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81 results for “Fluke”
Data from: Phylogeny of seven Bulinus species originating from endemic areas in three African countries, in relation to the human blood fluke Schistosoma haematobium
Background: Snails species belonging to the genus Bulinus (Planorbidae) serve as intermediate host for flukes belonging to the genus Schistosoma (Digenea, Platyhelminthes). Despite its importance in the transmission of these parasites, the evolutionary history of this genus is still obscure. In the present study, we used the partial mitochondrial cytochrome oxidase subunit I (cox1) gene, and the nuclear ribosomal ITS, 18S and 28S genes to investigate the haplotype diversity and phylogeny of seven Bulinus species originating from three endemic countries in Africa (Cameroon, Senegal and Egypt). Results: The cox1 region showed much more variation than the ribosomal markers within Bulinus sequences. High levels of genetic diversity were detected at all loci in the seven studied species, with clear segregation between individuals and appearance of different haplotypes, even within same species from the same locality. Sequences clustered into two lineages; (A) groups Bulinus truncatus, B. tropicus, B. globosus and B. umbilicatus; while (B) groups B. forskalii, B. senegalensis and B. camerunensis. Interesting patterns emerge regarding schistosome susceptibility: Bulinus species with lower genetic diversity are predicted to have higher infection prevalence than those with greater diversity in host susceptibility. Conclusion: The results reported in this study are very important since a detailed understanding of the population genetic structure of Bulinus is essential to understand the epidemiology of many schistosome parasites.
Fig. 4 in Digestive system of the marine blood fluke, Aporocotyle simplex (Odhner, 1900) (Digenea: Aporocotylidae) with consideration of the digenean digestive morphology
Fig. 4. Ultrastructure of the caecum of Aporocotyle simplex (A) Cross section through caecal portion showing relatively homogeneous and non-cellular content of the caecal lumen, note large dense inclusions and variable residual bodies; insert Type of residual body (B) Area of caecum showing different thickness of cytoplasmic lining, note nucleus, surface lamellae (C) Large residual body in the gastrodermal cytoplasm, note deep basal invaginations (D) Residual body occupying most of the thickness of the gastrodermal cytoplasm, note moderately dense body content and clumps of inclusions of different shapes (E) Tubular structure in the gastrodermal cytoplasm (F) Residual body, note Golgi vesicles within and in contact with it (G) Multivesiculate body and Golgi vesicles (H) Portion of syncytial gastrodermal cytoplasm showing developed stages of large residual bodies, insert Granular endoplasmic reticulum and Golgi vesicles (I, J) Gastrodermal vacuolated surface areas in a secretory-absorptive phase, note surface depressions and an agglomeration of residual material between lamellae (K) Portion of gastrodermal cytoplasm filled with different kinds of vesicles and residual bodies during secretory-absorptive phase. Abbreviations: arm, agglomeration of residual material; bi, basal infoldings; cl, caecal lumen; di, dense inclusion; dlb1, dlb2, developed residual bodies; dm, dense material; gc, gastrodermal syncytial cytoplasm; ger, granular endoplasmic reticulum; gv, Golgi vesicles; hm, haematin; lb, large residual body; mb, multivesiculate body; nb, nascent residual body; sl, surface lamellae; sd, surface depression; rb, residual body; other abbreviations in Figs. 1–3. Scale bars: A = 50 μm; inserts, E, F = 0.2 μm; B, С = 2 μm; D, G, H = 0.5 μm; I – K = 1 μm.
Fig. 3 in Digestive system of the marine blood fluke, Aporocotyle simplex (Odhner, 1900) (Digenea: Aporocotylidae) with consideration of the digenean digestive morphology
Fig. 3. Ultrastructure of middle and posterior esophagus of Aporocotyle simplex (A) Section through middle esophagus surrounded by large area of compact cellular aggregation, note esophageal lumen filled with epithelial cytoplasmic protrusions (B) Section through posterior esophagus surrounding compact cellular aggregation, note blood cells between esophageal cytoplasmic protrusions within duct lumen (C) Esophageal sunken perikaryon showing large area with different stages of secretory granule development in perinuclear cytoplasm, note muscle fibres near cell, insert Large secretory granule surrounded vacuolar area (D, F) Blood cell disintegration within lumen of posterior esophagus, note conglomerations of moderately dense substance around cells permeated with thin terminal protrusions (E) Esophageal perikariya and axonemal and muscle fibres (G) Nascent and forming secretory granules surrounding vacuolar areas, note cellular tubular structures (H) Esophageal perikaryon at the beginning stage of the development (I) Part of posterior esophageal cytoplasmic lining, note large scattered conglomerations of moderately dense substance. Abbreviations: anf, axonemal nerve fibres; bc, blood cells; fg, forming granules; mf, muscle fibres; n, nucleus; ng, nascent granules; tp, protrusion terminal portion; vm, vacuolated matrix around granules; other abbreviations in Figs. 1 and 2. Scale bars: A, B = 10 μm; С – E, G, I = 1 μm; insert, F, H = 0.5 μm.
