Ultrastructure of Spermatozoa in the Nematode Halalaimus dimorphus (Nemata: Oxystominidae)

The ultrastructure of spermatozoa in the free-living marine nematode Halalaimus dimorphus was studied with transmission electron microscopy. Spermatozoa in the posterior testis of the male had a large cavity filled with cellular processes, which contained a variable number of small tubules. Mitochondria and small tubules were the only cell structures observed in the cytoplasm. The spermatozoa had a bipolar structure. The anteriorly situated nucleus, which was electron-dense and homogeneous, was surrounded by a single membrane. The size of the small tubules in the cytoplasm (diam. 12-13 nm) and their relatively thick wall structure suggested that they were not normal microtubules (diam. 25 nm). The material of the small tubules was assumed to be major sperm protein (MSP). The cavity appeared to open on the surface of the spermatozoon at the posterior extremity of the cell, and also medially, at the level of the anterior end of the cavity. The pores apparently were closed by a special plug-like structure, which was an evagination of the cell. The wall of the cavity was characterized by longitudinal folds, which were mushroom-shaped in transverse section. Spermatids in the anterior testis of H. dimorphuswere characterized by fibrous bodies packed with small tubules and by cellular processes also containing small tubules. H. dimorphus sperm seem to perform swimming movements based on liquid currents commonly present in turbin-like systems. Spermatogenesis resembled that found in ticks.     

Light and electron microscopic investigation of Pelomyxa prima (Gruber, 1884) (Peloflagellatea, Pelobiontida)

Cell organization of a multinuclear pelobiont Pelomyxa prima has been studied at the light and electron microscopic levels. Motile individuals demonstrate a characteristic drop-like or pyriform shape and reach 550 microkm in length. The cell cover is represented by a well-developed, morphologically differentiated glycocalyx 80-100 nm thick. The cytoplasm contains many structural vacuoles. The nuclei are of vertical type, numbering up to several nuclei in large individuals. Numerous cytoplasmic microtubules are associated with the external membrane of the nuclear envelope. Separate non-motile flagella are distributed throughout the cell surface, being more numerous in the posterior body end and uroidal zone of the protist. Basal bodies of the flagella are extremely long, being deeply immersed into the cytoplasm. These bodies are surrounded by a muff of electron-dense material, with numerous microtubules radiating from it. A compact bundle of microtubules starts from the base of a basal body axially into the cytoplasm. Besides, a band-like lateral microtubular rootlet is present. The number of microtubules in the axoneme of undulipodia is unstable. Neither mitochondria, nor Golgi complex were found. Two species of bacterial endocytobionts are present in the cytoplasm in considerable numbers.     

Ultrastructure of feeding tubes formed in giant-cells induced in plants by the root-knot nematodeMeloidogyne incognita

Summary The plant pathogenic nematodeMeloidogyne incognita forms conspicuous tubular structures referred to as feeding tubes in special food cells, called giant-cells, induced and maintained in susceptible host roots by feeding nematodes. Feeding tubes are formed by nematode secretions injected into giant-cells via a stylet and apparently function to facilitate withdrawal of soluble assimilates by the parasite. In giant-cells in roots of the four host species examined in this study, feeding tube morphology was identical. Tubes were straight to slightly curved structures just less than 1 μm wide and up to slightly more than 70 μm long. At the ultrastructural level, each tube consisted of a 190–290 nm thick, electron-dense, crystalline wall surrounding an electron-transparent lumen with a diameter of 340–510 nm. The distal end of the tube was sealed with wall material. Older tubes were found free in the host cytoplasm while the proximal ends of young tubes were attached to the host cell wall via short wall ingrowths through which the nematode's stylet was inserted. An elaborate membrane system was associated with the feeding tubes and was most extensive around newly formed tubes. Contiguous to the feeding tube wall, this membrane system consisted of strands of smooth endoplasmic reticulum while rough endoplasmic reticulum predominated toward the outer margin of the membrane system. Vacuoles and mitochondria were excluded from a zone of cytoplasm surrounding feeding tubes. This zone of exclusion, as well as the membrane system noted above, tended to be less pronounced or absent around older tubes no longer being used by the nematode.     

