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78 results for “Taenia”
Presence of Echinococcus multilocularis and Taenia taeniaformis in muskrats (Ondatra zibethicus)
<p>This dataset describes the presence of <em>Echinococcus multilocularis</em> and <em>Taenia taeniaformis </em>in muskrats (<em>Ondatra zibethicus</em>) in Flanders, Belgium.</p> <p>From 1994 onward, muskrats from Flanders have been autopsied with the aim of understanding their demography. In 2008, we first detected EM in a muskrat from Lessines (Wallonia), just across the border with Flanders. Therefore, from 2009 onward, all available muskrats from Flanders and neighbouring regions were collected and examined.</p> <p>The dataset contains the following variables:</p> <ul> <li><code>date</code>: YYYY-MM-DD</li> <li><code>province</code>: Flemish province where the muskrat was captured, for locations outside of Flanders only a municipality is provided</li> <li><code>municipality</code>: the municipality where the muskrat was captured</li> <li><code>weight</code>: the weight of the animal in grams</li> <li><code>sex</code>: either M: male or F: female</li> <li><code>taen</code>: Infection with <em>Taenia taeniaformis</em>, scored as: <ul> <li>0: No <em>T. taeniaformis </em>present</li> <li>1: Few <em>T. taeniaformis </em>present</li> <li>2: Multiple <em>T. taeniaformis </em>present</li> <li>3: A high number of <em>T. taeniaformis </em>present</li> </ul> </li> <li><code>EM</code>: Infection with <em>Echinococcus multilocularis</em>, scored as: <ul> <li>N: negative, no parasites present</li> <li>P: positive, parasite present</li> <li>?: unsure</li> </ul> </li> </ul>
Figure 2. Dextrasepiola taenia n. gen. & n in Two new genera and species of sepioline squids (Cephalopoda: Sepiolidae) from Australia
Figure 2. Dextrasepiola taenia n. gen. & n. sp., female, paratype 1 (MOV F91359): a, dorsal view; b, ventral view; c, oral view of arm crown showing sucker arrangements of female.
Figure 5. Dextrasepiola taenia n. gen. & n in Two new genera and species of sepioline squids (Cephalopoda: Sepiolidae) from Australia
Figure 5. Dextrasepiola taenia n. gen. & n. sp. (grids in background: 1 mm × 1 mm): a, spermatophore from the holotype (MOV F80458); b, close-up of cement body; c, bursa copulatrix, paratype 1 (MOV F31359; bc: bursa copulatrix; rg: right gill; rsf: right side of funnel); d, bursa copulatrix, juvenile (MOV F31360; bc: bursa copulatrix; lflc: left funnel locking cartilage; rflc: right funnel locking cartilage; rg: right gill); e, bursa copulatrix, paratype 3 (MOV F31361; bc: bursa copulatrix; lsf: left side of funnel; ms: mantle septum; rsf: right side of funnel); f, close-up of a portion of e, arrow points to opening of bursa copulatrix.
Figure 4. Dextrasepiola taenia n. gen. & n in Two new genera and species of sepioline squids (Cephalopoda: Sepiolidae) from Australia
Figure 4. Dextrasepiola taenia n. gen. & n. sp. (grids in background: 1 mm × 1 mm): a, left tentacular club, female, paratype 3 (MOV F91361); b, inside mantle cavity: photophores (p), left gill (lg), male, holotype (MOVF80458); c, radula (paratype 1, MOV F91359); d, lateral view of upper beak (MOV F91361); e, lateral view of lower beak (MOV F91361); f, top view of lower beak (MOV F91361).
Figure 1. Dextrasepiola taenia n. gen. & n in Two new genera and species of sepioline squids (Cephalopoda: Sepiolidae) from Australia
Figure 1. Dextrasepiola taenia n. gen. & n. sp., male: a, dorsal view, holotype (MOV F80458); b, ventral view (MOV F80458); c, lateral view (MOV F80458); d, hectocotylised arm (right arm I; MOV F80458); e, diagram of the hectocotylised arm showing tape-like modification, paratype 2 (MOV F74469; drawn by T. Okutani); f, inside mantle cavity, showing photophores (p) and other organs (MOV F80458); g, diagram of opened funnel and inside mantle cavity showing dorsal funnel organ (dfo), ventral funnel organ (vfo) and photophores (p; MOV F80458; drawn by T. Okutani).
