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454 results for “Monogenea”
Figure 3 in Revision of the systematics of the Polystomoidinae (Platyhelminthes, Monogenea, Polystomatidae) with redefinition of Polystomoides Ward, 1917 and Uteropolystomoides Tinsley, 2017
Figure 3. Bayesian tree inferred from the analysis of COI sequences. Numbers at nodes indicate Bayesian Posterior Probabilities (BPP). Only BPP » 0.95 are indicated. Scale bar reflects expected changes per site. * designates haplotypes characterizing specimens of Polystomoides multifalx (Stunkard, 1924) that were, for some of them, collected from Pseudemys concinna (Le Conte), for the others, from P. floridana (Le Conte) (see Table 3 for more details).
Figure 3. Pseudorhabdosynochus cephalopholi n in Three new species of Pseudorhabdosynochus (Monogenea, Diplectanidae) from several species of Cephalopholis and Epinephelus (Perciformes, Serranidae) from Thailand
Figure 3. Pseudorhabdosynochus cephalopholi n. sp. from Cephalopholis sonnerati in the lower Gulf of Thailand. (A) Composite drawing (mainly from holotype), dorsal view. (B) Male quadriloculate organ, dorsal view. (C) Sclerotized vagina, dorsal view. (D) Egg. (E) Ventral hamulus. (F) Dorsal hamulus. (G) Dorsal (lateral) bar. (H) Ventral bar. (I) Dorsal squamodisc. (J) Ventral squamodisc. (K) Hooklet. Scale-bars: (A) 100 µm; (B)–(K) 50 µm.
Figure 5. Pseudorhabdosynochus samaesarnensis n in Three new species of Pseudorhabdosynochus (Monogenea, Diplectanidae) from several species of Cephalopholis and Epinephelus (Perciformes, Serranidae) from Thailand
Figure 5. Pseudorhabdosynochus samaesarnensis n. sp. from Epinephelus lanceolatus from Samaesarn Island in the Gulf of Thailand. (A) Composite drawing (mainly from holotype), dorsal view. (B) Male quadriloculate organ, dorsal view. (C) Sclerotized vagina, dorsal view. (D) Ventral hamulus. (E) Dorsal hamulus. (F) Dorsal (lateral) bar. (G) Ventral bar. (H) Dorsal squamodisc. (I) Ventral squamodisc. (J) Hooklet. Scale-bars: (A) 200 µm. (B)–(J): 50 µm.
Figure 1. Pseudorhabdosynochus suratthaniensis n in Three new species of Pseudorhabdosynochus (Monogenea, Diplectanidae) from several species of Cephalopholis and Epinephelus (Perciformes, Serranidae) from Thailand
Figure 1. Pseudorhabdosynochus suratthaniensis n. sp. from Cephalopholis argus in the lower Gulf of Thailand. (A) COMPOSITE drawing (mainly from holotype), dorsal view. (B) Male quadriloculate organ, dorsal view. (C) Sclerotized vagina, dorsal view. (D) Ventral hamulus. (E) Dorsal hamulus. (F) Ventral bar. (G) Dorsal (lateral) bar. (H) Ventral squamodisc. (I) Dorsal squamodisc. (J) Hooklet. Scale-bars: (A) 200 µm; (B)–(J) 50 µm.
Figure 1. A in Revision of the systematics of the Polystomoidinae (Platyhelminthes, Monogenea, Polystomatidae) with redefinition of Polystomoides Ward, 1917 and Uteropolystomoides Tinsley, 2017
Figure 1. A: Non-lethal procedure for retrieving a polystome from the pharyngeal pouches of a freshwater turtle; B: polystome collected on wooden stem cotton swab.
Figure 1 in Neohexostoma gymnosardae n. sp. (Monogenea, Hexostomatidae), a gill parasite of Gymnosarda unicolor (Valenciennes) (Teleostei, Scombridae) in the South China Sea
Figure 1. Maximum likelihood tree based on an analysis of 28S rDNA sequences. Bootstrap percentages with 1000 replicates.
