[Cestoda of the genus Raillietina Fuhrmann, 1920 (Cestoda-Davaineidae), parasites of Columbiforms].
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Caulobothrium longicolle (Linton, 1890) and Phyllobothrium gracile (Weld, 1855) (Cestoda: Tetraphyllidea, Phyllobothriidae) have the same embryonic development with the following characteristic data: --a small number of vitelline cells (2 or 3) pass with the zygote in the ootype;--a non operculate thin egg-shell;--the entire and equal zyhote cleavage following by unequal divisions leading to the formation of four blastomere types (Macromeres, secondary Macromere, Mesomeres and Micromeres);--the differentiation of two syncytial embryonic envelopes during the preoncospheral phase. The outer envelope encloses the vitelline material remnant and three Macromeres among which the secondary Macromere. The inner envelope or embryophore, originates from five or six Mesomeres;--the presence of the oncospheral membrane;--the Phyllobothriidae ontogenesis is similar to that of the Onchobothriidae. By their embryonic features, the Tetraphyllidea are close to the Cyclophyllidea. This similarity suggests a phylogenic relationship between those two Cestoda orders.
The manner in which the flatworm, Hymenolepis diminuta (Cestoda), regulates the transport of glucose and Na+ across the brush border was examined. While the presence of an unstirred region in the brush border may favor the reabsorption of leaked glucose, some leaked glucose was lost to the ambient medium. This loss was markedly enhanced by preloading the worms with glucose and by removing Na+ from the incubation medium. Since glucose and Na+ influxes are coupled, glucose leakage stimulated the influx of 22Na+. However, this 22Na+ influx was balanced by a simultaneous increased 22Na+ efflux. The presence of phlorizin inhibited both unidirectional fluxes of 22Na+ indicating that efflux of 22Na+ occurred by countertransport; countertransport of [14C] glucose appeared to be negligible. A model has been proposed in which the transport of glucose and compensating transfers of Na+ across the membrane occur via the same carrier.
Polyonchobothrium scleropagis (Cestoda: Pseudophyllidea) is described as a new species from the Australian osteoglossid fish Sclerophages leichardti Günther.
The embryonic development from the egg to the oncosphere is examined in three Cestoda: Acanthobothrium coronatum (Rud., 1819), Acanthobothrium filicolle, Zschokke, 1888 and Acanthobothrium zschokkei Baer, 1948 (Tetraphyllidea, Onchobothriidae). The three ontogeneses have in common the following data: -- Two vitelline cells pass with the zygote into the ootype where a thin shell is formed out of a material which comes from the vitelline cells. -- At first the cleavage is equal, then it becomes unequal resulting in the formation of four types of blastomeres: macromere, secondary macromere, mesomere and micromere. -- The preoncospheral phase is characterized first by the blastomere multiplication and later by their decreasing number and differentiation. -- The embryonic envelopes are formed within the shell. The vitelline layer includes the cytoplasm, a vitelline nucleus and possibly the secondary macromere, the nucleus of which always lies against the outer membrane of this envelope. The syncytial embryophore develops from mesomeres coming from the embryo. -- The oncosphere is limited by its owm membrane whose posterior region seems to double in order to form a kind of cap bending over the six hook tips. The final number of embryonic hexacantha cells is relatively low.
Aploparaksis borealis sp. n. (Cestoda: Hymenolepididae), from the long-tailed jaeger, Stercorarisu longicaudus Vieillot, on the Seward Peninsula, Alaska, and from the red-throated pipit, Anthus cervinus (Pallas), and the Lapland longspur, Calcarius lapponicus (Linnaeus), in Chukotka, northestern Siberia, is described. This cestode is distinguished by the structure of the cirrus and other morphologic characters from other species of Aploparaksis Clerc 1903 in which there are 10 rostellar hooks and the vitelline gland is aporal to the ovary. A. borealis is the first species of Aploparaksis to be reported from birds representing 2 orders (Passeriformes and Charadriiformes).
