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A protocol of the new method of DNA extraction from the ethanol fixed parasitic worms is described. The method is based on the use of the guanidine thiocyanate extraction buffer after evaporation of the ethanol from the tissues by drying. The method has been successfully used on several groups of parasitic Plathyhelminthes and provided higher DNA yield than a conventional phenol-chloroform extraction.
Unilatus irae sp. nov. (Dactylogyridae) is described from the gills of the armored catfish, Leporacanthicus galaxias Isbrücker et Nijssen (Loricariidae: Ancistrinae), from Guamá river, Pará State, Brazil. The new species can be differentiated from its cogeneners by the combination of the following features: anterior anchor with well-developed superficial root, inconspicuous deep root, shaft bent at midpoint, forming angle of approximately 60°, evenly short curved point; posterior anchor with inconspicuous roots, sclerotized cap of base with small protuberance for articulation to posterior bar; evenly curved shaft and short point; anterior bar broadly V-shaped, with small posteromedial projection; and posterior bar anteriorly expanded on it midportion, with expanded ends slightly curved in posterior direction.
A high infestation of the monogenean Gussevia tucunarense in a cultivation of bujurqui-tucunare was reported. The prevalence was 100%. The mean intensity and abundance of the parasite was 164.4 of parasites per individual. This is the first report of a high infestation by G. tucunarense in C. semifasciatus cultured from the Peruvian Amazon.
The most species rich order of tapeworms is the Cyclophyllidea and prior to wide-scale sampling of these worms for phylogenetics, we wished to develop reliable PCR primers that would capture fragments of mitochondrial (mt) DNA with phylogenetic utility across the order. Nuclear ribosomal RNA gene sequences are well-established and valuable markers for resolving flatworm interrelationships spanning a wide range of taxonomic divergences, but fail to provide resolution amongst recently diverged lineages. Entire mt genomes of selected cyclophyllidean tapeworms are available on GenBank, and we used these to design PCR primers to amplify mtDNA from cox1, rrnL and nad1 for a range of cyclophyllideans (7 davaineids, 1 hymenolepidid and 1 dilepidid) and selected outgroups (Tetrabothrius sp. and Mesocestoides sp.). A combined nuclear and mt gene data set was used to estimate a reference phylogeny and the performance of the individual genes was compared to this. Although nuclear and mt genes each contributed to the structure and stability of the phylogenetic estimate, strongest nodal support was provided by nuclear data amongst the basal lineages and by mt data amongst the most recently diverged lineages. The apparent complementarity afforded by combining nuclear and mt data was compromised by these data partitions providing conflicting signal at poorly supported nodes. Nevertheless, we argue for a combined evidence approach. PCR primers that amplify rrnL were designed and tested successfully against a diversity of cyclophyllideans; rrnL and nad1 appeared to be more informative than the fragment of cox1. The genus Raillietina was not supported by molecular evidence. The new primers will likely provide considerable resolution to estimates of cyclophyllidean interrelationships in future studies.
The spermiogenesis process in Wardula capitellata begins with the formation of a differentiation zone containing two centrioles associated with striated rootlets and an intercentriolar body. Each centriole develops into a free flagellum orthogonal to a median cytoplasmic process. Later these flagella rotate and become parallel to the median cytoplasmic process, which already exhibits two electron-dense areas and spinelike bodies before its proximodistal fusion with the flagella. The final stage of the spermiogenesis is characterized by the constriction of the ring of arched membranes, giving rise to the young spermatozoon, which detaches from the residual cytoplasm. The mature spermatozoon of W. capitellata presents most of the classical characters reported in digenean spermatozoa such as two axonemes of different lengths of the 9 + “1” trepaxonematan pattern, nucleus, mitochondrion, two bundles of parallel cortical microtubules and granules of glycogen. However, some peculiarities such as two lateral expansions accompanied by external ornamentation of the plasma membrane and spinelike bodies characterize the mature sperm. Moreover, a new spermatological character is described for the first time, the so-called cytoplasmic ornamented buttons.