Fig. 1 in Digestive system of the marine blood fluke, Aporocotyle simplex (Odhner, 1900) (Digenea: Aporocotylidae) with consideration of the digenean digestive morphology
Fig. 1. Anterior foregut of Aporocotyle simplex (A) SEM view of anterior body region, note mouth opening (B, C) LM view of mouth opening, anterior and posterior esophagus, two anterior. and two posterior caeca and caecum bifurcation, note compact cell mass around esophageal portion (D, G) TEM view of anterior foregut portion showing mouth cavity, behind which there is a foregut portion with developed circular and radial muscles and the following anterior esophageal portion, note longitudinal muscle fibres surrounded anterior esophagus (E) Continuation of syncytial tegumental lining of the body into mouth cavity and anterior foregut, note sensory ending around mouth cavity and surface knob-like outgrowths (F) Anterior foregut side showing lateral fold and bunds of circular and radial muscles surrounding foregut syncytial cytoplasm, note well developed nerve plexus (H) Portion of body tegumental cytoplasm, note dense tegumental bodies within cytoplasm and knob-like outgrowths on the surface (I) Anterior foregut syncytial cytoplasm surrounded by circular and radial muscles. Abbreviations: ac, anterior caecum; aes, anterior esophagus; bl, basal lamina; cb, caecum bifurcation; cm, circular muscles; db, dense tegumental bodies; dtc, distal tegumental cytoplasm of the body; elm, esophageal longitudinal muscle fibres; em, extracellular matrix; fsc, foregut syncytial cytoplasm; hd, hemidesmosomes; lf, lateral fold; ko, knob-like outgrowths; maf, muscular portion of anterior foregut; mo, mouth opening; nf, nerve fibers; pc, posterior caecum; pes, posterior esophagus; rm, radial muscles; se, sensory ending; sm, surrounding cell masses; vi, vesicular inclusions. Scale bars: A = 50 μm; B = 200 μm; С = 100 μm; D = 5 μm; E, H, I = 1 μm; F, G = 2 μm.
Fig. 2 in Digestive system of the marine blood fluke, Aporocotyle simplex (Odhner, 1900) (Digenea: Aporocotylidae) with consideration of the digenean digestive morphology
Fig. 2. Ultrastructure of esophageal epithelial lining of Aporocotyle simplex (A) Transition between muscular area of anterior foregut and anterior esophagus, note different kinds of cytoplasmic protrusions (B) Anterior esophagus showing luminal irregular, broad and angular cytoplasmic protrusions, note tegumental dense bodies in the syncytial cytoplasm (C) Cytoplasmic processes of sunken perikarya filled with dense bodies pass into esophageal syncytial cytoplasm, note vesicles localized close to surface membrane and discharged vesicles (D) Middle esophageal lining showing thinner and branched protrusions filling luminal area, note numerous cytoplasmic vesicles and rare dense secretory granules (insert) (E) Syncytial cytoplasmic layer of anterior esophagus, showing numerous vesicles, some tegumental dense bodies and tubular structures (F, G) Portion of middle esophageal cytoplasmic lining, note vesicles, discharged vesicles and rounded secretory granules. Abbreviatons: cp, cytoplasmic processes of the sunken perikarya; dv, discharged vesicles; esl, esophageal lumen; fl, flat epithelial layer; mt, microtubules; mw, membranous whorls; pr, cytoplasmic protrusions; sc, substance conglomeration; sec, syncytial esophageal cytoplasm; sg, secretory granules; ss, smooth surface; ts, tubular structures; other abbreviations in Fig. 1. Scale bars: A, В = 2 μm; B, E = 1 μm; C, insert, F, G = 0.5 μm.