Figure 3 in Neohexostoma gymnosardae n. sp. (Monogenea, Hexostomatidae), a gill parasite of Gymnosarda unicolor (Valenciennes) (Teleostei, Scombridae) in the South China Sea
Figure 3. Photographs of Neohexostoma gymnosardae n. sp. (A) Holotype, whole worm (ventral view); (B) Male copulatory organ; (C) Vaginal spines; (D) Haptor; (E)–(F) Eggs; (G) Clamp with sclerites in lateral view. (B)–(G) are paratypes.
Figure 2 in Revision of the systematics of the Polystomoidinae (Platyhelminthes, Monogenea, Polystomatidae) with redefinition of Polystomoides Ward, 1917 and Uteropolystomoides Tinsley, 2017
Figure 2. Micrograph of the reproductive system of Polystomoides multifalx (Stunkard, 1924). Abbreviations: Gb, genital bulb; Te, testis; Ut, Uterus with eggs; Va, vagina. Scale bar = 200 μm.
Figure 2 in Three new species of Pseudorhabdosynochus (Monogenea, Diplectanidae) from several species of Cephalopholis and Epinephelus (Perciformes, Serranidae) from Thailand
Figure 2. Variations (A)–(F) of the sclerotized vagina of Pseudorhabdosynochus suratthaniensis n. sp. from Cephalopholis argus in the lower Gulf of Thailand. Abbreviations: Tr – trumpet, Ca1 – primary canal, Ch1 – primary chamber, Ca2 – secondary canal. Scale-bar: 50 µm.
Figure 4 in Three new species of Pseudorhabdosynochus (Monogenea, Diplectanidae) from several species of Cephalopholis and Epinephelus (Perciformes, Serranidae) from Thailand
Figure 4. Variations (A)–(I) of the sclerotized vagina of Pseudorhabdosynochus cephalopholi n. sp. from Cephalopholis sonnerati in the lower Gulf of Thailand. Abbreviations: Tr – trumpet, Ca1 – primary canal, Ch1 – primary chamber, Ca2 – secondary canal, Ch2 – secondary chamber, As – accessory structure. Scale-bar: 50 µm.
Figure 7. Indopolystoma parvum n. gen. n in Indopolystoma n. gen. (Monogenea, Polystomatidae) with the description of three new species and reassignment of eight known Polystoma species from Asian frogs (Anura, Rhacophoridae)
Figure 7. Indopolystoma parvum n. gen. n. sp. from Zhangixalus omeimontis. Dorsal view of holotype. (A) A drawing; (B) A photograph. Scale bar: 1 mm.
Figure 5. Indopolystoma elongatum n. gen. n in Indopolystoma n. gen. (Monogenea, Polystomatidae) with the description of three new species and reassignment of eight known Polystoma species from Asian frogs (Anura, Rhacophoridae)
Figure 5. Indopolystoma elongatum n. gen. n. sp. from Zhangixalus arboreus. Ventral view of holotype. (A) A drawing; (B) A photograph. Scale bar: 1 mm.
Figure 4. Indopolystoma viridi n. gen. n in Indopolystoma n. gen. (Monogenea, Polystomatidae) with the description of three new species and reassignment of eight known Polystoma species from Asian frogs (Anura, Rhacophoridae)
Figure 4. Indopolystoma viridi n. gen. n. sp. from Zhangixalus viridis. Marginal hooklets from paratypes. (A) Marginal hooklet C1; (B) Marginal hooklet C8; (C) Marginal hooklets C2–C7. Scale bar: 20 µm.
Figure 3. SDS PAGE and Western blots with rEnSerp1 in Identification and partial characterization of a novel serpin from Eudiplozoon nipponicum (Monogenea, Polyopisthocotylea)
Figure 3. SDS PAGE and Western blots with rEnSerp1, ESP and CWE. Lines 1–3, 1D gel. Lines 4–10, Western blot. M, protein standard; 1, rEnSerp1; 2, ESP; 3, CWE sample; 4, rEnSerp1 with anti-HIS antibodies; 5, rEnSerp1 without primary antibodies; 6, rEnSerp1 with anti-rEnSerp1 sera; 7, rEnSerp1 with pre-immune sera; 8, ESP with anti-rEnSerp1 sera; 9, ESP with pre-immune sera; 10, CWE with anti-rEnSerp1 sera. Arrow points to the expected recombinant EnSerp1 band. Arrowhead points to the natural form of EnSerp1 in the ESP sample. Dots indicate fragmented parts of rEnSerp1.