Morphology of the air-breathing stomach of the catfish Hypostomus plecostomus

Histological and ultrastructural investigations of the stomach of the catfish Hypostomus plecostomus show that its structure is different from that typical of the stomachs of other teleostean fishes: the wall is thin and transparent, while the mucosal layer is smooth and devoid of folds. The epithelium lining the whole internal surface of the stomach consists of several types of cells, the most prominent being flattened respiratory epithelial cells. There are also two types of gastric gland cells, three types of endocrine cells (EC), and basal cells. The epithelial layer is underlain by capillaries of a diameter ranging from 6.1-13.1 microm. Capillaries are more numerous in the anterior part of the stomach, where the mean number of capillary sections per 100 microm of epithelium length is 4, compared with 3 in the posterior part. The cytoplasm of the epithelial cells, apart from its typical organelles, contains electron-dense and lamellar bodies at different stages of maturation, which form the sites of accumulation of surfactant. Small, electron-dense vesicles containing acidic mucopolysaccharides are found in the apical parts of some respiratory epithelial cells. Numerous gastric glands (2 glands per 100 microm of epithelium length), composed of two types of pyramidal cells, extend from the surface epithelium into the subjacent lamina propria. The gland outlets, as well as the apical cytoplasm of the cells are Alcian blue-positive, indicating the presence of acidic mucopolysaccharides. Zymogen granules have not been found, but the apical parts of cells contain vesicles of variable electron density. The cytoplasm of the gastric gland cells also contains numerous electron-dense and lamellar bodies. Gastric gland cells with electron-dense cytoplasm and tubulovesicular system are probably involved in the production of hydrochloric acid. Fixation with tannic acid as well as with ruthenium red revealed a thin layer of phospholipids and glycosaminoglycans covering the entire inner surface of the stomach. In regions of the epithelium where the capillaries are covered by the thin cytoplasmic sheets of the respiratory epithelial cells, a thin air-blood barrier (0.25-2.02 microm) is formed, thus enabling gaseous exchange. Relatively numerous pores closed by diaphragms are seen in the endothelium lining the apical and lateral parts of the capillaries. Between gastric gland cells, solitary, noninnervated endocrine cells (EC) of three types were found. EC are characterized by lighter cytoplasm than the surrounding cells and they contain dense core vesicles (DCV) with a halo between the electron-dense core and the limiting membrane. EC of type I are the most abundant. They are of an open type, reaching the stomach lumen. The round DCV of this type, with a diameter from 92-194 nm, have a centrally located core surrounded by a narrow halo. EC of type II are rarely observed and are of a closed type. They possess two kinds of DCV with a very narrow halo. The majority of them are round, with a diameter ranging from 88-177 nm, while elongated ones, 159-389 nm long, are rare. EC of type III are numerous and also closed. The whole cytoplasm is filled with large DCV: round, with a diameter from 123-283 nm, and oval, 230-371 nm long, both with a core of irregular shape and a wide, irregular halo. EC are involved in the regulation of digestion and probably local gas exchange. In conclusion, the thin-walled stomach of Hypostomus plecostomus, with its rich network of capillaries, has a morphology suggesting it is an efficient organ for air breathing.     

Ultrastructure of the colon of Locusta migratoria

The ultrastructure of the colon of Locusta migratoria is described. The colon is lined by a thick cuticle that, for the most part, adheres to the underlying epithelium. The cuboid epithelial cells are characterized by moderate invaginations of the apical and, to a lesser extent, basal plasma membranes; the lateral plasma membranes are relatively flat. The bulk of the mitochondria are located in the apical region of the cell and are not particularly associated with any of the plasma membranes. The basal region of the cells contains much rough endoplasmic reticulum, glycogenlike granules, and a predominance of spherical, electron-dense bodies of various sizes. Where muscle fibers make contact with the epithelium, the cells are much reduced; the cytoplasm is usually less electron-dense, and, typically, the nucleus has a thick layer of granular material associated with the inner nuclear membrane. The apical and basal plasma membranes of the reduced epithelial cells contain numerous hemidesmosomes. The apical hemidesmosomes occur in pairs around an extracellular space that contains electron-opaque material. The latter forms tonofibrillae that extend into the endocuticle. Bundles of microtubules are associated with the hemidesmosomes. The tubules traverse the cell from the apical to the basal region. The possible significance of these findings is discussed.     