Comparative studies of the larval development of Hymenolepis stylosa Rudolphi, 1809 (Cestoda : Cyclophyllidea), a parasite of Corvid birds are undertaken from three insect species. The development in the beetle, Tenebrio molitor shows that the scolex differenciation occurs before the invagination of the metacestode in the cystic vesicle. The cercomer is long, narrow and flexuous. In the grasshopper, Lousta migratoria, the development is the same one but the scolex invaganation begins early. In another beetle, Dermestes frischi, the oncosphere is stopped in the gut-wall. The morphology and development of the cysticercoids of avian species of Hymenolepis, which have a well known life cycle, are similar. Studies on the structure of the larval stages of avian and mammal species of Hymenolepis seem necessary to find the relations between the different species of this genus.
Monoecocestus thomasi sp. n. (Cestoda: Anoplocephalidae), from the northern flying squirrel, Glaucomys sabrinus (Shaw), in Oregon, is described and distinguished from its congeners. Monoecocestus thomasi is the sixth species of Monoecocestus to be described from nearctic rodents, and the first from a member of the family Sciuridae. Our comparisons of taxonomic characters of the nominal species of Monoecocestus in North American rodents have shown that M. giganticus Buhler 1970 is a synonym of M. americanus (Stiles 1895), both from the porcupine, Erethizon dorsatum (Linnaeus). Insemination in Monoecocestus ssp. is discussed, with the conclusion that it takes place only by way of the vagina in early immature segments.
Uptake and serosal transfer of the vitamins thiamine, riboflavin and folic acid have been studied in vivo in normal and parasitized rats infected with Hymenolepis diminuta (Cestoda). Regional differences in intestinal uptake of all three vitamins in both uninfected and parasitized animals were not satistically significant. In the parasitized intestine mucosal uptake and serosal transfer of thiamine were significantly inhibited, with increased mucosal accumulation of the vitamin as luminal thiamine concentration increased. Apparent increased riboflavin mucosal uptake in parasitized animals, was not matched by the reduced serosal transfer, suggesting adsorption of the vitamin in the unstirred aqueous layers. Mucosal uptake of folic acid increased in the parasitized gut; serosal transfer and mucosal accumulation were not affected. These results, indicating vitamin malabsorption associated with infection by H. diminuta, are consistent with the parasite inhibiting mucosal passive transport mechanisms. This conclusion is supported by the changes in net water fluxes associated with vitamin uptake in the parasitized intestine.
H. diminuta at different stages of development contained as many as five pyruvate kinase isozymes. Four of these were unusually sensitive to allosteric activation by fructose-1,6-P2. One isozyme which occurred only in adults or near-adults was insensitive but had a relatively low Km. All were inhibited by ATP and Ca2+, none by alanine, and the pH optimum was unaffected by fructose-1,6-P2. The five isozymes were present in gravid or reproductively active proglottids. Two of them occurred after eight days growth in the rat intestine, and three after four days. These three were also present in the immature, anterior proglottids of adult parasites. Hexacanth larvae from gravid proglottids, as well as cysticercoids developing from these larvae in Tenebrio molitor, possessed only two isozymes. It was inferred from information on tissue concentrations of ADP, ATP, phosphoenolypyruvate (PEP) and on K0.5S and Km that competition between pyruvate kinase and PEP carboxykinase is probably controlled by fructose-1,6-P2 concentrations. Since H. diminuta is an obligatory fermenter in which gluconeogenesis is minimal, the probable function of its L-type pyruvate kinases is to control the specific composition of lactic, acetic and succinic acid mixtures that are excreted at different stages of development.
The properties of pyruvate kinase (PK) and phosphoenol pyruvate carboxykinase (PEP CK), two enzymes that determine the preferrential accumulation of either succinate or lactate as endproducts of carbohydrate metabolism, are described in adult Hymenolepis diminuta. PK activity at Vmax and Km levels of PEP was unaffected by ATP, alanine, FDP4, OR H+ ions, but was inhibited by 50% at 6.3 mM L-lactate and 30 mM HCO3. The addition of 30 mM HCO3 increased the Km(PEP) by 6-fold but did not alter the Vmax. The inhibition of PK by HCO3 cannot be explained entirely by an effect of ionic strength, but probably represents a specific modulator-enzyme interaction. Under similar conditions PEP CK was maximally activated. Although L-lactate inhibited PEP CK (Ki(lac) = 1.8 mM), this effector may play a minor role in regulation of PEP flux. These results implicate the poise of the HCO3-:CO2 system as a major determiner of endproduct accumulation in H. diminuta.