Figure 4 in Philophthalmus hechingeri n. sp. (Digenea: Philophthalmidae), a Human-Infecting Eye Fluke from the Asian Mud Snail, Batillaria attramentaria
Figure 4. The adult stage of Philophthalmus hechingeri n. sp. Line drawing of ventral view. Abbreviations: c, cirrus; ca, caecum; cs, cirrus sac; gp, genital pore; mg, Mehlis' gland; mt, metraterm; o, ovary; os, oral sucker; p, pharynx; sr, seminal receptacle; sv, seminal vesicle; t, testis; u, uterus; v, vitellarium; vs, ventral sucker.
Figure 5 in Philophthalmus hechingeri n. sp. (Digenea: Philophthalmidae), a Human-Infecting Eye Fluke from the Asian Mud Snail, Batillaria attramentaria
Figure 5. The larval stages of Philophthalmus hechingeri n. sp. (A) Daughter redia. (B) Cercaria. (C) Excysted juvenile.
Figure 1. A in Philophthalmus hechingeri n. sp. (Digenea: Philophthalmidae), a Human-Infecting Eye Fluke from the Asian Mud Snail, Batillaria attramentaria
Figure 1. A map showing places related to Philophthalmus hechingeri n. sp. Black, gray, and white circles represent the occurrence of human philophthalmosis (Mimori et al., 1982; Sato et al., 2019), the snail collection site of this study, and the snail collection sites of Hechinger (2007), respectively.
Figure 3 in Philophthalmus hechingeri n. sp. (Digenea: Philophthalmidae), a Human-Infecting Eye Fluke from the Asian Mud Snail, Batillaria attramentaria
Figure 3. Mitochondrial DNA-based genetic analyses of philophthalmid species. (A) A maximum likelihood phylogenetic tree of the genus Philophthalmus. The tree was made using sequences of COI (693 nucleotide sites) under the substitution model HKYþG. The DNA accession number of each taxon is shown in parentheses. The tree was rooted by the outgroup taxon, Fasciola hepatica (M93388). The outgroup was removed from the tree to save space. Bootstrap percentages are indicated at branching points. A scale bar indicates the number of substitutions per nucleotide site. (B) A parsimony network of COI haplotypes (849 nucleotide sites) of Philophthalmus hechingeri n. sp. in a seashore of the Seto Inland Sea. The size of circles indicates the frequency of the haplotypes. Numerals within the circles mean the number of haplotypes. A closed circle indicates a haplotype, which is identical to that of Philophthalmus sp. from human in Aichi Prefecture (Sato et al., 2019). Tiny circles are hypothetical haplotypes.
Figure 2. A in Philophthalmus hechingeri n. sp. (Digenea: Philophthalmidae), a Human-Infecting Eye Fluke from the Asian Mud Snail, Batillaria attramentaria
Figure 2. A maximum likelihood phylogenetic tree of the family Philophthalmidae. The tree was made using sequences of 28S rDNA (874 nucleotide sites) under the substitution model GTRþI. The tree was rooted by the outgroup taxon, Sphaeridiotrema globulus (GQ890331). The outgroup was removed from the tree to save space. The isolates obtained in this study are highlighted in bold face. The DNA accession number of each philophthalmid is shown in parentheses. Bootstrap percentages are indicated at branching points. A scale bar indicates the number of substitutions per nucleotide site.
Data from: Phylogeny of seven Bulinus species originating from endemic areas in three African countries, in relation to the human blood fluke Schistosoma haematobium
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Figure 9 from: Montoya AL, Wolff M (2020) Description of five new large species of Argentinomyia Lynch-Arribálzaga, and redescription of Talahua fervida (Fluke) (Diptera, Syrphidae, Syrphinae). . https://doi.org/10.3897/zookeys.929.37666
Figure 9 Argentinomyia quimbaya sp. nov., male genitalia: A whole genitalia including epandrium, cercus, and surstylus, lateral view B epandrium, dorsal view C hypandrium, ventral view. Scale bar: 0.05 mm.
