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During a parasitological survey of Astyanax altiparanae captured in the Mogi Guaçú river, Pirassununga, state of São Paulo, Brazil, a new species of myxozoa was observed infecting the kidney of 30 of 42 specimens. Plasmodia of the new myxozoa, referred to herein as Unicauda whippsi n. sp. were spherical and varied from 450 to 1000 μm in length. The mature spore was elongated and measured 11 ± 1.2 (10–12) μm long by 5.4 ± 0.6 (4.7–7.2) μm wide. Polar capsules of unequal length with the filament coiled 7–9 times and a unique caudal process characteristic of the genus Unicauda, were recorded. Phylogenetic analysis demonstrated that U. whippsi n. sp. clustered with members of the genus Unicauda and Myxobolus, confirming it’s placement within the family Myxobolidae. This is the first record of a species of Unicauda infecting characiform fish, as well as the first registered occurrence of species of this genus in South America.

We describe three new Henneguya spp. (Myxobolidae) found parasitizing two species of cichlid fish from the Amazon basin, Brazil: H. tucunarei n. sp. from gill filaments of Cichla monoculus and H. tapajoensis n. sp. from gill filaments of Cichla pinima, both from the Tapajos River, Para State and H. jariensis n. sp. in the fins of Cichla monoculus from the Jari River, Amapa State. We based descriptions on myxospore morphology and small subunit ribosomal DNA sequences, and used a phylogenetic analysis to compare the new Henneguya species with known relatives. Spores of the three species had similar morphology and morphometrics, but differed molecularly 5–7.5%, and were no more than 94% similar to any other sequence in GenBank. Together with having different hosts, these data supported the diagnosis of the parasites as distinct, novel species. Maximum likelihood and Bayesian analyses showed that H. tucunarei n. sp., H. tapajoensis n. sp., and H. jariensis n. sp. plus Henneguya paraensis (which parasitizes Cichla temensis) formed a well-supported sub-clade of Henneguya parasites of cichlids from the Amazon basin, in a lineage sister to those in characiforms hosts. Our analysis was consistent with previous studies that suggest that aquatic environment and vertebrate host group are the strongest correlates with phylogenetic signals in the Myxobolidae.

Myxobolus miyairii Kudo, 1919 was first reported from the intestines of the Amur catfish (Silurus asotus) in Japan and then in China and Russia, but with incomplete description. During the investigation of fish myxosporean diversity in Poyang Lake, the biggest lake along the Yangtze River, China, two Amur catfish highly infected with M. miyairii in the intestine wall were sampled. So, the complete description of this species with morphological and molecular data was presented here. A large number of whitish, round or ellipsoidal pseudocysts 0.32-0.78 mm in diameter could be found in the external intestinal wall after dissecting the infected fish. Mature spores of M. miyairii were elongated and ellipsoidal in the frontal view and narrow fusiform in the lateral view, with a slightly pointed anterior end and a bluntly rounded posterior end and measured 13.3 ± 0.49 (12.5-14.7) μm × 6.6 ± 0.27 (6.2-7.4) μm × 5.0 ± 0.26 (4.4-5.7) μm in size. Spore surface was smooth and two spore valves symmetrical, with a thin and straight sutural ridge. Interestingly, two types of caudal appendage (single or bifurcated) were occasionally present on the posterior end of some spores which has not previously been reported. The two equal pyriform polar capsules measured 6.5 ± 0.30 (6.2-7.5) μm long and 1.9 ± 0.14 (1.5-2.3) μm wide and situated at the anterior end of the spore. Polar filaments coiled with eight to nine turns, perpendicularly to the longitudinal axis of the polar capsules. Histopathological analysis showed that the plasmodium developed in the circular muscle layer of intestinal wall of Amur catfish, but no obvious inflammatory responses were observed. Phylogenetic analysis based on the partial 18S small subunit ribosomal DNA sequences indicates that M. miyairii cluster within a clade of Siluriforme-infecting Henneguya species with the support of a high bootstrap value, but also evolutionarily independent from the Henneguya clade infecting the epithelium of fish of the Ictaluridae family. Additionally, Myxobolus species reported with caudal processes dispersed within the Henneguya-Myxobolus clade.

A new Myxobolus species, Myxobolus mucosus sp. n., was found in the basifilamental location of roach, Rutilus rutilus, and common dace, Leuciscus leuciscus, during the investigation of fish myxosporean fauna in Finnish Bay of Baltic Sea and Lake Ladoga in 2014. Plasmodia from the two hosts share similar morphometric and morphological features which are whitish and slightly elongated oval and measured 300-500 μm in diameter. Mature spores of M. mucosus sp. n. are ellipsoidal in frontal view and lemon shaped in sutural view, measuring 13.6 ± 0.62 (12.8-14.2) μm in length, 10.7 ± 0.51 (10.3-11.4) μm in width, 7.8 ± 0.41 (7.2-8.3) μm in thickness and 13.0 ± 0.89 (11.5-14.2) μm in length, 10.8 ± 0.77 (10.2-11.5) μm in width, 7.7 ± 0.52 (7.3-8.0) μm in thickness from roach and common dace, respectively. Polar capsules were pyriform, equal in size, converging anteriorly, with 5.9 ± 0.22 (5.7-6.3) μm in length and 3.9 ± 0.3 (3.5-4.1) μm in width and 5.6 ± 0.38 (5.1-6.2) μm in length and 3.8 ± 0.24 (3.5-4.0) μm in width from roach and common dace, respectively. Spore valves are relatively thin, symmetrical, and smooth. The most remarkable morphological character of this new Myxobolus species is the distinct mucous envelope, surrounding the full myxospore valves, up to 25 and 32 μm, respectively, in roach and common dace. The partial 18S ribosomal DNA (rDNA) sequence variation of myxospores from two hosts is very tiny (below 0.8 %) but significantly differing from all available sequences of myxosporeans in GenBank. Therefore, it can be concluded that this myxosporean from these two closely related cyprinids are conspecific by combining morphological characteristics, tissue specificity, and molecular data. Phylogenetic analysis showed that this newly described species cluster with several gill-infecting Myxobolus species from cyprinid fish inhabiting in Eastern Europe.

The common nase Chondrostoma nasus (L.) is a frequent cyprinid fish in the River Danube. In a survey on its infection with myxosporeans, eight different Myxobolus spp. spore types were found in the gills, swim bladder, fins and intestinal wall. Of these, spore types representing three species were studied in detail by morphological and molecular methods. Based on the differences in 18S rDNA sequences, two new species of Myxobolus Bütschli, 1882 from the gills and one from the swim bladder are described: M. arrabonensis n. sp., M. szentendrensis n. sp. and M. paksensis n. sp. The new species resembled M. muelleri Bütschli, 1882, M. intimus Zaika, 1965 and M. cycloides Gurley, 1893, all parasitic in leuciscine cyprinids, in spore size and location in the host, but exhibited differences in partial 18S rDNA sequences as follows: M. arrabonensis - M. muelleri (1.4%), M. szentendrensis - M. intimus (2.8%), M. paksensis - M. cycloides (2.4%). Based on the significant differences in rDNA sequences, the three forms are considered to represent new, hitherto undescribed species in spite of their morphological similarities to some Myxobolus spp. forming spores in identical locations in genetically closely related cyprinids of the subfamily Leuciscinae.