All enzymes of the tricarboxylic acid cycle are present in subcellular fractions of the plerocercoid of Ligula intestinalis but the low activity of aconitase and malate dehydrogenase in the forward direction suggests that the complete cycle may be of questionable importance to the parasite. As in other helminths and intertidal molluscs, succinate, formed via a partial reversal of the tricarboxylic acid cycle, is a major end-product of anaerobic glucose degradation.
In vitro studies revealed that the hatching of oncospheres of Moniezia expansa requires the mechanical breakage of the eggshell and subshell membrane and enzymic digestion of the pyriform apparatus. Removal of the outer two egg membranes elicits the activation of most oncospheres. Between pH 5.0-7.8, there is no significant difference in numbers of oncospheres activated by eggshell removal and the addition of sodium bicarbonate has no effect. Solutions of more extreme pH values (2.0 and 10.0) are harmful and render oncospheres immobile. The subshell membrane forms a barrier to the passage of water in an osmotic gradient and to several molecular and ionic substances. Between the eggshell and subshell membrane is a layer of droplets which have a strong affinity for Sudan stains and which are partially removed by lipase. The eggshell is resistant to a variety of proteolytic enzymes, amylases and lipase. The pyriform apparatus is digested by chymotrypsin and pepsin, though not by trypsin. Both eggshell and pyriform apparatus are dissolved by solutions of sodium sulphide and sodium hypochlorite, indicating that their structures are stabilized by disulphide bonds and other covalent linkages.
Hymenolepis microstoma grown in mice, treated with 1.25 mg cortisone acetate every second day, are heavier and have a significantly higher glycogen content than those in control mice. The dry/wet weight ratio and protein content however are unaffected. It is suggested that the increase in glycogen reserve and weight in H. microstoma from cortisone-treated mice is due to an immunosuppressive effect and better nutritional environment rather than hormonal action. Inclusion of 0.1 mg of cortisone per 100 ml of culture medium produces no change in worm weight in vitro. Single worm infections result in 100% recovery, but 30 worm infections provoke a rejection process which can be suppressed partially by administration of cortisone acetate.
The processes of spermatogenesis and spermiogenesis in Hymenolepis diminuta were studied by electron microscopy using improved preparative techniques. Spermatogonia (Type A) are characterized by nuclei 3.79 (+/- 0.17) micrometer in diameter, dense cytoplasm packed with free ribosomes and aggregates of mitochondria. After mitoses, certain spermatogonia (Type B) assume syncytial rosettes containing eight nuclei. Primary spermatocytes maintain the rosette syncytium and have large nuclei (4.28 +/- 0.24 micrometer in diameter), smooth endoplasmic reticulum, and polysomes. The secondary spermatocyte is short-lived and is characterized by nuclei (2.0 +/- 0.11 micrometer in diai (2.0 +/- 0.11 micrometer in diameter) and perinuclear membranous lamellae. The syncytial spermatid cluster contains avoid nuclei which condense and elongate to a final diameter of 0.22 +/- 0.04 micrometer. Once elongated, these nuclei become delimited from the syncytium by invaginations of the plasma membrane. During delimitation, cortical peripheral microtubules arise beneath the spermatozoon plasmalemma and a 9 + 1 axoneme extends the length of the mature lance-shaped spermatozoon.
The embryophore (inner capsule) of the tapeworm Shipleya inermis was studied with histochemistry and electron microscopy. It was found to be unique for the cestodes in that it has a laminated construction. During development lamina are added until there are 10 which are arranged in an irregular zig-zag pattern. The embryophore is positive to tests for acid and alkaline phosphatase, and the Hales test for acid mucopolysaccharides. Permeability of tapeworm egg coverings is discussed.
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