##plugins.themes.bootstrap3.article.main##

Katokhin A. V., Kornyychuk Yu. M. Genotyping of Black Sea trematodes of the family Opecoelidae by mitochondrial markers. Marine Biological Journal, 2020, vol. 5, no. 4, pp. 15-27. https://doi.org/10.21072/mbj.2020.05.4.02

##plugins.themes.bootstrap3.article.details##

Abstract

Opecoelidae Ozaki, 1925 (Trematoda: Opecoeloidea) is the biggest trematode family in the Black Sea in terms of species and genera number. Maritae of the most common Black Sea Opecoelidae trematodes are well described morphologically; nevertheless, information on their genomes structure is sketchy, and data on mitochondrial genomes are absent. The aim was to study the structure of mitochondrial genome fragments of Black Sea trematode species: Cainocreadium flesi Korniychuk & Gaevskaya, 2000, Gaevskajatrema perezi (Mathias, 1926) Gibson & Bray, 1982, and Helicometra fasciata (Rudolphi, 1819) Odhner, 1902. Sequences were made for CO1 (the cytochrome c oxidase subunit I) and 16S mitochondrial genes. To amplify CO1 gene fragment of Cainocreadium and Helicometra trematodes, primers were developed. Phylogenetic relationships within the analyzed part of the Opecoelidae family were reconstructed on the basis of our data and the corresponding GenBank data by the Maximum Likelihood algorithm, implemented in MEGA X program. To root the phylogenetic trees, the corresponding sequences of the closely related trematode Brachycladium goliath (Brachycladioidea: Brachycladiidae) were used. For the first time, nucleotide sequences of CO1 and 16S mitochondrial genes fragments of Black Sea trematodes C. flesi, G. perezi, and H. fasciata from different definitive fish hosts were identified and deposited in GenBank. In case of C. flesi, no host-specific lines were found in the structure of CO1 mitochondrial gene fragment, but high CO1 nucleotide diversity was noted. Black Sea H. fasciata, parasitizing peacock wrasse, Symphodus tinca, were revealed to be a host-specific CO1 haplogroup; its taxonomic status requires further clarification, and ecological and genetic studies of the putative H. fasciata species complex from different water areas are needed. No host-specific genetic lines were found when analyzing the sequences of H. fasciata 16S rRNA mitochondrial gene fragment. No significant differences in 16S fragment were registered between G. perezi trematodes from different Black Sea definitive hosts; however, the intraspecific 16S nucleotide diversity was rather high.

Authors

A. V. Katokhin

senior researcher, PhD

https://orcid.org/0000-0003-4537-456X

https://elibrary.ru/author_items.asp?id=88361

Yu. M. Kornyychuk

leading researcher, PhD

https://orcid.org/0000-0003-3095-6436

https://elibrary.ru/author_items.asp?id=696720

References

Гаевская А. В., Корнийчук Ю. М. Паразитические организмы как составляющая экосистем черноморского побережья Крыма // Современное состояние биоразнообразия прибрежных вод Крыма (черноморский сектор) / под ред. В. Н. Еремеева, А. В. Гаевской ; НАН Украины, Институт биологии южных морей. Севастополь : ЭКОСИ-Гидрофизика, 2003. С. 425–490. [Gaevskaya A. V., Kornyychuk Yu. M. Paraziticheskie organizmy kak sostavlyayushchaya ekosistem chernomorskogo poberezh’ya Kryma. In: Sovremennoe sostoyanie bioraznoobraziya pribrezhnykh vod Kryma / V. N. Eremeev, A. V. Gaevskaya (Eds) ; NAN Ukrainy, Institut biologii yuzhnykh morei. Sevastopol : EKOSI-Gidrofizika, 2003, pp. 425–490. (in Russ.)].

Гаевская А. В., Солонченко А. И. Новые данные о трематодах черноморских рыб // Биологические науки: научные доклады высшей школы. 1989. № 5. С. 43–47. [Gaevskaya A. V., Solonchenko A. I. Novye dannye o trematodakh chernomorskikh ryb. Biologicheskie nauki: nauchnye doklady vysshei shkoly, 1989, no. 5, pp. 43–47. (in Russ.)]

