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[Experimental evolutive cycle of Diphyllobothrium erinaceieuropei in Paracyclops fimbriatus, tadpoles of Bufo arenarum and dogs].

Experiments were performed in order to develop the life cycle of Diphyllobothrium erinaceieuropei Rudolphi 1819 (Cestoda, Pseudophyllidea) in Paracyclops fimbriatus and Bufo arenarum as intermediate hosts and dogs as definitive hosts. The eggs of Diphyllobothrium erinaceieuropei from faeces of naturally infected dogs were kept refrigered, in water. In order to obtain coracidiums they were incubated at 25 degrees C, and then were placed in a flask which contained Paracyclops fimbriatus. The copepods were observed to be infected with procercoids 12 days after, (mean temperature 22.6 degrees C) and then, ten tadpoles of Bufo arenarum were put into the same flask. The tadpoles were examined 22, 23, 61 and 107 days later, finding plerocercoids in all them (mean temperature 24.9 degrees C). On the 23rd day, 49 plerocercoids were removed from 6 tadpoles and 28 of them were fed to a bitch. On the 107th day, 11 plerocercoids were recovered from a dead tadpole and 3 of them were fed to another bitch. In the faeces of the first bitch there were observed the eggs of Diphyllobothrium erinaceieuropei 22 days post infection (d.p.i.) and part of the strobila 30 d.p.i.. In the faeces of the second bitch the eggs were found 30 d.p.i..

Animals

Protein profiles as an aid to taxonomy in the genus Diphyllobothrium.

Specific and distinct protein profiles were demonstrated by isoelectric focusing performed on soluble whole-body proteins of four Diphyllobothrium species. The protein patterns differed in number, position and relative density of the fractions separated. Altogether 31-36 protein bands per species were separated by isoelectric focusing in thin-layer polyacrylamide gels. The results show that sensitive chemotaxonomic methods can be used to help characterize and delimit species in the troublesome Diphyllobothrium group.

Animals

Comparison of restriction fragment length polymorphisms of ribosomal DNA between Diphyllobothrium nihonkaiense and D. latum.

Restriction fragment length polymorphisms (RFLPs) of ribosomal DNA (rDNA) were compared between Diphyllobothrium latum and D. nihonkaiense using seven kinds of restriction endonucleases. No intra-specific variation in restriction fragment profiles was shown within both species of Diphyllobothrium. Digestion of the genomic DNA with three endonucleases. SmaI, HinfI and HhaI, provided one or two different bands between two species, although the hybridization patterns generated with the others. HindIII, XbaI, StyI and HaeIII, were the same in both. RFLPs in the digested profiles with SmaI, HinfI and HhaI could be used as species-specific markers even if only fragments of strobilae with morphological similarity were available. Other cestodes, Spirometra erinacei and Taenia saginata, used as controls showed quite different restriction fragment patterns with all the enzymes used.

Animals

The development of the tapeworm Diphyllobothrium latum (L. 1756) (Cestoda; Pseudophyllidea) in its definitive hosts, with special references to the growth patterns of D. dendriticum (Nitzsch, 1824) and D. ditremum (Creplin, 1827).

When Diphyllobothrium latum develops from larva to adult in a definitive host, it first sheds the entire larval 'body' before growth of an adult strobila starts. This process of shedding off the entire larval abothrial extremity, piece by piece, takes about 48 h. By this time the larva has usually reached the anterior third of the small intestine of the host. D. dendriticum and D. ditremum develop quite differently, although exhibiting similar anterior migrations. In these two species the larvae develop directly into adults without the larval 'body' first being shed. The implications of the observed differences in growth pattern between these three species of Diphyllobothrium to the classification of diphyllobothriid cestodes is discussed briefly.

Aging

[Causative agent of human diphyllobothriasis--Diphyllobothrium klebanovskii sp. n].

A new cestode species, Diphyllobothrium klebanovskii sp. n., is described on the basis of experimental examination and morphological study of 51 specimens expelled from men in lower part of the Amur river and 18 specimens expelled from golden hamsters. The larval stage of this cestode is plerocercoid of type F, which is localized in muscles of Oncorhynchus keta and O. gorbuscha. D. klebanovskii sp. n. is a marine species, it differs from D. latum and other species of the genus Diphyllobothrium.

Animals

Use of praziquantel for treatment of Diphyllobothrium sp infection in a dog.

