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99 results for “Myxosporea”
Fig. 1 in A new Myxobolus (Cnidaria: Myxosporea) infecting the ornamental catfish Corydoras schwartzi from the Purus River in Brazil
Fig. 1. Corydoras schwartzi Rössel, 1963 infected by Myxobolus adrianoi sp. nov. A. Sampled fish captured in the Purus River near Lábrea Municipality, Amazonas State, Brazil. B. Histological sections of the fish intestine showing large cyst in the serosa layer (black arrow).
Fig. 2. A in Molecular Characterization of Two Myxosporean Species, Henneguya namae Haldar et al. 1983 and Myxobolus sophorae Jayasri, 1982 (Myxosporea: Myxobolidae)
Fig. 2. A schematic drawing of Henneguya namae and Myxobolus sophorae myxospores found infect Chanda nama and Puntius sophore. In frontal view: A – H. namae, C – M. sophorae. In sutural view: B – H. namae, D – M. sophorae. Scale bars (A–D) 10 µm.
Fig. 1 in Molecular Characterization of Two Myxosporean Species, Henneguya namae Haldar et al. 1983 and Myxobolus sophorae Jayasri, 1982 (Myxosporea: Myxobolidae)
Fig. 1. Photographs of myxobolids: A – Cysts of H. namae of different sizes between gill filaments of the host fish show by arrows, B – Spores released from ruptured cysts of H. namae, C – H. namae frontal view, D – H. namae sutural view, E – M. sophorae frontal view, F – M. sophorae sutural view. Scale bars (A) 300 µm, (B) 50 µm, (C–F) 10 µm.
Fig. 1 in Myxobolus opsaridiumi sp. nov. (Cnidaria: Myxosporea) infecting different tissues of an ornamental fish, Opsaridium ubangiensis (Pellegrin, 1901), in Cameroon: morphological and molecular characterization
Fig. 1. Photomicrographs of Myxobolus opsaridiumi sp. nov. infecting skin, muscle and spleen of Opsaridium ubangiensis (Pellegrin, 1901). A. Fresh myxospores in frontal view. B. Fresh myxospore in lateral view. C. Giemsa-stained myxospores. D. Diagrammatic drawing of a mature myxospore.
Fig. 2 in Myxobolus opsaridiumi sp. nov. (Cnidaria: Myxosporea) infecting different tissues of an ornamental fish, Opsaridium ubangiensis (Pellegrin, 1901), in Cameroon: morphological and molecular characterization
Fig. 2. Photomicrographs of plasmodia of Myxobolus opsaridiumi sp. nov. developing on Opsaridium ubangiensis (Pellegrin, 1901). A. Plasmodium development on the skin. B. Histological section stained with hematoxylin and eosin showing plasmodium situated in the dermis. C. Plasmodium developing within muscle fibers (hematoxylin and eosin). D. Higher magnification of a plasmodium from the muscle fibers.
Fig. 3. A–C in Myxobolus opsaridiumi sp. nov. (Cnidaria: Myxosporea) infecting different tissues of an ornamental fish, Opsaridium ubangiensis (Pellegrin, 1901), in Cameroon: morphological and molecular characterization
Fig. 3. A–C. Photomicrographs of plasmodia of Myxobolus opsaridiumi sp. nov. affecting a spleen of Opsaridium ubangiensis (Pellegrin, 1901). A. Spleen harbouring large plasmodia. B. Whitish plasmodia isolated from each other (black arrows) or arranged in grape-like clusters (white arrow). C. Spleen completely filled with plasmodia. – D–G. Histological sections stained with hematoxylin and eosin of spleens of O. ubangiensis infected with plasmodia of M. opsaridiumi sp. nov. D. Plasmodia implanted on the external region of the spleen. E. Asynchronous development of plasmodia within the spleen. F. Mechanical compression of the cells adjacent to the cysts. G. Higher magnification of plasmodia showing each surrounded by a wall and full of myxospores. Abbreviation: P = plasmodium.
Fig. 4 in Myxobolus opsaridiumi sp. nov. (Cnidaria: Myxosporea) infecting different tissues of an ornamental fish, Opsaridium ubangiensis (Pellegrin, 1901), in Cameroon: morphological and molecular characterization
Fig. 4. Maximum likelihood phylogenetic tree based on the SSU rDNA sequences showing the position of Myxobolus opsaridiumi sp. nov. (in bold) and related species. Accession numbers and infected tissues are listed adjacent to the species names. Numbers at the nodes represent Bayesian posterior probabilities and ML bootstrap percentages. Kudoa thyrsites (Gilchrist, 1924) was used as the outgroup.
