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Differences in biological characteristics of two strains of the cestode Hymenolepis diminuta.

Biological characteristics of infectivity, growth rate and fecundity of Hymenolepis diminuta isolated from wild Rattus rattus in Japan were compared with parasites of Texas origin maintained for several generations in this and many other laboratories in laboratory bred Rattus norvegicus. The timing of development and maturation was similar in parasites from both sources, but the mean parasite dry weight was less and the mean egg production lower in Japanese parasites in both single and multiple infections. The differences persisted over 10 weeks in single infections, and were unaffected by rat strain. In all experiments there was much greater variation and heterogeneity in the biological characteristics of the Japanese parasites. It was concluded that the Texas parasites were better adapted to R. norvegicus and in the course of adaptation had become more homogeneous, and that the difference between the parasite strains had a complex genetic basis. Some Japanese parasites of the early isolated generations failed to produce normal eggs, but the proportion of these decreased in later generations. However, selected individual Japanese parasites whose egg production was equal to that of parasites of Texas origin did not produce offspring of larger mean size or higher mean fecundity, and heterogeneity of these characteristics was maintained. In the intermediate host, the mean number of cysticercoids of the Japanese isolate per beetle was higher than that of the Texas strain in Tribolium confusum but lower in Tenebrio molitor. The greater heterogeneity exhibited by Japanese parasites and the genetic basis of the strain difference are discussed with particular reference to geographical isolation, differences in definitive hosts and co-evolution of wild and laboratory host and parasite populations.

Animals↗

Cysteine metabolism in the cestode Hymenolepis diminuta.

The major pathways for cysteine catabolism in Hymenolepis diminuta have been investigated. The parasite has an active cystathionine-beta-synthase and, as in other tissues, this enzyme has a wide substrate specificity. However, the enzyme from H. diminuta differs significantly from the mammalian enzyme in showing a high serine sulphydrase activity and a high serine lyase activity. There was only low gamma-cystathionase activity in H. diminuta and again the enzyme showed a range of substrate specificities. Cysteine aminotransferase activity was readily demonstrated in the tapeworm, but there was no evidence for 3-mercaptopyruvate sulphotransferase activity. An oxidative pathway for cysteine catabolism in H. diminuta was shown by the presence of cysteine dioxygenase and cysteine sulphinate transaminase. The properties of the helminth cysteine dioxygenase were very similar to those of rat liver. H. diminuta was able to reduce cystine to cysteine via a glutathione-cysteine transhydrogenase system.

Animals↗

The role of sex steroids in the complex physiology of the host-parasite relationship: the case of the larval cestode of Taenia crassiceps.

Sex steroids play a significant role in regulating the parasite load in experimental intraperitoneal Taenia crassiceps cysticercosis of male and female Balbc/anN mice. Briefly, oestrogens increase parasite loads and androgens decrease them (1) by acting directly on the parasite, favouring or hindering its reproduction, respectively, and (2) by biasing the hosts' immune response towards a parasite-permissive Th2 or a parasite-restrictive Th1 response. The infected male host also undergoes drastic endocrinological and behavioural changes that may impinge upon the course of infection, and the host's mating behaviour and its exposure to predators. In addition, at different times of infection, significant changes occur in the expression of c-fos in the host's hyppocampus, hypothalamus and preoptic area. Thus, the host's brain seems to sense and/ or react to intraperitoneal infection. The physiological domains of the network affected by the infection, which classically included the hypothalamus-pituitary-axis and the immune system, must now incorporate the host's sexual hormones and other areas of the brain. The network's complex circuitry and functions may help understand some basic questions of parasitology (i.e. the hosts' sexual dimorphism in parasite infections, host-parasite specificity, heterogeneity in the course and outcome of infections at different stages of parasite and host development). The plurality of elements and the complexity of the network that regulates the host-parasite relationship also point to additional strategies for the treatment and control of infections.

Animals↗

The neuropeptide F (NPF) encoding gene from the cestode, Moniezia expansa.

