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Six young tortoises Testudo marginata Schoepff, 1792 were experimentally infected with Hemolivia mauritanica (Sergent et Sergent, 1904). The prepatent period ranged from 6 to 8 weeks. Young, smaller, club-like forms (6-9 × 3-6 µm) of gametocytes appeared in the peripheral blood first, whereas mature, elongated, cylindrical forms (9-12 × 5-7 µm) were detected after 1-2 weeks and predominated during later patency. Three of the infected tortoises were euthanized and dissected to study the endogenous stages. Meronts occurred in the cells of the reticulo-endothelial system and in the erythrocytes; these were observed mostly in parenchymatous organs. Mature forms measured 14.2 × 9.3 µm and contained 7-12 merozoites. Cysts with two (exceptionally one) cystozoites were also found predominantly in parenchymatous organs and measured 14.8 × 7.9 µm. Pathological changes attributable to Hemolivia were mild and limited to liver and kidneys. The role of individual developmental stages of haemogregarines is discussed with respect to evolution of heteroxenous life cycle and long-term persistence of parasites in their intermediate hosts.

The cystidicolid nematode Metabronema magnum (Taylor, 1925) is redescribed from specimens collected from the swimbladder of the fish (golden trevally) Gnathanodon speciosus (Forsskål) (Carangidae, Perciformes) off New Caledonia, South Pacific (a new geographical record). The light and scanning electron microscopical examination made it possible to study in detail the morphology of this so far little-known species. Its pseudolabia were found to possess distinct anterior protrusions (protuberances), sublabia are absent, only four cephalic papillae are present, deirids are bifurcated, and the male possesses six pairs of postanal papillae. By its morphology, M. magnum seems to be most similar to species of Salvelinema Trofimenko, 1962, also from the swimbladder of fishes, differing from them mainly in the presence of median wedge-shaped outgrowths in the mouth, lateral alae, the longer spicule on the right side, and a fewer number of pairs of preanal papillae in the male. Since the morphology of M. magnum considerably differs from that of other representatives of the Cystidicolidae, Metabronema in Rasheed's (1966) conception is considered a valid genus.

Gyrodactylus thymalli Žitňan, 1960 and G. salaris Malmberg, 1957 have an indistinguishable ribosomal internal transcribed spacer (ITS) DNA sequence, but exhibit surprisingly high levels of intra- and interspecific sequence variation of the mitochondrial cytochrome oxidase I (CO1) gene. To test whether different populations of these reportedly very similar species could be discriminated using morphometric methods, we examined the morphometry of four different populations representing different mitochondrial clades. Twenty five point-to-point measurements, including five new characters of the attachment hooks, were recorded from three Norwegian laboratory populations (G. salaris from the Rivers Lierelva and Rauma, and G. thymalli from the River Rena), and from one wild population of G. thymalli from the River Test, UK. The Norwegian populations were kept under identical environmental conditions to control for the influence of temperature on the haptoral attachment hooks. Data were subsequently subjected to univariate and linear stepwise discriminant analyses. The model generated by the linear stepwise discriminant analysis used 18 of the 25 original variables, the first two roots accounting for 96.6% of the total variation between specimens. The hamulus shaft length accounts for 66.7% of the overall correct classification efficiency. Based on morphometry, all specimens were assigned to the correct species. Apart from three specimens of G. salaris from the River Lierelva population which were misclassified as belonging to the G. salaris Rauma population, all specimens were assigned to the correct population. Thus, populations of Gyrodactylus identified by mtDNA can also be discriminated using morphometric landmark distances.

Ailinella gen. n. (Pseudophyllidea: Triaenophoridae) is proposed to accommodate Ailinella mirabilis sp. n. from Galaxias maculatus (Jenyns, 1842), a freshwater fish inhabiting the Andean lakes in Argentinean Patagonia. Ailinella belongs to the Triaenophoridae because it has a marginal genital pore, a follicular vitelline gland, and a ventral uterine pore. The new genus can be distinguished from other triaenophorids by the following combination of characters: a small body size, a low number of proglottides, which are longer than wide, a truncated pyramidal to globular scolex, a rectangular apical disc, presence of the neck, lack of internal longitudinal musculature separating the cortex from the medulla, testes distributed in one central field surrounding the ovary laterally and posteriorly, the vagina predominantly anterior to the cirrus sac, vitelline follicles circum-medullary, the genital pores post-equatorial, a saccate uterus, and operculate eggs. Blade-like spiniform microtriches were present on all tegument surfaces, and tumuli on all surfaces of the scolex and the anterior surface of the neck. Microtriches were characterized according to their size and density, and tumuli according to their size, inter-tumulus distance and density. Ailinella mirabilis is the first cestode described from G. maculatus and the second triaenophorid species recorded from a South American freshwater fish.

