Ultrastructure, surface topography, morphology and histological observations of a new parasitic cnidarian of the marbled swamp eel from the world's largest tropical wetland area, Pantanal, Brazil.

Myxosporeans are a diverse group of microscopic cnidarians of wide distribution that evolved into a parasitic lifestyle. A new myxosporean species, Myxobolus sp., is herein described infecting the mandible of wild specimens of Synbranchus marmoratus, caught in the world's largest tropical wetland area, Pantanal, Brazil. Light, scanning, transmission electron microscopy and histological observations unveiled detailed taxonomic information of the new myxosporean cnidarian. Ultrastructural analysis revealed a detailed description of plasmodia structures which can be used for comparison with plasmodia from other species of myxobolids. Both histological and ultrastructural observations evidenced a connective tissue capsule surrounding the plasmodia of Myxobolus sp. as a histopathological host reaction to the infection of this parasitic cnidarian. Histology showed that tissue tropism of the new myxosporean occurs in a well-defined part of the mandible, with development of plasmodia occurring in the epidermis layer. Mature myxospores from the valvular view featured an ovoid shape and had a short prolongation of the spore valves in the posterior end. Myxospores measured 22.7 ± 1.2 µm (21.5-23.9 µm) in length, 12.5 ± 0.4 µm (12.1-12.9 µm) in width and 11.3 ± 0.5 (10.8-11.8 µm) in thickness. Polar capsules were pyriform equally-sized and measuring 4.6 ± 0.3 µm (3.9-4.3 µm) in length and 2.9 ± 0.1 µm in width (2.8-3.0 µm). Finally, this study substantiates the still hidden myxosporean diversity from South America.

A new myxozoan parasite, Myxobolus allami sp. n. (Myxozoa: Myxobolidae) from the intestinal wall of Sparidentex hasta (Valenciennes) in Arabian Gulf.

Myxobolus allami sp. n. is described from the intestinal wall of the silvery black porgy, Sparidentex hasta (Valenciennes), off Saudi Arabian coast of Arabian Gulf. Two of 20 examined fish were found to be infected with irregular-shaped plasmodia 3-8 mm long × 2-3 mm wide. Mature myxospores are subspherical to elliptical in the valvular view and oval in the sutural view, and are 11-13 (12) µm long, 7-8 (7.5) µm wide and 10-12 (10.8) µm thick. Spores have relatively thin valves and mostly (~ 72%) end with short caudal appendages of ~3 µm long. The spores also have two polar capsules, which are oval to elliptical and measure 5-7 (5.7) µm in length and 2-3 (2.7) µm in width. Polar filaments are coiled, with three turns. Transmission electron microscopy revealed that caudal appendages originated from the sutural edge at the posterior pole of the myxospore with density similar to that of its valves. The SSU rRNAgene sequence of the present species does not match any available sequences in GenBank. Phylogenetically, this species is sister to Myxobolus khaliji Zhang, Al-Qurausihy et Abdel-Baki, 2014 within a well-supported clade of Myxobolus-Henneguya with species infecting marine fishes. The combination of molecular data and morphological differences between this and other species of Myxobolus Bütschli, 1882 lead us to propose that the present form be established as a new species, M. allami. The present study also provides more evidence for the idea that caudal appendages cannot be reliably used to distinguish the species of the genera Myxobolus and Henneguya Thélohan, 1892.

Involvement of sphaeractinomyxon in the life cycle of mugiliform-infecting Myxobolus (Cnidaria, Myxosporea) reveals high functionality of actinospore morphotype in promoting transmission.

Four new actinospore types belonging to the sphaeractinomyxon collective group (Cnidaria, Myxosporea) are described from the coelomic cavity of a marine Baltidrilus sp. (Oligochaeta, Naididae) inhabiting a northern Portuguese estuary. Host identification supports the usage of marine oligochaetes, namely of the family Naididae Ehrenberg, 1828, as definitive hosts for myxosporeans inhabiting estuarine/marine environments. The absence of mixed infections in the host specimens analysed is suggested to reflect the influence of host-, parasite- and environmental-related factors regulating myxosporean-annelid interactions. Molecular analyses matched the SSU rDNA sequences of three of the four new types with those of mugiliform-infecting Myxobolus spp., namely Myxobolus mugiliensis and a Myxobolus sp. from flathead grey mullet Mugil cephalus, and Myxobolus labrosus from thicklip grey mullet Chelon labrosus. These results directly link, for the first time, the sphaeractinomyxon collective group to a myxospore counterpart, further confirming their previously hypothesized specific involvement in the life cycle of myxobolids that infect mullets. Acknowledging this life cycle relationship, the functionality of the sphaeractinomyxon morphotype is suggested to have been decisive for the evolutionary hyperdiversification of the genus Myxobolus in mullets. Unlike other actinospore morphotypes, sphaeractinomyxon lack valvular processes, which implies a limited capability for buoyancy. Considering the benthic-feeding nature of mullets, this feature is most likely crucial in promoting successful transmission to the vertebrate host.

