Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “CESTODA”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 37 records · Page 2Linked to original sources

Comparative analysis of amino acids of three species of gangesia (Cestoda: Proteocephalata).

A total of 21 amino acids were detected in the present investigations on three species of Gangesia (Cestoda: Proteocephalata) viz. G. bengalensis Woodland, 1924, G. hanumanthai Seth & Capoor, 1982 and G sanehensis Malhotra et al., 1981. The study was conducted in a sub-humid region around Allahabad, India. The implications of amino acid utilization in metabolic activities of fish tapeworms have been discussed.

Amino Acids↗

Description and morphometric variability of Paranoplocephala serrata n. sp. (Cestoda: Anoplocephalidae) in collared lemmings (Dicrostonyx spp., Arvicolinae) from Arctic Siberia and North America.

We describe Paranoplocephala serrata n. sp. (Cestoda, Anoplocephalidae) from collared lemmings Dicrostonyx torquatus and D. groenlandicus (Arvicolinae, Rodentia) in Arctic Siberia and North America. The new species was recorded from the Yamal Peninsula (type-locality), Yana Delta, Kolyma Delta, Wrangel Island, Alaska and Victoria Island/Kent Peninsula (Northwest Territories). P. serrata n. sp. is characterised by a long, ribbon-like strobila, distinctly serrated segments, a small scolex, unilateral or infrequently alternating genital pores and testes confined to the antiporal part of the segment. It differs from the related species (Andrya bairdi, Parandrya feodorovi and Paranoplocephala manseri) by several morphological features, including the distribution of testes (several testes antiporal to ventral longitudinal osmoregulatory canal), structure of the cirrus-sac and vagina, and large eggs (0.053-0.068 mm in the type-material). The material of P. serrata n. sp. from North America differs from the Siberian material by the shorter cirrus-sac, smaller dimensions of the female reproductive organs, larger seminal receptacle and larger eggs. However, the statistical differences in the dimensions of reproductive organs mainly reflect the larger size of mature segments in Siberian specimens compared with North American specimens. The main diagnostic features, i.e. the size and form of scolex and suckers, number and distribution of testes, position of female glands, vagina/cirrus-sac ratio and morphology of reproductive organs, do not differ markedly between the Palaearctic and Nearctic specimens. According to the structure of the early-stage uterus, A. bairdi Schad, 1954 belongs to the genus Paranoplocephala. Parandrya Gulyaev & Chechulin, 1996 is probably a synonym of Paranoplocephala. A redescription is provided for Paranoplocephala bairdi n. comb.

Animals↗

Wardium canarisi n. sp. (Cestoda: Hymenolepididae) parasite of Arenaria melanocephala (Aves: Charadrii) of Alaska.

The authors describe and illustrate Wardium canarisi n. sp. (Cestoda: Hymenolepididae), an intestinal parasite of Arenaria melanocephala (Aves: Charadrii) from Alaska, characterised by a strobila 20-40 mm long, 10 aploparaksoid hooks 19-21 microm long, a short cylindrical cirrus (40 microm) covered with very minute spines (0.2 microm), and a short (8-18 microm) and extremely narrow (1 microm) copulatory vagina. These characters have no equivalent, even approximate, among the 27 species of Wardium parasitic in the Charadrii which are reviewed. The genus Debrosia Spassky, 1987 appears to be justified.

Alaska↗

[Wardium longosacco (Joyeux & baer, 1939) n. comb. (Cestoda: Hymenolepididae) parasite of Charadrius marginatus (Aves: Charadrii) of South Africa].

The authors describe and illustrate Wardium longosacco (Joyeux & Baer, 1939) n. comb. (Cestoda: Hymenolepididae) collected from Charadrius marginatus from South Africa. The species with a strobila 7 cm long is characterised by one crown of ten aploparaksoid hooks 27-30 microm long, a simple genital atrium, a long evaginated cirrus (120 microm) which is glabrous, regularly cylindrical and slender (12-6.5 microm in diameters) and a simple, tubular, membranous vagina. The species Hymenolepis clandestina sensu Deblock (1964) nec (Krabbe, 1869) is a synonym of W. longosacco (Joyeux & Baer, 1939) n. comb.

