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13 results for “Spirometra”
Fig. 3 in Molecular identification and phylogenetic analysis of Cryptosporidium, Hepatozoon and Spirometra in snakes from central China
Fig. 3. Maximum likelihood phylogenetic tree of Spirometra based on the cox1 gene. The tree was constructed with the cox1 sequences (444bp) by using the Kimura 2-parameter model with MEGA 7.0; we calculated bootstrap values with 1000 replicates. The representative sequence of Spirometra spagarnas isolated from snakes in this study are in bold print and marked by circles. Scale bar indicates nucleotide substitutions per site.
Fig. 2 in Molecular identification and phylogenetic analysis of Cryptosporidium, Hepatozoon and Spirometra in snakes from central China
Fig. 2. Maximum likelihood phylogenetic tree based on the 18S rRNA gene of Hepatozoon. The phylogenetic tree was constructed with the 18S rRNA gene sequences (670bp) by using the General time reversible model with MEGA 7.0; the bootstrap values were calculated with 1000 replicates. Representative sequences of Hepatozoon detected in this study are in bold print and marked by circles. Scale bar indicates nucleotide substitutions per site.
Fig. 1 in Molecular identification and phylogenetic analysis of Cryptosporidium, Hepatozoon and Spirometra in snakes from central China
Fig. 1. Maximum likelihood phylogenetic tree based on the SSU gene of Cryptosporidium. The phylogenetic tree SSU gene (834bp) was constructed by using the Kimura 2-parameter model with MEGA 7.0 and the bootstrap values were calculated with 1000 replicates. Representative sequences of Cryptosporidium detected in snakes in this study are in bold print and marked by circles. Scale bar indicates nucleotide substitutions per site.
Fig. 2. Maximum likelihood tree constructed from partial cox1 in Spirometra infection in a captive Samar cobra (Naja samarensis) in the United States: An imported case?
Fig. 2. Maximum likelihood tree constructed from partial cox1 gene sequences of Spirometra samples and related taxa. HKY + G + I was used as the best substitution model. Schistocephalus solidus and Dibothriocephalus nihonkaiensis were used as outgroups. (JPN – Japan; KOR – South Korea; CHI and CHN – China; AUS – Australia; IRA – Iran; USA – United States; THA – Thailand; MMR – Myanmar; TZA – Tanzania; IND – India; VNM – Vietnam; KHM – Cambodia; LAO – Laos; COL – Colombia; NZL – New Zealand; IDN – Indonesia; ROU – Romania; SSD – South Sudan; ETH – Ethiopia; POL – Poland; UKR – Ukraine; FIN – Finland; CHL – Chile; BRA – Brazil).
Fig. 1. A in Spirometra infection in a captive Samar cobra (Naja samarensis) in the United States: An imported case?
Fig. 1. A) Presence of Spirometra plerocercoid in subcutaneous tissue of a male Samar cobra (Naja samarensis) from a zoological facility in the USA; B) Plerocercoids isolated from de subcutaneous tissue of the same specimen.
Fig. 8 in Diversity and biology of Spirometra tapeworms (Cestoda: Diphyllobothriidea), zoonotic parasites of wildlife: A review
Fig. 8. Map of the distribution of Spirometra spp. in the world (in yellow). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 4 in Diversity and biology of Spirometra tapeworms (Cestoda: Diphyllobothriidea), zoonotic parasites of wildlife: A review
Fig. 4. Microphotographs of Spirometra spp. from North and South America. A–C – Scolex and gravid proglottids of S. decipiens syntype from Puma concolor, Brazil (NMW 2682, 2699). D, E – gravid proglottids of S. decipiens syntype from Herpailurus yagouaroundi (NMW 12781). F–J – Gravid proglottids and sagittal section of S. decipiens hologenophore from Chrysocyon brachyurus, Bolivia (USNM 1233899). K–O – Scolex and proglottids of S. mansonoides syntype from Felis catus, USA (USNM 1333923). P – Immature proglottid of Spirometra sp. 2 hologenophore from Lynx rufus, USA Illinois (IPCAS C-987).