Myxobolus balatonicus n. sp. was detected in the gill filaments of the common carp Cyprinus carpio L. collected in Lake Balaton, Hungary. Its oval plasmodia measuring 600-800 × 300-400 µm were located intravasally in the filamental arteries. The spores measured 11.2 ± 0.92 × 9.5 ± 0.41 × 7.4 ± 0.33 µm and had two equal polar capsules with six filamental turns. Both morphology and DNA sequence analysis revealed that M. balatonicus n. sp. is distinct from the ten species of Myxobolus Bütschli, 1882 described from the European common carp and the 21 species described from the Asian common carp subspecies. Phylogenetic analysis placed M. balatonicus n. sp. in a clade of gill-infecting myxobolids.

A new species of Myxosporea, Henneguya aequidens sp. n. (Myxozoa: Myxobolidae), was described based on its ultrastructural features. This is a parasite of the freshwater fish Aequidens plagiozonatus, in the Peixe-boi River, Pará, Brazil. This parasite was found in the gills, in the form of whitish ellipsoid cysts with mature spores inside them. The average spore body was 15 ± 0.9 μm in length (n = 30) and 6 ± 0.8 μm in width (n = 30), and the tail measured 27 ± 0.5 μm in length (n = 15). The spores showed typical features of the genus Henneguya with two valves of equal size and two symmetrical polar capsules of 3 ± 0.3 μm in length and 2 ± 0.3 μm in width. Each polar capsule had a polar filament forming a helix from the apical region to the polar caps, with four to six turns. Based on the ultrastructural differences in morphology of these spores, the location of the parasite, and its host specificity, this parasite was described as a new species.

Fish mortality and poor growth in surviving fish contribute substantial losses to the ornamental fish farms of India and revealed an infection of a new myxosporidian parasite Thelohanellus indiana n. sp. which has become one of the most important limiting factors for successful aquaculture management. The parasite infects Carassius auratus, an Indian goldfish, described on the basis of myxospores morphology and amplification of a part of 18 S rDNA gene. Three major attaching site of fish body have been explored for showing the location of attachment for the parasites. The whitish cysts of the parasites are about 2.5–3.5 mm contains large amount of lemon shaped mature myxospores measuring 12.1–15.2 (13.8) × 7.5–8.8 (8) μm. A single round or elliptical polar capsule located only at the anterior pole of the spore having 6.2–7.2 (6.8) × 3.3–4.7 (4.0) μm in diameter. The morphological characters have been assessed by both the light and scanning electron microscope. The most differentiating feature from closely related species was carried out by morpho-taxonomic affinities with previously described species which are tremendously supported by molecular taxonomy by partial sequencing of the 18 S rDNA gene resulted in a total of 2101 bp fragment of newly obtained SSU rRNA gene sequence of the new species which exhibit 79–91% homogeneity with other closely related species available in GenBank. The BLAST search of Thelohanellus sp. did not matches with any available sequences in GenBank and the phylogenetic analysis revealed that the novel species were sister to T. habibpuri and T. caudatus, in the Thelohanellus clade and form a closest neighboring branch as a subclade in phylogenetic tree from which the new Thelohanellus parasite is being placed. Both the branches are originating from monophyletic clade that are strongly supported by bootstrap values which indicate clearly about independent position of T. indiana n. sp.

We used microscopy and molecular biology to provide the first documentation of infections of Myxobolus cerebralis (Myxozoa: Myxobolidae), the etiological agent of whirling disease, in trout (Salmonidae) from North Carolina (USA) river basins. A total of 1085 rainbow trout Oncorhynchus mykiss, 696 brown trout Salmo trutta, and 319 brook trout Salvelinus fontinalis from 43 localities across 9 river basins were screened. Myxospores were observed microscopically in pepsin-trypsin digested heads of rainbow and brown trout from the Watauga River Basin. Those infections were confirmed using the prescribed nested polymerase chain reaction (PCR; 18S rDNA), which also detected infections in rainbow, brown, and brook trout from the French Broad River Basin and the Yadkin Pee-Dee River Basin. Myxospores were 9.0-10.0 µm (mean ± SD = 9.6 ± 0.4; N = 119) long, 8.0-10.0 µm (8.8 ± 0.6; 104) wide, and 6.0-7.5 µm (6.9 ± 0.5; 15) thick and had polar capsules 4.0-6.0 µm (5.0 ± 0.5; 104) long, 2.5-3.5 µm (3.1 ± 0.3; 104) wide, and with 5 or 6 polar filament coils. Myxospores from these hosts and rivers were morphologically indistinguishable and molecularly identical, indicating conspecificity, and the resulting 18S rDNA and ITS-1 sequences derived from these myxospores were 99.5-100% and 99.3-99.8% similar, respectively, to published GenBank sequences ascribed to M. cerebralis. This report comprises the first taxonomic circumscription and molecular confirmation of M. cerebralis in the southeastern USA south of Virginia.

The third part of the catalogue of type material in the Helminthological Collection of the Oswaldo Cruz Institute/FIOCRUZ (CHIOC), comprising types deposited between 1979 and 2016, is presented to complement the first list of all types that was published in 1979. This part encompasses Acanthocephala, Nematoda and the other non-helminth phyla Cnidaria, Annelida, and Arthropoda. Platyhelminthes was covered in the first (Monogenoidea) and second (Rhabditophora Trematoda and Cestoda) parts of the catalogue published in September 2016 and March 2017, respectively. The present catalogue comprises type material for 116 species distributed across five phyla, nine classes, 50 families, and 80 genera. Specific names are listed systematically, followed by type host, infection site, type locality, and specimens with their collection numbers and references. Species classification and nomenclature are updated.

Myxosporean Myxobolus saladensis sp. nov. in the gills ofMugil liza Valenciennes, 1836 from Samborombón Bay was described by light and electron microscopy studies. Spores were pyriform and binucleated, measuring 10.63±0.36 pm (n=20) long, 9.24±0.50 pm (n=20) wide and 4.13±0.36 pm (n=20) thick, included in polysporic cyst-like plasmodia. Elongated pyriform polar capsules were of equal size (3.84±0.27 pm long and 2.30±0.12 pm wide). The sporoplasm contained some sporoplasmosomes. Each PC contained a polar filament with 4-5 coils obliquely arranged in relation to the polar capsules axis. The PC wall was composed of two layers of different electron densities. Based on the morphological and ultrastructure differences of the spore to those of previously described species of Myxobolus, we describe a new species, Myxobolus saladensis sp. nov., Facultad de Ciencias Naturales y Museo

This study provides morphological and molecular data of a new parasite species found in the muscle layer of the intestinal tract of the South American silver catfish, Rhamdia quelen from Marajó Island region (Pará State, Brazil), an important fishery resource with recognized potential for fish farming. The morphology of these parasites was reanalyzed and phylogenetic analyses were run on their 18S rDNA gene sequences. The spores were morphologically distinct from those of other Myxobolus species described previously. The obtained partial sequence of the 18S rDNA gene sequences of the new species were compared to those of 24 other Myxobolus and Henneguya species available in GenBank. The results of morphological and molecular analyses indicated clearly the existence of a new species, Myxobolus marajoensis sp. n. Resumo Este estudo fornece dados morfológicos e moleculares de um novo parasita encontrado na parede intestinal do jandiá, Rhamdia quelen coletado na região da ilha do Marajó (Estado do Pará, Brasil), um importante recurso pesqueiro com potencial para aquicultura. Foram realizadas comparações morfológicas deste parasita e análises filogenéticas da região do gene 18S rDNA sequenciada. Os esporos foram morfologicamente distintos das espécies de outros Myxobolus descritos anteriormente. A sequência parcial obtida do gene 18S rDNA da nova espécie foi comparada com outras 24 espécies de Myxobolus e Henneguya retiradas do GenBank. Os resultados de análises morfológica e molecular indicaram claramente a existência de uma nova espécie, Myxobolus marajoensis sp. n.