Eggs of a tapeworm, Diphyllobothrium sp (probably D dendriticum), were detected in feces of a healthy, 5-month-old, Siberian Husky. The dog acquired its infection in northern Canada while consuming a diet that included raw salmonid fish. Such fish serve as intermediate hosts for Diphyllobothrium spp. The infection was successfully eliminated by oral administration of a single dose of praziquantel (7.5 mg/kg of body weight.

Animals

Immunocytochemical evidence for the presence of "mammalian" neurohormonal peptides in neurones of the tapeworm Diphyllobothrium dendriticum.

In the nervous system of the obligatory endoparasite Diphyllobothrium dendriticum immunoreactivity (IR) to growth hormone-releasing factor (GRF), peptide histidine isoleucine (PHI), bovine pancreatic polypeptide (BPP), gastrin, gastrin-releasing peptide (GRP), oxytocin, FMRFamide (FMRF) and serotonin (5HT) was demonstrated by immunocytochemical methods. A very strong GRF-IR was observed in the CNS and PNS of larvae and of the constantly growing adult worms. GRF-IR axon terminals occur beneath the basal lamina of the tegument along the inside of the bothridia, the holdfast organ of the worm. GRF-IR fibres surround the yolk producing vitelline glands and occur in the wall of the vagina. PHI-IR was observed in the CNS and PNS of larvae and adult worms. PHI-IR terminals occur beneath the basal lamina of the tegument along the strobila, the nutrient absorbing surface of the worm. PHI-IR fibres seem to innervate the testicular follicles. FMRF-IR fibres and perikarya occur close to the vitelline glands and the uterine pore and in the male copulatory organ. Numerous large 5HT-IR perikarya with long varicose fibres were observed in the nervous system of the worm. 5HT-IR perikarya occur close to the genital atrium. D. dendriticum is the phylogenetically lowest organism in which IR to PHI has been demonstrated.

Animals

Immunocytochemical demonstration of neuropeptides and serotonin in the tapeworm Diphyllobothrium dendriticum.

The present immunocytochemical study concerns the distribution of four neuropeptides, FMRF-amide, vasotocin, leu-enkephalin and neurotensin, and of the bioamine serotonin in the plerocercoid larva of Diphyllobothrium dendriticum. Anti-FMRF-amide and vasotocin-reactivity occurs in perikarya and nerve fibres in the CNS and PNS of this worm. The peptide-containing fibres surround and seem to innervate the musculature and to terminate beneath the basal lamina of the tegument at the inner surface of the bothridia, suggesting a neurotransmitter function. Anti-leu-enkephalin reaction occurs in perikarya and fibres in the main nerve cords and in the PNS. Anti-neurotensin reactive fibres were observed in the neuropile of the nerve cords. Serotonin immunoreactivity was found in neurons in the ganglionic commissure of the brain and along the main nerve cords. This study is the first immunocytochemical identification of neuropeptides and serotonin in a parasitic flatworm and the information gained may be of importance for the development of new antihelminthics.

Animals

A marine Diphyllobothrium plerocercoid (cestoda, pseudophyllidea) from blue whiting (micromestius poutasson).

A type of Diphyllobothrium plerocercoid found in blue whiting, Micromestius poutasson, caught near the north edge of the Faeroe Banks, is described. The most dominant characters of these larvae are their typical dorsoventrally flattened body and their fully extruded and "adult"-like scolex. A morphological comparison with perocercoids of D. dendriticum, D. ditremum and D. latum is given.

Animals

Early development of four Diphyllobothrium species in the final host.

The early development of four Diphyllobothrium species, D. latum, D. dendriticum, D. ditremum, and D. vogeli, are described. D. latum sheds the entire larval body easily and shows a high shedding rate of 82.1% on average. On the other hand, D. dendriticum exhibits a different developmental pattern, with a low shedding rate of 8.7% in the hamster and a high shedding rate of 34.9% in the rat. D. ditremum is difficult to recover from hamsters but shows a high shedding rate of 42.9%. D. vogeli shows a constant recovery rate of 38.3% without shedding. The species specificity of these four diphyllobothriids is discussed briefly in relation to the early developmental pattern and the growth rate.

Animals

Trace element content in two species of whale tapeworms, Diphyllobothrium macroovatum and Diplogonoporus balaenopterae.

Trace elements in two species of whale tapeworms, Diphyllobothrium macroovatum and Diplogonoporus balaenopterae, were analysed by atomic absorption spectroscopy. Six elements (Fe, Cu, Zn, Mn, Cd, Ca) were assayed from different regions of two tapeworms: scolex, neck, immature, mature and gravid proglottids. Whole strobilae at different stages of maturity were also examined. The relationship between the trace element content and the physiological significance is discussed.