Figure 14 from: Montoya AL, Wolff M (2020) Description of five new large species of Argentinomyia Lynch-Arribálzaga, and redescription of Talahua fervida (Fluke) (Diptera, Syrphidae, Syrphinae). . https://doi.org/10.3897/zookeys.929.37666
Figure 14 Talahua fervida, male genitalia: A whole genitalia including epandrium, cercus and surstylus, lateral view B hypandrium, dorsal view C cerci, and surstyli, ventral view D cerci and surstyli, dorsal view. Scale bar: 0.05 mm.
Figure 11 from: Montoya AL, Wolff M (2020) Description of five new large species of Argentinomyia Lynch-Arribálzaga, and redescription of Talahua fervida (Fluke) (Diptera, Syrphidae, Syrphinae). . https://doi.org/10.3897/zookeys.929.37666
Figure 11 Argentinomyia talamanca sp. nov., male genitalia: A whole genitalia including epandrium, cercus, and surstylus, lateral view B epandrium, dorsal view C hypandrium, ventral view. Scale bar: 0.05 mm.
Figure 10 from: Montoya AL, Wolff M (2020) Description of five new large species of Argentinomyia Lynch-Arribálzaga, and redescription of Talahua fervida (Fluke) (Diptera, Syrphidae, Syrphinae). . https://doi.org/10.3897/zookeys.929.37666
Figure 10 Argentinomyia talamanca sp. nov., male (USNM ENT 00036926): A head, frontal, male B dorsal view C lateral view. Female (INBio CRI002462383): D head, frontal view E dorsal view F lateral view. Scale bars: 5 mm.
Figure 2 from: Montoya AL, Wolff M (2020) Description of five new large species of Argentinomyia Lynch-Arribálzaga, and redescription of Talahua fervida (Fluke) (Diptera, Syrphidae, Syrphinae). . https://doi.org/10.3897/zookeys.929.37666
Figure 2 Argentinomyia andina sp. nov., male genitalia: A whole genitalia including epandrium, cercus, and surstylus, lateral view B epandrium, dorsal view C hypandrium, ventral view. Abbreviations used in male genitalia structures are as follows: Ahp = apex of hypandrium (superior lobes; Cer = cercus; Epd = epandrium; Hyp = hypandrium; Led = aedeagal lobe; Sur = surstyle. Scale bar: 0.05 mm.
Figure 8 from: Montoya AL, Wolff M (2020) Description of five new large species of Argentinomyia Lynch-Arribálzaga, and redescription of Talahua fervida (Fluke) (Diptera, Syrphidae, Syrphinae). . https://doi.org/10.3897/zookeys.929.37666
Figure 8 Argentinomyia quimbaya sp. nov., male (USMN ENT 000035733): A head, frontal, male B dorsal view C lateral view. Female, Paratype (CEUA 87109): D head, frontal view E dorsal view F lateral view. Scale bars: 5 mm.
Figure 16 from: Montoya AL, Wolff M (2020) Description of five new large species of Argentinomyia Lynch-Arribálzaga, and redescription of Talahua fervida (Fluke) (Diptera, Syrphidae, Syrphinae). . https://doi.org/10.3897/zookeys.929.37666
Figure 16 Biogeographical distribution of Argentinomyia huitepecensis sp. nov. (green), A. talamanca sp. nov. (red) and A. puntarenas sp. nov. (blue).
Figure 13 from: Montoya AL, Wolff M (2020) Description of five new large species of Argentinomyia Lynch-Arribálzaga, and redescription of Talahua fervida (Fluke) (Diptera, Syrphidae, Syrphinae). . https://doi.org/10.3897/zookeys.929.37666
Figure 13 Talahua fervida, male (CEUA 95345): A dorsal view, male B lateral view (Paratype USNM). Female (CEUA 93328): C lateral view D dorsal view E posterior view, detail of maculae on sixth tergum. Scale bars: 5 mm.
Figure 12 from: Montoya AL, Wolff M (2020) Description of five new large species of Argentinomyia Lynch-Arribálzaga, and redescription of Talahua fervida (Fluke) (Diptera, Syrphidae, Syrphinae). . https://doi.org/10.3897/zookeys.929.37666
Figure 12 Genus Talahua Fluke: A head, frontal, male B basoflagellomere, frontal view C metacoxa pile tuft, ventral view D scutellum emarginated, dorsal view E male genitalia, lateral view F holotype, AMNH G paratype label, USNM. Scale bars: 5 mm.
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