Species of the cnidarian genus Henneguya Thélohan, 1892 (Myxosporea: Myxobolidae) are histozoic parasites commonly found in freshwater and, more rarely, in marine fish. The development of these parasites in fish tissues includes the formation of plasmodia within which occurs the sporogony originating spores with two caudal processes, which are usually randomly distributed within the plasmodia. In this report the authors present some cases of non-random distribution of the spores of six species of Henneguya within their plasmodia. Two different patterns of non-random distribution were found based on a literature survey. These patterns and their origin are discussed. Apparently this non-random distribution of the spores is due to both internal and external factors.

In this report, a new myxosporean species, Myxobolus linzhiensis n. sp. (Cnidaria: Myxozoa: Bivalvulida), was described from the endemic cyprinid Schizothorax oconnori inhabiting the Yarlung Tsangpo River in the Tibetan plateau, China. The whitish ellipsoidal plasmodia of M. linzhiensis n. sp. grew under the epithelium of gill filaments, 1.7-mm long and 0.4-mm wide, and were found in the 3 of 8 examined S. oconnori (37.5%). Mature spores appeared suborbicular in frontal view, fusiform shaped in lateral view with tapering anterior, measuring 11.4 ± 0.7 (10.1–13.0) μm in length, 10.6 ± 0.4 (10.0–11.3) μm in width, and 6.6 ± 0.3 (6.2–7.0) μm in thickness. Two equal polar capsules were pyriform with an apophysis at its top end, measuring 5.7 ± 0.5 (4.8–6.7) μm in length, 3.8 ± 0.2 (3.2–4.2) μm in width, and polar filaments coiled 4 turns. Spore valves were symmetrical, and sutural ridge was straight and thin, running near the middle of the valves. Although Myxobolus linzhiensis n. sp. showed similar morphological characteristics with Myxobolus chushi Dar Kaur & Chishti 2017 from Schizothorax niger, Myxobolus kienweiensis Ma, 1976 from Schizothorax davidi, the new myxosporean was distinguished with them in spore shape, polar filament, and host-tissue tropism. Homology search by BLAST in GenBank indicated that the obtained 18S rDNA sequence of M. linzhiensis n. sp. (KY965935) did not match any available myxozoan sequence, most similar to Henneguya zikaweiensis, and showing less than 93% sequence similarity. Phylogenetical analyses demonstrated that M. linzhiensis n. sp. was firmly clustered in the clade consisting of myxosporeans Thelohanellus, Myxobolus, Henneguya from Asian cyprinids. This study is the first report on myxosporean parasitizing in endemic fish in the Tibetan Plateau, China.

This paper describes light and ultrastructural observations and molecular analysis of a fish-infecting myxosporean, Henneguya gilbert n. sp., which was found infecting the gill epithelium of the commercially important freshwater teleost fish Cyphocharax gilbert (Curimatidae) collected in the estuarine region of Guandu River, Rio de Janeiro State, Brazil. The parasite occurs in the gills, forming whitish spherical to ellipsoidal polysporic cysts measuring up to ~ 750 μm, and displaying asynchronous development. Mature myxospores are ellipsoidal with a bifurcated caudal process. The length, width and thickness of the body of the myxospore are 12.0 × 5.3 × 3.6 μm, respectively; two equal caudal processes are 16.8 μm long, and the total length of the myxospore is 27.2 μm. There are two unequal polar capsules: the larger measures 5.5 μm length × 1.3 μm width and has a polar filament with 9–10 coils; the smaller is 4.0 μm long × 1.3 μm wide and has a polar filament with 7–8 coils. The sporoplasm is binucleated and presents a spherical vacuole surrounded by numerous globular sporoplasmosomes. Phylogenetic analysis, based on the small subunit rRNA sequencing, using maximum likelihood method reveals the parasite clustering together with other myxobolids that are histozoic and parasitize freshwater fish of the order Characiformes, thereby strengthening the contention that the host phylogenetic relationships and aquatic environment are the strongest evolutionary signals for myxosporeans of the family Myxobolidae.

Made available in DSpace on 2018-12-11T17:15:25Z (GMT). No. of bitstreams: 0 Previous issue date: 2017-12-01 Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Plasmodia containing myxospores belonging to the genus Myxobolus Bütschli, 1882 were found in the ovaries and liver of Salminus hilarii. Despite its economic value, this fish host has no previous reports of myxozoan infections. Herein, we describe Myxobolus batalhensis n. sp. using morphological and ultrastructural data, as well as histological and SSU rDNA molecular data. The mature myxospores were elongated, measuring in average 15.2 ± 0.8 μm in length, 8.4 ± 0.4 μm in width, and 5.1 ± 0.2 μm in thickness. Polar capsules were elongated and measured 5.3 ± 0.3 μm in length and 2.8 ± 0.3 μm in width. Polar filaments had 6–9 coils. Histopathological analysis showed coagulation necrosis associated with cell lysis as a response of the host cell to the parasite in the ovaries. No inflammatory reaction was observed in the liver, although the presence of the plasmodia caused changes in tissue structure. The phylogenetic analysis of South American myxobolid species showed M. batalhensis n. sp. as sister species of Myxobolus aureus. This is the first report of a myxozoan species parasitizing S. hilarii and the first myxozoan species described in the Batalha river. Department of Parasitology Universidade Estadual Paulista “Júlio de Mesquita Filho” – UNESP, Botucatu Department of Microbiology Oregon State University Center for Applied Research and Technology Transference in Marine Resources Almirante Storni (CIMAS-CCT CONICET) & ESCiMar National University of Comahue Department of Environmental Sciences Universidade do Sagrado Coração – USC, Bauru Department of Parasitology Universidade Estadual Paulista “Júlio de Mesquita Filho” – UNESP, Botucatu FAPESP: 2013/25623-0 FAPESP: 2014/12862-0 FAPESP: 2015/01361-2 FAPESP: 2015/24901-2

Microscopic and molecular procedures are used to describe a new myxosporean species, Henneguya carolina sp. nov., found infecting the intestine of the marine teleost fish Trachinotus carolinus on the southern Atlantic coast of Brazil. Spherical to ellipsoid cysts, measuring up to ~750 µm, display synchronous development. Mature myxospores are ellipsoidal with a bifurcated caudal process. Myxospore body length, width, and thickness are 12.7 ± 0.8 (12.0-13.4) µm, 8.8 ± 0.6 (7.5-9.6) µm, and 5.8 ± 0.4 (5.0-6.4) µm, respectively; 2 equal caudal processes are 16.8 ± 1.1 (15.9-18.0) µm long, and the total myxospore length is 29.4 ± 0.8 (28.4-30.4) µm. Two pyriform polar capsules measure 5.0 ± 0.5 (4.6-5.6) × 2.4 ± 0.4 (1.9-2.9) µm, and each contains a polar filament forming 3 to 4 coils. Sporoplasm is binucleated and presents a spherical vacuole surrounded by numerous globular sporoplasmosomes. Molecular analysis of the small subunit rRNA gene by maximum parsimony, neighbor joining, and maximum likelihood reveals the parasite clustering together with other myxobolids that are histozoic in marine fish of the order Perciformes, thereby strengthening the contention that the host phylogenetic relationships and aquatic environment are the strongest evolutionary signal for myxosporeans of the family Myxobolidae.