Figure 1 in Identification and partial characterization of a novel serpin from Eudiplozoon nipponicum (Monogenea, Polyopisthocotylea)
Figure 1. (A) Alignment of the EnSerp1 sequence with four of the most similar serpin sequences of other platyhelminths: 1, EnSerp1 from Eudiplozoon nipponicum (GenBank: MF288891.1); 2, Echinococcus multilocularis (GenBank: CDS35969.1); 3, Schistosoma haematobium (GenBank: XP_012797533.1); 4, Echinococcus granulosus (GenBank: CDS22753.1); 5, Taenia solium (GenBank: ATG83400.1). Conserved motifs characteristic for serpins are highlighted. The serpin motif (E342 – E346) shown in red is part of the reactive centre loop (RCL, A347 – N365), shown in green. Immediately after RCL, follows serpin signature (F366 – I376) in yellow. Scissile bond is situated within the RCL between P1 (F358) and P1' (C359) residue, shown in magenta. (B) Predicted 3D structure of EnSerp1. Coloured areas of the molecule correspond to the sequence highlighted in Figure 1A. (C) RCL and β-sheet A. After the peptidase cleaves the scissile bond within RCL (in orange), the residual part of RCL is incorporated as a new strand into β-sheet A (in cyan).
Figure 3. Indopolystoma viridi n. gen. n in Indopolystoma n. gen. (Monogenea, Polystomatidae) with the description of three new species and reassignment of eight known Polystoma species from Asian frogs (Anura, Rhacophoridae)
Figure 3. Indopolystoma viridi n. gen. n. sp. from Zhangixalus viridis. Hamuli from holotype and paratypes. (A–A') Holotype; (B–H) Paratypes. Scale bar: 100 µm.
Figure 6. Indopolystoma elongatum n. gen. n in Indopolystoma n. gen. (Monogenea, Polystomatidae) with the description of three new species and reassignment of eight known Polystoma species from Asian frogs (Anura, Rhacophoridae)
Figure 6. Indopolystoma elongatum n. gen. n. sp. from Zhangixalus arboreus. Hamuli and marginal hooklets from holotype and paratypes. (A–A') Holotype; (A''–A''') Paratypes; (B) Marginal hooklet C1; (B') Marginal hooklet C3; (B'') Marginal hooklet C8. Scale bar: 100 µm (A–A'''), 20 µm (B–B'').
Figure 4 in Identification and partial characterization of a novel serpin from Eudiplozoon nipponicum (Monogenea, Polyopisthocotylea)
Figure 4. The inhibitory effect of rEnSerp1 on selected SPs. (A) trypsin; (B) factor Xa; (C) plasmin; (D) plasma kallikrein. Results of assays with a bacterial lysate instead of rEnSerp1: (E) factor Xa and F, trypsin. Data are expressed as a mean value ± standard deviation.
Figure 1 in Indopolystoma n. gen. (Monogenea, Polystomatidae) with the description of three new species and reassignment of eight known Polystoma species from Asian frogs (Anura, Rhacophoridae)
Figure 1. Bayesian tree for neobatrachian polystomes inferred from the analysis of four concatenated genes, namely 18S, 28S, COI and 12S. Numbers on nodes indicate Bayesian Posterior Probabilities. Indopolystoma spp. were regarded earlier as Polystoma spp. in Badets et al. [2] and Héritier et al. [22]. B. w. refers to Blommersia wittei and Z. s. to Zhangixalus smaragdinus. See also Table 1 for other host species. Scale bar represents 0.1 substitution/site.
Figure 2. A in Identification and partial characterization of a novel serpin from Eudiplozoon nipponicum (Monogenea, Polyopisthocotylea)
Figure 2. A phylogram of platyhelminth serpin homologs, Bayesian inference analysis. Values along the branches indicate posterior probabilities and bootstrap values resulting from Bayesian inference and Maximum likelihood analyses, respectively. Proportional lengths of the branches correspond to the expected number of amino acid substitutions per site. The resulting tree is mid-point rooted in order to visualise the clustering of representative subfamilies. Newly obtained Eudiplozoon nipponicum serpin homolog (EnSerp1) is labelled red.
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