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.     

The Fine Structure of Some Developmental Stages of Mattesia grandis McLaughlin (Sporozoa, Neogregarinida), a Parasite of the Boll Weevil Anthonomus grandis Boheman

SYNOPSIS Sporozoites, macronuclear schizonts, merozoites and gamonts of Mattesia grandis were examined by electron microscopy. A conoidal complex, consisting of conoid, polar rings and subpellicular microtubules was present in all of these stages. The conoidal complex was similar in structure to the same organelle of other Sporozoa. The conoidal complex in mono- to quadrinucleate macronuclear schizonts is transformed into an organelle similar to the mucron of some eugregarines.
This mucron consists of a specialized area of the cell membrane from which fine fibers extend into a large vacuole situated directly beneath the cell membrane. The top part of the vacuole is encircled by 2 ring-like structures formed by the dilatation of the original apical rings. The vacuole of the mucron contains many anastomosing protrusions of the cytoplasm, suggesting a nutritional role. The mucron disappears when the schizont reaches the multinucleate state. Later the merozoites bud from the surface of the schizont as in the coccidia. Each merozoite again has a conoidal complex, which persists thru the gamont stage and usually serves as the point of contact between 2 gamonts during their pairing.
The presence of a conoidal complex thru a major portion of the life cycle, its transformation into a mucron and the mode of formation of merozoites indicate that the Neogregarinida combine the fine structure characters of both the Eugregarinida and the Eucoccida, thereby suggesting a phylogenetic relationship between these sporozoans, with the neogregarines as a link between eugregarines and coccidia.     

Potential of high‐density pheromone‐releasing microtraps for control of codling moth Cydia pomonella and obliquebanded leafroller Choristoneura rosaceana

Recent large‐cage studies with codling moth Cydia pomonella (L.) reveal that the removal of moths from an apple orchard using pheromone‐releasing traps is more effective at reducing capture in a central monitoring trap than is a mating disruption protocol without kill/capture. The present study uses open orchard 0.2‐ha plots comparing a high‐density trapping scenario with mating disruption to confirm those results. Two tortricid moth pests of tree fruit are studied: codling moth and obliquebanded leafroller Choristoneura rosaceana (Harris). Codling moth treatments include Isomate CM FLEX (ShinEtsu Ltd, Japan), nonsticky traps baited with Trécé CM lures (Trécé, Inc., Adair, Oklahoma), and sticky traps baited with Trécé CM lures, all at equal application rates of 500 dispensers ha^?1, as well as a no pheromone control. These microtraps are of a novel design, small and easy to apply, and potentially inexpensive to produce. Mating disruption using Isomate CM FLEX and nonsticky traps reduces codling moth capture in standard monitoring traps by 58% and 71%, respectively. The attract‐and‐remove treatment with sticky traps reduces capture by 92%. Obliquebanded leafroller treatments include Isomate OBLR/PLR Plus and Pherocon IIB microtraps baited with Trécé OBLR lures, both applied at 500 dispensers ha^?1, as well as a no pheromone control. Mating disruption reduces capture in monitoring traps by 69%. The attract‐and‐remove treatment reduces capture by 85%. Both studies suggest that an attract‐and‐remove approach has the potential to provide superior control of moth populations compared with that achieved by mating disruption operating by competitive attraction.     

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.     

“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).