Ophiotaenia echidis n. sp. (Cestoda: Proteocephalidae) from the saw-scaled viper, Echis carinatus sochureki Stemmler (Ophidia: Viperidae), one of the world's deadliest snakes, from the United Arab Emirates
Status PubMed-not-MEDLINE Jazyk angličtina Země Velká Británie, Anglie Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
33898236
PubMed Central
PMC8056141
DOI
10.1016/j.ijppaw.2021.03.006
PII: S2213-2244(21)00038-9
Knihovny.cz E-zdroje
- Klíčová slova
- Morphology, Onchoproteocephalidea, Phylogenetic relationships, Snakes, Tapeworms, Taxonomy, United Arab Emirates,
- Publikační typ
- časopisecké články MeSH
Ophiotaenia echidis n. sp. (Cestoda: Proteocephalidae) is described from the intestine of one of the world's deadliest snakes, the saw-scaled viper Echis carinatus sochureki Stemmler (Ophidia: Viperidae) in the United Arab Emirates. The new species differs from other species of the non-monophyletic Ophiotaenia by the position of testes in two longitudinal lines on both sides of the uterus, and by the large size of an embryophore (diameter of 44-55 μm versus less than 40 μm in other species). Phylogenetic reconstructions based on lsrDNA and concatenated lsrDNA + COI datasets place the new species among proteocephalids from unrelated zoogeographical realms but mostly infecting venomous snakes. In all analyses, O. echidis n. sp. exhibited a strongly supported sister relationship with O. lapata Rambeloson, Ranaivoson et de Chambrier, 2012, a parasite of a pseudoxyrhophiid snake endemic to Madagascar. Despite a shared close evolutionary history between these taxa, morphological synapomorphies remain unclear, which impedes the erection of a new genus to accommodate them. A list of the 71 tapeworms of the former, non-monophyletic subfamily Proteocephalinae, parasitising snakes and lizards, including species inquirendae, and the phylogenetically closely related Thaumasioscolex didelphidis from opossum, with selected characteristics, is also provided, together with a checklist of helminth parasites reported from E. carinatus.
Central Veterinary Research Laboratory Dubai PO Box 597 United Arab Emirates
Natural History Museum PO Box 6434 CH 1211 Geneva 6 Switzerland
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Alencar L.R.V., Quental T.B., Grazziotin F.G., Alfaro M.L., Martins M., Venzon M., Zaherb H. Diversification in vipers: phylogenetic relationships, time of divergence and shifts in speciation rates. Mol. Phylogenet. Evol. 2016;105:50–62. PubMed
Barlow A., Pook C.E., Harrison R.A., Wüster W. Coevolution of diet and prey specific venom activity supports the role of selection in snake venom evolution. Proc. Roy. Soc. B. 2009;276:2443–2449. PubMed PMC
Biserkov V., Kostadinova A. Development of the pleroceroid I of Ophiotaenia europaea in reptiles. Int. J. Parasitol. 1997;27:1513–1516. PubMed
Bogdanov O.P., Markov G.S. Parasitic worms of some reptiles of Middle Asia. Izv. Akad. Nauk Uzb. SSR. 1955;8:59–68. (In Russian)
Bogdanov O.P., Markov G.S. Venomous Animals of Middle Asia and their Venoms. Tashkent. 1960. Parasite fauna of venomous snakes of Middle Asia and Kazakhstan; pp. 38–45. (In Russian)
Cañeda-Guzmán I.C., de Chambrier A., Scholz T. Thaumasioscolex didelphidis n. gen. and n. sp. (Cestoda: Proteocephalidae) from the black-eared opossum Didelphis marsupialis from Mexico, the first proteocephalidean tapeworm from a mammal. J. Parasitol. 2001;87:639–647. PubMed
de Chambrier A. A new tapeworm from the Amazon, Amazotaenia yvettae n. gen., n. sp. (Eucestoda: Proteocephalidea) from the siluriform fishes Brachyplatystoma filamentosum and B. vaillanti (Pimelodidae) Rev. Suisse Zool. 2001;108:303–316.