Figure 3. Dextrasepiola taenia n. gen. & n in Two new genera and species of sepioline squids (Cephalopoda: Sepiolidae) from Australia
Figure 3. Dextrasepiola taenia n. gen. & n. sp. male, paratype 2 (MOV F74469). Oral view of arms (grids in background: 1 mm × 1 mm): a, right arm I, arrow points to remnant of a tiny sucker; b, right arm II; c, right arm III; d, right arm IV; e, left arm I; f, left arm II; g, left arm III; h, left arm IV.
Fig. 2 in Absorbing Hybridization Of Cobitis Taenia And Sabanejewia Aurata (Cypriniformes, Cobitidae) In Water Reservoirs Of Northern Ukraine Connected With Diploid-Polyploid Complex Formation
Fig. 2. Electrophoretic spectra of enzymes coding by allozymic loci: aspartate amynotransferase (1 — Aat- 1100/100, 2 — Aat-1100/110-110, 3 — Aat-195/110-110, 4 — Aat-1100-100/110, 5 — Aat-195-95/110, 6 — Aat-195-100/110), lactate dehydrogenase (1 — Ldh-B90/90, 2 — Ldh-B100/100, 3 — Ldh-B90/100-100, 4 — Ldh-B90/100/110), malate dehydrogenase (1 — Mdh-1A100/100, 2 — Mdh-1A100/110-110, 3 — Mdh-1A100-100/110).
Fig. 5 in Spatial Segregation of Diploid and Polyploids Spined Loaches (Сobitis elongatoides-taenia-tanaitica) in the River Systems of Western and Central Ukraine
Fig. 5. Changes in the frequency of polyploids in samples of spined loaches from the Teteriv River, depending on the distance from the mouth. The approximation is performed with a polynomial function.
Fig. 4 in Spatial Segregation of Diploid and Polyploids Spined Loaches (Сobitis elongatoides-taenia-tanaitica) in the River Systems of Western and Central Ukraine
Fig. 4. Frequencies of polyploids and its standard errors in different parts of the first and second-order tributaries of the Dnipro River system: Lower — lower third of the channel, Middle — middle part of the channel, Upper — upper third of the channel. The approximation is performed with a polynomial function.
Fig. 3 in Spatial Segregation of Diploid and Polyploids Spined Loaches (Сobitis elongatoides-taenia-tanaitica) in the River Systems of Western and Central Ukraine
Fig. 3. Frequency of polyploids in spined loach settlements and its standard errors of rivers with different channel lengths, as well as in accessory systems of the rivers (ASR) of the Western and Central Ukraine. The approximation is performed with a polynomial function.
Fig. 2 in Spatial Segregation of Diploid and Polyploids Spined Loaches (Сobitis elongatoides-taenia-tanaitica) in the River Systems of Western and Central Ukraine
Fig. 2. Frequencies of polyploids in spined loach settlements and its standard errors depending on the type of water system of the Western and Central Ukraine. M — main channel, Tr-1, Tr-2, Tr-3 — first, second, and the third-order tributaries, L — lakes. The approximation is performed with a polynomial function.
Fig. 1 in Spatial Segregation of Diploid and Polyploids Spined Loaches (Сobitis elongatoides-taenia-tanaitica) in the River Systems of Western and Central Ukraine
Fig. 1. Distribution of polyploid frequencies in spined loach settlements of the water systems of the Western and Central Ukraine. The approximation is performed with a polynomial function.
Figure 2 in Expression and immunolocalisation of TpFABP as a candidate antigen for the serodiagnosis of rabbit Taenia pisiformis cysticercosis
Figure 2. Expression of rTpFABP and identification by rabbit antisera in western blotting. Lane (1) molecular weight markers; (2) purified rTpFABP protein; (3) rTpFABP protein reacted with negative rabbit serum (1:100 v/v dilutions) by western blotting analysis; (4) rTpFABP protein reacted with rabbit antisera (1:100 v/v dilutions) by western blotting analysis. Molecular masses (kDa) are indicated on the left.