A synopsis of the species of Myxobolus Bütschli, 1882 (Myxozoa, Myxosporea, Myxobolidae) described between 2005 and 2013 is presented, including 112 nominal species. For each species the most important morphological and morphometric features are indicated in tabulated format. Included are also accession numbers for molecular data (when available), site of the infection within the host, features of the vegetative stage, organ infected, etc., plus a full bibliography of the original records for these species.

Henneguya jocu n. sp. (Myxosporea, Myxobolidae) is described from the gill lamellae of the marine teleost fish Lutjanus jocu, with a focus on ultrastructural and molecular features. This myxosporean forms subspherical cysts up to ∼260 μm × 130 μm long, and develops asynchronously. Mature myxospores ellipsoidal with a bifurcated caudal process. Myxospore length 10.9 ± 0.4 μm (n = 50); width, 8.2 ± 0.3 μm (n = 50); and thickness, 2.9 ± 0.5 μm (n = 50). Two equal caudal processes, 34.1 ± 1.0 μm long (n = 50); and total myxospore length, 45.2 ± 1.0 μm (n = 50). Two symmetric valves surround two ellipsoidal polar capsules, 5.0 ± 0.3 × 1.4 ± 0.2 μm (n = 20), each containing an isofilar polar filament forming 4–5 coils along the inner wall of these structures, as well as a binucleated sporoplasm presenting a spherical vacuole and several globular sporoplasmosomes. Both the morphological data and molecular analysis of the SSU rDNA gene identify this parasite as a new species of the genus Henneguya. Maximum Likelihood and Maximum Parsimony analyses further indicate that the parasite clusters within others marine Myxobolidae species, forming a group alongside other Henneguya species described from marine hosts.

Two new myxosporean species, Myxobolus marumotoi n. sp. and Cardimyxobolus japonensis n. sp. (Myxozoa: Myxosporea: Bivalvulida), are described from the dark sleeper, Odontobutis obscura, in Japan, based on their morphological and molecular characterizations. Plasmodia of M. marumotoi n. sp. (Myxobolidae) grew in the myofiber of trunk muscles, forming pseudocysts. The rounded spore was relatively large, measuring 13.3-15.0 μm (average 13.8) in length, 14.2-15.0 μm (14.6) in width, and 10.0-11.7 μm (10.8) in thickness, with two subspherical polar capsules of 7.9-9.6 μm (8.4) in length by 5.4-6.3 μm (5.9) in width (n = 15). The polar capsules were directed toward the apex of the spore, packing five to six spirals of the polar filament. Plasmodia of C. japonensis n. sp. (Ortholineidae) were surrounded by thin fibrous tissue, forming cysts in the lamina propria of the alimentary tract. The spore was ovoid, wider than long, in valvular view and spindle-shaped in sutural view. It measured 8.8-10.4 μm (9.4) in length, 11.3-12.5 μm (11.9) in width, and 5.2-6.7 μm (5.8) in thickness, with two ovoid polar capsules of 4.2-5.0 μm (4.7) in length by 2.9-3.8 μm (3.3) in width (n = 15). The shell valves of spores often showed a flattened anterior border and semicircular posterior border, and the two polar capsules were directed toward opposite lateral sides. In addition, the sporoplasm contained an iodinophilous vacuole. Almost complete small-subunit (SSU) rDNA sequences, except for primer flanking regions, were obtained for both species; 1,996 bp long for the former and 1,588 bp long for the latter. On phylogenetic trees based on the SSU rDNA sequences of representative species of Bivalvulida, M. marumotoi n. sp. and C. japonensis n. sp. formed a distinct branch in the Henneguya/Myxobolus clade or near but outside this clade, respectively. This study is the first report of the genetic characterization for the genus Cardimyxobolus.

Made available in DSpace on 2019-10-06T16:35:48Z (GMT). No. of bitstreams: 0 Previous issue date: 2019-09-01 Plasmodia containing spores of a new species of myxozoan, Henneguya jundiai n. sp., were found in the gill arches of Rhamdia quelen catfish. The present study describes H. jundiai n. sp. based on morphological and molecular analysis. The mature spores were elongated and measured 26.9 ± 1.9 (22.9–29.2) μm in total spore length, 9.5 ± 0.4 (8.8–10.0) μm in spore body length, 4.6 ± 0.4 (4.1–5.5) μm in spore body width, 17.3 ± 1.8 (14.1–19.8) μm in tail length, 4.9 ± 0.3 (4.6–5.5) μm in polar capsule length and 1.4 ± 0.2 (1.2–1.7) μm in polar capsule width. The polar filaments had 6–7 coils. Histological analysis revealed the formation of a large plasmodium connected to the gill arch through the epithelial tissue. Ultrastructural analysis revealed the presence of a binucleated sporoplasm, as well as the polar capsules and the coils of the polar filament. Phylogenetic analysis found that H. jundiai n. sp. is located within a subclade formed by species of Henneguya which parasitize siluriform fish from Brazil. Henneguya jundiai n. sp. appears as a sister species of H. quelen. The results of the analyzes clearly indicated the existence of a new species, H. jundiai. Departament of Parasitology Universidade Estadual Paulista “Júlio de Mesquita Filho” – UNESP, Botucatu Docente do Programa de Pós-graduação em Análise de Sistemas Ambientais Centro Universitário CESMAC Departament of Parasitology Universidade Estadual Paulista “Júlio de Mesquita Filho” – UNESP, Botucatu

The present study was performed to trace the decisive evidence for mixed infection of 2 Myxobolus species, M. episquamalis and Myxobolus sp., in the gray mullet, Mugil cephalus, from Korean waters. Mullets with whitish cyst-like plasmodia on their scales were collected near a sewage plant in Yeosu, southern part of Korea, in 2009. The cysts were mainly located on scales and also found in the intestine. The spores from scales were oval in a frontal view, tapering anteriorly to a blunt apex, and measured 7.2 µm (5.8-8.0) in length and 5.3 µm (4.7-6.1) in width. Two polar capsules were pyriform and extended over the anterior half of the spore, measuring 3.5 µm (2.3-4.8) in length and 2.0 µm (1.5-2.2) in width. In contrast, the spores from the intestine were ellipsoidal, 10.4 µm (9.0-11.9) in length and 8.4 µm (7.3-10.1) in width. The polar capsules were pyriform but did not extend over the anterior half of the spore, 3.7 µm (2.5-4.5) in length and 2.2 µm (1.8-2.9) in width. The nucleotide sequences of the 18S rDNA gene of the 2 myxosporean spores from scales and intestine showed 88.1% identity to each other and 100% identity with M. episquamalis and 94.5% identity with M. spinacurvatura from mullet, respectively. By the above findings, it is first confirmed that mullets from the Korean water are infected with 2 myxosporean species, M. episquamalis and Myxobolus sp.

The myxozoan Henneguya friderici is a parasite of the gills, intestine, kidney and liver of Leporinus friderici, a characiform fish belonging to the family Anostomidae. Forty-two specimens of L. friderici that had been caught in the Mogi Guaçú River, state of São Paulo, were studied. Elongated white plasmodia were found in the gill filaments of 10 host specimens (24%). The mature spores had an ellipsoidal body with polar capsules of equal size and caudal length greater than body length. This study also described 18S rDNA sequencing of H. friderici infecting the gill filaments. This produced a sequence of 1050 bp that demonstrated significant genetic differences with previously described species of Henneguya. Similarity analysis using sequences from species that clustered closest to those produced by this study showed that the species with greatest genetic similarity to H. friderici was H. leporinicola, with 94% similarity.