Ultrastructure of the Anterior Body Region of Marine Nematode Deontostoma californicum

The ultrastructure of the anterior body region of the free-living marine nematode Deontostoma calilornicum was studied by electron microscopy. The body wall consists of a nine-layered cuticle, a cellular hypodermis containing eight nerve bundles, and a well-developed coelomyarian somatic musculature. Nerves in the dorsal, lateral, ventral, and submedian hypodermal chords anterior to the nerve ring were observed with regularity. Structure of subventral somatic setae suggests a mechanoreceptive function. The esophagus is cellular and consists of three marginal cells alternating with an equal number of radial muscle cells, three esophageal glands, and three enteric nerves. The membranes of adjacent esophageal cells are sinuous. Apices of the triradiate lumen are connected with the outer wall of each marginal cell by bands of electron-dense nonmyofibrils, whereas two types of myofilaments run radially between the apophyses of the lumen and the outer walls of radial cells. Each myofibril, which forms hemidesmosomes at both ends, is interpreted to be the morphological equivalent of one sarcomere. Synaptic junctions between the processes of muscles, gland cells, and axons of the enteric nerves are described in detail.     

The Surface Coat of Plant-Parasitic Nematodes: Chemical Composition,Origin, and Biological Role—A Review

Chemical composition, origin, and biological role of the surface coat (SC) of plant-parasitic nematodes are described and compared with those of animal-parasitic and free-living nematodes. The SC of the plant-parasitic nematodes is 5-30 nm thick and is characterized by a net negative charge. It consists, at least in part, of glycoproteins and proteins with various molecular weights, depending upon the nematode species. The lability of its components and the binding of human red blood cells to the surface of many tylenchid plant-parasitic nematodes, as well as the binding of several neoglycoproteins to the root-knot nematode Meloidogyne, suggest the presence of carbohydrate-recognition-domains for host plants and parasitic or predatory soil microorganisms (Pasteuria penetrans and Dactylaria spp., for example). These features may also assist in nematode adaptations to soil environments and to plant hosts with defense mechanisms that depend on reactions to nematode surfaces. Surface coat proteins can be species and race specific, a characteristic with promising diagnostic potential.     

Morphology and Ultrastructure of the Intestine in a Plant-Parasitic Nematode,Tylenchorhynchus dubius

An unusual feature of the intestine in Tylenchorhynchus dubius is the presence, within the intestinal cytoplasm, of an extensive system of fibrillar bundles consisting of thin (14 nm diam) filaments and thick (70-90 nm diam), rod-like elements arranged in closely packed arrays. The larger of the fibrillar bundles, for which the term "intestinal fasciculi" is proposed, are evident in whole mounts and apparently correspond to the lateral or sinuous canals described in some other tylenchids. The nature and function of fasciculi are not known, but some possibilities are considered. Fasciculi were found in at least seven other species of Tylenchorhynchus. The intestinal cytoplasm also contains the usual sub cellular organelles and large amounts of reserve materials in the form of particulate glycogen and three types of globules. The surface of the cells bordering the lumen is elaborated into numerous microvilli which have central filaments and often bear regular external projections. Although terminal bars delimit the apical margins between cells, the frequent lack of complete lateral boundaries and extensive length of the fasciculi indicate that the intestinal epithelium is a multinucleate mosaic or syncytium.     