Taxonomy, phylogeny and host-parasite interaction of two novel Myxobolus species infecting Brycon orthotaenia from the São Francisco River, Brazil.

Two new Myxobolus species were described infecting Brycon orthotaenia from the São Francisco River, in the state of Minas Gerais, Brazil. From a total of 39 B. orthotaenia collected, two specimens (5.1%) exhibited infection of the ovary and 12 specimens (30.8%) displayed infection of the liver. The plasmodia of both Myxobolus species were white and spherical measuring around 1 mm in length. The plasmodium found in the ovary showed mature myxospores, which were oval shaped from the frontal view and measured 9.2-11.0 (9.8 ± 0.4) µm in length, 5.9-6.9 (6.5 ± 0.3) µm in width and 4.6-5 (4.9 ± 0.1) µm in diameter. The two polar capsules were the same size and measured 3.9-6.2 (4.7 ± 0.5) µm in length and 1.8-2.4 (2.1 ± 0.2) µm in width. The polar tubules had 9 coils. The plasmodium found in the liver showed mature myxospores which were ellipsoidal in shape from the frontal view and measured 10.0-11.4 (10.7 ± 0.5) µm in length, 7.3-8.6 (8.1 ± 0.4) µm in width and 5.3-7.0 (6.8 ± 0.4) µm in diameter. The two polar capsules were the same size and measured 4.2-5.4 (4.9 ± 0.3) µm in length and 1.9-2.9 (2.7 ± 0.3) µm in width. The polar tubules had 8 coils. Ultrastructural analysis revealed an asynchronous sporogenesis process, with young developmental myxospore stages more often found in the periphery of the plasmodium and mature myxospores in the centre of the plasmodium. The plasmodial wall was formed by a single membrane which was not surrounded by a layer of host tissue. A thick layer of fibrous material was found in the peripheral ectoplasm close to the plasmodial wall of the plasmodium found in the ovary. Phylogenetic analysis based on the small-subunit ribosomal DNA - ssrDNA sequences and using the closest myxozoan sequences to each one of the species studied here based on previous GenBank data and Henneguya/Myxobolus/Thelohanellus species parasitizing fish from South American, revealed that the new species are grouped in a subclade together with other Myxobolus species parasitizing bryconid hosts.

Ultrastructural morphology of the Myxobolus dermatobius Ishii 1915 (Mixosporea: Myxobolideae) microspores infecting eyes of Nile tilapia (Oreochromis niloticus) in Egypt.

A total of 1,000 cultured Nile tilapia (Oreochromis niloticus) were collected from different governmental and private fish farms and examined for detection of myxosporean parasites infection. The infected fishes showed slight unilateral exophthalmia with whitish cyst in the eye. Numerous white cysts like plasmodia of Myxobolus dermatobius were recovered from the eye of the examined fishes with low prevalence rate (1%). Small intact cyst was isolated, fixed in 3% glutaraldehyde in 0.1 M sodium cacodylate (pH 7.4) and prepared for transmission electron microscopy examination. Ultrathin sections myxospores of M. dermatobius revealed pair of capsulogenic cells at the apical pole of the developing myxospore. Single sporoplasm containing a single nucleus and sporoplasmosomes fills nearly all the space beneath the polar capsules. The later were pyriform in shape, each one had homogenous dense core and 4 turns of polar filaments. Ultrastructural characteristics of the present myxospore were described and discussed in detail.

New data on Myxobolus imparfinis (Cnidaria, Myxosporea): host, distribution, and ultrastructural morphology.