A parasitological survey of freshwater fishes in the Big Thicket National Preserve in southeast Texas revealed myxozoan infections in two species of sunfish, Lepomis marginatus Holbrook and Lepomis miniatus Jordan (Perciformes: Centrarchidae). Pseudocysts were elongate-oval, 988 × 485 µm (ex L. marginatus) and 800 × 606 µm (ex L. miniatus) and demonstrated a predilection to the edge of the primary gill lamellae. Myxospores consistent with the genus Myxobolus were oblong, 16.8-21.3 (19.0 ± 0.9) µm long, 7.0-8.8 (7.9 ± 0.5) µm wide and 5.3-6.1 (5.8 ± 0.3) µm thick (ex L. marginatus) and 17.2-20.3 (18.8 ± 0.7) µm long, 7.5-9.9 (8.7 ± 0.6) µm wide, and 6.8-7.2 (7.0 ± 0.2) µm thick (ex L. miniatus); with 2 pyriform polar capsules 8.3-9.8 (9.0 ± 0.5) µm long, 2.2-2.7 (2.5 ± 0.2) µm wide (ex L. marginatus) and 9.2-10.5 (10.0 ± 0.4) µm long, 2.2-3.0 (2.8 ± 0.2) µm wide (ex L. miniatus). Statistically, the measurements of spore body width, polar capsule length, and polar capsule width were significantly different between myxospores from L. marginatus and L. miniatus. However, intraspecific genetic variability between isolates at the 18S rRNA gene was negligible, with0.8% variability across2,000 bp of sequence. The isolates shared no significant sequence similarity with any myxozoan deposited in the GenBank nucleotide database. Phylogenetic analysis inferred from the 18S rRNA gene from both L. marginatus and L. miniatus placed the isolates within a clade of myxozoan parasites of perciform fishes. Based on shared tissue and host family tropism, overlapping morphological characters and high degrees of sequence conservation at the 18S rRNA gene, we propose these isolates as morphologically distinct, genetically conspecific representatives of M. lepomis n. sp. from the gills of L. marginatus and L. miniatus in the Big Thicket National Preserve in Texas, USA.

An investigation of mortalities in a group of cardinal tetras Paracheirodon axelrodi Meyers, 1936, a popular ornamental fish, revealed myxozoan parasites in ventricles of the brains in 3/10 fish and the ocular retina of a fourth. Parasite impacts were unclear, as additional histopathological findings were present, including bacterial dermatitis and meningitis. Ethanol-preserved specimens pooled from multiple fish were used for morphological characterization of myxospores. Elongate, teardrop myxospores were 20.5 ± 0.7-μm (mean ± SD; range = 19.0–21.8 μm) long, 6.6 ± 0.5-μm (5.7–7.9 μm) wide, and 5.1 ± 0.4-μm (4.8–5.9 μm) thick (valvular width). Two, unequally sized, apical, pyriform polar capsules were in the same plane as the sutural ridge. The larger measured 9.9 ± 0.8-μm (8.0–11.2 μm) long and 3.8 ± 0.3-μm (3.2–4.8 μm) wide. The smaller was 4.1 ± 0.3-μm (3.5–4.5 μm) long and 2.0 ± 0.1-μm (1.8–2.3 μm) wide. Identical 1912 bp 18S rRNA sequences were obtained from two pooled spore samples from tetra brains, which did not match any sequences in the NCBI nr/nt database. Phylogenetically, these parasites grouped loosely within a clade containing Myxobolus spp. from other South American characins and Unicauda spp. from siluriform catfish. Myxospores shared some morphological similarities with Myxobolus inaequus from the unrelated glass knifefish (Order: Gymnotiformes), but were genetically divergent (

Allogynogenetic gibel carp is one of the most important freshwater cultured species in China. However, myxosporidiosis represents a severe threat to prevent the sustainable development of aquaculture of this species. During the investigation of myxosporean diversity of reared allogynogenetic gibel carp in East China, a new myxosporean with typical characteristics of Myxobolus was found from 169 out of 210 (80.4 %) examined samples, designated as Myxobolus sheyangensis n. sp. by combing comparative analysis of morphological and molecular data. The diagnostic features of this species are reminiscent with Myxobolus pyramidis Chen, 1958 as follows: round or ellipsoidal, grayish white, cyst-like polysporous plasmodia, averaging 219.3 ± 11.9 (98.7-421.7) × 158.4 ± 9.7 μm (79.9-191.8) in size; spores flat-pear shaped in frontal view with tapering anterior and rounded posterior ends and lemon-shaped in sutural view, averaging 11.0 ± 0.31 (10.5-11.9) × 10.2 ± 0.25 (9.2-10.7) × 6.3 ± 0.23 μm (5.9-6.9) in size; and two equal pyriform polar capsules averaging 5.5 ± 0.3 (4.5-6.1) × 3.4 ± 0.26 μm (2.9-4.0) in size with convergent longitudinal axes and polar filaments wounded in seven to eight coils, perpendicularly to the longitudinal axis of the polar capsules. Spore surface was smooth and two spore valves were symmetrical, with a thin and straight sutural ridge. Occasionally, abnormal spores with typical Henneguya-like caudal appendage and atypical papillary caudal appendage could be observed. The sporogenesis is asynchronous. Histopathological investigation showed that the plasmodia developed inside the capillary network of gill lamellae, belonging to the intralamellar vascular type, and no significant inflammatory responses were provoked by the infection. Homology search by BLAST showed that the newly obtained sequence did not match any available sequences in GenBank. Phylogenetic analysis of the aligned sequences indicated that M. sheyangensis n. sp. positioned in a clade composed of Myxobolus species infecting the gill of several freshwater cyprinid fish.

Myxosporeans of the genus Henneguya have a global distribution and infect organs and tissues of both marine and freshwater fishes. Here we describe the morphological, histological and molecular characteristics of Henneguya sinova sp. nov. parasitizing the gill arches of tentacled blenny Parablennius tentacularis (Perciformes: Blenniidae) collected from the coast of Sinop on the Black Sea in Turkey. Several oval whitish plasmodia of different sizes in the gill arches of fish were found. The mature spores were rounded oval in frontal view, with a mean (range) total length 57.5 (51.5-68.0) µm; the spore body was 11.7 (11.3-12.0) µm in length by 7.6 (7.3-8.3) µm in width and 6.7 (6.6-6.8) µm in thickness. The caudal appendages, measuring 46.0 (40.0-55.0) µm in length, were very thin at the tapered end. The prevalence of infection by H. sinova sp. nov. was 35.5%. Phylogenetic analysis of nuclear small subunit ribosomal DNA (SSU rDNA) clearly suggested H. sinova as a new species which is clustered within the marine Henneguya lineage. Pairwise nucleotide similarities and DNA distance values of SSU rDNA between H. sinova sp. nov. and other related Henneguya species also supported this suggestion.

Myxobolus Butschli, 1882 (Myxozoa, Myxosporea, Bivalvulida, Myxobolidae) is an important parasitic protozoan of freshwater fishes reported from almost all over the world. The severity of infection may lead to mortality of the host fish. The present paper deals with the description of three new species of Myxobolus Butschli, 1882, Myxobolus sonarpurensis sp. nov., Myxobolus elongatum sp. nov. and Myxobolus petalum sp. nov. from a freshwater minor carp Labeo bata (Hamilton, 1822) and major carp Labeo rohita (Hamilton, 1822) respectively from West Bengal, India. Spores of Myxobolus sonarpurensis sp. nov. measures 12.16 µm × 6.74 µm, with two elongated unequal sized polar capsules measuring, 8.84 µm × 3.019 µm and 7.71 µm × 3.12 µm. Spores of Myxobolus elongatum sp. nov. are 16.23 µm × 7.9 µm with two equal polar capsules 8.896 µm × 3.468 µm and 6.51 µm × 3.46 µm. In comparison to aforementioned two new species, Myxobolus petalum sp. nov. have two equal polar capsules, 7.905 µm × 2.975 µm (2.9 µm) in each spore, 12.07 µm × 5.95 µm.