Animals↗

Prochristianella spinulifera n. sp. (Cestoda: Trypanorhyncha) from Australian dasyatid and rhinobatid rays.

Prochristianella spinulifera n. sp. (Cestoda: Trypanorhyncha: Eutetrarhynchidae) is described from the spiral valves of the rays Rhinobatos typus (Rhinobatidae) and Himantura fai (Dasyatidae) from Heron Island, Queensland, Australia. The new species is distinguished from all congeners by the deltoid microtriches covering the anterior 80% of the scolex and the presence of a dorsoventrally elongate genital atrium. The species occurred in the anteriormost section of the spiral valve of R. typus. The orientation of the armature of this and other congeners is such that principal rows of hooks begin on the bothridial surface of the tentacle and end on the antibothridial surface.

Animals↗

The genus Biuterina Fuhrmann, 1902 (Cestoda, Paruterinidae) in the Old World: redescriptions of four species from Afrotropical passeriformes.

Four species of Biuterina Fuhrmann, 1902 (Cestoda, Cyclophyllidea, Paruterinidae), originally described from Afrotropical passeriform birds, are redescribed and figured on the basis of their type-specimens. These are B. pentamyzos (Mettrick, 1960) from Prionops plumata (Laniidae) in Zimbabwe, B. quelea (Mettrick, 1963) from Quelea quelea (Ploceidae) in Zimbabwe, B. ugandae Baylis, 1919 from Chalcomitra senegalensis (Nectariniidae) in Uganda and B. zambiensis (Mettrick, 1960) from Campephaga flava (Campephagidae) in Zimbabwe. The rostellum of B. quelea is a spherical structure filled with strongly-developed glandular tissue and possessing a weak musculature. The remaining three species have a sucker-like rostellar apparatus with moderately developed glandular tissue in the rostellum and around it. It is considered that the glandular elements are an inherent part of the rostellar apparatus of the paruterinids. An armament consisting of fine, punctiform, spine-like structures arranged in transverse rows on the inner surface of suckers is observed in B. pentamyzos. This is the first record of sucker armature in the Paruterinidae.

Africa↗

Alcataenia fraterculae sp. n. from the horned puffin, Fratercula corniculata (Naumann), Alcataenia cerorhincae sp. n. from the rhinoceros auklet, Cerorhinca monocerata (Pallas), and Alcataenia larina pacifica ssp. n. (Cestoda: Dilepididae) in the North Pacific basin.

Three Cestodes representing two species of the genus Alcataenia Spasskaia, 1971 and a subspecies of Alcataenia larina (Krabbe, 1869) are described. Alcataenia fraterculae sp. n. (Cestoda: Dilepididae) was found in horned puffins, Fratercula corniculata (Naumann), and other species of seabirds from localities in the western Aleutian Islands, Gulf of Alaska, Bering Sea, and Chukchi Sea. Alcataenia cerorhincae sp. n. is described from the rhinoceros auklet, Cerorhinca monocerata (Pallas) in the eastern North Pacific Ocean and western Aleutian Islands. Alcataenia larina pacifica ssp. n. is recognized from species of Laridae and other seabirds in the North Pacific Ocean, Sea of Okhotsk, Bering Sea and the region of the Arctic Ocean near Bering Strait. It is distinguished from A. larina larina (Krabbe, 1869) by a greater number of testes, a longer cirrus sac, and variation in the position of the genital ducts which may be either dorsal to or between the osmoregulatory canals. A fraterculae and A. cerorhincae are most similar to A. larina and particularly to the North Pacific form A. l. pacifica. Generally specimens of A. fraterculae can be distinguished from the other taxa by larger rostellar hooks, a longer cirrus sac, and a combination of other characters. A. fraterculae, A. cerorhincae, and A. l. pacifica however represent a complex of cryptic species in which there is extensive overlap in some morphological characters. Results of a discriminant analysis among these nominal taxa were significant and, in combination with data about other morphological characters and host and geographic distribution, clearly indicated that these represent three species in the North Pacific basin.