Дмитриева Е. В., Полякова Т. А., Корнийчук Ю. М., Пронькина Н. В., Плаксина М. П., Юрахно В. М., Лебедовская М. В., Лозовский В. Л., Белоусова Ю. В. Паразиты морских гидробионтов // Биология Чёрного моря у берегов Юго-Восточного Крыма / под ред. Н. С. Костенко. Симферополь : ИТ «Ариал», 2018. Гл. 3.1.4. С. 96–130. [Dmitrieva E. V., Polyakova T. A., Kornyychuk Yu. M., Pron’kina N. V., Plaksina M. P., Yurakhno V. M., Lebedovskaya M. V., Lozovskii V. L., Belousova Yu. V. Parazity morskikh gidrobiontov. In: The Biology of the Black Sea Offshore Area at the South-Eastern Crimea / N. S. Kostenko (Ed.). Simferopol : PP “Arial”, 2018, chap. 3.1.4, pp. 96–130. (in Russ.)]

Катохин А. В., Корнийчук Ю. М. Первые данные генотипирования черноморских трематод родов Cainocreadium и Helicometra (Trematoda: Opecoelidae) // Морской биологический журнал. 2018. Т. 3, № 4. С. 36–42. [Katokhin A. V., Kornyychuk Yu. M. First data of ITS1-genotyping of the Black Sea trematodes Cainocreadium and Helicometra (Trematoda: Opecoelidae). Morskoj biologicheskij zhurnal, 2018, vol. 3, no. 4, pp. 36–42. (in Russ.)]. https://doi.org/10.21072/mbj.2018.03.4.04

Корнийчук Ю. М. О морфологической изменчивости черноморских представителей рода Helicometra (Trematoda: Opecoelidae) // Экология моря. 2000. Вып. 51. С. 40–44. [Korniychuk J. M. Morphological variability of genus Helicometra (Trematoda: Opecoelidae) maritae from the Black Sea. Ekologiya morya, 2000, iss. 51, pp. 40–44. (in Russ.)]

Корнийчук Ю. М. О структуре трематодофауны черноморских губановых рыб (Pisces: Labridae) // Экология моря. 2001. Вып. 58. С. 32–36. [Korniychuk J. M. Structure of the trematode fauna of the Black Sea labrid fishes (Pisces: Labridae). Ekologiya morya, 2001, iss. 58, pp. 32–36. (in Russ.)]

Корнийчук Ю. М. Трематоды рода Cainocreadium (Opecoelidae) в Чёрном и Средиземном морях // Паразитология в XXI веке – проблемы, методы, решения : материалы IV Всерос. съезда Паразитологического общества при Российской академии наук. Санкт-Петербург, 2008. Т. 2. С. 77–80. [Kornyychuk Yu. M. Trematody roda Cainocreadium (Opecoelidae) v Chernom i Sredizemnom moryakh. In: Parazitologiya v XXI veke – problemy, metody, resheniya : materialy IV Vseros. s"ezda Parazitologicheskogo obshchestva pri Rossiiskoi akademii nauk. Saint Petersburg, 2008, vol. 2, pp. 77–80. (in Russ.)]

Корнийчук Ю. М. Дополненное описание гермафродитного поколения трематоды черноморских рыб Helicometra fasciata (Trematoda, Opecoelidae) // Вестник зоологии. 2009. Отд. вып. № 23. С. 63–68. [Korniychuk Yu. M. Additional description of hermaphroditic generation of trematodes Black Sea fishes, Helicometra fasciata (Trematoda, Opecoelidae). Vestnik zoologii, 2009, spec. iss. 23, pp. 63–68. (in Russ.)]

Корнийчук Ю. М., Гаевская А. В. Cainocreadium flesi sp. n. (Trematoda, Opecoelidae) – новый вид трематод черноморских рыб // Вестник зоологии. 2000. Т. 34, № 6. С. 89–91. [Kornyychuk Yu. M., Gaevskaya A. V. Cainocreadium flesi sp. n. (Trematoda, Opecoelidae) – A new trematode from the Black Sea fishes. Vestnik zoologii, 2000, vol. 34, no. 6, pp. 89–91. (in Russ.)]