Specimens of the elasmobranch, Isurus oxyrinchus Rafinesque, captured in 1999 in the state of Santa Catarina, Brazil, were parasitized with the poecilacanthoid trypanorhynch cestode Gymnorhynchus isuri Robinson, 1959, that is redescribed here. New details of scolex and proglottid morphology are given. These details are mainly related to tentacle armature, terminal genitalia and observations of external morphology of proglottids.

Previous studies have recorded Spironucleus torosus Poynton et Morrison, 1990 from several species of gadoid fishes, including the only freshwater gadoid, the burbot Lota lota (L.). Two morphologically different isolates of S. torosus have been described (elongate and pyriform). Both have been found in saltwater, while only the elongate has been found in freshwater. To address the conspecificity of the two morphs of S. torosus, and to identify the source of S. torosus in burbot in Norway, we have sequenced the small subunit ribosomal RNA (SSU rRNA) gene from 43 isolates of S. torosus from six species of gadoid fishes sampled at 15 localities in Norway, Sweden and the Baltic Sea. Phylogenetic analyses of the SSU rRNA gene sequence data recovered two major clades, one containing mainly isolates from burbot, while the other contained isolates from marine gadoid fishes only. The genetic distance (based on 25 nucleotide substitutions in 789 base pairs) separating the two assemblages was not large enough to consider the two groups separate species. Spironucleus torosus isolated from burbot displayed limited genetic variation in the small subunit ribosomal RNA (SSU rRNA) gene along the post-Pleistocene migration route of its host. The present study is the first report of S. torosus in tusk Brosme brosme (Ascanius), whiting Merlangius merlangus (L.), and fourbeard rockling Enchelyopus cimbrius (L.).

Polylabris lingaoensis sp. n. is described from the gills of the bald glassy, Ambassis gymnocephalus (Chandidae), from the Gulf of Tonkin (South China Sea), near Lingao, Hainan Province, China. The new species is characterized by a midventral vaginal pore, comparatively few (5-7) testes, and 2 parallel rows each comprised of 30-43 microcotylid clamps in the haptor. Polylabris lingaoensis is the only member of the genus known to parasitize a chandid host. Polylabris cf. mamaevi is described from the gills of the mottled spinefoot, Siganus fuscescens (Siganidae), from the South China Sea, which represents new host and locality records for the helminth. The gill parasites from S. fuscescens are tentatively assigned to P. mamaevi pending new collections and restudy of microcotylid species from siganid fishes.

Soricimyxum fegati gen. et sp. n. is a new myxosporean (Myxozoa) species discovered in the liver of shrews, Sorex araneus L., collected in the Bialowieza primeval forest (Poland). Both developmental stages and mature spores were found during a histological study. The infection had about 40% prevalence at the investigated locality. Plasmodia were polysporic. Elongated plasmodia with an average size of 30 by 8 µm occupied bile ducts and larger rounded plasmodia up to 80 µm in diameter were found in liver parenchyma where they most probably entered after the ducts had been destructed. Plasmodia in both locations elicited a vigorous inflammatory reaction. Spores were of an ovoid shape, 7 µm long, 5.4 µm wide and about 3.5 µm thick. They had two shell valves and two equal polar capsules, located in opposite ends of the spore.

Marssoniella elegans Lemmermann, 1900, a parasite of ovarial tissues of the copepod Cyclops vicinus Uljanin, 1875, was studied as a representative of aquatic-clade microsporidia which form "heteroinfectious spores" (spores not infective to the original host as opposed to "homoinfectious spores" which are infective for the original host) and which thus should require an alternate host. Several structural characters of this microsporidian are similar to those of copepod morphs of microsporidia infecting mosquitoes. However, small subunit ribosomal DNA phylogeny indicates that caddis flies (Insecta, Trichoptera) might be the alternate hosts of Marssoniella. Ultrastructural data obtained are used to redefine the genus Marssoniella Lemmermann, 1900 and its type species Marssoniella elegans.