A mass of free myxozoan spores was found in the gill filaments of specimens of Cetopsorhamdia iheringi Schubart and Gomes, 1959, popularly known as "three-barbeled catfishes" (Heptapteridae, Siluriformes) collected in streams of the Middle Paranapanema River, Upper Paraná River basin, in the state of São Paulo, Brazil. Morphological and molecular analysis identified the spores as Myxobolus imparfinis Vieira, Tagliavini, Abdallah and Azevedo, 2018. The ultrastructural morphology of this parasite is described here for the first time. Differences were observed in the number of coils of the polar filament as well as some organelles not previously described for this species. Asynchronous development was also observed, with the presence of both mature and immature spores. This is the first report of a myxozoan parasitizing C. iheringi and the first geographical record of myxozoan parasites in streams of the Middle Paranapanema River. The new data improve the original description of the species and add to the knowledge of host-parasite interactions and distribution.

Phylogeny and comprehensive revision of mugiliform-infecting myxobolids (Myxozoa, Myxobolidae), with the morphological and molecular redescription of the cryptic species Myxobolus exiguus.

Mullets inhabit a wide range of habitats from tropical to temperate regions and play a critical role in their ecosystems. This commercially important fish group constitutes a significant source of food in several geographic regions, and the production of some species for consumption is an increasing trend. About 64 myxosporean species have been reported in mullets, some of which are cryptic, as is the case of Myxobolus exiguus, and M. muelleri. This paper provides, for the first time, a detailed and critical revision of the data available for myxobolids reported in mullets, determining the species that have bona fide mugiliform fish hosts, in accordance with the original species descriptions, the available molecular data and the currently accepted taxonomic and phylogenetic criteria. Phylogenetic analyses using Bayesian inference and maximum-likelihood methodologies suggest that the evolutionary history of myxobolids with bona fide mugiliform fish hosts reflects that of its vertebrate hosts, while reinforcing known evolutionary factors and old systematic issues of the clade of myxobolids. A comprehensive morphological, ultrastructural and molecular redescription is also provided for the cryptic species M. exiguus, from infections in the visceral peritoneum of the thinlip-grey mullet Chelon ramada in the River Minho, Portugal.

The light microscopy and ultrastructural characteristics of Myxobolus naffari (Myxosporea, Myxobolidae) infecting the Nile carp Labeo niloticus (Cyprinidae) and its histological impact

During a survey of myxosporean parasites infecting freshwater fishes from the River Nile at Giza Governorates, Egypt between March and September 2016, nine out of 30 specimens of the Nile carp Labeo niloticus (Cyprinidae) were found to be naturally infected with Myxobolus naffari (Myxobolidae). Small macroscopic plasmodia appeared embedded in the host gill tissue accompanied with fusion of the gill epithelia, and atrophy was observed at the site of infection. The host reaction was manifested by the encapsulation of the plasmodia with a thick layer of connective tissue. The plasmodia appeared as white, elongated rods between gill filaments with an intensity ranging from three to eight cysts/fish. The average dimensions of plasmodia were 1.2­2.0 (1.8 ± 0.2) mm long × 0.4­0.7 (0.6 ± 0.2) mm wide. The spores were oval, reaching 9.56­11.2 (10.2 ± 0.2) µm long and 6.5­7.7 (7.0 ± 0.4) µm wide with two equal-sized polar capsules regularly arranged at the anterior pole of each spore. They were 4.51­5.5 (5.1 ± 0.4) µm in length and 1.5­2.0 (1.7 ± 0.2) µm in width. Histological, semi-thin sections were taken through parasite plasmodia and transmission electron microscopic examination of ultrathin sections was performed to describe the developmental stages of the recorded parasite within the host fish.

Histological and ultrastructural study of Myxobolus mugchelo (Parenzan, 1966) with initial histopathology survey of the Liza ramada host intestine.

This paper provides histological and ultrastructural data on Myxobolus mugchelo (Myxozoa), a parasite of the intestinal wall of thinlip mullet Liza ramada from the Comacchio lagoons (Northern Adriatic Sea, Italy). About 80% of the examined mullets were infected with this myxozoan. In histological sections, the plasmodia appeared rounded to ovoid and spindle shaped, measured 181.61 ± 97 × 122.79 ± 53.16 µm (mean ± standard deviation, SD) in size. Early sporogenic plasmodia were located primarily in the muscle layer where no pronounced inflammatory response was detected. Plasmodia containing mature spores were situated closer to mucosal folds and were encircled by numerous immune cells, especially mast cells. Mature spores were generally oval and 6.06 ± 0.40 × 3.48 ± 0.92 µm in size. The spores showed symmetrical and smooth valves. The anterior end of the spores contained two equal pyriform polar capsules measuring 2.19 ± 0.47 × 1.59 ± 0.29 µm. Inside the polar capsules, an isofilar polar filament displayed 5-6 coils perpendicular or slightly oblique to the longitudinal axis. The wall of the polar capsule was filled with a hyaline substance contrasting with the very dense internal matrix. The mucus layer surrounded the spore surface. A thorough comparison with the Myxobolus species infecting intestine of fish is provided. This is the first report on occurrence of this myxozoan species in L. ramada population of the North Adriatic Sea.