Animals↗

[Description of Scalithrium n. gen. (Cestoda, Tetraphyllidea) with Scalithrium minimum (Van Beneden, 1850) n. comb., a parasite of Dasyatis pastinaca (Elasmobranchii, Dasyatidae), as type species].

Scalithrium gen. n. (Cestoda, Tetraphyllidea) is proposed with Scalithrium minimum (Van Beneden, 1850) n. comb., parasite of Dasyatis pastinaca (Elasmobranchii, Dasyatidae) as type-species. The new genus Scalithrium (Tetraphyllidea, Phyllobothriidae, Rhinebothriinae) is erected for several species previously included in the genus Rhinebothrium. These species have a scolex with four bothridia, the distal surface of which is divided by transverse septa in a single row of loculi. Scalithrium minimum (Van Beneden, 1850) n. comb. is redescribed from specimens collected from the type-host Dasyatis pastinaca in Tunisia and becomes the type-species of the new genus. After Braun (1900) Echeneibothrium variabile Van Beneden, 1850 is considered as type-species of the genus Echeneibothrium. Species of Rhinebothriinae to be transferred into the genus Scalithrium are discussed and a key is proposed for the eight species.

Animals↗

Progamotaenia capricorniensis sp. nov. (Cestoda: Anoplocephalidae) from wallabies (Marsupialia: Macropodidae) from Queensland, Australia.

Progamotaenia capricorniensis sp. nov. (Cestoda: Anoplocephalidae) is described from the wallabies Macropus dorsalis (Gray, 1837) and Petrogale assimilis Ramsay, 1877 from Queensland, Australia. The new species is characterised by a fimbriated velum composed of 26-32 digitiform to triangular projections on each side of the proglottis, paired uteri and 140-190 testes distributed in a single band across the medulla. Minor variation occurs in the distribution of the testes. The above characters distinguish the new species from its most closely related congeners P. lagorchestis (Lewis, 1914), P. proterogyna (Fuhrmann, 1932), P. spearei Beveridge, 1980 and P. villosa (Lewis, 1914). P. capricorniensis appears to exhibit a highly disjunct distribution within its usual host, M. dorsalis.

Animals↗

Description of Paranoplocephala yoccozi n. sp. (Cestoda: Anoplocephalidae) from the snow vole Chionomys nivalis in France, with a review of anoplocephaud cestodes of snow voles in Europe.

We describe Paranoplocephala yoccozi n. sp. (Cestoda: Anoplocephalidae) from the snow vole Chionomys nivalis in Bourg-Saint-Maurice, French Alps, compare it with several related species from rodents, and review the anoplocephalid cestodes of snow voles in Europe. Paranoplocephala yoccozi n. sp. is primarily distinguished from the related species by its large scolex of characteristic shape, robust neck region, and the structure of the cirrus sac, vitellarium and vagina. We show that the anoplocephalid cestodes of snow voles in Europe, representing the genera Anoplocephaloides and Paranoplocephala, include at least seven species. This fauna consists primarily of species that snow voles share with other voles inhabiting the high-mountain areas. Some of the species, including P. yoccozi n. sp., appear to have a very localized distribution, which is assumed to be a consequence of the historical fragmentation of snow vole populations.

Animals↗

Evolutionary relationships of sibling tapeworm species (Cestoda) parasitizing teleost fishes.

DNA/DNA hybridization and sequencing of rDNA (partial 18S rDNA and ITS1) were used to investigate phylogenetic relationships among seven host-specific Bothriocephalus parasites (Cestoda, Pseudophyllidae). The small nucleotide divergence between six of the seven bothriocephalids suggests that isolation and differentiation of Bothriocephalus lineages in the different host species probably occurred recently and over a short time span. Comparison of the molecular phylogeny of the parasite species to the phylogeny of their hosts (teleostean fishes) revealed little congruence between the branching patterns of hosts and parasites, suggesting that bothriocephalids have not cospeciated with their hosts.