Fig. 3 in Molecular Characterization of Two Myxosporean Species, Henneguya namae Haldar et al. 1983 and Myxobolus sophorae Jayasri, 1982 (Myxosporea: Myxobolidae)
Fig. 3. Phylogenetic relationship of H. namae and M. sophorae based on the 18S gene sequences. Numbers at nodes indicates ML bootstrap values (1000 replications) and posterior probabilities (BI) respectively. Unsupported nodes by BI are marked with a hyphen. The scale bar indicates the number of substitution per site. Newly generated sequences in this study shown as bold. GenBank accession numbers are listed before the species names.
Fig. 4 in Henneguya (Cnidaria: Myxosporea: Myxobolidae) infections of cultured barramundi, Lates calcarifer (Perciformes: Latidae) in an estuarine wetlands system of Malaysia: description of Henneguya setiuensis n. sp., Henneguya voronini n. sp. and Henneguya calcarifer n. sp.
Fig. 4 Histological sections of gill filaments from Lates calcarifer infected by plasmodia of H. setiuensis n. sp. and H. voronini n. sp. (a) Plasmodia of H. setiuensis n. sp. (arrows) producing compression and damage to the lamellae (*). (b) Development of plasmodia of H. voronini n. sp. (arrows) in the sub-epithelial layer at the base of the filament. Note that the plasmodia also impinge into the gill arch (g)
Fig. 5 in Henneguya (Cnidaria: Myxosporea: Myxobolidae) infections of cultured barramundi, Lates calcarifer (Perciformes: Latidae) in an estuarine wetlands system of Malaysia: description of Henneguya setiuensis n. sp., Henneguya voronini n. sp. and Henneguya calcarifer n. sp.
Fig. 5 Phylogenetic tree generated by maximum likelihood analysis of 18S ribosomal DNA sequences of Henneguya species from perciform hosts and other closely related myxosporean species identified by BLAST; GenBank accession numbers shown after the species name, including the three novel data in bold (H. setiuensis n. sp., H. voronini n. sp. and H. calcarifer n. sp.). Numbers at nodes indicate the bootstrap confidence values (ML). Taxonomic orders of the fish hosts are shown at right: Char Characiformes, Sil Siluriformes, Esoc Esociformes, Mug Mugiliformes, Gob Gobiiformes, Per Perciformes and Acti Actinospores. Chloromyxum cyprini was used as an outgroup
Fig. 2 Henneguya voronini n in Henneguya (Cnidaria: Myxosporea: Myxobolidae) infections of cultured barramundi, Lates calcarifer (Perciformes: Latidae) in an estuarine wetlands system of Malaysia: description of Henneguya setiuensis n. sp., Henneguya voronini n. sp. and Henneguya calcarifer n. sp.
Fig. 2 Henneguya voronini n. sp. (a–b) Line drawings of mature myxospores in frontal view showing polar capsules with coiled polar tubules. (c) Fresh, unstained myxospores in frontal view showing the two pyriform polar capsules. (d) Scanning electron microscope image of the spores showing simple, smooth valve cell surfaces, each contiguous with a caudal process; features typical of the genus
Fig. 1 Henneguya setiuensis n in Henneguya (Cnidaria: Myxosporea: Myxobolidae) infections of cultured barramundi, Lates calcarifer (Perciformes: Latidae) in an estuarine wetlands system of Malaysia: description of Henneguya setiuensis n. sp., Henneguya voronini n. sp. and Henneguya calcarifer n. sp.
Fig. 1 Henneguya setiuensis n. sp. (a–b) Line drawings of mature myxospores in frontal view showing polar capsules with coiled polar tubules. (c) Fresh, unstained myxospores in frontal (arrow) and sutural (*) views, with divergent caudal appendages
Fig. 2 in Data on Ten New Myxosporean Parasites (Myxozoa, Myxosporea, Bivalvulida) from the Yellow Sea, China
Fig. 2. Schematic illustrations of Ceratomyxa kareus sp. n. A–L – from Kareius bicoloratus; M–N – from Zebrias zebra; A–D – lateral view of mature spore; E–F, N – plasmodia with two spores; G–J – earlier stage plasmodia; K – plasmodium with one spore; L–M – plasmodia with mature spores. Scale bars: 10 µm.