Neuropeptide F (NPF) is an abundantly expressed neuropeptide in platyhelminth nervous systems, and exhibits a moderate, myogenic effect on muscle preparations of parasitic flatworms. NPF displays structural similarities to peptides from molluscs and vertebrate members of the neuropeptide Y (NPY)-superfamily of peptides. NPY is one of the most abundant and highly conserved neuropeptides within vertebrates and similarities between the gene organization of NPY, pancreatic polypeptide (PP) and peptide tyrosine tyrosine (PYY), suggest a common evolutionary origin of this peptide family. Dual localization analyses coupled with confocal scanning laser microscopy revealed a close spatial relationship between NPF-containing nerves and muscle fibres in M. expansa. Molecular cloning techniques identified the M. expansa NPF (mxNPF) precursor and characterized the isolated transcript which encodes an open reading frame of 57 amino acids. The transcript possesses a 17 amino acid signal peptide and the mature NPF sequence (39 amino acids) followed by a carboxyterminal glycyl extension. Sequence analysis of genomic DNA identified a product which possessed a 54 base pair intron with consensus sequences for 5' and 3' splice sites. The M. expansa npf gene possesses a phase 2 intron within the penultimate arginyl residue, a characteristic feature of NPY superfamily peptide-genes. The intron-exon organization of the npf gene, coupled with the abundant expression of NPF within the nervous systems of flatworms, suggests an early evolutionary origin for this peptide transmitter family within the nervous systems of basal bilaterian metazoans.

Amino Acid Sequence↗

Observations on the phylogeny of the cestode order Pseudophyllidea Carus, 1863.

A preliminary phylogenetic analysis of the Pseudophyllidea, based on the 16 type-genera of putative families, indicates that a division into two suborders is reasonable. The subordinal grouping are, on the whole, congruent with those suggested by earlier workers, but the positions of three genera, Hexagonoporus, Cephalochlamys and Parabothriocephalus, are somewhat anomalous with respect to earlier work.

Animals↗

Preliminary cladistic analysis of genera of the cestode order Trypanorhyncha Diesing, 1863.

A preliminary cladistic analysis was carried out on the 49 currently recognised genera of the order Trypanorhyncha. Forty-four characters were analysed; a functional outgroup was used for scolex and strobilar characters, while Nybelinia was utilised to polarise characters related to the rhyncheal system. Eight well-resolved clades were evident in the resultant cladogram, which is compared with existing phenetic classifications. An analysis of families resulted in a similar clustering of taxa to that observed in the case of the genera. The results suggest that two key characters used in existing classifications, namely the presence of sensory fossettes on the bothridia and the development of atypical heteroacanth and poeciloacanth armatures from typical heteroacanth armatures, have occurred on several occasions. Some clades provide support for the arrangements used in current classifications. Suggestions are made for future avenues of research which might provide more robust phylogenetic data for the Trypanorhyncha.

Animals↗

Cestodes of the family Dilepididae (Cestoda:Cyclophyllidea) from fish-eating birds in Mexico: a survey of species.

A survey of adults of dilepidid tapeworms (Cyclophyllidea) from piscivorous birds from Mexico is presented on the basis of the taxonomic evaluation of freshly collected and voucher specimens. The following species are reported (first records from Mexico marked with an asterisk): Cyclustera capito (Rudolphi, 1819); *C. ibisae (Schmidt & Bush, 1972); *Dendrouterina ardeae Rausch, 1955; *D. herodiae Fuhrmann, 1912; *D. papillifera (Fuhrmann, 1908); Glossocercus auritus (Rudolphi, 1819); *Neogryporhynchus cheilancristrotus (Wedl, 1855); Paradilepis caballeroi Rysavy & Macko, 1973; Paradilepis sp.; Parvitaenia cochlearii Coil, 1955; and Valipora mutabilis Linton, 1927. Dendrouteria herodiae is reported from America for the first time. New definitive hosts are Phalacrocorax olivaceus for C. capito, N. cheilancristrotus and P. caballeroi; Casmerodius albus and Egretta thula for G. auritus; and E. thula for D. herodiae. Data on the morphology of the rostellar hooks of all species, their hosts and distribution in Mexico are provided.

