda, Caryophyllidea]

76%

Swiderski Z. , Mlocicki D. , Mackiewicz J. S. , Miquel J. , Ibraheem M. H. , Brunanska M.

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nr 2

131-142

EN

Vitellogenesis in Wenyonia virilis was examined by transmission electron microscopy (TEM), including the cytochemical detection of glycogen at the ultrastructural level with the periodic acid-thiosemicarbazide-silver proteinate (PA-TSC-SP) technique. Mature vitelline follicles have cells in various stages of development, progressing from immature cells of gonial type near the periphery of the follicle to maturing and mature vitellocytes towards the centre. Maturation is characterized by: (1) increase in cell volume; (2) increase in nuclear surface area restoring the N/C (nucleo-cytoplasmic) ratio; (3) nucleolar transformation; (4) extensive development of parallel cisternae of GER, the shell-protein producing units; (5) development of Golgi complexes, engaged in shell-granule/shell-globule formation and packaging; (6) synthesis and storage of glycogen in the cytoplasm; (7) simultaneous, independent formation and storage of intranuclear glycogen; (8) continuous fusion of small shell-granules into larger shell-globules and fusion of these into large shell-globule clusters with a progressive increase in the number and size of the latter; and (9) disintegration of GER in the medial layer of vitellocyte cytoplasm, degenerative changes and accumulation of glycogen and shell-globule clusters within the cytoplasm. The functional significance of numerous shell-globule clusters and the relatively small amount of nuclear and cytoplasmic glycogen is analysed. Unlike vitellogenesis of other caryophyllids, the nuclear glycogen of mature vitellocytes in W. virilis is randomly dispersed in the nucleoplasm and never forms a high central accumulation, the so-called “nuclear vacuole”. The nutritive function of vitellocytes appears greatly reduced in W. virilis, a fact perhaps related to the intrauterine development of the early embryos. The ultrastructure of vitellogenesis in W. virilis is compared with that in other lower cestodes, both monozoic and polyzoic. Conclusions concerning interrelationships of the vitellogenesis pattern of the ultrastructural cytochemistry of mature vitellocytes of W. virilis to intrauterine embryonation, absence of uterine glands and an extensive uterus characteristic for this species, are drawn and discussed.

4

Post-embryonic development and ultrastructural characteristics of the polycephalic larva of Taenia parva Baer, 1926 [Cyclophyllidea, Taeniidae]

75%

Swiderski Z. , Miquel J. , Mlocicki D. , Georgiev B. B. , Eira C. , Grytner-Ziecina B. , Feliu C.

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tom 52

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nr 1

EN

Post-embryonic development and fully-formed polycephalic larvae of Taenia parva Baer, 1926 were examined by light (LM) and transmission electron microscopy (TEM). Three developmental stages were recognised: (1) an early stage of exogenous budding at the surface of the central vesicle; (2) a stage of polycephalic cyst development accompanied by segmentation of the growing larval strobile and an obvious decrease in the size of the central vesicle; (3) fully-formed larval strobile and invaginated scoleces. In fully-developed encysted polycephalic larvae, there are usually 14–24 segmented larval strobilae, each terminating with an invaginated scolex; larval strobilae arise from a common central vesicle and remain attached posterior to it during the entire development. The number of segments varies between 109 and 120 per larval strobila. The polycephalic larvae examined closely resemble the strobilocercus type of taeniid larvae. The structure of developing and fully-formed larvae was examined by TEM. The tegument, scolex, subtegumental musculature of the strobilar segments, protonephridial system, calcareous corpuscles and medullary parenchyma of larvae exhibit general similarity with the same structures in adults at both LM and TEM levels. The morphogenesis of the larva of T. parva is compared with that of the polycephalic larvae of other Taenia spp. (T. krepkogorski, T. twitchelli and T. endothoracica) and with other asexually-multiplying cestode larvae (mesocestoidids, hymenolepidids and dilepidids).