A recent infestation of Gyrodactylus cichlidarum Paperna, 1968 on yolk sac fry of Nile tilapia, Oreochromis niloticus niloticus (L.), in an isolated aquarium system in the UK resulted in high mortalities and provided an opportunity to study this species in greater detail. A tentative identification was made using the measurements and drawings of the ventral bar and hamuli provided in the original description; however, details on the morphology of the marginal hooks were lacking. A comparison of the gyrodactylid material collected from O. n. niloticus with the holotype of G. cichlidarum, the only known available specimen, from Mango tilapia, Sarotherodon galilaeus galilaeus (L.), confirmed its identity. Proteolytic digestion and image analysis of the opisthaptoral hard parts were used to obtain tissue-free, accurate measurements as part of a complete revised description of G. cichlidarum. Further, a comparison of G. cichlidarum from both hosts with the holotype and several paratypes of Gyrodactylus niloticus Cone, Arthur et Bondad-Reantaso, 1995 cited as parasitizing captive stocks of Nile tilapia in the Philippines revealed the two species to be synonymous. An 803 bp fragment of the ribosomal internal transcribed spacers 1 and 2 and the 5.8S was obtained and is provided with the revised description. This is the first DNA sequence from a Gyrodactylus species originating from the African continent. The sequence is very divergent from other species in the genus and only the 5.8S sequence places it unambiguously in the genus Gyrodactylus. In addition to G. cichlidarum, two specimens of another morphological similar species of Gyrodactylus were also found on the UK held stock of O. n. niloticus. These latter specimens, Gyrodactylus sp., differed from G. cichlidarum in having a longer hamulus point with a smaller hamulus aperture and possessing marginal hook sickles that had a shorter shaft with a longer point giving the sickles a more rounded, closed appearance.

About 300 species belonging to four superfamilies (Gnathostomatoidea, Habronematoidea, Physalopteroidea and Thelazioidea) of the nematode suborder Spirurina are known as the adult parasites of freshwater, brackish-water and marine fishes. They are placed in four families, of which the Gnathostomatidae, including Echinocephalus with a few species and the monotypic Metaleptus, are parasites of elasmobranchs, whereas Ancyracanthus contains one species in teleosts; the Physalopteridae is represented in fish by four genera, Bulbocephalus, Heliconema, Paraleptus and Proleptus, each with several species in both elasmobranchs and teleosts. The majority of fish spirurines belongs to the Rhabdochonidae, which includes 10 genera (Beaninema, Fellicola, Hepatinema, Heptochona, Johnstonmawsonia, Megachona, Pancreatonema, Prosungulonema, Rhabdochona and Vasorhabdochona) of species parasitizing mainly teleosts, rarely elasmobranchs, and the Cystidicolidae with about 23 genera (Ascarophis, Caballeronema, Capillospirura, Comephoronema, Crenatobronema, Cristitectus, Ctenascarophis, Cyclozone, Cystidicola, Cystidicoloides, Johnstonmawsonoides, Metabronema, Moravecnema, Neoascarophis, Parascarophis, Prospinitectus, Pseudascarophis, Pseudoproleptus, Salvelinema, Similascarophis, Spinitectoides, Spinitectus, Sterliadochona), with many species parasitic in teleosts only. Because of difficulties in studying fish spirurines, associated with their morphological and biological peculiarities, most species of these parasites are poorly known. It is apparent that their present classification system does not reflect phylogenetic relationships and a taxonomic revision of this nematode group, based on detailed morphological (including SEM and TEM), life history and molecular studies of individual species, is quite necessary. In Cystidicolidae, several genera have been based on details in the cephalic structures visible only with the aid of SEM, but it will be evident whether or not these tiny features are of generic importance only when more cystidicolids are described using SEM and comparative molecular data become available. Data on the biology of fish spirurines are scarce. In known cases, their life cycles involve aquatic arthropods (crustaceans or insects) as intermediate hosts, in which, sometimes, the larvae undergo a precocious development and may even attain adulthood and become gravid in these invertebrates; sometimes, fish paratenic hosts are known to occur in cystidicolids parasitizing as adults piscivorous definitive hosts. Some spirurine species are pathogenic and are known as causative agents of serious fish diseases. Consequently, further detailed studies on fish spirurines are significant not only from the theoretical viewpoint, but they may also have practical implications.