THE FINE STRUCTURE OF NERVE CELL BODIES AND THEIR MYELIN SHEATHS IN THE EIGHTH NERVE GANGLION OF THE GOLDFISH

The eighth cranial nerve ganglion consists of bipolar nerve cell bodies each occupying part of an internodal segment. The perikaryal sheaths range from a single layer of Schwann cell cytoplasm on the smallest cells to typical thick compact myelin on the largest. On most perikarya, the sheath displays an intermediate form, consisting of multiple layers of Schwann cell cytoplasm (loose myelin), or of loose and compact myelin continuous with each other. Internodes beyond the one containing the cell body bear only compact myelin. In loose myelin the thickness of each layer of Schwann cell cytoplasm is about 100 A. It may be much greater (~ 3000 A) particularly in the outermost layers of the sheath, or the cytoplasm may thin and even disappear with formation of a major dense line. The cytoplasmic layers are separated from each other by a light zone, 40 to 200 A wide, which in its broader portions may contain an intermediate line. Desmosomes sometimes occur between lamellae. In addition to the usual organelles, the perikaryal cytoplasm contains granular and membranous inclusions. Large cells covered by compact myelin have a consistently higher concentration of neurofilaments, and some of the largest cells, in addition, show a reduced concentration of ribosomes. The functional significance and possible origins of perikaryal myelin sheaths are discussed.     

Structure of the sulfur inclusion envelopes from four beggiatoas

The sulfur inclusions from four strain ofBeggiatoa alba were observed by using a ruthenium red-glutaraldehyde technique and a modified Ryter-Kellenberger technique. Three of the four strains contained 4-to 5-nm-thick, single, electron-dense, layered sulfur inclusion envelopes. The fourth strain (B15LD) contained a complex pentalaminar sulfur inclusion envelope, 12–14 nm thick. The sulfur inclusions from all four strains were external to the cytoplasmic membrane but internal to the complexBeggiatoa cell walls. Freeze-etching of theB. alba strain B18LD trichomes revealed the unusual cross-fracture morphology of the sulfur in the inclusions. Fractures around the sulfur inclusions revealed a surface similar to that of the fractured cytoplasmic membrane.     

Mitotic Schwann cells in developing nerve: their changes in shape, fine structure, and axon relationships

The shape of mitotic Schwann cells and their relationships with axons and their interphase neighbors were studied in electron micrographs of longitudinally and transversely sectioned newborn rat sciatic nerves. During prophase, the radial extent of sheetlike processes surrounding axons was progressively reduced until the Schwann cell was spindle shaped. Numerous 100 nm vesicles were found in the cytoplasm as the surface area decreased; they disappeared during subsequent reextension of the radial processes. The axis of mitosis was parallel to the long axis of the cell and transverse cleavage of the cytoplasm occurred between the daughter nuclei. The earliest cytoplasmic outgrowth was identified in serial sections through an anaphase cell which was traced distally from its mid nuclear region. A slender process, originating near the spindle pole, arched over and grew longitudinally beside and beyond the dividing nucleus. Observed also in telophase, this process was thought to represent a daughter cell's new axial process and to be important in establishing the cell's longitudinal symmetry. Radial processes that surrounded axons reappeared in telophase; they began forming in the nuclear region and subsequently grew radially and extended peripherally toward both ends of the cell. Our results show that the changes in shape that occur in dividing Schwann cells and their interphase neighbors increase contacts between these Schwann cells and the axons they surround. These surface interactions probably are important in the selection of axons to be myelinated.     

Electron tomographic analysis of cytoskeletal cross-bridges in the paranodal region of the node of Ranvier in peripheral nerves

