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78 results for “Taenia”
Fig. 1. Hare 36 in Cysticercosis by Taenia pisiformis in Brown Hare (Lepus europaeus) in Northern Italy: Epidemiologic and pathologic features
Fig. 1. Hare 36/2013, liver and stomach. Cysticercosis (T. pisiformis) in liver surface and gastric peritoneum.
Fig. 3 in Molecular identification of Taenia hydatigena and Mesocestoides species based on copro-DNA analysis of wild carnivores in Mongolia
Fig. 3. Phylogenetic tree based on a partial sequence of tapeworms obtained by the maximum likelihood method was conducted using the HKY + G + I nucleotide substitution model. Numbers above branches are percent bootstrap values based on 1,000 replicates. Bootstrap value> 70% are shown. (a) Phylogenetic tree based on the cox1 sequences of T. hydatigenaand Mesocestoides sp. isolates available in the GenBankṜ database were included. Hymenolepis nana served as an out-group. (b) Phylogenetic analysis of the 12SrRNA partial sequence of T. hydatigena, Mesocestoides sp., and M. lineatus inferred using the sequence distance method and maximum likelihood. Hymenolepis nana was used as an out-group.
Fig. 1 in Molecular identification of Taenia hydatigena and Mesocestoides species based on copro-DNA analysis of wild carnivores in Mongolia
Fig. 1. Map of Mongolia showing the distribution of Taenia hydatigena (pentangle), Mesocestoides sp.-1 (square), and Mesocestoides sp.-2 (circle) by province detected by molecular identification of fecal samples from wild carnivores. Mongolia consists of 21 provinces: Arkhangai (Akh), Bayankhongor (Bkh), Bayan-Ulgii (BU), Bulgan (BG), Darkhan-Uul (DU), Dornogobi (DoG), Dundgobi (DuG), Govi-Altai (GA), Khentii (KhE), Khovd (KhO), Khuvsgul (KhU), Orkhon-Uul (OU), Selenge (SE), Sukhbaatar (SB), Tuv (TU), Umnu-Gobi (UG), Uvs (Uv), Uvurkhangai (Ukh), Zavkhan (ZKh), Dornod (D), and Gobi-Sumber (GS). The field survey was conducted in all provinces, unless Dornod (D), and GS (Gobi-Sumber). Ulaanbaatar (U) is the capital city of Mongolia. The field survey was conducted in all provinces, unless Dornod (D), and GS (Gobi-Sumber). Ulaanbaatar (U) is the capital city of Mongolia located in Tuv Province.
Fig. 7 in The morphological and molecular identification of the tapeworm, Taenia lynciscapreoli, in intermediate and definitive hosts in Poland
Fig. 7. Large rostellar hooks: A - larvae T. lynciscapreoli from roe deer; B – larvae T. hydatigena from wild boar, C - larvae T. hydatigena from moose.
Fig. 6 in The morphological and molecular identification of the tapeworm, Taenia lynciscapreoli, in intermediate and definitive hosts in Poland
Fig. 6. Phylogenetic tree of Taenia lynciscapreoli haplotypes, constructed by Bayesian inference (BI) analysis using MrBayes version 3.2. The HKY + G + I model was chosen as the best-fitting nucleotide substitution model using JModelTest version 2.1.10 software (Guindon and Gascuel, 2003; Darriba et al., 2012). Sequences of Echinococcus granulosus sensu stricto GenBank accession number AB688619 and Echinococcus multilocularis GenBank accession number AB461413 were used as the outgroup. Analysis was run for 1,000,000 generations, with 250,000 generations discarded as 'burn-in'. Nodal support is indicated as Bayesian posterior probabilities. Sequences generated in this study are shown in bold. The scale bars are proportional to the number of substitutions per site.
Fig. 5 in The morphological and molecular identification of the tapeworm, Taenia lynciscapreoli, in intermediate and definitive hosts in Poland
Fig. 5. Four crowns of T. lynciscapreoli, A – C larvae, D – adult; A – AM1 (32 hooks), B – APS3 (38 hooks), C – APS2 (34 hooks), D – R17 (36 hooks).
Fig. 4 in The morphological and molecular identification of the tapeworm, Taenia lynciscapreoli, in intermediate and definitive hosts in Poland
Fig. 4. The crown of T. lynciscapreoli; examples of empty spaces, from where hooks have been lost are indicated (arrows).
Fig. 3. A in The morphological and molecular identification of the tapeworm, Taenia lynciscapreoli, in intermediate and definitive hosts in Poland
Fig. 3. A – lung of roe deer with cyst of tapeworm T. lynciscapreoli; B – Cysticercoid of T. lynciscapreoli.
Fig. 1 in Morphological and molecular analyses of Taenia and Mesocestoides species from red foxes (Vulpes vulpes) in northwestern China
Fig. 1. Phylogenetic relationships of Taenia and Mesocestoides species from red foxes based on cox1 sequences.
