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99 results for “Myxosporea”
Fig. 2. A in The occurrence of known Myxobolus and Thelohanellus species (Myxozoa, Myxosporea) from Indian major carps with the description of Myxobolus bandyopadhyayi n. sp. in West Bengal
Fig. 2. A plasmodium (P) of Thelohanellus caudatus in the fin of a rohu in close contact with the cartilaginous fin ray (Fr). Mount picture. Bar = 200 μm.
Fig. 15 in The occurrence of known Myxobolus and Thelohanellus species (Myxozoa, Myxosporea) from Indian major carps with the description of Myxobolus bandyopadhyayi n. sp. in West Bengal
Fig. 15. Spores of M. rewensis from the fin of mrigal. Arrow is indicating the characteristic globule inside the intercapsular appendix. Mount picture. Bar = 10 μm.
Fig. 6 in New data on Thelohanellus nikolskii Achmerov, 1955 (Myxosporea, Myxobolidae) a parasite of the common carp (Cyprinus carpio, L.): The actinospore stage, intrapiscine tissue preference and molecular sequence
Fig. 6. Phylogenetic position of Thelohanellus nikolskii spores from the fins and scales of common carp based on SSU rDNA analysis by the Maximum Likelihood algorithm. Myxobolus cerebralis was used as the outgroup. Bootstrap values are given at the nodes. The scale-bar indicates the number of expected substitutions per site.
Fig. 5 in New data on Thelohanellus nikolskii Achmerov, 1955 (Myxosporea, Myxobolidae) a parasite of the common carp (Cyprinus carpio, L.): The actinospore stage, intrapiscine tissue preference and molecular sequence
Fig. 5. Microphotograph of fresh, unstained actinospore of Aurantiactinomyxon type (AUM5) from Nais sp. Insert – apical view of spore with protruding polar capsules.
Fig. 7 in New data on Thelohanellus nikolskii Achmerov, 1955 (Myxosporea, Myxobolidae) a parasite of the common carp (Cyprinus carpio, L.): The actinospore stage, intrapiscine tissue preference and molecular sequence
Fig. 7. Schematic illustration of T. nikolskii life cycle: Aurantiactinomyxon-type actinospores (A) infect the vertebrate host C. carpio (V) in which they develop myxospores (M) that infect the invertebrate host Nais sp. (I).
Fig. 2. A in New data on Thelohanellus nikolskii Achmerov, 1955 (Myxosporea, Myxobolidae) a parasite of the common carp (Cyprinus carpio, L.): The actinospore stage, intrapiscine tissue preference and molecular sequence
Fig. 2. A: Section of an infected fin, containing T. nikolskii cysts, stained with hematoxilin-eosin. Cartilage of finray (cf) is next to the cyst. Plasmodium (p) is in the achromatic tegument, mature myxospores (s) are in the middle, sporoblasts (sb) are at the edges. Around the plasmodium, there is a thick connective tissue (ct) layer, containing cartilaginous elements (c). Multilayer epithelium (e) is the outer layer. B: T. nikolskii myxospores from the plasmodium.
Fig. 4. A in New data on Thelohanellus nikolskii Achmerov, 1955 (Myxosporea, Myxobolidae) a parasite of the common carp (Cyprinus carpio, L.): The actinospore stage, intrapiscine tissue preference and molecular sequence
Fig. 4. A: Cross section of infected scales, stained with hematoxilin-eosin. The plasmodia (p) are filled with myxospores (s) and are surrounded by cartilaginous tissue (c) of the scales, covered by the epithelium layer (e). B: T. nikolskii myxospores from a plasmodium in the scale.
Fig. 1 in Effect of 80% ethanol or 10% formalin fixation, freezing at - 20 C and staining on Myxobolus (Myxosporea) spores to be deposited in parasitological collections
Fig. 1. Myxospores of Myxobolus bramae treated in different ways. (a) Fresh spore, (b) Spore fixed in 80% ethanol, (c) Spore fixed in 10% formalin solution, (d) Spore freezing at – 20 ◦C for 3 months, (e) Spore stained with Giemsa stain, (f) Spore stained with Ziehl–Neelsen stain.
Fig. 3 in Effect of 80% ethanol or 10% formalin fixation, freezing at - 20 C and staining on Myxobolus (Myxosporea) spores to be deposited in parasitological collections
Fig. 3. Myxospores of Myxobolus bliccae treated in different ways. (a) Fresh spore, (b) Spore fixed in 80% ethanol, (c) Spore fixed in 10% formalin solution, (d) Spore freezing at – 20 ◦C for 3 months, (e) Spore stained with Giemsa stain, (f) Spore stained with Ziehl–Neelsen stain.
Fig. 4 in Effect of 80% ethanol or 10% formalin fixation, freezing at - 20 C and staining on Myxobolus (Myxosporea) spores to be deposited in parasitological collections
Fig. 4. Length and width (n = 795 and 729, respectively) of differently treated spores of Myxobolus bramae. Medians and interquartile ranges are indicated by thick middle lines and boxes, respectively, whereas the whiskers represent maximum and minimum values, and the open circles refer to outliers.