The node of Ranvier is a site for ionic conductances along myelinated nerves and governs the saltatory transmission of action potentials. Defects in the cross-bridging and spacing of the cytoskeleton are a prominent pathological feature in diseases of the peripheral nerve. Electron tomography was used to examine cytoskeletal–cytoskeletal, membrane–cytoskeletal, and heterologous cell connections in the paranodal region of the node of Ranvier in peripheral nerves. Focal attachment of cytoskeletal filaments to each other and to the axolemma and paranodal membranes of the Schwann cell via narrow cross-bridges was visualized in both neuronal and glial cytoplasm. A subset of intermediate filaments associates with the cytoplasmic surfaces of supramolecular complexes of transmembrane structures that are presumed to include known and unknown junctional proteins. Mitochondria were linked to both microtubules and neurofilaments in the axoplasm and to neighboring smooth endoplasmic reticulum by narrow cross-bridges. Tubular cisternae in the glial cytoplasm were also linked to the paranodal glial cytoplasmic loop juxtanodal membrane by short cross-bridges. In the extracellular matrix between axon and Schwann cell, junctional bridges formed long cylinders linking the two membranes. Interactions between cytoskeleton, membranes, and extracellular matrix associations in the paranodal region are likely critical not only for scaffolding, but also for intracellular and extracellular communication.     

An Ultrastructural Study of the Hemocytes of the Pericardial Body in the Ascidian Ciona intestinalis (L.)

Abstract The hemocytes of the pericardial body of Ciona intestinalis were studied by electron microscopy. Our findings showed that stem cells, clear vesicular granulocytes, microgranulocytes, unilocular granulocytes and globular granulocytes are present at the periphery of the smaller-sized pericardial bodies. The stem cells are small round cells with a large nucleus, with or without nucleolus, and homogeneous cytoplasm containing numerous ribosomes. The clear vesicular granulocytes are characterized by an ameboid shape and cytoplasm containing several large electron-lucent vacuoles and small electron-dense granules. The microgranulocytes are variable in shape and contain numerous large electron-dense granules. The unilocular granulocytes show a single large vacuole with an electron-dense or electron-lucent content and a thin layer of peripheral cytoplasm that contains the flattened nucleus. The globular granulocytes are characterized by the presence of large vacuoles containing either fibrogranular material or electron-dense aggregates.     

Presence of the myelin-associated glycoprotein correlates with alterations in the periodicity of peripheral myelin

The myelin-associated glycoprotein (MAG) is an integral membrane protein (congruent to 100,000 mol wt) which is a minor component of purified peripheral nervus system (PNS) myelin. In the present study, MAG was localized immunocytochemically in 1-micrometer thick Epon sections of 7-d and adult rat peripheral nerves, and its localization was compared to that of the major structural protein (Po) of PNS myelin. To determine more precisely the localization of MAG, immunostained areas in 1 micrometer sections were traced on electron micrographs of identical areas from adjacently cut thin sections.l MAG was localized in periaxonal membranes. Schmidt-Lantermann incisures, paranodal membranes, and the outer mesaxon of PNS myelin sheaths. Compact regions of PNS myelin did not react with MAG antiserum. The results demonstrate MAG's presence in "'semi-compact" Schwann cell or myelin membranes that have a gap of 12-14 nm between extracellular leaflets and a spacing of 5 nm or more between cytoplasmic leaflets. In compact regions of the myelin sheath which do not contain MAG, the cytoplasmic leaflets are "fused" and form the major dense line, whereas the extracellular leaflets are separated by a 2.0 nm gap appearing as paired minor dense lines. Thus, it is proposed that MAG plays a role in maintaining the periaxonal space, Schmidt-Lantermann incisures, paranodal myelin loops, and outer mesaxon by preventing "complete" compaction of Schwann cell and myelin membranes. The presence of MAG in these locations also suggests that MAG may serve a function in regulating myelination in the PNS.     

Early events in fibroblast adhesion to glass : An electron microscopic study

Electron micrographs of trypsinized fibroblasts settling on glass in protein-free buffer show, after 15 min, areas of cell/substrate relationship characterized by obliteration of the gap between cell and substrate. The thickness of the plasma membrane at these points of adhesion is reduced from 7–8 to 3–5 nm the trilaminar structure being reduced to a single electron-dense layer. After 15 min, cells spreading in the presence of serum have small areas of cell/substrate specialization, which are characterized by an electron-transparent gap of 7–8 nm and by increased density of the cortical cytoplasm. The addition of manganese to the media results in an increase in spreading, but has little effect on the ultrastructure of adhesion. The possibility of introduction of artefacts by the technique used for removal of the glass substrate during processing is discussed.     