Groups of female BALB/c mice infected by intravenous injection with 50 erythrocytes containing Plasmodium berghei Vincke et Lips, 1948 were sacrificed on days 3 through 12 after infection. Rheumatoid factor-like IgM (RF-IgM) and parasite-specific IgG levels were determined by enzyme-linked immunosorbent assay in serum specimens and in culture medium removed from spleen cell cultures established at sacrifice. All four mouse IgG subisotypes were recognized by RF-IgM molecules induced by Plasmodium berghei infection, and in this regard, the parasite-induced RF-IgM response resembled that induced by lipopolysaccharide polyclonal activation. Plasmodium berghei infection resulted in a biphasic RF-IgM response, with infected animals demonstrating significantly increased levels of RF-IgM early in the infection and significantly decreased levels late in the infection, compared to uninfected control mice. The decreased levels of RF-IgM observed late in infection correlated with increasing parasitaemia levels, and were primarily due to a decrease in RF-IgM specific for mouse IgG2a. Late infection levels of RF-IgM specific for IgG1, IgG2b, and IgG3 were not significantly different from those of control animals.

A sample of over 6,000 specimens of frogs belonging to about 120 species of all families occurring in West Africa and Madagascar were screened for parasitic mites. Three species of Endotrombicula Ewing, 1931 were found in representatives of two African and two Madagascan frog families. All Trombiculidae found in African frogs belonged to Endotrombicula pillersi (Sambon, 1928), whereas in Madagascar E. madagascariensis (Sambon, 1928) and E. ptychadenae sp. n. were sampled. These three species are described, data about their parasitic associations are provided, and their zoogeographical distribution is discussed. Only those frog species that spend a considerable time in terrestrial ground habitats were parasitized; neither arboreal nor strictly aquatic frogs were infected. The geographic distribution of Endotrombicula, restricted to Africa, the Arabian Peninsula and Madagascar, suggests that these mites invaded Madagascar from the African continent. This is supported by the observation that the ancestors of Ptychadena mascareniensis (Duméril et Bibron) (Ptychadenidae), the host of E. ptychadenae, colonized Madagascar from the African continent quite recently, possibly accompanied by its Endotrombicula parasites.

The first ultrastructural description of Ceratomyxa tenuispora Kabata, 1960 (Myxozoa, Bivalvulida) from Madeira Island (Portugal), a parasite found in the gall bladder of the commercially important black-scabbard fish, Aphanopus carbo Lowe is presented. This parasite possesses spherical to ellipsoidal disporous trophozoites. Spores have a central crescent-shaped body averaging 11.0 µm in length, 28.5 µm in thickness and 12.1 µm in width. The valves have two long opposite lateral processes (ribbon-like structures or tails), each averaging 173 µm in length. The total thickness of the spore averages 375 µm. The spore has two sub-spherical polar capsules (∼5.2 × 4.1 µm), each with a polar filament with 7 to 8 coils. Some ultrastructural aspects of the sporogonic stages are described. The trophozoites develop without contact with epithelial cells. The cytoplasmic membrane has numerous evenly distributed external slender projections about 0.3 to 0.7 µm long. The sporogenesis produces two spores without pansporoblast formation. In the matrix of the capsular primordium, microtubules with an unusual organisation were observed. A binucleate sporoplasm that contains several sporoplasmosomes and dense bodies fills the spore cavity and extends to the tails without penetrating them.

A new nematode species, Cucullanus pargi sp. n., is described from the intestine and pyloric caeca of the grey snapper, Lutjanus griseus (Linnaeus), off the southern Quintana Roo coast, Mexico. This species shows similar morphological features as cucullanids occurring in marine and brackish-water fishes; however, it differs from all other species in the length of spicules, arrangement and number of caudal papillae, position of the excretory pore and deirids. Cucullanus pargi is the third species of this genus described from fishes in Mexico and the second one from Mexican marine fishes.