Fig. 3 in Data on Ten New Myxosporean Parasites (Myxozoa, Myxosporea, Bivalvulida) from the Yellow Sea, China
Fig. 3. Schematic illustrations of Ceratomyxa spp. A–E – Ceratomyxa lomi sp. n.; A – mature spore viewed from the perspective of the capsule; B–D – lateral view of mature spore; E – plasmodium with two mature spores; F–J – Ceratomyxa lateolabrax sp. n.; F – plasmodium with two spores; G–J – lateral view of mature spore; K–N – Ceratomyxa qingdaoensis sp. n.; K–L, N – showing a lateral view of a mature spore; M – lateral view of an immature spore. Scale bars: 10 µm.
Fig. 1 in Data on Ten New Myxosporean Parasites (Myxozoa, Myxosporea, Bivalvulida) from the Yellow Sea, China
Fig. 1. Schematic illustrations of three myxosporean species. A–E – Sphaerospora sebasta sp. n.; A – mature spore from a frontal view; B–C – spore viewed from the perspective of the capsule; D – spore from a sutural view; E – spore from an oblique sutural view; F–H – Ceratomyxa sebastisca sp. n., showing mature spores with coarse sporoplasm; I–O – Ceratomyxa hemitriptera sp. n.; I–J – mature spore from a lateral view; K–L – plasmodium with one mature spore; M–N – early stage plasmodium with one developing spore; O – plasmodium with one developing spore from a capsule view. Scale bars: 10 µm.
Fig. 5 in Data on Ten New Myxosporean Parasites (Myxozoa, Myxosporea, Bivalvulida) from the Yellow Sea, China
Fig. 5. Microphotographs of myxosporean species. A–B – Sphaerospora sebasta sp. n.; C – Ceratomyxa sebastisca sp. n.; D–E – Ceratomyxa hemitriptera sp. n.; F–H – Ceratomyxa kareus sp. n.; I–J – Ceratomyxa lomi sp. n. Scale bars: 10 µm.
Fig. 4 in Data on Ten New Myxosporean Parasites (Myxozoa, Myxosporea, Bivalvulida) from the Yellow Sea, China
Fig. 4. Schematic illustrations of Ceratomyxa spp. A–G – Ceratomyxa saurida sp. n.; A–D, G – lateral view of mature spore; E – lateral view of abnormal spore; F – lateral view of immature spore; H–L – Ceratomyxa simplex sp. n.; H, J – lateral view of mature spore; I – immature spore viewed from the perspective of the capsule; K–L – plasmodia with one spore; M–T – Ceratomyxa triacantha sp. n.; M–N, P – plasmodia with two spores; O, Q – early stage plasmodia with many nuclei; R–T – sutural view of mature spores. Scale bars: 10 µm.
Fig. 6 in Negative effects of Kudoa islandica n. sp. (Myxosporea: Kudoidae) on aquaculture and wild fisheries in Iceland
Fig. 6. SSU rDNA maximum likelihood phylogenetic tree of 16 Kudoa spp. Kudoa islandica is robustly and consistently placed with other Kudoa taxa in all analyses, but is not well supported in the clade it is placed in. Numbers at the nodes represent bootstrap support from 1000 samplings, nodes with a support of <50 are considered not supported (ns).
Fig. 4 in Negative effects of Kudoa islandica n. sp. (Myxosporea: Kudoidae) on aquaculture and wild fisheries in Iceland
Fig. 4. Line drawings of Kudoa islandica n. sp. in apical view (A) and lateral view (B). Scanning electron microscope images of K. islandica n. sp. (C–E). Mature spore in lateral view showing extruded polar filaments (arrow) (C). Single spore in apical view (D) showing the sutures of the four valves (broad arrows), the four apical projections (thin arrow) and cytoplasmic projections (arrowhead). Single spore in posterior view (E) showing the suture of the four valves (broad arrows), Scale bars: (A) and (B) = 2 µm; (C), (D) and (E) = 1 µm.
Fig. 3 in Negative effects of Kudoa islandica n. sp. (Myxosporea: Kudoidae) on aquaculture and wild fisheries in Iceland
Fig. 3. Fresh mature spores of Kudoa islandica n. sp. as seen in fresh squash preparations from muscular tissue of Atlantic wolffish, Anarhichas lupus. Note the protruding polar filament of one of the spores (arrow). Nomarski differential interference contrast. Scale bar = 10 µm.
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International Brain Laboratory public data
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OpenNeuro
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