Enterocytozoon hepatopenaei sp. nov. (Microsporida: Enterocytozoonidae), a parasite of the black tiger shrimp Penaeus monodon (Decapoda: Penaeidae): Fine structure and phylogenetic relationships

A new microsporidian species, Enterocytozoon hepatopenaei sp. nov., is described from the hepatopancreas of the black tiger shrimp Penaeus monodon (Crustacea: Decapoda). Different stages of the parasite are described, from early sporogonal plasmodia to mature spores in the cytoplasm of host-cells. The multinucleate sporogonal plasmodia existed in direct contact with the host-cell cytoplasm and contained numerous small blebs at the surface. Binary fission of the plasmodial nuclei occurred during early plasmodial development and numerous pre-sporoblasts were formed within the plasmodium. Electron-dense disks and precursors of the polar tubule developed in the cytoplasm of the plasmodium prior to budding of early sporoblasts from the plasmodial surface. Mature spores were oval, measuring 0.7 × 1.1 μm and contained a single nucleus, 5-6 coils of the polar filament, a posterior vacuole, an anchoring disk attached to the polar filament, and a thick electron-dense wall. The wall was composed of a plasmalemma, an electron-lucent endospore (10 nm) and an electron-dense exospore (2 nm). DNA primers designed from microsporidian SSU rRNA were used to amplify an 848 bp product from the parasite genome (GenBank FJ496356). The sequenced product had 84% identity to the matching region of SSU rRNA from Enterocytozoon bieneusi. Based upon ultrastructural features unique to the family Enterocytozoonidae, cytoplasmic location of the plasmodia and SSU rRNA sequence identity 16% different from E. bieneusi, the parasite was considered to be a new species, E. hepatopenaei, within the genus Enterocytozoon.     

Ultrastructure of the sense receptors of adult Multicotyle purvisi (Trematoda, Aspidogastrea)

The following presumptive sense receptors of adult Multicotyle purvisi from the intestine of freshwater turtles in Malaya are described by transmission electron microscopy: disc-like receptor with many electron-dense collars and modified ciliary rootlet forming a 'disc'; non-ciliate receptor with long rootlet; non-ciliate receptor with branching rootlet and dense mass of irregularly arranged microtubules; non-ciliate receptor with rootlet fanning out from basal body, cross-striated in its upper and with electron-dense structures in its lower part; uniciliate receptor with thick layer of cytoplasm around axoneme; receptor with short cilium, at base of deep invagination of tegument; receptor with short cilium terminating in an electron-dense apical cap; and uniciliate receptor with long cilium. In addition, there may be a small non-ciliate receptor with a long ciliary rootlet at the base of the thick dorsal tegument, and uniciliate receptors differing from the uniciliate receptor with long cilium in the number of electron-dense collars and the length of the cilium and ciliary rootlet. Implications of the findings for the phylogeny of the parasitic Platyhelminthes and for evolutionary trends within that group arc discussed. The considerable degree of divergence of receptor types between the species of one family is attributed to the archaic nature of the group.     

Histopathological effects of larval digenea on the digestive epithelia of the marine prosbranch Cerithidea californica: Fine structural changes in the intestine

Light and electron microscopy were employed to study the effects of infection by sporocysts of Renicola buchanani on the posterior intestine of the marine snail Cerithidea californica. Columnar intestinal epithelium in close contact with renicolid sporocysts usually are compressed by growing larval stages resulting in the reduction of epithelial height, the disruption of cell-cell junctions, and the formation of convolutions in the supporting basal lamina. Intestinal cells of infected snails are further characterized by a reduction of rough endoplasmic reticulum, microtubules and microfilaments, and the formation of cytoplasmic vacuoles and electron-dense lysosome-like inclusions. Mitochondria of degenerating intestinal and smooth muscle cells show signs of cristolysis. In addition, the cytoplasm of smooth muscle cells often display a fine grainy appearance due to the breakdown of actin and paramyosin filaments.     