A new species, Sphaeromyxa noblei sp. n., is described from Heteroclinus whiteleggii (Perciformes: Clinidae), a marine fish from the coast of New South Wales in Australia. This raises the number of Sphaeromyxa species to 38; their list is presented. The species is characterised by a layer of branched glycostyles, which is about 2.4 µm thick and is a feature rather unique in Myxosporea. Pansporoblasts form one or two spores. The study of ultrastructure of this species and of those described to date result in recognition of a combination of patterns characterising the genus: plasmodia have marked surface projections, the endoplasm is full of vacuoles larger than in any other myxosporean genus, and contains a special kind of cells, the lobocytes. Sections through polar capsule reveal different appearance of subsequent stretches of the polar filament unlike in other Myxosporea.

The Microsporidia are a group of obligate intracellular parasites, now thought to be derived fungi. Presented here is a comparative small subunit rDNA (ssrDNA) analysis of 125 species of Microsporidia (sequences obtained from GenBank). This analysis shows that groups or clades are formed based largely on habitat and host. This result is supported by comparative molecular analyses of the past decade, and indicates that structural and ultrastructural characters are unreliable for distinguishing among higher-level microsporidian taxa. Our findings indicate the presence of five major clades of Microsporidia which group according to habitat. We present three new classes of Microsporidia based on natural phylogenetic groupings as illustrated by the ssrDNA analysis: Aquasporidia, Marinosporidia and Terresporidia. The names of the proposed classes reflect the habitat of each group. The class Aquasporidia, found primarily in freshwater habitats, is a paraphyletic group consisting of three clades. The Marinosporidia are found in hosts of marine origin and the Terresporidia are primarily from terrestrial environments.

Species of Rhamnocercinae Monaco, Wood et Mizelle, 1954 are gill parasites of sciaenid fishes (Perciformes). Seven are marine species (three in the western Atlantic and four in oriental Pacific) and one is a neotropical freshwater species (Rio Doce Basin, Brazil). While the status of the subfamily may be questioned, this assemblage of species is apparently supported by several shared apomorphic and plesiomorphic characters, such as: (1) peduncular spines with anterior and posterior roots; (2) haptor laterally expanded, armed with anchors (two pairs); bars (one ventral, two dorsal); 14 hooks and haptoral accessory spines; and (3) double (nested) tubes of the male copulatory organ (MCO), directed posteriorly with the genital pore lying posterior to the MCO. The phylogenetic hypothesis for the eight known species of this clade is: (Spinomatrix penteormos (Rhamnocercoides stichospinus, Rhamnocercoides menticirrhi) Rhamnocercus oliveri (Rhamnocercus rhamnocercus (Rhamnocercus stelliferi, Rhamnocercus bairdiella, Rhamnocercus margaritae)). This hypothesis indicates that Spinomatrix penteormos represents the sister group of all remaining rhamnocercines. The resulting phylogenetic sister-group relationships support the transfer of Rhamnocercus stichospinus Seamster et Wood, 1956 to Rhamnocercoides Luque et Iannacone, 1991 as Rhamnocercoides stichospinus (Seamster et Wood, 1956) n. comb.

The nematode superfamily Dracunculoidea includes 166 recognized species, of which 150 (90%) are parasitic in about 300 species of freshwater, brackish-water and marine fishes. Fish dracunculoids are placed in 31 genera (86% of all dracunculoid genera) belonging to eight of the nine dracunculoid families: Anguillicolidae, Daniconematidae, Guyanemidae, Lucionematidae, Micropleuridae, Philometridae, Skrjabillanidae, and Tetanonematidae; the genus Lockenloia is considered incertae sedis. Because of difficulties in studying fish dracunculoids, associated with their morphological and biological peculiarities, most species of these largely histozoic parasites are poorly known and males of the majority of species and of eight genera have not yet been discovered. It is apparent that the present classification system of dracunculoids as a whole does not reflect phylogenetic relationships and a taxonomic revision of this nematode group, based on detailed morphological (including SEM and TEM), life history and molecular studies of individual species, is quite necessary. Data on the biology of fish dracunculoids is scarce. In known cases, their life cycles involve copepods, ostracods or branchiurids as intermediate hosts and, sometimes, fish paratenic hosts are known to occur in dracunculoid species parasitizing as adults piscivorous definitive hosts. However, nothing is known about the life cycles of representatives of 20 genera. Some species of dracunculoids, particularly of philometrids, are highly pathogenic and are known as agents of serious fish diseases. During recent years, especially the importance of Philometra spp. parasitizing the gonads of many species of marine fishes has increased due in particular to the rapid development of marine aquaculture, because they may significantly decrease fish reproduction or even cause full parasitic castration. Therefore, further detailed studies on fish dracunculoids are significant not only from the theoretical viewpoint, but they may also have practical implications.

