A new myxosporean species, Kudoa inornata sp. n. (Myxosporea: Multivalvulida), is described from skeletal muscles of the spotted seatrout Cynoscion nebulosus (Cuvier), collected in estuarine waters along the coast of South Carolina, USA. Light microscopic and ultrastructural characters rank this species to the group of Kudoa species with simple-shaped spores. The uniqueness of the SSU and LSU rDNA sequences justifies its status of a new species with sister relationship to Kudoa paniformis. The 100% prevalence in seatrout from four out of five localities sampled and pathogenicity of K. inornata recognized in this study should motivate further screening for infections in its host, which is considered a commercially important game fish with a wide distribution in the Western North Atlantic.
The presence of terminal carbohydrate residues in Enteromyxum leei (Diamant, Lom et Dyková, 1994) Palenzuela, Redondo et Álvarez-Pellitero, 2002 stages in gilthead seabream intestines was studied at light microscopy (LM) and transmission electron microscopy (TEM) level using lectin histochemical techniques. Abundant mannose and/or glucose residues were demonstrated by the intense staining caused by binding of biotinylated concanavalin A (Con A), at both LM and TEM. A clear positivity was also obtained with Ulex europaeus (UEA I) agglutinin specific for fucose residues. Both lectins stained E. leei proliferative and sporogonic stages, though glycan patterns varied between these developmental stages. Wheat germ agglutinin (WGA) and Bandeiraea simplicifolia lectin I (BSL I) recognised only structures in the sporogonic stages. Faint labelling occurred with Glycine max (SBA) lectin. No staining was obtained with Sambucus nigra (SNA) agglutinin. The TEM studies demonstrated a restricted presence of N‑acetyl-D-galactosamine and α-D-galactose, whereas glucose/mannose and fucose, the dominant structures, were also present at the parasite membranes and host-parasite interface, suggesting a role in host-parasite interaction.
Myxobolus porofilus sp. n. is described infecting the visceral cavity of Prochilodus lineatus (Valenciennes, 1836) cultivated in São Paulo State, Brazil. The plasmodial form of the parasite is 3-5 mm in length and appeared compressed between the wall of the visceral cavity and the pyloric caecum, reposing on this organ. The spores are small (length 5.7 ± 0.3 µm, width 4.8 ± 0.2 µm; mean ± SD) and round to elliptical in frontal view. The valve surfaces are smooth and have sutural folds. The polar capsules are ovoid, small (length 1.6 ± 0.1 µm, width 1.1 ± 0.1 µm) and equal in size. The polar filaments have three turns aligned perpendicularly to the longitudinal axis of the capsule. A conspicuous polar filament pore is arranged at the anterior end of the spore. The only reaction observed upon histological analysis was the presence of a capsule of connective tissue surrounding the plasmodia. This is the first report of a myxosporean parasite in the Prochilodontidae.
Kudoid parasites are known to infect a large variety of fish. A significant proportion of Kudoa species have relatively low host specificity, with a single species able to infect multiple host species representing various host families even from different host orders. Since DNA sequences have been associated with myxosporean species characterisations, it has become far easier to determine host range of new species and validate host records from earlier descriptions. This study investigated the host specificity of a kudoid parasite, Kudoa thalassomi Adlard, Bryant, Whipps et Kent, 2005, from the Great Barrier Reef in Australia using DNA sequence analysis and morphology. The results revealed the host specificity to be broad, with K. thalassomi identified in 18 different fish species representing six different fish families. This study also compares current genetic information from different host isolates of Kudoa Meglitsch, 1947 to their host ranges recorded in existing literature. From this analysis, only half of the Kudoa species with multiple host records (27 Kudoa species) have half or more isolates that are genetically characterised, and thus specifically identified with a high confidence, from their known hosts. Only five kudoid species have genetically characterised isolates from all of their recorded hosts.
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.
Four new species of Ceratomyxa Thélohan, 1892 are described from the gall bladders of fishes collected off Lizard Island, Australia. These species are characterised using a combination of morphometric and molecular data. Ceratomyxa bartholomewae sp. n. is described from Hyporhamphus dussumieri (Valenciennes) (family Hemirhamphidae); C. koieae sp. n. is described from Sphyraena forsteri Cuvier (family Sphyraenidae); C. pantherini sp. n. is described from Bothus pantherinus (Rüppell) (family Bothidae) and C. reidi sp. n. is described from Chaetodon vagabundus Linnaeus (family Chaetodontidae). A fifth species from Zebrasoma veliferum (Bloch) (family Acanthuridae) is also reported but due to limited material is not formally described here.