de Chambrier A., Zehnder M.P., Vaucher C., Mariaux J. The evolution of the Proteocephalidea (Platyhelminthes, Eucestoda) based on an enlarged molecular phylogeny, with comments on their uterine development. Syst. Parasitol. 2004;57:159–171. PubMed
de Chambrier A., Ammann M., Scholz T. First species of Ophiotaenia (Cestoda: Proteocephalidea) from Madagascar: O. georgievi n. sp., a parasite of the endemic snake Leioheterodon geayi (Colubridae) Folia Parasitol. 2010;57:197–205. PubMed
de Chambrier A., Binh T.T., Scholz T. Ophiotaenia bungari n. sp. (Cestoda), a parasite of Bungarus fasciatus (Schneider) (Ophidia: Elapidae) from Vietnam, with comments on relative ovarian size as a new and potentially useful diagnostic character for proteocephalidean tapeworms. Syst. Parasitol. 2012;81:39–50. PubMed
de Chambrier A., Waeschenbach A., Fisseha M., Scholz T., Mariaux J. A large 28S rDNA-based phylogeny confirms the limitations of established morphological characters for classification of proteocephalidean tapeworms (Platyhelminthes, Cestoda) ZooKeys. 2015;500:25–59. PubMed PMC
de Chambrier A., Scholz T., Mariaux J., Kuchta R. Onchoproteocephalidea I Caira, Jensen, Waeschenbach, Olson & Littlewood, 2014. In: Caira J.N., Jensen K., editors. Planetary Biodiversity Inventory (2008–2017): Tapeworms from Vertebrate Bowels of the Earth. University of Kansas, Natural History Museum, Special Publication No. 25; Lawrence: 2017. pp. 251–277.
de Chambrier A., Beveridge I., Scholz T. Tapeworms (Cestoda: Proteocephalidae) of Australian reptiles: hidden diversity of strictly host-specific parasites. Zootaxa. 2018;4461:477–498. PubMed
de Chambrier A., Brabec J., Tran B.T., Scholz T. Revision of Acanthotaenia von Linstow, 1903 (Cestoda: Proteocephalidae), parasites of monitors (Varanus spp.), based on morphological and molecular data. Parasitol. Res. 2019;118:1761–1783. PubMed
de Chambrier A., Brabec J., Scholz T. Molecular data reveal unexpected species diversity of tapeworms of Australasian reptiles: revision of Kapsulotaenia (Cestoda: Proteocephalidae) Zootaxa. 2020;4869:529–561. PubMed
Coquille S.C., de Chambrier A. Cairaella henrii gen. n., sp. n., a parasite of Norops trachyderma (Polychrotidae), and Ophiotaenia nicoleae sp. n. (Eucestoda: Proteocephalidea), a parasite of Thecadactylus rapicauda (Gekkonidae), in Ecuador. Folia Parasitol. 2008;55:197–206. PubMed
Dereeper A., Guignon V., Blanc G., Audic S., Buffet S., Chevenet F., Dufayard J.F., Guindon S., Lefort V., Lescot M., Claverie J.M., Gascuel O. Phylogeny.fr: robust phylogenetic analysis for the non-specialist. Nucleic Acids Res. 2008;36:W465–W469. PubMed PMC
Farooq M., Khanum Z., Ansar R. Helminth parasites of fresh water tortoise and poisonous snake from Sind, Pakistan. Pakistan J. Zool. 1983;15:31–37.
Freze V.I. vol. V. 1965. (Essentials of Cestodology). [Proteocephalata in fish, amphibians and reptiles.] Nauka, 538 pp. (In Russian: English translation: Israel Program of Scientific Translation, Jerusalem, 1969, Cat. No. 1853, v + 597pp.)
Gibson D.I., Bray R.A., Harris E.A. (Compilers) 2005. Host-Parasite Database of the Natural History Museum.http://www.nhm.ac.uk/research-curation/scientific-resources/taxonomy-systematics/host-parasites/ London. accessed on December 2020.
Guindon S., Dufayard J.-F., Lefort V., Anisimova M., Hordijk W., Gascuel O. New algorithms and methods to estimate maximum likelihood phylogenies: assessing the performance of PhyML 3.0. Syst. Biol. 2010;59:307–321. PubMed
Hoang D.T., Chernomor O., von Haeseler A., Minh B.Q., Vinh L.-S. UFBoot2: improving the ultrafast bootstrap approximation. Mol. Biol. Evol. 2018;35:518–522. PubMed PMC
Holt B.G., Lessard J.-P., Borregaard M.K., Fritz S.A., Araújo M.B., Dimitrov D., Fabre P.-H., Graham C.-H., Graves G.R., Jønsson K.A., Nogués-Bravo D., Wang Z., Whittaker R.J., Fjeldså J., Rahbek C. An update of Wallace's zoogeographic regions of the world. Science. 2013;339:74–78. PubMed
Kalyaanamoorthy S., Minh B.Q., Wong T.K.F., von Haeseler A., Jermiin L.S. ModelFinder: fast model selection for accurate phylogenetic estimates. Nat. Methods. 2017;14:587–589. PubMed PMC
Katoh K., Standley D.M. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol. Biol. Evol. 2013;30:772–780. PubMed PMC
Kearse M., Moir R., Wilson A., Stones-Havas S., Cheung M., Sturrock S., Buxton S., Cooper A., Markowitz S., Duran C., Thierer T., Ashton B., Meintjes P., Drummond A. Geneious Basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data. Bioinformatics. 2012;28:1647–1649. PubMed PMC
Markov G.S., Bogdanov O.P. Parasite fauna of reptiles of Turkmenistan. Tr. Inst. Biol. Akad. Nauk Turkm. SSR. 1956;4:260–277. (In Russian)
Markov G.S., Bogdanov O.P. Helminths and ticks – parasites of snakes of Middle Asia. Uzb. Biol. Zhurnal. 1960;2:35–41. (In Russian)
Markov G.S., Bogdanov O.P., Persianova L.A. Venomous Animals of Middle Asia and their Venoms. Tashkent. 1970. Helminth fauna of saw-scaled viper; pp. 46–60. (In Russian)
Marsella C.M., de Chambrier A. Ophiotaenia alessandrae sp. n. (Eucestoda: Proteocephalidea), a parasite of Hyla boans (Anura: Hylidae) from Amazonia in Ecuador. Rev. Suisse Zool. 2008;115:553–563.