Animals↗

Experimental infection of Atlantic salmon (Salmo salar) with marine Eubothrium sp. (Cestoda: Pseudophyllidea): observations on the life cycle, aspects of development and growth of the parasite.

The life cycle of marine Eubothrium sp. (Cestoda: Pseudophyllidea), from Atlantic salmon (Salmo salar L.) was experimentally completed in one year and included only one intermediate host (Acartia tonsa Dana) (Copepoda: Calanoida). Adult cestodes were collected from farmed salmon, and ripe eggs released by the cestodes were fed to Acartia tonsa. Ingested eggs hatched in the gut and the larvae developed in the haemocoel of the copepod for 15 days at 16 degrees C. A total of 170 seawater-reared salmon were exposed to infected copepods and the total prevalence of Eubothrium sp. in the salmon after infection was 95.3%, with a mean intensity of 15.0 (range 1-87). The infected salmon were kept in the laboratory where the growth of the cestodes was studied for eleven months. Mean length of the cestodes increased with time, but a large variation among the cestodes was observed. Growth and maturation of the cestodes were dependent on host size and the number of worms present in the intestine. No evidence of mortality of Eubothrium sp. was observed during the experimental period.

Animals↗

Redescription of Andrya cuniculi (Blanchard, 1891) (Cestoda: Anoplocephalidae), a parasite of Oryctolagus cuniculus (Lagomorpha) in Spain.

Andrya cuniculi (Blanchard, 1891) (Cestoda: Anoplocephalidae) is redescribed from Oryctolagus cuniculus (L.) from Spain. Large ranges of variability in body length and width, testes number and position of the cirrus sac were observed. An external seminal vesicle covered with small glandular cells is present. The pattern of development of the uterus is similar to that of Andrya rhopalocephala (Riehm, 1881). The only reliable differential characters to distinguish A. cunliculi from A. rhopalocephala are the position of the uterus in gravid segments and the position of the testes in mature segments. The uterus of A. cuniculi occupies the median field and parts of the lateral fields but is restricted to the median field in A. rhopalocephala. Testes are distributed more symmetrically lateral to the female organs in A. cuniculi but are mostly antiporal in A. rhopalocephala.

Animals↗

Review of the Rhopalothylacidae Guiart, 1935 (Cestoda: Trypanorhyncha), with a description of the adult of Pintneriella musculicola Yamaguti, 1934 and a redescription of P. gymnorhynchoides (Guiart, 1935) comb. n.

The family Rhopalothylacidae (Cestoda: Trypanorhyncha) is reviewed. The type species, Rhopalothylax gymnorhynchoides Guiart, 1935, is redescribed from the type specimens and belongs within the genus Pintneriella Yamaguti, 1934, previously described only from the plerocercus. Rhopalothylax therefore becomes a junior synonym of Pintneriella. The adult of Pintneriella musculicola Yamaguti, 1934 is described for the first time, from the shark Carcharias taurus Rafinesque from Australia. Pintneriella is characterised by two bothridia, a typical heteroacanthous armature, a unique, bipartite external seminal vesicle and a uterus deviated porally, terminating at a uterine pore. It belongs within the Heteracanthoidea but is distinguishable both from the Eutetrarhynchidae and the Gilquiniidae, the two families which it most closely resembles. Cladistic analyses align Pintneriella within the clade containing the families Gilquiniidae, Gymnorhynchidae and Molicolidae rather than with the Eutetrarhynchidae. The family Rhopalothylacidae is therefore retained provisionally to accommodate Pintneriella within the Heteracanthoidea. The second genus of the Rhopalothylacidae, Clujia Guiart, 1935, is unrecognisable from its description and cannot be redescribed from its holotype. It is therefore considered a genus inquirendum.