Redescription and phylogenetic position of Myxobolus aeglefini and Myxobolus platessae n. comb. (Myxosporea), parasites in the cartilage of some North Atlantic marine fishes, with notes on the phylogeny and classification of the Platysporina.

Myxobolus 'aeglefini' Auerbach, 1906 was originally described from cranial cartilage of North sea haddock (Melanogrammus aeglefinus), but has subsequently been recorded from cartilaginous tissues of a range of other gadoid hosts, from pleuronectids and from lumpsucker (Cyclopterus lumpus) in the North Atlantic and from a zoarcid fish in the Japan Sea (Pacific). We obtained partial small-subunit rDNA sequences of Myxobolus 'aeglefini' from gadoids and pleuronectids from Norway and Iceland. The sequences from gadoids and pleuronectids represented two different genotypes, showing 98.2% identity. Morphometric studies on the spores from selected gadids and pleuronectids revealed slight but statistically significant differences in spore dimensions associated with the genotypes, the spores from pleuronectids were thicker and with larger polar capsules. We identify the morpho- and genotype from gadoids with Myxobolus 'aeglefini' sensu Auerbach, and the one from pleuronectids with Sphaerospora platessae Woodcock, 1904 as Myxobolus platessae n. comb. The latter species was originally described from Irish Sea plaice (Pleuronectes platessa). Myxobolus albi Picon et al., 2009 described from the common goby Pomatoschistus microps in Scotland is a synonym of M. 'aeglefini'. The Pacific Myxobolus 'aeglefini' represents a separate species, showing only 97.4-97.6% identity to the Atlantic species. In phylogenetic analyses based on SSU rDNA sequences, these and some related marine chondrotropic Myxobolus spp. form a distinct well supported group. This clusters with freshwater and marine myxobolids and Triangula and Cardimyxobolus species, in a basal clade in the phylogeny of the Platysporina. Members of family Myxobilatidae, Ortholinea spp. (currently Ortholineidae) and sequences of some other urinary system infecting myxosporeans form a well supported clade among members of the suborder Platysporina. Based on phylogenetic analyses, we propose the following changes to the classification of Myxosporea: i) Ortholineidae is dismantled and Ortholinea spp. transferred to Myxobilatidae, and ii) Myxobilatidae is transferred from suborder Variisporina to Platysporina.

Morphological and ultrastructural characteristics of Myxobolus ridibundae n. sp. (Myxosporea: Bivalvulida) infecting the testicular tissue of the marsh frog Rana ridibunda (Amphibia: Ranidae) in Egypt.

Myxozoans are one of the most economically important groups of protozoan parasites causing many serious diseases of their hosts. In the present study, a total of 60 live adult male specimens of the marsh frog Rana ridibunda have been randomly captured during the period of January-December 2015 in different areas at Kafr El-Sheikh Governorate, Egypt and were examined for infection by myxosporidian parasites. A total of 48 (80.0 %) out of 60 frog specimens were found to be infected with Myxobolus species. Parasitic infection was restricted to the testicular tissue of the examined frogs. Macroscopic cysts (plasmodia) which heavily infested different parts of the testes were recovered. Morphological and ultrastructural characteristics of these myxosporidian species were carried out using light and transmission electron microscopy. Plasmodia measured 0.16-0.53 (0.34 ± 0.01) mm in diameter. Mature spores appeared oval in frontal view, measuring 8.9-11.5 (9.6 ± 0.1) µm in length and 7.5-9.1 (8.4 ± 0.1) µm in width containing 5-6 turns of polar filaments. Morphometric characterization revealed that the very small size of the present Myxobolus species was the most distinctive feature that separates them from all previously described Myxobolus species. Ultrastructural analysis showed that the plasmodia are surrounded by a plasma membrane with numerous pinocytotic protrusions extending toward the host cell. The generative cells and the different developmental stages are arranged at the periphery of the plasmodia, while immature and mature spores are centrally located. Sporogenesis, capsulogenesis, valvogenesis, and spore maturation of the present parasite are also described. The present species is described as Myxobolus ridibundae and represents a new species.