A checklist of the new species of Henneguya described since 2002 (43 species) is presented. Included are the main features of each species, the type-host, the type-locality and the original references. In addition, accession numbers to sequences in GenBank are indicated whenever possible.

Myxosporean genera Henneguya and Myxobolus (Bivalvulida: Myxobolidae) are closely related in morphology and molecular phylogeny, speciose with approximately 1,000 nominal species. The majority of them are recorded from freshwater fish worldwide, and few are known from marine fish. In this study, three myxobolid spp. are described from marine fish around Japan. Two novel Henneguya spp., Henneguya ogawai sp. n. and Henneguya yokoyamai sp. n., are described from two black sea breams (Acanthopagrus schlegelii) fished in the Inland Sea (Setonaikai), Japan. Plasmodia of the former species were localized in the esophageal or intestinal wall, and those of the latter species were in the wall of the gall bladder and peritoneum. Spore development in plasmodia of these two species was synchronous. The spore body of H. ogawai sp. n. was 11.0 (8.9-12.2) μm in length, 6.9 (6.3-7.5) μm in width, 5.9 (5.2-6.6) μm in thickness, with a bifurcated caudal process of equal length, 10.0 (8.4-12.7) μm long; total spore length, 21.1 (19.2-23.4) μm. It contained two polar capsule, 4.3 (3.8-5.2) × 1.9 (1.4-2.3) μm. The spore body of H. yokoyamai sp. n. was 11.0 (10.1-13.7) μm in length, 7.1 (6.6-7.5) μm in width, and 5.6 (4.5-6.4) μm in thickness, with a bifurcated caudal process of equal length, 14.1 (10.8-17.0) μm long; total spore length, 25.0 (21.9-29.2) μm. It contained two polar capsules, 3.7 (3.1-4.2) × 2.0 (1.8-2.4) μm. A novel Myxobolus sp., Myxobolus machidai sp. n., is described from a spotted knifejaw (Oplegnathus punctatus) fished in the Sea of Japan, off Shimonoseki, Yamaguchi Prefecture, Japan. Plasmodia were embedded in the esophageal wall. Its round spore was small in size, 9.0 (8.1-9.4) μm in length, 7.8 (7.5-8.3) μm in width, and 5.5 (5.1-6.0) μm in thickness. It contained two polar capsules, 3.5 (3.2-3.8) × 2.3 (2.2-2.5) μm. Spore development in a plasmodium was asynchronous. Nucleotide sequencing of the small subunit ribosomal RNA gene (SSU rDNA) of these two novel Henneguya spp. revealed a close phylogenetic relationship with the marine clade of Henneguya spp.; however, they were distinct in morphology and SSU rDNA sequence from any known species. M. machidai sp. n. was grouped with freshwater Henneguya spp. in a phylogenetic tree based on the SSU rDNA, distant from a known marine clade of Myxobolus spp. reported mainly from the Mediterranean Sea. This is the first record of Henneguya-Myxobolus spp. from natural marine water in Japan.

A synopsis of 131 nominal species of Myxobolus Butschli, 1882 (Myxozoa: Myxosporea: Myxobolidae) reported from India is presented. For each species, the relevant morphometric and morphological data are indicated, as well as the host(s), site(s) of infection within the host and locality data. A revised dichotomous key of 59 genera of the class Myxosporea has also been included. This key incorporates 10 additional genera to that proposed in 1991 by Lom & Dykova.

Echinactinomyxon-type actinospores were found in a mixed-species oligochaete culture originating from the Temperate Water Fish Hatchery near Budapest, Hungary. On the basis of DNA sequence analysis, the actinospores were identified as Myxobolus pavlovskii (Akhmerov, 1954), the 18S rDNA sequence from myxospores of which is available in GenBank. Silver carp Hypophthalmichthys molitrix (Valenciennes) fry specimens were successfully infected by cohabitation with the echinactinomyxon-releasing oligochaetes, which confirmed the molecular data congruence. The echinactinomyxons and the myxospores that developed in the gills of exposed fish fry were analysed morphologically and on DNA basis. The infected gill tissue was examined histologically. As typical characters of M. pavlovskii, numerous small plasmodia were observed in the epithelia of gill lamellae. Plasmodia contained thousands of myxospores with polar capsules unequal in size and witl; large intercapsular processes. The 18S rDNA sequence from actinospores and those from myxospores originating from the experimentally infected fish were identical. The oligochaete species releasing actinospores was morphologically determined as Limnodrilus sp. This is the first record of an echinactinomyxon as an alternate stage within the genus Myxobolus.

During a study of myxosporean parasites of freshwater fishes of Punjab Wetlands, India, one new myxosporean species, Myxobolus harikensis sp. nov. was recorded from the caudal fin of Cirrhina mrigala (Ham.) (Cypriniformes: Cyprinidae). Plasmodia are small, white, spherical-to-rounded and are present on the caudal fin (in between the fin rays) having two to five spores per plasmodium. Spores of M. harikensis measure 10.1 × 8.5 μm in size, pyriform in valvular view and lenticular in sutural view pointing in the direction to the plane of slightly bent sutural line. Shell valves are thick, smooth, asymmetric and flattened at the sutural plane. Parietal folds are absent. Polar capsules are two, prominently unequal, broadly pyriform-to-rounded in shape and lie at different levels in the spore body cavity. The larger polar capsule is 5.0 × 3.1 μm in size, placed anteriorly on the sutural plane and opening to the exterior anteriolaterally. The smaller polar capsule measures 1.7 × 1.4 μm in size, placed posteriorly, perpendicular to the sutural plane and opening to the exterior mediolaterally. Spores of M. harikensis closely resembles to that of Myxobolus africanus in having polar capsules placed at different levels in the spore body cavity, however, are unique in having unequal polar capsules both discharging laterally.

A new myxosporean species, Myxobolus supamattayai n. sp., was isolated from wild mullet (Valamugil seheli) from the Andaman Sea, Thailand and described based on its morphology and molecular data. The myxosporean produced black plasmodia-like unique clinical sign on the skin with sporogonic stages and mature spores. Polysporous plasmodia, up to 2.5 mm in diameter, were found in epithelium tissue in the scale pocket. The spores measured 6.6 (6.2-7.0) μm in length, 6.5 (6.2-6.7) μm in width, smooth, and round board to ellipsoidal in valvular view. Spores were enclosed with intracapsular process which represents 5-7 and 11-12 in amount revealed in light microscopy and ultrastructure, respectively. The polar capsules were pyriform and of equal size, measuring 3.5 (3.4-3.6) μm in length and 2.0 (1.9-2.2) μm in width, with four to five turns of polar filament arranged perpendicularly to longitudinal axis of the polar capsule. In conclusion, this new species is entirely different from those previously described; however, this finding was assured by the partial sequence of SSU rRNA gene (1,666 bp) analysis that differed from all known species of Myxobolus Bütschli, 1882. The phylogenetic tree of the sequence data sets including those of freshwater and marine of Myxobolus spp. and the sister group (Henneguya spp.) was constructed to establish the relationship of this new species in Myxobolus clade and to explore its relations between their sister groups. Phylogenetic analysis indicated that a monophyletic group with Myxobolus spp. which infected mullet represents the newly formed species. These results suggested the presumably nearby evolution prospecting of Myxobolus species that were found in the same host.