Figure 1 in Expression and immunolocalisation of TpFABP as a candidate antigen for the serodiagnosis of rabbit Taenia pisiformis cysticercosis
Figure 1. Structural analysis of TpFABP. Alignment of the amino acid residue sequences of Taenia pisiformis FABP with T. solium and Echinococcus granulosus in primary structures. The secondary structure of the TpFABP amino acid residue sequence was predicted and is shown at the top of the alignment. The light-grey shading indicates the identical amino acid sequences, and locations of linear B-cell epitopes are marked with open boxes. TpFABP1, GU205472; TsFABP1, HQ259679; TsFABP2, AFS64570; EgFABP1, 1O8V_A; EgFABP2, AAK12095; H-FABP, NP_004093.
Figure 4 in Expression and immunolocalisation of TpFABP as a candidate antigen for the serodiagnosis of rabbit Taenia pisiformis cysticercosis
Figure 4. Dot-ELISA of naturally infected rabbit experimental sera with rTpFABP. The tan-yellow tint shows the positive reaction: A, negative control sera; B, positive antisera; C, sera at 0 day postinfection; D, sera at 7 days post-infection; E, sera at 14 days post-infection; F, sera at 21 days post-infection; G, sera at 28 days post-infection; H, sera at 35 days post-infection; I, sera at 42 days post-infection; J, sera at 49 days post-infection.
Figure 3 in Expression and immunolocalisation of TpFABP as a candidate antigen for the serodiagnosis of rabbit Taenia pisiformis cysticercosis
Figure 3. Immunolocalisation of TpFABP in T. pisiformis tapeworm and cysticercus. The yellowish-brown tint shows the TpFABP protein location. (A) negative sera in cysticercus; (B) antisera in cysticercus; (C) negative sera in adult tapeworm; (D) antisera in adult tapeworm. Arrows indicate the areas of the parasite: MT, microthrix; DC, distal cytoplasm; PC, perinuclear cytoplasm; GD, gathering duct; M, microtrichia; ICW, inside the layer of cystic wall; OCW, outer layer of cystic wall; MCW, middle layer of cystic wall. Scale bars: 20 µm.
Fig. 3 in First report of pulmonary cysticercosis caused by Taenia crassiceps in a Cape fur seal (Arctocephalus pusillus)
Fig. 3. Alignment result for the partial sequence of the COX 1 gene (fur seal) with an exemplary T. crassiceps COX 1 gene sequence (accession no. KY321321.1), obtained from NCBI BLASTN tool. Homology was 100% (query: KY321321.1, sbject: herein obtained sequence).
Fig. 1 in Wildlife-transmitted Taenia and Versteria cysticercosis and coenurosis in humans and other primates
Fig. 1. Taenia crassiceps metacestodes (case 8, Table 2). A. Cysticerci isolated at surgery (wet preparation, scale bar 5mm). B. HE stained section of an invaginated scolex with suckers (S) and hooks (H) (scale bar 500μm). C. Large and small hooks, calcareous corpuscules (wet preparation, scale bar 200μm). D. Calcareous corpuscules in the parenchyma and microvilli like structures (microtriches) on the outer surface of a metacestode wall (HE stain, scale bar 20μm).
Fig. 1 in Severe coenurosis caused by larvae of Taenia serialis in an olive baboon (Papio anubis) in Benin
Fig. 1. Clinical presentation of the baboon with the clear presence of swellings in various areas of the body: ventral abdominal and thoracic parts, inner part of forearms, intermandibular region (arrow heads) and dorsal region also.
Fig. 2. Hare 19 in Cysticercosis by Taenia pisiformis in Brown Hare (Lepus europaeus) in Northern Italy: Epidemiologic and pathologic features
Fig. 2. Hare 19/2015. Histological image of a hepatic cyst (T. pisiformis), visible on the left. Focal infiltrate of eosinophil granulocytes with few lymphocytes, macrophages and plasma cells on the right. H&E, Bar = 200 μm.
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