Histopathological and ultrastructural studies of Myxobolus turpisrotundus from allogynogenetic gibel carp Carassius auratus gibelio in China.

During an ongoing systematic survey on species diversity of myxozoans parasitising allogynogenetic gibel carp Carassius auratus gibelio (Bloch) in China, plasmodia were detected in the fins, lip, jaw, gill chamber, gill arches, operculum and oral cavity of infected fish. Combining the morphological and molecular data, the present species was identified as Myxobolus turpisrotundus Zhang, Wang, Li et Gong, 2010. Histopathological examination revealed that despite infecting different organs, M. turpisrotundus always occurred in dermis, demonstrating its affinity to this tissue. Histopathological effect of M. turpisrotundus on the host is relatively mild except parasites in the gill arches producing compression of the adipose tissue and heavy adductor muscles deformation with lymphohistiocytic infiltrates. In addition, the plasmodia in different sites were with the same complex structure arrangement: cup-like cells with unknown derivation, a thin collagenous fibril layer, areolar connective tissue, basement membrane and host epithelial cell. Ultrastructural analysis showed that the parasite has monosporic pansporoblast and sporogenesis followed the usual pattern of most of the myxosporeans.

Ultrastructural, ssrDNA sequencing of Myxobolus prochilodus and Myxobolus porofilus and details of the interaction with the host Prochilodus lineatus.

Myxobolus prochilodus and Myxobolus porofilus are parasites of Prochilodus lineatus, an economically important South American fish found in La Plata and Paraiba do Sul river basins. This study focusing on parasite-host interaction provides an ultrastructural and phylogenetic analysis, the latter based on ssrDNA sequencing of these parasites respectively infecting the gill filaments and fins of P. lineatus taken from the Mogi Guaçu River, São Paulo, Brazil. A total of 13 adult specimens were examined in this study. The prevalence of infection was 7.69 % for M. prochilodus and 15.38 % for M. porofilus. Phylogenetic analysis showed M. prochilodus and M. porofilus clustered in a subclade composed of parasites of the Prochilodontidae family. In M. prochilodus infecting gill filaments, where cellular degeneration in the epithelium was observed, the plasmodia were surrounded by a capsule composed of layers of fibrocyte-like cells, with cellular projections joined to the projections of other fibrocyte-like cells by desmosomes, and more externally typical fibroblast layers. Some granular leukocytes were seen interspersed among these layers. In M. porofilus infecting the fins, the capsule of connective tissue was represented only by loosely arranged collagen fibers, and no granular leucocytes were observed. Finally, several unusual vacuoles with filamentous content and some characteristics usually described as degenerative alterations, as myelin figure, were noted in plasmodia and pansporoblasts of both myxosporean species. The possible influence of inflammatory response and xenobiotics was considered to be the explanation for the alterations observed in Myxobolus species and its host.

Ultrastructural description of Myxobolus cuneus (Myxosporea) in the skeletal muscle and kidney of tropical farmed fish Piaractus mesopotamicus (Characiformes: Characidae).

This study characterizes by transmission electron microscopy (TEM) and morphometric features the myxozoan Myxobolus cuneus (Myxosporea) in Piaractus mesopotamicus and reports the skeletal muscle and kidney as site of infection. The register was based in 21 young fish from intensive fish farming in Southeast Brazil and the spores were analyzed in fresh-mounted slides of the infected organs stained with Toluidine blue and processed as usual for TEM. It differs from Myxobolus cunhai from the fish host and different polar capsule size, and from Myxobolus serrasalmi on the pyriform spore shape and an oval macrospore, differently to that reported in this study. Morphometric characteristics and TEM study confirmed the present material as M. cuneus.

Morphological and ultrastructural aspects of Myxobolus niger n. sp. (Myxozoa) gill parasite of Corydoras melini (Siluriformes: Callichthyidae) from Brazilian Amazon.