Animals

Development of immunoreactivity to the invertebrate neuropeptide small cardiac peptide B in the tapeworm Diphyllobothrium dendriticum.

Neurons immunoreactive to small cardiac peptide B (SCPb) occur in the scolex and neck region of adult Diphyllobothrium dendriticum. The localisation of the SCPb-IR neurons in the peripheral nervous system is very pronounced; they are closely associated to the bothridial musculature in the scolex. SCPb-IR neurons were not observed in plerocercoid larvae but appeared after cultivation in vitro at 37 degrees C for 30 h. Functional and developmental aspects of the SCPb-IR neurons are discussed.

Animals

Scanning electron microscopic study of four Diphyllobothrium species.

Three-dimensional observation was carried out on plerocercoids and adults of Diphyllobothrium dendriticum, D. ditremum, D. latum, and D. vogeli using scanning electron microscopy. The species-specific differences between plerocercoids were recognized in the shapes of the whole body, scolex, and bothrium and the wrinkle pattern on the body surface. The differences between adult worms were also observed in the shapes of the scolex, neck, and genital papillae around the genital pore and the pattern on the egg surface. The significance of species specificity in the three-dimensional morphology of diphyllobothriid cestodes is briefly discussed.

Animals

Observations on the histogenesis of nervous tissue in Diphyllobothrium dendriticum Nitzsch, 1824 (Cestoda, Pseudophyllidea).

The mode of growth of the populations of cells within and immediately surrounding the main lateral nerve cords in the actively growing, immature Diphyllobothrium dendriticum was studied by the use of 3H-thymidine autoradiography. The population of nerve cells within the nerve cord grows only on account of cell migration from the surrounding parenchyma. No mitotic figures were observed in the nerve cords. The rate of growth is high. Within a period of cultivation for 2 days in hamster 34% of the nerve cells within the nerve cords have arrived from the parenchyma. These cells can be considered as cells at the starting point for differentiation into nerve cells. The protective layer of binding cells around the nerve cords also grows on a-count of cells migrating from the parenchyma. The binding cells actively move from the outer regions of the layer inwards close to t-e nerve cord. As stem cells for these types of cell differentiation serve the highly basophilic, actively dividing germinative cells.

Animals

Leucocyte migration in rainbow trout (Oncorhynchus mykiss [Walbaum]): optimization of migration conditions and responses to host and pathogen (Diphyllobothrium dendriticum [Nitzsch]) derived chemoattractants.

A rainbow trout leucocyte-derived chemoattractant(s) was prepared and tested as a stimulant of leucocyte migration. It was used to optimize an in vitro leucocyte migration assay using a 48-well micro chemotaxis chamber. This assay has subsequently been used to test the chemoattractant activity of antigen extracts from the tegument of Diphyllobothrium dendriticum plerocercoids and conditioned medium obtained after in vitro maintenance of live plerocercoids. Leucocytes were found to have an increased directional motility (chemotactic response) to the host-derived chemoattractant(s) but a random increased motility (chemokinetic response) following stimulation/contact with parasite-derived antigens.

Animals

Tests with a new compound (Praziquantel) against Diphyllobothrium latum.

Praziquantel (Droncit) is a new anthelminthic agent with a strikingly wide therapeutic index. The efficiency of the drug against Diphyllobothrium latum was tested in vivo and in vitro. With a drug dose of 50 mg/kg, artificially infected hamsters were completely cured. The threshold value of the active dose was between 2-5 and 10-0 mg/kg. Clinical trials with Praziquantel against human diphyllobothriasis show great promise, all of ten patients treated with 25-0 mg/kg of the drug being cured. Praziquantel had little effect on larval or adult diphyllobothriids in vitro.

Animals

A hidden break in the 28.0S rRNA from Diphyllobothrium dendriticum.

Nondenatured and denatured total RNA from the tapeworm Diphyllobothrium dendriticum (Cestoda) was analysed by agarose gel electrophoresis. It was found that the large subunit ribosomal RNA (lrRNA) is 28.0S and the small subunit ribosomal RNA (srRNA) is 19.5S. Following denaturation the 28.0S rRNA was disrupted into a 19.5S subfragment and a 20.7S subfragment due to the presence of a centrally located hidden break. By hybridization of Northern blot membranes with oligonucleotide probes specific for the 5'- and 3'-ends of the lrRNA respectively, we have shown that the 19.5S subfragment is from the 5'-end (the alpha-subfragment) and the 20.7S subfragment from the 3'-end (the beta-subfragment) of the 28.0S rRNA of D. dendriticum.

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