Larvae (metacestodes) of tapeworms of the cyclophyllidean family Gryporhynchidae (previously included in the Dilepididae) occur in different internal organs of fresh- and brackish water fish (110 fish species of 27 families in 12 orders reported), which serve as the second intermediate hosts. The species composition, spectrum of fish hosts, sites of infection, and geographical distribution of gryporhynchids recorded from fish are reviewed here on the basis of literary data and examination of extensive material from helminthological collections. Metacestodes of the following genera have been found in fish: Amirthalingamia Bray, 1974 (1 species), Ascodilepis Guildal, 1960 (1), Cyclustera Fuhrmann, 1901 (4), Dendrouterina Fuhrmann, 1912 (1), Glossocercus Chandler, 1935 (3), Neogryporhynchus Baer et Bona, 1960 (1), Paradilepis Hsü, 1935 (5), Parvitaenia Burt, 1940 (2), and Valipora Linton, 1927 (3). However, most published records concern only three species, namely Neogryporhynchus cheilancristrotus (Wedl, 1855) from the intestinal lumen, Paradilepis scolecina (Rudolphi, 1819) from the liver and mesenteries, and Valipora campylancristrota (Wedl, 1855) from the gall bladder of cyprinids and other fish in the Palaearctic Region. Data on other species as well as reports from other regions are very scarce and almost no information is available from Australia, tropical Asia and South America. A recent study of gryporhynchid metacestodes from Mexico (Scholz and Salgado-Maldonado 2001), which reported 13 species, suggested that they may be more common than indicated by records in the literature. Although only a few cases of pathogenic influence of larvae on fish hosts have been reported, the veterinary importance of gryporhynchids remains to be assessed on the basis of more detailed studies. The data available indicate a strict host and site specificity of some species whereas others occur in a wide spectrum of fish hosts and are not strictly site-specific. Evaluation of Paradilepis larvae from the liver of salmonid fish from British Columbia, Canada, identified as P. simoni Rausch, 1949 by Ching (1982), has shown that they probably belong to two species, P. simoni and P. rugovaginosus Freeman, 1954. Metacestodes of the latter species and those of Cyclustera magna (Baer, 1959) from the intestinal wall of Tilapia zillii (Gervais) from Kenya are reported from fish for the first time.

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As part of a metazoan parasite survey of elasmobranchs from Malaysian Borneo, specimens of Rhoptrobothrium Shipley et Hornell, 1906 were collected from the eagle rays Aetomylaeus maculatus (Gray) and Aetomylaeus niehofii (Bloch et Schneider). The type species is redescribed from its type host, and a neotype specimen is designated. In addition, three new species of Rhoptrobothrium are described: R. chongi sp. n., R. gambangi sp. n. and R. limae sp. n. Rhoptrobothrium myliobatidis conspicuously differs from the three new species in its lack of a secondary areola; R. limae is distinguished from R. chongi and R. gambangi based on its greater total length; R. chongi possesses conspicuously stalked remi, while R. gambangi possesses short remi, often folded anteriorly. Rhoptrobothrium is somewhat unusual among tetraphyllideans in its possession of a "metascolex," a character it shares with other taxa in the Thysanocephalinae (i.e., Myzocephalus Shipley et Hornell, 1906, Myzophyllobothrium Shipley et Hornell, 1906 and Thysanocephalum Linton, 1889). The morphology of the "metascolex" of Rhoptrobothrium is investigated and new terminology is suggested to standardise the names given to structures constituting a metascolex. As a result, Rhoptrobothrium is considered to possess cephalic peduncle extensions, termed remi. In Rhoptrobothrium, each remus bears, at its distal end, a primary areola, and, in the case of the three new species, also a secondary areola proximal to the primary areola. Myzocephalus and Myzophyllobothrium are tentatively considered to possess remi; the configuration of the "metascolex" of Thysanocephalum, however, is not considered homologous to the condition in the other three genera currently placed in the Thysanocephalinae.