Myxobolus niger n. sp. (Myxozoa) is described in the connective tissue of the serosa layer of the gill arch of Corydoras melini (Callichthyidae) captured from the Negro River, Amazonas State, Brazil. The prevalence of the parasite was 20% and the range intensity was 1-2 cysts per fish. The plasmodia were white and spherical to ellipsoidal, measuring 175 µm in diameter and were surrounded by a well-defined capsule of host connective tissue, with distinct delicate and interlaced collagen fibers. The myxospores body was ellipsoidal in frontal view and biconvex in sutural view. Spore dimensions were 11.3 ± 0.4 µm in length, 6.8 ± 0.2 µm in width and 4.1 ± 0.2 µm in thickness. The valves were symmetrical and smooth. The two polar capsules were elongated as pyriform and equal in size, measure 5.0 ± 0.3 µm in length and 2.0 ± 0.1 µm in width. The polar capsule had six to seven polar filament turns. Some aberrant spores were round in shape and had three polar capsules. The sporoplasm was binucleated and contained moderated number of sporoplasmosomes. The development of the plasmodia was asynchronic, with mature and immature spores. The plasmodium had moderated pynocitic channels. There were no projections, no invaginations and no microvilli in the plasmodial wall. This study is the first description of Myxobolus species in the fish of the Callichthyidae family.

Morphological, ultrastructural and phylogenetic analyses of Myxobolus hilarii n. sp. (Myxozoa, Myxosporea), a renal parasite of farmed Brycon hilarii in Brazil.

Myxobolus hilarii n. sp. was described, based on morphology, histology, ultrastructure and 18S rDNA sequencing, infecting the kidney of Brycon hilarii (Valenciennes 1850) (Characiformes: Bryconidae) taken from fish farms in the state of São Paulo, Brazil. Thirteen specimens of B. hilarii were examined and 100% had round, white plasmodia in the kidney. The mature myxospores were rounded, measuring 11.5 ± 0.8 (9.8-13.4) µm in length, 11.0 ± 0.7 (9.7-12.4) µm in width and 7.6 ± 1.0 (6.7-9.0) µm in thickness. Polar capsules were elongated and of equal size, with 6.5 ± 0.4 (6.0-7.2) µm in length and 4.0 ± 0.2 (3.6-5.3) µm in width and their polar filaments had 5 to 7 coils. Histological analysis revealed plasmodial development in the renal tubules, causing compression and deformation of adjacent tissues and destruction of renal tubule cells. Ultrastructural analysis showed direct contact between the plasmodial wall and the host tissue and asynchronous plasmodial development. The phylogenetic analysis of South American myxobolids, based on 18S rDNA sequencing, showed the myxosporeans grouping into two main clades. M. hilarii n. sp. appears as sister species of Myxobolus piraputangae.

Testicular myxosporidiasis and ultrastructural characteristics of Myxobolus bufonis (Myxobolidae) infecting the Egyptian toad Bufo regularis (Bufonidae). A light and electron microscopic study.

The phylum Myxozoa comprises more than 2180 species, almost all of which are considered to be obligate parasites of aquatic fishes and amphibians. They are dangerous pathogens responsible for severe economic losses. From March to September 2014, 40 adult male Bufo regularis (Bufonidae) captured from different areas at Giza province, Egypt, were surveyed for myxosporean parasitic infection. Of these, 22 (55%) were infected by histozoic plasmodia, which produced spores after rupture belonging to Myxosporidia. The present investigation introduced a new data for the recorded parasite observed by light and transmission electron microscopy. The infection was diagnosed as large clusters of macroscopic plasmodia embedded in the testicular tissue causing distortion at the site of infection. The host reaction was manifested by the encapsulation of the plasmodia with a thick layer of connective tissue. Plasmodia were whitish in color, elliptical to ovoid in shape measuring 0.54 ± 0.2 (0.34-0.63) mm in diameter. The spores were subspherical, reaching 7.1 ± 0.2 (6.2-8.4) µm in length and 6.3 ± 0.2 (5.8-7.0) µm in width with two equal-sized polar capsules regularly arranged at the anterior pole of each spore. They were 3.4 ± 0.2 (3.0-4.2) µm in length and 1.9 ± 0.2 (1.6-2.4) in width with 6-8 turns of polar filaments. Ultrastructural analysis showed that the plasmodia were surrounded by a plasma membrane with numerous projections and pinocytotic channels extended toward the host cell. The generative cells and the different developmental stages were arranged at the periphery of the plasmodia while immature and mature spores were centrally arranged. Sporogenesis, capsulogenesis, valvogenesis, and spore maturation of the present parasite were also described.