Miller M.A., Pfeiffer W., Schwartz T. Proceedings of the Gateway Computing Environments Workshop. GCE; 2010. Creating the CIPRES Science Gateway for inference of large phylogenetic trees; pp. 1–8. 14 Nov. 2010.
Minh B.Q., Nguyen M.A.T., von Haeseler A. Ultrafast approximation for phylogenetic bootstrap. Mol. Biol. Evol. 2013;30:1188–1195. PubMed PMC
Nama H.S. Faunistic survey of helminth parasites of vertebrates of Rajasthan with special reference to arid zone. Sci. Rev. Arid Zone Res. 1984;2:187–225.
Pook C.E., Joger U., Stümpel N., Wüster W. When continents collide: phylogeny, historical biogeography and systematics of the medically important viper genus Echis (Squamata: Serpentes: Viperidae) Mol. Phylogenet. Evol. 2009;53:792–807. PubMed
Rambeloson V.R., Ranaivoson H.C., de Chambrier A. Ophiotaenia lapata sp. n. (Eucestoda: Proteocephalidea) from Madagascar: a parasite of the endemic snake Madagascarophis colubrinus (Colubridae) Rev. Suisse Zool. 2012;119:547–559.
Rego A.A. Order Proteocephalidea Mola, 1928. In: Khalil L.F., Jones A., Bray R.A., editors. Keys to the Cestode Parasites of Vertebrates. CAB International; Wallingford: 1994. pp. 257–293.
La Rue G.R. A revision of the cestode family Proteocephalidae. Zool. Anz. 1911;38:473–482.
La Rue G.R. A revision of the cestode family Proteocephalidae. Ill Biol. Monogr. 1914;1(1–2):3–351.
Scholz T., de Chambrier A. Taxonomy and biology of proteocephalidean cestodes: current state and perspectives. Helminthologia. 2003;40:65–77.
Scholz T., de Chambrier A., Kuchta R., Littlewood D.T.J., Waeschenbach A. Macrobothriotaenia ficta (Cestoda: Proteocephalidea), a parasite of sunbeam snake (Xenopeltis unicolor): example of convergent evolution. Zootaxa. 2013;3640:485–499. PubMed
Schuster R.K., Sivakumar S. 24th Conference of the World Association for the Advancement of Veterinary Parasitology, 25–29 August 2013, Perth, Australia. 2013. Reptiles as paratenic hosts of feline parasites.
Sela I., Ashkenazy H., Katoh K., Pupko T. GUIDANCE2: accurate detection of unreliable alignment regions accounting for the uncertainty of multiple parameters. Nucleic Acids Res. 2015;43:W7–W14. PubMed PMC
Sharpilo V.P. Naukova Dumka; Kiev: 1976. Parasitic Worms of Reptiles of the Fauna of the USSR. Systematics, Chorology, Biology; p. 288. (In Russian)
Trifinopoulos J., Nguyen L.T., von Haeseler A., Minh B.Q. W-IQ-TREE: a fast online phylogenetic tool for maximum likelihood analysis. Nucleic Acids Res. 2016;44:W232–W235. PubMed PMC
Uetz P., Freed P., Hošek J., editors. The Reptile Database. 2020. http://www.reptile-database.org Available.
Velikanov V.P. Larval forms of the Acuarioidea superfamily (Nematoda, Spirurata). Parasites of reptiles in Turkmenistan. Vestnik Zool. 1984;1984(1):3–8. (In Russian)
World Health Organization Venomous snakes distribution and species risk categories. 2020. https://apps.who.int/bloodproducts/snakeantivenoms/database/default.htm Available.