Animals↗

Review of the genus Progrillotia Dollfus, 1946 (Cestoda: Trypanorhyncha), with a redescription of Progrillotia pastinacae Dollfus, 1946 and description of Progrillotia dasyatidis sp. n.

Progrillotia pastinacae Dollfus, 1946 (Cestoda: Trypanorhyncha) is redescribed from the spiral valve of Dasyatis pastinaca (Linnaeus) (Dasyatididae) from the coast of France. Progrillotia dasyatidis sp. n. is described from the spiral valves of Dasyatis tortonesei Capapé (Dasyatididae) from the Mediterranean in the Gulf of Gabès (Tunisia) and D. pastinaca from the Bassin d'Arcachon (France). The new species differs from congeners in having, on the tentacles, a single rather than two rows of intercalary hooks and fewer testes. The generic definition is emended based upon the new species, the redescription of P. pastinacae Dollfus, 1946 and re-examination of the type specimen of P. louiseuzeti Dollfus, 1969. Important additional characters noted are that the tentacular hooks are solid, a prebulbar organ is present and that there are gland cells attached to the retractor muscle within the bulb. A cladistic analysis suggests that the genus is closely allied with the Eutetrarhynchidae. Progrillotia dollfusi Carvajal et Rego, 1983 is provisionally excluded from the genus as the adult of the species is unknown and a key character of the genus is that the testes are pre-ovarian.

Animals↗

Effect of Triaenophorus crassus (Cestoda) infection on behavior and susceptibility to predation of the first intermediate host Cyclops strenuus (Copepoda).

Some parasites have been shown to manipulate host behavior so that parasite transmission to the next host is enhanced. Infection with Triaenophorus crassus Forel (Cestoda) caused alterations in the activity and microhabitat selection of the first intermediate host Cyclops strenuus Fischer (Copepoda) in the laboratory. Infected copepods made more starts to swim but spent less time swimming than uninfected copepods. These changes were independent of the intensity of infection. In a water column illuminated from above, infected copepods approached the surface, whereas uninfected ones remained close to the bottom. In the dark both infected and uninfected copepods stayed near the bottom. Finally, infection with T. crassus increased the probability of C. strenuus being eaten by the second intermediate host, whitefish (Coregonus lavaretus L. s.l.), in the laboratory. In experimental infections, 10-day-old procercoids had significantly lower infectivity for whitefish than older (12-, 14-, and 21-day-old) procercoids. Behavioral changes were detected in infected copepods containing procercoids 12 days old or older but not in experiments with 10-day-old procercoids. These results may indicate that T. crassus changes the behavior of the copepod host only after it has become infective to the next host, which is consistent with the active manipulation hypothesis.

Analysis of Variance↗

Identification of life cycle stages of Cyathocephalus truncatus (Cestoda: spathebothriidea) using molecular techniques.

Morphological identification of tapeworm species at larval stages (procercoids and cysticercoids) is often difficult because few diagnostic characters are available. In the present study, a molecular approach (sequencing of partial 18S rDNA gene) was used to evaluate the genetic similarity between adult specimens of Cyathocephalus truncatus (Pallas, 1871) (Cestoda: Spathebothriidea) found in fish, its definitive host, and procercoids of the same species recovered from amphipod, Echinogammarus stammeri (Karaman, 1931). Furthermore, cestode cysticercoids of uncertain species were found in the amphipod's hemocoel. The sequences obtained from adults and procercoids were identical, and even very similar to those of C. truncatus available in GenBank, whereas the sequences obtained from cysticercoids differed significantly from those of adults and procercoids, indicating that these larvae belong to another species; later it was demonstrated that they were cysticercoids of Microsomacanthus pachycephala (Linstow, 1972), a cestode of the Hymenolepididae (Cyclophyllidea). The results of this investigation show that the comparison of nucleotide sequence data may avoid misclassification of developmental stages of parasites, which use the same intermediate host.

Animals↗