5

Ultrastructural and cytochemical studies on vitellogenesis in trypanorhynch cestode Dollfusiella spinulifera Beveridge, Neifar et Euzet, 2004 [Eutetrarhynchidae]

75%

Swiderski Z. , Miquel J. , Mlocicki D. , Neifar L. , Grytner-Ziecina B. , Mackiewicz J. S.

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nr 3

EN

The first description of vitellogenesis in the Trypanorhyncha is presented in this paper. Though the type of vitellogenesis and mature vitellocyte in Dollfusiella spinulifera appear to be unique among the Eucestoda, to some extent they resemble that observed in the lower cestodes, namely the Tetraphyllidea and Pseudophyllidea. Maturation is characterized by: (1) an increase in cell volume; (2) extensive development of large, parallel, frequently concentric cisternae of GER that produce proteinaceous granules; (3) development of Golgi complexes engaged in packaging this material; (4) continuous enlargement of proteinaceous granules within vesicles and their transformation into shell globule clusters; and (5) progressive fusion of all vesicles, with flocculent material containing the proteinaceous granules and shell globule clusters, into a single very large vesicle that characterises mature vitellocytes of this tapeworm. Cell inclusions in and around the large vesicle consist of flocculent material of a very low density, a few shell globule clusters, moderately dense proteinaceous granules and numerous large droplets of unsaturated lipids. A new previously unreported mode of transformation of proteinaceous granules into shell globule clusters, that evidently differs from that of pseudophyllideans and tetraphyllideans, is described. Cytochemical staining with periodic acid-thiosemicarbazide-silver proteinate for polysaccharides indicates a strongly positive reaction for membrane-bound glycoproteins in all membranous structures such as GER, mitochondria, Golgi complexes, nuclear and cell plasma membranes. Similar staining revealed β-glycogen particles scattered in the cytoplasm of maturing vitellocytes. Typical cytoplasmic β-glycogen particles appear mainly during early vitellocyte maturation but it is characteristic for this species that they are only seldom visible in mature cells. Some working hypotheses concerning the interrelationship between this particular pattern of vitellogensis, possible mode of egg formation in D. spinulifera, its embryonic development and trypanorhynchean life cycle, are drawn and discussed.

6

Ultrastructure of oncospheral hook formation in the cestode Mosgovoyia ctenoides [Railliet, 1890] Beveridge, 1978 [Cyclophyllidea, Anoplocephalidae]

75%

Mlocicki D. , Swiderski Z. , Conn D. B. , Eira C. , Miquel J. , Baranowska-Korczyc A.

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tom 50

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nr 2

EN

The ultrastructure of oncospheral hook formation in the anoplocephalid cestode Mosgovoyia ctenoides (Railliet, 1890) Beveridge, 1978, is described. The hook morphogenesis takes place inside the six symmetrically arranged hook-forming cells, the oncoblasts. They show characteristic large nuclei of semilunar shape, localized at one pole of the embryo. At the beginning of the hook formation, the "hook-forming centre" appears in the cytoplasmic part of each oncoblast. It consists of numerous free ribosomes and polyribosomes surrounded by several mitochondria and Golgi complexes. The hook-forming centre is involved in synthesis of an electron-dense, undifferentiated hook primordium, which undergoes progressive differentiation and elongation into the fully developed hook. A fully formed oncospheral hook consists of the three parts: blade, shank, and base. Each hook, at the site of its protrusion from the oncosphere, is surrounded by two electron-dense rings interconnected by a circular septate junction. The hook material consists of two or three layers that differ in electron density: (1) a moderately electron-dense core, (2) a middle layer of low electron density, and (3) a highly osmiophilic cortex. Wide bands of hook muscles are attached to the basal and collar parts of the hook. The hook blades project outside of the oncospheral body into a large cavity delimited by the hook region membrane attached at this pole directly to the oncospheral surface. In the fully developed oncosphere of M. ctenoides, the three pairs of oncospheral hooks and their muscles form a complex "hook muscle system", responsible for coordinated hook action. The differentiation and ultrastructure of oncospheral hooks in the oncospheres of M. ctenoides are compared to those described in other cestode species.