Fig. 7 in Diversity and biology of Spirometra tapeworms (Cestoda: Diphyllobothriidea), zoonotic parasites of wildlife: A review
Fig. 7. Microphotographs of Spirometra spp. and Dibothrium folium from Africa. A–D – Scolex, proglottids and sagittal section of S. theileri from Panthera leo, DR Congo material of Baer (1959) (RMCA 32316). E – Scolex of D. folium, type specimen (NMW No. 2616). F, G – Gravid proglottid and sagittal section of hologenophore from Panthera pardus, South Africa (IPCAS C-986). H, I – Gravid proglottid and sagittal section from P. pardus, Siera Leone (NHMUK 1924.6.12.116). J – Gravid proglottid from P. pardus, DR Congo (NHMUK 1934.12.18.51). K, P – Gravid proglottid and mounted specimen from Crocuta crocuta, Tanzania (NHMUK 1937.10.20.26–30). L, M – Gravid proglottid and sagittal section from P. leo (RMCA 32316). N, O – Gravid proglottid and sagittal section from P. pardus, DR Congo (1934.12.18.51–54). Q, R – Syntype slides of Diphyllobothrium theileri from Leptailurus serval, South Africa (MHNG-PLAT 40726). S – Syntype slide of Lueheella pretoriensis from Otocyon megalotis, South Africa (MHNG-PLAT 41517).
Fig. 6 in Diversity and biology of Spirometra tapeworms (Cestoda: Diphyllobothriidea), zoonotic parasites of wildlife: A review
Fig. 6. Line drawing of gravid proglottid of the neotype of Spirometra mansoni from Canis familiaris, Japan (IPCAS C-988), ventral view; note the shape of the ovary, which is long, with narrow lateral wings. Vitelline follicles and testes illustrated in one side of proglottids only, except for lateral-most and median-most vitelline follicles.
Fig. 5 in Diversity and biology of Spirometra tapeworms (Cestoda: Diphyllobothriidea), zoonotic parasites of wildlife: A review
Fig. 5. Microphotographs of Spirometra mansoni neotype from experimentally infected dog Canis familiaris, Japan. A – Whole unstained neotype. B, C – SEM photo of scolex and gravid proglottid. D – Whole mounts with part of neotype. E, F – Mature proglottids. G, H, K – Gravid proglottids. I, J – Sagittal section of gravid proglottid.
Fig. 3 in Diversity and biology of Spirometra tapeworms (Cestoda: Diphyllobothriidea), zoonotic parasites of wildlife: A review
Fig. 3. Line drawings of Spirometra erinaceieuropaei from Canis lupus, Poland. A, B – ovarian region and terminal genitalia; ventral (A) and dorsal (B) view of the same proglottid. C, D – gravid proglottids; dorsal (C) and ventral (D) view; note the shape of the ovary, which is short, but with wide lateral wings. Vitelline follicles and testes illustrated in one side of proglottids only, except for lateral-most and median-most vitelline follicles. Abbreviations: ci – cirrus; cs – cirrus sac; doc – dorsal osmoregulatory canal; eg – eggs; esv – external seminal vesicle; mp – male genital pore; Mg – Mehlis' gland; oc – oocapt; ov – ovary; rc – receptaculum seminis; te – testes; up – uterine pore; ut – uterus; va – vagina; vd – vas deferens; vf – vitelline follicles; vp – vaginal pore; vr – vitelline reservoir.
Fig. 1 in Diversity and biology of Spirometra tapeworms (Cestoda: Diphyllobothriidea), zoonotic parasites of wildlife: A review
Fig. 1. Phylogenetic tree of the interrelationships of the genus Spirometra based on selected cytochrome c oxidase subunit I (cox1) gene data (long sequences), maximum likelihood. The branch length scale bar indicates number of substitutions per site. Colours highlight specimens of different species; samples without colour represent undescribed species. See Supplementary Fig. 1 for more data based on larger dataset, but based on shorter sequences. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2 in Diversity and biology of Spirometra tapeworms (Cestoda: Diphyllobothriidea), zoonotic parasites of wildlife: A review
Fig. 2. Microphotographs of Spirometra erinaceieuropaei from Canis lupus. A – Scolex from Ukraine. B–F – Gravid and mature proglottids from Poland. G – Sagittal section of gravid proglottid from Poland.
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OpenNeuro
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