Morphological study of cysts of Pelomyxa palustris Greeff, 1874

Pelomyxa palustris Greeff, 1874, is the only representative of pelomyxoid amoebae with rest cysts in its life cycle. The morphology of the P. palustris cysts was studied using light and electron microscopy. The encystation of P. palustris under the climatic conditions of northwestern Russia occurs in August through September. The rest of the cysts have complex, trilaminar walls. The most developed are the two inner layers, i.e., the electron-dense structureless endocyst and the laminated mesocyst; the thickness of each layer can reach 0.6–0.7 μm. The thickness of the superficial electron-dense ectocyst lamina usually does not exceed 0.1–0.2 μm. The encysted cell of P. palustris has a unique structure. About 60% of its cell volume is occupied by a giant central vacuole filled with prokaryotic cytobionts. This vacuole has also been found to contain vacuoles and vesicles of different natures, restricted by vacuole membranes, autophagosomes, and lipid droplets. The amoeba cytoplasm occupies the space between the endocyst inner surface and the central vacuole. It contains no inclusions, prokaryotic cytobionts and most of cell organelles. In the cytoplasm there are 4 large nuclei filled with relatively homogeneous karyoplasm. The nuclear envelope forms numerous long tubular outgrowths, piercing the cytoplasm and underlining the central vacuole membrane. In this state the encysted pelomyxoids survive until the beginning of excystation. The excystation of P. palustris in the studied region occurs in spring, during the second half of April through the beginning of May. The cysts undergo complex morphofunctional changes due to reorganization of the wall and formation of young multinucleate amoebae. Out of the three initial lamina of the wall, only one persists until the moment of encystation. The central vacuole is destroyed and its content penetrates into the cytoplasm. Pelomyxoid nuclei divide twice. Prokaryotic cytobionts are localized in the cytoplasm and in the perinuclear area. Young multinuclear P. palustris individuals exiting cysts do not differ from the adult forms by their organization.     

Ultrastructural study of spermiogenesis and the spermatozoon of the proteocephalidean cestode Barsonella lafoni de Chambrier et al., 2009, a parasite of the catfish Clarias gariepinus (Burchell, 1822) (Siluriformes, Clariidae)

Spermiogenesis in the proteocephalidean cestode Barsonella lafoni de Chambrier et al., 2009 shows typical characteristics of the type I spermiogenesis. These include the formation of distal cytoplasmic protrusions forming the differentiation zones, lined by cortical microtubules and containing two centrioles. An electron-dense material is present in the apical region of the differentiation zone during the early stages of spermiogenesis. Each centriole is associated to a striated rootlet, being separated by an intercentriolar body. Two free and unequal flagella originate from the centrioles and develop on the lateral sides of the differentiation zone. A median cytoplasmic process is formed between the flagella. Later these flagella rotate, become parallel to the median cytoplasmic process and finally fuse proximodistally with the latter. It is interesting to note that both flagellar growth and rotation are asynchronous. Later, the nucleus enlarges and penetrates into the spermatid body. Finally, the ring of arching membranes is strangled and the young spermatozoon is detached from the residual cytoplasm.The mature spermatozoon presents two axonemes of the 9 + ‘1’ trepaxonematan pattern, crested body, parallel nucleus and cortical microtubules, and glycogen granules. Thus, it corresponds to the type II spermatozoon, described in almost all Proteocephalidea. The anterior extremity of the gamete is characterized by the presence of an apical cone surrounded by the lateral projections of the crested body. An arc formed by some thick and parallel cortical microtubules appears at the level of the centriole. They surround the centriole and later the first axoneme. This arc of electron-dense microtubules disorganizes when the second axoneme appears, and then two parallel rows of thin cortical microtubules are observed. The posterior extremity of the male gamete exhibits some cortical microtubules. This type of posterior extremity has never been described in proteocephalidean cestodes. The ultrastructural features of the spermatozoon/spermiogenesis of the Proteocephalidea species are analyzed and compared.