Myxidium biliare sp. n., a new myxosporean species parasitizing the gall bladder of Galaxias maculatus (Jenyns), in Patagonia, is described. Its coelozoic plasmodia were floating free in the bile. Spores are fusiform 13.7 ± 0.9 µm long and 6.9 ± 0.6 µm wide, with rounded ends in frontal view and slightly pointed ends in sutural view; shell with ridges and sinuous sutural line. Both maximum prevalence and maximum percentage of immature plasmodia occurred in summer. In winter the prevalence and the percentage of immature plasmodia fell to their lowest values. Prevalence was independent of host sex but increased with host length. Prevalence in 15 Patagonian Andean lakes (situated from 39°25'S to 41°30'S) ranged between 4.2% and 70%.
Four myxosporean species were found on the gills of Ictiobus bubalus from Illinois (USA). Myxobolus endovasus (Davis, 1947) Grinham et Cone, 1990 is revised. Three new species are recorded. Myxobolus enoblei sp. n. has spores ovoid in frontal view, 14.3 x 13 pm in size. Myxobolus morrisonae sp. n. has spores subcircular in frontal view, 10 x 9.5 pm in size; the surface of shell valves appears hairy when studied by SEM. Triangula illinoisensis sp. n. has spores rounded semicircular in frontal view, 10.2 x 12.8 pm in size. Triangula illinoisensis is the fourth species of its genus to be described from fishes.
Three new myxosporean species are described from Tetraodon fluviatilis (Osteichthyes: Tetraodontidae) imported from Southeast Asia to the Czech Republic. Zschokkella tetrafluvi sp. n. lives in the gall bladder. Di- or monosporic plasmodia produce ellipsoidal spores averaging 11.3 x 7.2 pm. Zschokkella pleomorpha sp. n. infects renal tubules and renal corpuscles; mono- to polysporic plasmodia produce spores averaging 15.7 x 7.1 pm. In the process of maturation, immature subspherical spores assume elongated shape. In both species, extremely curved suture line does not bisect poles of the spore. Ortholinea tetrafluvi sp. n. occurs as a rule in mixed infections with Z. pleomorpha sp. n. in the renal tubules. Mono- to polysporic plasmodia produce spores with a wide anterior and a narrow posterior end, averaging 8.3 x 7.8 pm. Both Z. pleomorpha sp. n. and O. tetrafluvi sp. n. have also limited number of stages located within the renal tubule epithelium, where they can complete sporogony. In one of the fish specimens, a myxosporean tentatively identified with Sinuolinea tetraodoni El-Matbou)i et Hoffmann, 1994 was found. A new genus is proposed for Ortholinea alata Kent et Moser, 1990 - Kentmoseria gen. n., and its diagnosis is presented.
Two myxosporean species, Zschokkella pleomorpha Lom et Dyková, 1995 (Zp) and Ortholinea fluviatilis Lom et Dyková, 1995 (Of) from the kidney of Tetraodon fluviatilis were studied by transmission electron microscope. Coelozoic sporogonie plasmodia of both species use pseudopodia-like projections for attachment to the epithelial cells of renal tubules. These projections either attach to host microvilli forming an interface reminiscent of septate junction (Zp) or are embedded into the epithelial cell surface (Of) or are inserted into gaps between epithelial cells (Zp, Of). Zp produces spores only by direct division of generative cells while in Of pansporoblasts prevail over direct division of generative cells. Sporogonie plasmodia of Zp greatly differ in size and in the variety of cytoplasmic constituents. A special feature in capsulogenesis is a transient envelope encasing the capsular primordium; there are fine fibres on the surface of the nascent filament spaced at 11 nm. In Of, vegetative nuclei of the plasmodium adhere to generative cells in a way reminding of sporoplasmic plasmodium of actinospores. In Of plasmodia, several unusual cytoplasmic structures were observed (membrane bound bodies with fuzzy radial contents or with a central dense inclusion, and endoplasmic reticulum cistemae forming a scalloped network). Of may also form intracellular coelozoic sporogonie plasmodia in the epithelial cells of renal tubules; these stages do not seem to constitute an important part of the life cycle.