Proctocaecum blairi sp. nov. is described from specimens found in the intestine of an Australian freshwater crocodile, Crocodylus johnstoni, from Northern Territory, Australia. The most important diagnostic features of the new species are the body proportions and size, the position of the pharynx (relative length of the prepharynx and oesophagus), the relative length and position of the vitelline fields, and the number, shape and size of the circumoral spines. The new species is morphologically most similar to Proctocaecum atae, P. elongatum, P. crocodili, P. gairhei and Acanthostomum slusarskii. It differs from all of these species in having a much longer prepharynx, and differs from both P. atae and P. crocodili in having a much longer body and posteriorly situated vitelline fields. Proctocaecum blairi sp. nov. differs from P. elongatum in having a shorter body, a greater forebody to hindbody ratio, a much smaller ventral sucker, and a higher number of circumoral spines (23 vs 21 in P. elongatum). The new species differs from P. gairhei in possessing a much larger body length:width ratio and an ovary separated from the anterior testis by a seminal receptacle. Acanthostomum slusarskii lacks a gonotyl and has fewer circumoral spines than the new species. Proctocaecum blairi sp. nov. is the third species of Proctocaecum and the fourth cryptogonimid species known from crocodiles in Australia.
Free-living Plathelminthes constitute an important component of meiobenthic communities in various marine benthic environments, but research focusing on this group is generally scarce. The current study investigated the free-living interstitial flatworms of the shallow sandy sublittoral zone of the southern Baltic coast. Sediment samples were taken at Hel Peninsula at water depths of 1.5 m and 7 m, and the plathelminths were identified alive to the species level. In total, 22 species were identified. The majority of the species belonged to Kalyptorhynchia and Proseriata, but Acoela recently moved from Plathelminthes into their own phyllum and represented by Mecynostomidae, was the most numerous group. The average total plathelminth densities ranged between 6 and 74 ind. 10 cm–2. The vertical distribution of the plathelminth fauna in the sediments was usually limited to the upper 3–4 cm, except for acoels which penetrated deeper into the sediment layers. The role of both sediment water saturation and oxygen availability appeared to be the main factors limiting flatworm occurrence in the sediments investigated in this study.
The opecoelid species Macvicaria jagannathi (Gupta et Singh, 1985) Bijukumar, 1997 (new syn. Plagioporus deeghaensis Gupta et Gupta, 1988) and Neolebouria lineatus Aken’Ova et Cribb, 2001 are redescribed from Nemipterus furcosus, from the waters off New Caledonia. Provisional keys to the genera Macvicaria Gibson et Bray, 1982 and Neolebouria Gibson, 1976 are presented. The following new combinations are made: Macvicaria yamagutii (Gupta et Ahmad, 1977), M. puriensis (Gupta et Govind, 1984) and M. chilkai (Gupta et Govind, 1984).
The phylogenetic relationships of representative species of the superfamily Lepocreadioidea were assessed using partial lsrDNA and nad1 sequences. Forty-two members of the family Lepocreadiidae, six putative members of the Enenteridae, six gyliauchenid species and one Gorgocephalidae, were studied along with 22 species representing 8 families. The Lepocreadioidea is found to be monophyletic, except for the two species of the putative enenterid genus Cadenatella, which are found to be only distantly related to the lepocreadioids. The Lepocreadioidea is formed of five clades in a polytomy, the Gorgocephalidae, a clade containing the Enenteridae and Gyliauchenidae, a small clade of atypical lepocreadiines and the deep-sea lepidapedine lepocreadiids, a small clade consisting of a freshwater form and a group of shallow-water putative lepidapedines and the final clade includes the remaining lepocreadiids. Thus, the generally accepted concept of the Lepocreadiidae is polyphyletic. The Enenteridae (minus Cadenatella) and the Gyliauchenidae are jointly and individually monophyletic, and are sister groups. The nad1 gene on its own places a deep-sea lepocreadiine with the deep-sea lepidapedines, whereas lsrDNA, combined sequences and morphology place this deep-sea lepocreadiine within a group of typical lepocreadiids. It could not be demonstrated that a significant proportion of sites in the nad1 gene evolved under positive selection; this anomalous relationship therefore remains unexplained. Most deep-sea species are in a monophyletic group, a few of which also occur in shallow waters, retaining some characters of the deep-sea clade. Many lepocreadioid species infect herbivorous fish, and it may be that the recently discovered life-cycle involving a bivalve first intermediate host and metacercariae encysted on vegetation is a common life-cycle pattern. The host relationships show no indication of co-speciation, although the host-spectrums exhibited are not random, with related worms tending to utilize related hosts. There are, however, many exceptions. Morphology is found to be of limited value in indicating higher level relationships. For example, even with the benefit of hindsight the gyliauchenids show little morphological similarity to their sister group, the Enenteridae.