Fig. 2 in Effect of 80% ethanol or 10% formalin fixation, freezing at - 20 C and staining on Myxobolus (Myxosporea) spores to be deposited in parasitological collections
Fig. 2. (a) Myxospore of M. bramae treated with Lugol's solution. (b) Myxospore of M. bliccae treated with Lugol's solution.
Fig. 3 in Description of Cystodiscus elachistocleis sp. nov. (Cnidaria: Myxosporea) parasitizing the gallbladder of Elachistocleis cesarii from Brazil, based on morphological and molecular analyses
Fig. 3. Phylogenetic tree of Bayesian analysis based on partial SSU rDNA partial sequences showing the position of Cystodiscus elachistocleis sp. nov. (INPA79) among genetically similar species. Node numbers represent the Bayesian posterior probabilities and bootstrap (BI/ML). Values less than 0.7 are represented by dashes. The scale bar represents the number of substitutions per site.
Fig. 1 in Description of Cystodiscus elachistocleis sp. nov. (Cnidaria: Myxosporea) parasitizing the gallbladder of Elachistocleis cesarii from Brazil, based on morphological and molecular analyses
Fig. 1. Myxospores and pseudoplasmodia of Cystodiscus elachistocleis sp. nov. (INPA79) found parasitizing the gallbladder of Elachistocleis cesarii (Miranda-Ribeiro, 1920) from Araguaiana, Mato Grosso State, Brazil. A. Front view of C. elachistocleis sp. nov. B. Front and side view of C. elachistocleis sp. nov. C. Pseudoplasmodium (P) containing several myxospores of C. elachistocleis sp. nov. highlights myxospores (M) through the pseudoplasmodium-forming tissue.
Fig. 2 in Description of Cystodiscus elachistocleis sp. nov. (Cnidaria: Myxosporea) parasitizing the gallbladder of Elachistocleis cesarii from Brazil, based on morphological and molecular analyses
Fig. 2. Schematic drawing of Cystodiscus elachistocleis sp. nov. (INPA79) found parasitizing the gallbladder of Elachistocleis cesarii (Miranda-Ribeiro, 1920) in front and side view.
Figure 4 in Morphological and Molecular Characteristics of Kudoa viseuensis n. sp. (Myxosporea: Multivalvulida), Found in the Muscle of Batrachoides surinamensis (Teleostei: Batrachoididae) in the Brazilian Amazon Region
Figure 4. Phylogenetic tree derived from Bayesian Inference (BI), based on the partial sequences of the SSU rDNA gene of Kudoa vi- seuensis n. sp. and closely-related myxosporans. The GenBank access numbers are shown next to the species names, and the numbers at each node are the BI posterior probabilities. The new species is highlighted in bold type. Abbreviations: Msl – muscle; Dtr – digestive tract; Nsy – nervous system.
Figure 2 in Morphological and Molecular Characteristics of Kudoa viseuensis n. sp. (Myxosporea: Multivalvulida), Found in the Muscle of Batrachoides surinamensis (Teleostei: Batrachoididae) in the Brazilian Amazon Region
Figure 2. Light photomicrograph: (A) longitudinal histology section of the skeletal musculature of B. surinamensis containing a pseudocyst (*), along the axis of the muscle, showing the substitution of the fiber by the parasite; (B) transversal section showing the pseudocyst of the mixosporean occupying the central portion of the muscle fiber (arrowhead), typical of an individual infection; (C) Multiple infection of pseudocysts within a single muscle fiber, separated from one another and the muscle tissue by a fine conjunctive membrane (arrows). Scale bars: 40 µm.
Figure 1 in Morphological and Molecular Characteristics of Kudoa viseuensis n. sp. (Myxosporea: Multivalvulida), Found in the Muscle of Batrachoides surinamensis (Teleostei: Batrachoididae) in the Brazilian Amazon Region
Figure 1. Light photomicrograph: (A) Whitish pseudocyst (arrowhead) found in the musculature of B. surinamensis. Scale bar: 1000 µm; (B) pseudocyst (c) and numerous mature spores (e) observed following the rupture of the pseudocyst. Scale bar: 100 µm; (C) Fresh, pseu- do-square spores (e) of Kudoa viseuensis n. sp. Scale bar: 20 µm; Inset: polar capsules (PC) in lateral (L) and apical (A) views (DIC). Scale bar: 10 µm.
Fig. 8 in The occurrence of known Myxobolus and Thelohanellus species (Myxozoa, Myxosporea) from Indian major carps with the description of Myxobolus bandyopadhyayi n. sp. in West Bengal
Fig. 8. Myxobolus dermiscalis plasmodia (P) in the scale of a rohu. Mount picture. Bar = 500 μm.
Fig. 3 in The occurrence of known Myxobolus and Thelohanellus species (Myxozoa, Myxosporea) from Indian major carps with the description of Myxobolus bandyopadhyayi n. sp. in West Bengal
Fig. 3. Spores of T. caudatus. Mount picture. Bar = 10 μm.
Fig. 4 in The occurrence of known Myxobolus and Thelohanellus species (Myxozoa, Myxosporea) from Indian major carps with the description of Myxobolus bandyopadhyayi n. sp. in West Bengal
Fig. 4. Schematic drawing of spore of T. caudatus, a: frontal view, b: sutural view. Bar = 10 μm.
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OpenNeuro
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