Animals↗

Life-cycles of cestodes of the genus Branchiopodataenia Bondarenko & Kontrimavichus, 2004 (Cestoda: Hymenolepididae) from gulls in Chukotka.

Data are presented on the life-cycles and the postembryonal development of four species of Branchiopodataenia Bondarenko & Kontrimavichus, 2004, B. anaticapicirra Bondarenko & Kontrimavichus, 2004, B. arctowskii (Jarecka & Ostas, 1984), B. haldemani (Schiller, 1951) and B. pacifica (Spassky & Jurpalova, 1968), which are specific parasites of gulls. The investigation was carried out in Chukotka (Chaun Bay) between 1971 and 1981 under natural and experimental conditions. Branchiopod crustaceans were exclusive natural and experimental intermediate hosts of all of the species studied; this fact provided additional evidence for the erection of Branchiopodataenia. The metacestodes exhibit a pattern of postembryonal development and a typical larval form, termed a 'cercocyst', which is a modification of a cysticercoid. This modification of the metacestode does not occur in species of Wardium Mayhew, 1925, the genus with which species of Branchiopodataenia had previously been affiliated.

Animals↗

Eutetrarhynchid cestodes from Atlantic and Mediterranean elasmobranch fishes, with the description of two new species of Dollfusiella Campbell & Beveridge, 1994 and redescriptions of Prochristianella papillifer (Poyarkoff, 1909) Dollfus, 1957 and Parachristianella trygonis Dollfus, 1946.

Dollfusiella elongata n. sp. is described from the spiral valves of Rhinobatos rhinobatos (Linnaeus) and R. cemiculus Geoffroy St-Hilaire off the coast of Tunisia, while D. aculeata n. sp. is described from the spiral valves of Dasyatis pastinaca (Linnaeus) off the western coast of France, Dasyatis tortonesei Capape off the coast of Tunisia and Dasyatis chrysonota (Smith) var. marmorata off the coast of Senegal. A redescription of Dollfusiella spinifer (Dollfus, 1969) Campbell & Beveridge, 1994 is included based on the type-specimens from Myliobatis aquila (Linnaeus) from the Mediterranean coast of France. Prochristianella papillifer (Poyarkoff, 1909) Dollfus, 1957 is redescribed from specimens from Dasyatis pastinaca off Tunisia and the scolex and mature segments are described for the first time. Parachristianella trygonis Dollfus, 1946 is redescribed from Dasyatis pastinaca off the coast of France and Dasyatis tortonesei off Tunisia, with the mature and gravid segments being described for the first time. Parachristianella monomegacantha Kruse, 1959 is reported for the first time from the elasmobranchs Dasyatis pastinaca , Myliobatis aquila , Rhinobatos cemiculus and R. rhinobatos . Definitions of the related genera Dollfusiella Campbell & Beveridge, 1994 and Prochristianella Dollfus, 1946 are revised. Prochristianella spinulifera Beveridge & Jones, 2000 is transferred to Dollfusiella as D. spinulifera n. comb. New combinations proposed formally for the first time are: D. aetobati (Beveridge, 1990) n. comb., D. bareldsi (Beveridge, 1990) n. comb., D. lineata (Linton, 1909) n. comb., D. litocephalus (Heinz & Dailey, 1974) n. comb., D. macrotrachelus (Heinz & Dailey, 1974) n. comb., D. michiae (Southwell, 1929) n. comb., D. musteli (Carvajal, 1974) n. comb., D. schmidti (Heinz & Dailey, 1974) n. comb. and D. vooreemi (Sao Clemente & Gomes, 1989) n. comb. The type-specimens of Prochristianella tenuispinis (Linton, 1890) Dollfus, 1946 were re-examined and the species is transferred to Dollfusiella as D. tenuispinis (Linton, 1890) n. comb. Features of known species of Dollfusiella are presented in tabular form.

Africa↗