During a survey on fishes from Hungarian freshwaters, the occurrence of eight Myxobolus species was registered in roach (Rutilus rutilus L.). Most species had a specific location within the fish host. Of the known species infecting roach, the intramuscularly developing species Myxobolus pseudodispar was found to be the most common. Besides Myxobolus intimus and Myxobolus diversicapsularis infecting the capillary network of gill lamellae, Myxobolus feisti infecting the cartilaginous gill rays were observed. Of the "muelleri-type" Myxobolus spp, Myxobolus rutili and Myxobolus sommervillae sp. n. formed elongated plasmodia in the gill filaments outside and inside the arteria efferens, respectively, while Myxobolus wootteni sp. n. developed cysts in fins. Plasmodia and spores of Myxobolus fundamentalis sp. n. were detected in the cartilaginous gill arch under the basis of gill filaments. Despite similarities of some species in spore morphology, 18S rDNA sequences and phylogenetic analyses showed clear differences among all species examined. The findings of the study demonstrate that morphologically similar spores could only be correctly identified by considering the location of plasmodia and the genetic characters of the myxozoan species.

Thelohanellus magnacysta n. sp. (Bivalvulida: Myxobolidae) infects the skeletal muscle of blacktail shiner, Cyprinella venusta Girard, 1856 (Cypriniformes: Cyprinidae) in Bull Creek, Chattahoochee River Basin, eastern Georgia. Although numerous members of ThelohanellusKudo, 1933 have overlapping myxospore dimensions with the new species, it differs from all nominal congeners by polar filament coil number and polar capsule width as well as by lacking a mucous envelope, iodinophilic vacuole, and sutural markings. With the use of novel primers for Myxozoa, a phylogenetic analysis of the small subunit ribosomal DNA (SSU rDNA) suggests that the new species shares a recent common ancestor with a clade of cyprinid-infecting species of Myxobolus Bütschli, 1882 (Bivalvulida: Myxobolidae) and Thelohanellus. Consistent with other published research concerning the systematics of Thelohanellus, this result suggested that Thelohanellus and Myxobolus are polyphyletic and need revision. Histological sections of infected blacktail shiners confirmed that myxospores were only found within a plasmodium and only infected skeletal muscle and that plasmodia were encapsulated by a granuloma comprising varying degrees of acute granulomatous inflammation. The new species is the fourth of Thelohanellus reported from North America and the first reported from Cyprinella, as well as the first myxozoan described from the blacktail shiner.

Myxobolus franciscoi sp. nov. (Myxozoa: Myxosporea: Myxobolidae) is described from the "curimatá-pacú" fish, Prochilodus argenteus Spix & Agassiz, 1829 (Actinopterygii: Prochilodontidae) from the Upper São Francisco River, Brazil. This parasite forms whitish plasmodia (about 1 x 1 mm) that develop in the connective tissue of fins. The spores are more or less round in frontal view and ellipsoidal in lateral view, measuring 6.4 (6.0-6.9) µm in length, by 6.0 (5.8-6.4) µm in width and 3.2 µm in thickness. The polar capsules are very small, measuring about 2 µm in length by 1.5 µm in width and ending in a tapered anterior neck. The polar filament makes three turns in a plane at right angles with the longitudinal axis of the spore. Thorough comparisons with the remaining species of Myxobolus Bütschli, 1882 described from South American fish, as well as with almost all species of Myxobolus described so far, are provided. This paper also includes a revision of Myxobolus species from South American fish hosts.

While investigating the parasite fauna of wild coho salmon. Oncorhynchus kisutch (Walbaum, 1792), histological examination provided evidence of a new species of Myxobolus (Myxozoa: Myxosporea) infecting nerves of skeletal muscle. Spores were morphologically similar to those of the intramuscular Myxobolus insidiosus Wyatt and Pratt, 1963, both having pyriform spores with clavate polar capsules. However, the former developed exclusively in the nerves of skeletal muscle rather than in myocytes. We examined both species of Myxobolus derived from coho salmon; Chinook salmon, Oncorhynchus tshawytscha (Walbaum, 1792); cutthroat trout, Oncorhynchus clarkii (Richardson, 1836); and rainbow trout Oncorhynchus mykiss (Walbaum, 1792) from freshwater in Oregon. Spore morphology, small subunit ribosomal RNA gene (rDNA) sequences, and site of infection were compared. Myxobolus arcticus Pugachev and Khokhlov, 1979 has pyriform spores, infects the central nervous system of many salmonids, and is found in the Pacific Northwest. It was therefore included in the analyses to rule out conspecificity with the new species. Together, these data show that the Myxobolus sp. from peripheral nerves in the skeletal musculature of coho salmon, rainbow trout, and cutthroat trout is a new species, described herein as Myxobolus fryeri n. sp.

Channel catfish Ictalurus punctatus from a commercial farming operation in the Mississippi Delta were submitted for examination for the presence of infection by the trematode Bolbophorus damnificus. The fish were instead found to possess skin nodules suggestive of Henneguya pellis, a species previously described in the blue catfish I. furcatus. Despite the dermal location and distribution of lesions, morphological characteristics of the myxospores were inconsistent with H. pellis. Spores possessed a lanceolate spore body 15.4 +/- 1.5 microm (mean +/- SD; range = 12.2-19.3 microm) in length and 5.5 +/- 0.6 microm (range = 4.5-6.8 microm) in width in valvular view, and 4.7 +/- 0.2 microm (range = 4.2-5.0 microm) in width in sutural view. Polar capsules were pyriform and unequal in both length and width and contained polar filaments with six coils. Polar capsules measured 6.1 +/- 0.8 microm (range = 4.0-7.9 microm) long and 1.7 +/- 0.3 microm (range = 1.0-2.2 microm) wide. The caudal appendages were 50.5 +/- 8.3 microm (range = 34.8-71.4 micorm) long and the total length of the spore was 65.9 +/- 8.6 microm (range = 48.2-90.0 microm). The "blister like" plasmodia were round or ovoid, up to 2 mm in diameter, and randomly distributed throughout the epidermis of the fish. Histologically, plasmodia were confined to the dermis and elicited no inflammatory reaction from the fish. A blast search of the 18S small subunit rDNA sequence obtained by polymerase chain reaction amplification resulted in no identical sequence matches but indicated a close relationship to H. gurlei, H. ictaluri, and H. exilis. The unique host record, spore morphology, and novel genetic sequence derived from this isolate lead us to propose this isolate as a novel species, H. sutherlandi.

Myxobolus ampullicapsulatus n. sp. was isolated from the gills of Carassius auratus auratus (L., 1758) in Chongqing, China. Myxospores were pyriform, measuring 16.5-19.5 microm long x 8.5-10.0 microm wide x 7.0 microm thick. Two equal polar capsules were ampullaceous, measuring 7.0-10.0 microm long x 2.5-4.0 microm wide, containing polar filaments coiled 9-10 turns. Spore length of this species exceeds that of the majority of other Myxobolus spp., and those overlapping in this dimension can be differentially diagnosed by other characters. Furthermore, the small subunit ribosomal DNA (SSU rDNA) of M. ampullicapsulatus n. sp. is unique among myxozoans sequenced to date. Phylogenetic analyses of the SSU rDNA gene sequence placed this species in a clade composed exclusively of gill parasites, most closely related to Myxobolus longisporus, which also infects the gills of cyprinid fishes in China.

