Etude Cytologique, Systématique et Pathologique d'Ichtyobodo necator (Henneguy, 1883) Pinto, 1928 (Zooflagelle)

SYNOPSIS. The free form of Ichtyobodo necator is typically quadrangular, with rounded corners, and flattened dorso-ventrally. Its dorsal surface is strongly convex and its ventral surface somewhat concave. A longitudinal groove traverses the posterior 2/3 of the ventral surface near its right margin. The part of the organism anterior to the groove is rather thick; that containing the depression thins out progressively toward the posterior end. Most of the organelles are in the major part of the cytoplasm to the left of the groove. Anteriorly this depression continues into a rather short canal. Two (4 in predivision stages) flagella originate near the anterior end of the canal, from which they run posteriorly. The cytostome is also near the anterior part of the canal. The cytostome, canal, and cell membrane are reinforced by microtubules. The chondriome, undoubtedly represented by a single very elongated mitochondrion, contains numerous dilated areas rich in deoxyribonucleic acid. The fixed form of the flagellate is highly modified. Its anterior part becomes attached to the host cell by forming a plate. A type of sucking organelle that contains the cytostome forms from the plate and penetrates the host cell. I. necator belongs in the family Bodonidae. RESUME La forme libre d'Ichtyobodo necator est quadrangulaire avec des angles arrondis, et présente un aplatissement dorsoventral. Sa surface dorsale est fortement convexe et sa surface ventrale légèrement concave. Une gouttiére longitudinale traverse les 2/3 postérieurs de la face ventrale sur le bord droit. La région cellulaire antérieure à, la gouttiére est plus épaisse que celle qui contient la dépression et s'amincit progressivement vers la partie terminale. La plupart des organites cellulaires occupent la partie gauche de la cellule. Dans la région antérieure la gouttiére se prolonge par un canal assez court. Deux (quatre dans les stades de prédivision) flagelles partent de ce canal et se dirigent vers la région postérieure. Le cytostome est également localisé près de la région antérieure du canal. Le cytostome, le canal et la membrane cellulaire sont jouxtés de microtubules. Le chondriome, sans doute représenté par une seule mitochondrie très allongée, présente de nombreuses dilatations riches en acide désoxyribonucléique. La forme fixée du flagellé est très modifiée. Sa partie antérieure adhère à la cellule hǒte par l'intermédiaire d'un plateau. Une sorte de suçoir, qui contient le cytostome, se forme à partir de ce plateau et pénètre dans la cellule hǒte. Ichtyobodo necator appartient à la famille des Bodonidae.     

Monoclonal Antibodies Identify a Subset of Dense Granules in Cryptosporidium parvum Zoites and Gamonts

ABSTRACT. Two monoclonal antibodies raised against purified oocysts and excysted sporozoites of Cryptosporidium parvum identified antigens located in the anterior half of sporozoites by indirect immunofluorescence microscopic assay. The monoclonal antibodies also reacted with Triton X-100-insoluble antigens of asexual and sexual stage parasites developing in epithelial cells in vitro and identified a 110 kilodalton antigen on immunoblots of sodium dodecyl sulfate-extracted oocysts. Immunoblotting reactivity was abolished by prior treatment of blotted antigen with periodic acid suggesting that the monoclonal antibodies recognize a carbohydrate or carbohydrate-dependent epitope(s). By immunoelectron microscopy, the antibodies reacted with a family of small, electron-dense granules located predominantly in the central region of merozoites and also with a population of cytoplasmic inclusions in macrogamonts. In addition, the monoclonal antibodies prominently labeled the parasitophorous vacuole membrane of all intracellular stages examined suggesting that the corresponding antigen(s) may be exocytosed from the granules to become associated with Triton X-100-insoluble components of the vacuolar membrane or cytoskeleton.     

Fine Structure of Triactinomyxon Early Stages and Sporogony: Myxosporean and Actinosporean Features Compared

ABSTRACT. 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.     

Recognition of Neurohormones of the NPY Family by Their Receptors

In this review a structural approach developed to answer the question whether hormones from the neuropeptide Y (NPY) family are recognized directly from solution or from the membrane-bound state is described. The chosen strategy is built onto a comparison of a set of peptides with well-known pharmacology and investigates whether similarities of structures of pharmacologically related peptides are higher in solution or in the membrane-bound state. Moreover, we have established the membrane-association mode of these peptides and contributed to our understanding of the structural features of these hormones both when placed in bulk solution and when bound to membranes. As a result we propose a receptor recognition pathway that includes initial association with the membrane and requires the peptides to come off the membrane to diffuse into the binding pocket of the receptor. This review also presents methodology recently developed by us to simulate the structural transition the peptides undergo when diffusing from bulk solution onto the membrane.     

Visual deprivation and distance estimation in the praying mantis larva

Abstract. Young larvae of the praying mantis, Tenodera sinensis Saussure, were placed on an off-centre island surrounded by a round arena with six black bars painted on a white inner wall. In this situation, it was shown that the horizontal peering movements of the head often seen in mantids are in fact used to measure distances; motion parallax may be involved in this process. Aimed jumps that followed peering were taken to be the distinct result of an absolute distance measurement. Specific visual deprivation such as painting over of certain parts of the eye with opaque black varnish or degeneration of the fovea with sulforhodamine showed that: absolute evaluation of distance is only possible with two fully intact eyes; the peering mechanism is under visual control; and visual experience has a long-term effect on distance measurement involving peering movements.     

“Unidentified” Mobile Protozoans from the Blood of Carp and Some Unsolved Problems of Myxosporean Life Cycles1

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).