Glochidia are the larval stage of freshwater unionid mussels that parasitize the fins and gill apparatus of fish. A total of 22 fish species were examined for the presence of glochidia whose distribution on individual hosts was studied on three common fish species, the roach Rutilus rutilus (L.), perch Perca fluviatilis L. and bitterling Rhodeus sericeus (Pallas). Between 1997 and 1999, the fish were obtained from the rivers Morava and Kyjovka and surrounding water pools in the Czech Republic. The glochidia of two genera, Unio and Anodonta, were found. Anodonta glochidia were observed on 10 fish species, Unio glochidia on 17 fish species. There was a difference in spatial distribution of glochidia on the body of the host fish. Unio glochidia were predominantly located on the gills, whereas most Anodonta glochidia were found on the fins, with the highest numbers of glochidia were observed on the margin of the pectoral fins. For the gill apparatus, Unio glochidia were found predominantly on the second and third arch. Anodonta glochidia were predominantly found during winter and spring (November-May), whereas Unio glochidia were more abundant during May and June. The number of glochidia was positively correlated with fish length in perch highly infected by Anodonta glochidia and perch infected by Unio glochidia. Of the three fish species, the highest occurrence of parasites was found on perch with fewer observed on roach. In spite of the close relationship between bitterling and unionid mussels, glochidiosis was rare on this fish species.

Seven species of fishes, Catostomus commersonii (Lacépède), Etheostoma nigrum Rafinesque, Micropterus dolomieu Lacépède, Notemigonus crysoleucas (Mitchill), Notropis hudsonius (Clinton), Perca flavescens (Mitchill), and Percina caprodes (Rafinesque) from the St. Lawrence River, Quebec, Canada, were found infected with progenetic specimens of Neochasmus spp. in the orbits and/or the body musculature. Worms displayed varying degrees of maturation. Eggs occupied the entirety of the worm in late stages of development and persisted as distinct clusters in situ after worm death. Populations of parasites were studied monthly in E. nigrum from one site between May and October in order to follow parasite recruitment, development and maturation. Recruitment of parasites was observed in young-of-the-year fish primarily in July and continued through October. Worms matured rapidly, displaying egg production within a month. Later developmental stages, in which eggs occupied most of the worm, and clusters of eggs became abundant by September. Infections in overwintered fish collected in May consisted mainly of worms in early stages of egg production and of clusters of eggs. When hatched artificially, eggs from the clusters released viable miracidia, indicating that they survive beyond the lifespan of the adult worm. It is suggested that progenesis is a fixed characteristic of the life cycle of these species, that egg dispersal requires the death of the host and that it is facilitated by predation. All prior records of Neochasmus spp. are examined, leading us to conclude that the role of the putative definitive host (primarily basses) has been reduced to that of a dispersal agent. Current hypotheses concerning the evolution and maintenance of progenesis are considered, but it is concluded that they do not apply to this host-parasite system.

In order to elucidate the transmission and dispersion routes used by the myxozoan parasite Enteromyxum scophthalmi Palenzuela, Redondo et Alvarez-Pellitero, 2002 within its host (Scophthalmus maximus L.), a detailed study of the course of natural and experimental infections was carried out. Purified stages obtained from infected fish were also used in in vitro assays with explants of uninfected intestinal epithelium. The parasites can contact and penetrate loci in the intestinal epithelium very quickly. From there, they proliferate and spread to the rest of the digestive system, generally in an antero-posterior pattern. The dispersion routes include both the detachment of epithelium containing proliferative stages to the intestinal lumen and the breaching of the subepithelial connective system and local capillary networks. The former mechanism is also responsible for the release of viable proliferative stages to the water, where they can reach new fish hosts. The finding of parasite stages in blood smears, haematopoietic organs, muscular tissue, heart and, less frequently, skin and gills, suggests the existence of additional infection routes in transmission, especially in spontaneous infections, and indicates the role of vascular system in parasite dispersion within the fish. The very high virulence of this species in turbot and the rare development of mature spores in this fish may suggest it is an accidental host for this parasite. This may also question the existence of a two-host life cycle involving an actinosporean stage in this species. Further studies are needed to clarify this open point of the life cycle.