Myxobolus gayerae sp. n. and M. leuciscini Gonzalez-Lanza & Alvarez-Pellitero, 1985 (Myxozoa: Myxobolidae) have been described and re-described from European chub Leuciscus cephalus L. from the Hungarian stretch of the river Danube. The ellipsoidal plasmodia of M. gayerae sp. n. were found in the mucosa of the intestinal wall, whereas the large, elongated plasmodia of M. leuciscini infected the afferent arteries of the gill filaments. The spores of M. gayerae sp. n. are relatively large, slightly oval and almost rectangular in shape. On the basis of spore morphology and 18S rDNA sequences, the most similar species was M. cycloides Gurley, 1893, but the 2 species differed in host and tissue tropism as well as in the size of the spores. The spores of M. leuciscini from L. cephalus, having no intercapsular appendix or occasionally a very small one, showed a high morphological similarity to spores collected from L. cephalus cabeda, Chondrostoma polylepis and Rutilus arcasi in Spain and described as M. leuciscini Gonzalez-Lanza & Alvarez-Pellitero, 1985.

Myxobolus platanus n. sp. infecting the spleen of Mugil platanus Günther, 1880 (Osteichthyes, Mugilidae) from Lagoa dos Patos, Brazil is described The parasites formed round or slightly oval whitish plasmodia (about 0.05-0.1mm in diameter) on the surface of the organ. The spores were round in frontal view and oval in lateral view, 10.7µm (10-11) long, 10.8µm (10-11) wide and 5µm thick, and presented four sutural marks along the sutural edge. The polar capsules, equal in size, were prominent, surpassing the mid-length of the spore, and were oval with the posterior extremity rounded, and converging with their anteriorly tapered ends. They were 7.7µm (7-8) long and 3.8µm (3.5-4) wide. A small intercapsular appendix was present. The polar filament formed five to six coils obliquely placed to the axis of the polar capsule. No mucous envelope or distinct iodinophilous vacuole were found.

Morphometric data from spores of ten myxosporean species were statistically analysed to explore myxosporean intraspecific variation in measurements when obtained from a sample from: (1) the same plasmodium, (2) different plasmodia from the same host and (3) different host individuals and localities. In some cases, significant differences in spore dimensions were found between samples from the same plasmodium, highlighting the difficulty of obtaining representative measurements of myxosporean spore. In addition, significant differences in spore dimensions were found when plasmodia from the same site of infection were compared, suggesting that measurements of spores should come from several different plasmodia of the sampling to increase the reliability of the morphology data. Moreover, significant differences in spore dimensions were observed for most spore dimensions when data were compared between localities. In all cases, there was clear overlap in ranges of dimensions even when means differed significantly. The present statistical analysis shows that intraspecific morphometric variation of myxosporean species commonly occurs, highlighting the importance of reporting ranges of measurements for a species, not just the mean dimensions, and taking into account all evidence when assigning or describing myxosporean species.

The present study describes light microscopy, transmission electron microscopy, and molecular analyses of a myxosporid found parasitizing the gill region of the teleost fish Cichla temensis, collected from the Tocantins River, near Cameta, Para State, Brazil. The prevalence of infection was 60 %. The spore-containing cysts that were located in the gill lamellae were oval and whitish. The spores had a mean length of 42.3 ± 0.65 μm; fusiform body, 12.8 ± 0.42-μm long and 8.6 ± 0.32-μm wide; each of the two valves exhibited a tapering tail of 29.5 ± 0.73 μm length. The spores had two polar capsules, 7.4 ± 0.16-μm long by 2.6 ± 0.08-μm wide, containing a polar filament with 5-7 twists. The spores differ from the species previously described, and phylogenetic analysis based on spore morphology and molecular aspects indicated that the fish parasite Henneguya sp. has a strong trend to form clades mainly based on the environment and host order/family. Thus, we conclude that the species belongs to the family Myxobolidae, genus Henneguya, which comprises a new species: Henneguya paraensis n. sp.

The smallmouth buffalo Ictiobus bubalus Rafinesque (Catostomidae) is native to North American waterways and occasionally grown in pond aquaculture. Species of Myxobolus Butschli, 1882 have been reported from the gills, integument, and intestinal tract of buffalo fish, although there is ambiguity in some host records. In the summer of 2013, thirteen adult smallmouth buffalo were seined from a 0.1-acre (0.04-hectare) experimental research pond at the Thad Cochran National Warmwater Aquaculture Center in Stoneville, Mississippi, USA, and examined for the presence of parasitic infection. Two previously unknown species of Myxobolus were observed parasitising the gills. Plasmodia of the two species differed from each other in both size and shape. Morphologically the two species were distinct from one another and from other Myxobolus spp. previously reported from buffalo fish. Myxospores of Myxobolus ictiobus n. sp. were spherical and measured 12.7–14.5 (13.9 ± 0.4) µm in length and 10.7–13.6 (12.5 ± 0.7) µm in width with a thickness of 10.3–14.8 (12.6 ± 2.3) µm. Polar capsules measured 5.6–7.4 (6.6 ± 0.4) µm in length and 3.7–4.9 (4.5 ± 0.8) µm in width and each contained a coiled polar filament with 5–6 turns. Myxospores of Myxobolus minutus n. sp. were circular in shape and measured 7.4–9.6 (8.6 ± 0.7) µm in length and 7.5–9.9 (8.8 ± 0.7) µm in width with a thickness of 6.5–7.3 (6.7 ± 0.3) µm. Polar capsules measured 3.6–4.9 (4.3 ± 0.3) µm in length and 2.8–3.8 (3.3 ± 0.3) µm and each contained a coiled polar filament with 5–6 turns. Supplemental 18S rRNA gene sequencing identified unique sequences for each isolate. Phylogenetic analysis of 18S rRNA sequences demonstrated a strong clustering of both isolates with other species of Myxobolus from cypriniform fish.

The channel catfish Ictalurus punctatus is a known host for 10 species of Henneguya, but few other myxozoan genera are described from this species. Unicauda is a genus of myxozoan parasites within the family Myxobolidae that consists of 10 valid species from freshwater fish. Herein, we describe a novel species of Unicauda from the intestinal tract of farm-raised channel catfish in Mississippi. Myxospores were consistent with the genus Unicauda but exhibited a unique branching at the terminal end of the caudal process that has not previously been reported. Myxospores measured 90.39 ± 14.97 μm (mean ± SD; range = 70.88-126.02 μm) in total length. The spherical spore body measured 7.31 ± 0.26 μm (6.75-7.84 μm) in length and 7.01 ± 0.63 μm (6.1-8.01 μm) in width. The 2 polar capsules measured 3.45 ± 0.33 μm (3.02-4.03 μm) in length and 2.65 ± 0.32 μm (2.18-3.11 μm) in width. The single caudal process measured 82.98 ± 14.97 μm (63.39-118.63 μm) in length from the base of the spore body to the end of the most terminal projection. Terminal projections measured 26.83 ± 8.8 μm (12.34-42.29 μm) in length and 0.95 ± 0.23 μm (0.52-1.6 μm) in width. The 18S rRNA gene sequence obtained did not match any published sequences. Given the uniqueness of the myxospore morphology, histological presentation, and gene sequence data, we describe this as an unreported species, Unicauda fimbrethilae n. sp.