Whirling disease revisited: pathogenesis, parasite biology and disease intervention.

Whirling disease (WD) is an ecologically and economically debilitating disease of rainbow trout Oncorhynchus mykiss caused by the actinosporean spores of the parasite Myxobolus cerebralis. M. cerebralis has a complex, 2-host life cycle alternating between salmonid fish and the oligochaete host Tubifex tubifex. The parasite alternates between 2 spore forms as transmission stages: an actinosporean triactinomyxon spore that is produced in the oligochaete host and a myxosporean spore that develops in the salmonid host. Waterborne triactinomyxon spores released from infected T. tubifex oligochaetes attach to the salmonid host by polar filament extrusion elicited by chemical (nucleoside) and mechanical (thigmotropy) stimuli-a process which is rapidly followed by active penetration of the sporoplasms into the fish epidermis. Upon penetration, sporoplasms multiply and migrate via peripheral nerves and the central nervous system to reach the cartilage where they form trophozoites which undergo further multiplication and subsequent sporogenesis. M. cerebralis myxospores are released into the aquatic environment when infected fish die and autolyse, or when they are consumed and excreted by predators. Myxospores released into the water are ingested by susceptible T. tubifex where they develop intercellularly in the intestine over a period of 3 mo through 4 developmental stages to give rise to mature actinospores. In this article, we review our current understanding of WD-the parasite and its alternate hosts, life cycle and development of the parasite in either host, disease distribution, susceptibility and resistance mechanisms in salmonid host and strategies involved in diagnosis, prevention and control of WD.

The resurrection of Myxobolus toyamai with a validation of a stunted polar capsule based on morphological evidence.

Myxobolus toyamai has long been known as a gill parasite of the common carp Cyprinus carpio in Europe, Asia and North America. Recently, a controversy was raised regarding whether this organism was synonymous with Thelohanellus toyamai because of ambiguity regarding the validity of the second stunted polar capsule. In the present study, detailed morphological examinations were conducted to reconfirm the presence of the small polar capsule of M. toyamai. The addition of potassium hydroxide or the application of drying treatment to fresh spores resulted in the extrusion of long and short polar filament from the spores. Transmission electron microscopy of M. toyamai plasmodia revealed that the polar filament coiled inside the small capsule. Molecular analysis of the 18S rDNA identified that the present myxosporean isolate was the same organism as the American and Japanese isolates that have previously been registered as T. toyamai and M. toyamai, respectively (99.5-99.8% similarities). These results demonstrate that the second small polar capsule was indeed present in the myxosporean isolate, which indicates that M. toyamai is a valid scientific name.

[THE DESCRIPTION OF MYXOBOLUS PELECICOLA SP. NOV. (MYXOZOA: MYXOBOLIDAE) FROM PELECUS CULTRATUS (CYPRINIFORMES, CYPRINIDAE)].

Morphological study of myxosporean parasites Myxobolus pelecicola sp. n. from Pele- cus cultratus (L., 1758), is presented. Presporogenic stage not observed. Polysporous, el- lipsoidal. plasmodia up to 1.2 mm in length and 0.1 to 0.4 mm in width develop in the ske- letal musculature. Mature spores elongate oval or oval form in frontal view, lens-shaped in sutural view. Length of spores 16.5 ± 0.83 (14.9-18.0), width 12.1 ± 0.63 (11.6-13.3) (n = 50), thickness 7.8 ± 0.3 (7.4-8.3) µm (n = 10). Polar capsules pyriform, unequal, length of large 8.0 ± 0.44 (7.5-8.8), small 7.6 ± 0.26 (7.2-7.8), width of large 4.5 ± 0.22 (4.2-4.7), small 4.0 ± 0.21 (3.8-4.3) µm. Five to 6 distinct filament coils oriented obli- quely to capsule length, found in polar capsule. The length of extruded (in water) filament up to 130 µm. Large, but indistinct triangular intercapsular appendix present in spores. Single rodlet inclusion is very often observed in the posterior part of spore. Mucous enve- lope is absent. The type host of Myxobolus pelecicola sp. n. is sabrefish Pelecus cultratus (L., 1758). Type locality: Finnish Bay (60°05' N 29°55' E) and Ladoga lake (60°07' N 32°19' E), Russia.