The taxonomical status of Paranoplocephala bairdi (Schad, 1954)-like cestodes (Anoplocephalidae) in heather voles Phenacomys spp. and tree voles Arborimus spp. (Muridae: Arvicolinae) and their discrimination from five related species of Paranoplocephala is assessed using uni- and multivariate morphometrics. The analyses support the independent status and conspecificity of specimens from Phenacomys spp. and Arborimus spp., and P. bairdi is therefore suggested to be a host-specialist species of heather and tree voles with a wide geographical distribution in North America. A redescription is presented for P. bairdi.

The feeding success of sand flies (Diptera: Phlebotominae) is linked to the vast array of pharmacological substances in their saliva, which interferes with the host haemostasis and immune response. Modification of feeding site plays also an important role in Leishmania transmission. In naive hosts, co-inoculation of saliva and Leishmania parasites increases the chance of successful transmission. Disease exacerbation seems to be associated with enhanced production of type 2 cytokines and selective inhibition of some macrophage functions including the production of NO and H₂O₂. On the other hand, hosts repeatedly exposed to sand fly bites develop anti-saliva immune response that results in a protection against Leishmania infection. This led to a new interesting approach to anti-Leishmania vaccine - using salivary components to block parasite transmission. The review is therefore focused on the interactions that run between immunomodulatory molecules in sand fly saliva and host immune response, with the impact on Leishmania infection development. Recent studies revealed that saliva-based vaccine for leishmaniasis might be effective and feasible, however, several questions still require to be solved. The knowledge based on experimental mouse model cannot be fully extrapolated to dogs or humans and due to differences in salivary antigens between sand fly species the protective effect is species-specific. On the other hand, the specificity of salivary antigens enables the use of anti-saliva antibodies for monitoring the exposure of hosts to sand fly bites and might be used as a marker of risks for Leishmania transmission in endemic areas.

The microsporidium Vittaforma corneae (Shadduck, Meccoli, Davis et Font, 1990) develops within the target cell cytoplasm. In the present study, green monkey kidney (E6) cells infected at 30°C, 35°C or 37°C with V. corneae developed enlarged multinucleate structures of up to 200 µm in any horizontal dimension made up either of a single cell or of multiple fused cells. A number of epithelial cell types (SW-480, HT-29, Caco-2 and HCT-8) were infected with V. corneae but did not induce the same highly organized structures, suggesting that for the structure to develop, the host cell must be capable of continued mitosis, and not be differentiated or be detaching from the surface matrix. Live cell imaging of infected E6 cells revealed large, multinucleate infected cells characterized by a central focus from which radiated parasite stages and host cell mitochondria. Immunocytochemistry identifying γ and α tubulin suggested that a single centrally-located microtubule organizing centre governed the distribution of parasite stages and host cell organelles, with mitochondria and parasites being eventually transported towards the periphery of the structure. Whole cell patch clamp analysis of infected cells indicated an average five-fold increase in total membrane capacitance, consistent with an enlarged single cell. Scanning electron microscopy revealed cell-like protrusions around the periphery of the structure with the intervening space being made up of parasites and cell debris. Clearly in the case of V. corneae-infected E6 cells the parasite-host cell relationship involves subverting the host cell cytoskeleton and cell volume control, providing the parasite with the same protected niche as does a xenoma.

Coprological examination of 71 samples from a breeding colony of veiled chameleons, Chamaeleo calyptratus Duméril et Duméril, 1851, revealed a presence of two species of coccidia. In 100% of the samples examined, oocysts of Isospora jaracimrmani Modrý et Koudela, 1995 were detected. A new coccidian species, Choleoeimeria hirbayah sp. n., was discovered in 32.4% of samples from the colony. Its oocysts are tetrasporocystic, cylindrical, 28.3 (25-30) × 14.8 (13.5-17.5) µm, with smooth, bilayered, ~1 µm thick wall. Sporocysts are dizoic, ovoidal to ellipsoidal, 10.1 (9-11) × 6.9 (6-7.5) µm, sporocyst wall is composed of two plates joined by a meridional suture. Endogenous development is confined to the epithelium of the gall bladder, with infected cells being typically displaced from the epithelium layer towards lumen. A taxonomic revision of tetrasporocystic coccidia in the Chamaeleonidae is provided.