Fig. 1 in Taenia laticollis and a potentially novel Taenia species from the Eurasian lynx (Lynx) in Northwestern China
Fig. 1. Phylogenetic relationships of Taenia species from two Eurasian lynxes (marked with black circle and triangle) based on 16S rDNA sequences.
Fig. 2 in Taenia laticollis and a potentially novel Taenia species from the Eurasian lynx (Lynx) in Northwestern China
Fig. 2. Phylogenetic relationships of Taenia species from two Eurasian lynxes (marked with black circle and triangle) based on cox1 sequences.
Fig. 6 in Theileria, Hepatozoon and Taenia infection in great gerbils (Rhombomys opimus) in northwestern China
Fig. 6. Phylogenetic analysis of Hepatozoon ayorgbor-like based on 18S rRNA gene with MEGA7.0. The tree was constructed with the Neighbor-Joining method (NJ; bootstrap replicates: 1000). Branch lengths correlate to the number of substitutions inferred according to the scale shown. Sequence of Hepatozoon ayorgbor-like obtained in this study is indicated by triangles ().
Fig. 2. A-C in Theileria, Hepatozoon and Taenia infection in great gerbils (Rhombomys opimus) in northwestern China
Fig. 2. A-C Piroplasmic forms of Candidatus Theileria xinjiangensis in a microscopic field by Giemsa staining method [A single annular forms; B single circular form]. C The macroscopic appearance of splenomegaly in piroplasm-positive the great gerbil.
Fig. 5 in Theileria, Hepatozoon and Taenia infection in great gerbils (Rhombomys opimus) in northwestern China
Fig. 5. Phylogenetic analysis of "Taenia sp. Rhombomys opimus" based on cox1 gene with MEGA7.0. The tree was constructed with the Neighbor-Joining method (NJ; bootstrap replicates: 1000). Branch lengths correlate to the number of substitutions inferred according to the scale shown. Sequences of "Taenia sp. Rhombomys opimus" obtained in this study are indicated by triangles ().
Fig. 1 in Theileria, Hepatozoon and Taenia infection in great gerbils (Rhombomys opimus) in northwestern China
Fig. 1. Map showing the sampling sites in Alataw City (China-Kazakhstan border), Manas County (center of Gurbantungut Desert).
Fig. 4 in Theileria, Hepatozoon and Taenia infection in great gerbils (Rhombomys opimus) in northwestern China
Fig. 4. Phylogenetic analysis of Candidatus Theileria xinjiangensis based on 18S rRNA gene with MEGA7.0. The tree was constructed with the Maximum Likelihood method (ML; bootstrap replicates: 1000). Branch lengths correlate to the number of substitutions inferred according to the scale shown. Sequences of Candidatus Theileria xinjiangensis obtained in this study are indicated by triangles ().
Fig. 3. A-C A in Theileria, Hepatozoon and Taenia infection in great gerbils (Rhombomys opimus) in northwestern China
Fig. 3. A-C A Three kinds of cyst in thoracic cavity of great gerbils. The a-type cyst, belonging to Taenia sp. Rhombomys opimus A, contained 7 protoscolices. The btype cyst, belonging to Taenia sp. Rhombomys opimus B, contained 13 protoscolices. The c-type cyst, belonging to Taenia sp. Rhombomys opimus C, contained 4 protoscolices. B A cyst attaching to the liver of a great gerbil in Manas County, XUAR. C Cysticercoids in cyst from the great gerbil in microscopic field by malachite green stain-method.. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 5 in Identification and phylogenetic analysis of Taenia spp. parasites found in wildlife in the Emilia-Romagna region, northern Italy (2017-2022)
Fig. 5. Geographical location of animals resulted positive for Taenia spp. Icons placed around circles are located in the same position, represented by the yellow point. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Identification and phylogenetic analysis of Taenia spp. parasites found in wildlife in the Emilia-Romagna region, northern Italy (2017-2022)
Fig. 1. Schematic representation of Taenia spp. life cycle in wildlife with accidental involvement of humans as intermediate hosts. Animals images taken from www. phylopic.org (Authors: Tracy Heath, Ferran Sayol, Anthony Caravaggi, Katy Lawler). The Figure was partly generated using Servier Medical Art, provided by Servier, licensed under a Creative Commons Attribution 3.0 unported license.
Fig. 6 in Identification and phylogenetic analysis of Taenia spp. parasites found in wildlife in the Emilia-Romagna region, northern Italy (2017-2022)
Fig. 6. Phylogenetic tree with the sequences of small ribosomal RNA subunit (rrnS) of T.hydatigena (yellow), T. serialis (orange), T. pisiformis (magenta), T. crassiceps (purple) sequenced at the IZSLER, compared with public sequences deposited in Gen- Bank (black). The tree was obtained using the HKJ + G substitution model. Chain length = 10 million iterations. Node labels are posterior probabilities ≥0.9. Squares = sequence from intermediate host; circles = sequence from definitive host. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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