Demidospermus annulus sp. nov. (Platyhelminthes, Monogenea, Ancyrocephalidae) is described from the gills of the catfish Parapimelodus valenciennis Lütken collected in Samborombón Bay, Argentina. The new species differs from all congeneric species mainly by the structure of the accessory piece of the male copulatory organ, the sclerotized ring-shaped vaginal aperture and the dorsal bar articulation.
Ultrastructural aspects of fertilization were studied in three cestode species: one proteocephalid with biflagellate spermatozoa, Proteocephalus longicollis, and two cyclophyllideans with uniflagellate spermatozoa, Inermicapsifer madagascariensis (Anoplocephalidae) and Mesocestoides lineatus (Mesocestoididae). Fertilization in all three species occurs in the oviduct lumen or in the fertilization canal proximal to the ootype, where the formation of the embryonic capsule precludes sperm contact with the oocyte. Cortical granules are not present in the oocytes of any of the three species. Spermatozoa coil spirally around the oocytes and syngamy occurs by lateral fusion of oocyte and sperm plasma membranes. In the ootype one (Proteocephalus and Inermicapsifer) or two (Mesocestoides) vitellocytes associate with the fertilized oocyte, forming a membranous capsule which encloses both cell types. In this stage, spirally coiled sperm flagella adhere partly to the external oocyte surfaces, and partially penetrate into the perinuclear cytoplasm. Usually, several loops of the spermatozoon occur within the oocyte cytoplasm. The electron-dense sperm nucleus within the oocyte cytoplasm becomes progressively electron lucent after penetration. Simultaneously with chromatin decondensation, the elongate sperm nucleus changes shape, forming a spherical male pronucleus, which attains the size of the female pronucleus. Cleavage begins immediately after pronuclear fusion.
Eggs within paruterine capsules of gravid proglottids of Distoichometra bufonis were examined by light and transmission electron microscopy. The embryonic capsule was membranous, but was immediately underlain by a non-uniform subcapsular lamina that was an intracellular component of the outer embryonic envelope. The subcapsular lamina was thick and semi-rigid on anterior and posterior poles, but thin and membranous laterally, giving the entire egg a laterally oblong shape. In contrast, the embryophore was spherical and uniform in thickness. The paruterine capsule walls were derived from layers of flattened processes of medullary parenchyma cells lined internally with a layer of uterine epithelium. All these layers extended inward to form parenchyma-uterine partitions segregating each egg into an individual chamber. The uterine epithelium was very thin, syncytial, and contained numerous vesicles. Little uterine secretory product occurred in the uterine lumen or on the outer surface of the embryonic capsule. Except for the unique subcapsular lamina, most features of the eggs and paruterine capsule resembled those of other nematotaeniid species. The paruterine capsule wall was similar to that of Mesocestoides lineatus, a species whose paruterine organ lacks parenchyma-uterine partitions.
A new species of Microdalyellia Gieysztor, 1938 is described from a temporal freshwater pool in Utah, USA. This new species is characterized by the detailed structure of the stylet, which is of the Microdalyellia-type and consists of a crossbeam that carries two proximal shafts, two distal branches each carrying 5-7 hollow spines, and a median process in between both these spiniferous branches. The most remarkable feature is the presence of a second connection (or crossbeam) between both shafts, giving the proximal part of the stylet the appearance of a plate with a large window. The species’ affinities within the taxon Dalyelliidae Graff, 1905 are discussed. Following the discussion, Gieysztoria rastafariae Therriault and Kolasa, 1999 is transferred to the taxon Microdalyellia, because of the presence of a Microdalyellia-type stylet, which closely resembles that of the newly described species.
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