Определитель паразитов позвоночных Чёрного и Азовского морей : Паразитические беспозвоночные рыб, рыбоядных птиц и морских млекопитающих / [сост. А. В. Гаевская, А. В. Гусев, С. Л. Делямуре и др.] ; АН УССР, Ин-т биологии юж. морей им. А. О. Ковалевского. Киев : Наукова думка, 1975. 551 с. [Opredelitel’ parazitov pozvonochnykh Chernogo i Azovskogo morei : Paraziticheskie bespozvonochnye ryb, ryboyadnykh ptits i mlekopitayushchikh / [A. V. Gaevskaya, A. V. Gusev, S. L. Delyamure, etc. (Eds)] ; AN USSR, In-t biologii yuzh. morei im. A. O. Kovalevskogo. Kiev : Naukova dumka, 1975, 551 p. (in Russ.)]

Световидов А. Н. Рыбы Чёрного моря. Москва ; Ленинград : Наука, 1964. 551 с. [Svetovidov A. N. Ryby Chernogo morya. Moscow ; Leningrad : Nauka, 1964, 551 p. (in Russ.)]

Andres M. J., Ray C. L., Pulis E. E., Curran S. S., Overstreet R. M. Molecular characterization of two opecoelid trematodes from fishes in the Gulf of Mexico, with a description of a new species of Helicometra. Acta Parasitologica, 2014, vol. 59, iss. 3, pp. 405–412. https://doi.org/10.2478/s11686-014-0258-7

Bandelt H.-J., Forster P., Röhl A. Median-joining networks for inferring intraspecific phylogenies. Molecular Biology and Evolution, 1999, vol. 16, iss. 1, pp. 37–48. https://doi.org/10.1093/oxfordjournals.molbev.a026036

Blasco-Costa I., Cutmore S. C., Miller T. L., Nolan M. J. Molecular approaches to trematode systematics: ‘Best practice’ and implications for future study. Systematic Parasitology, 2016, vol. 93, iss. 3, pp. 295–306. https://doi.org/10.1007/s11230-016-9631-2

Born-Torrijos A., Kostadinova A., Raga J. A., Holzer A. S. Molecular and morphological identification of larval opecoelids (Digenea: Opecoelidae) parasitising prosobranch snails in a Western Mediterranean lagoon. Parasitology International, 2012, vol. 61, iss. 3, pp. 450–460. https://doi.org/10.1016/j.parint.2012.03.002

Bray R. A., Cribb T. H., Littlewood D. T., Waeschenbach A. The molecular phylogeny of the digenean family Opecoelidae Ozaki, 1925 and the value of morphological characters, with the erection of a new subfamily. Folia Parasitologica, 2016, vol. 63, art. no. 013 (11 p.). https://doi.org/10.14411/fp.2016.013

Briscoe A. G., Bray R. A., Brabec J., Littlewood D. T. The mitochondrial genome and ribosomal operon of Brachycladium goliath (Digenea: Brachycladiidae) recovered from a stranded minke whale. Parasitology International, 2016, vol. 65, iss. 3, pp. 271–275. https://doi.org/10.1016/j.parint.2016.02.004

Donald K. M., Kennedy M., Poulin R., Spencer H. G. Host specificity and molecular phylogeny of larval Digenea isolated from New Zealand and Australian topshells (Gastropoda: Trochidae). International Journal for Parasitology, 2004, vol. 34, iss. 5, pp. 557–568. https://doi.org/10.1016/j.ijpara.2003.11.027

Donald K. M., Spencer H. G. Host and ecology both play a role in shaping distribution of digenean parasites of New Zealand whelks (Gastropoda: Buccinidae: Cominella). Parasitology, 2016, vol. 143, iss. 9, pp. 1143–1156. https://doi.org/10.1017/S0031182016000494

González M. T., Henriquez V., Lopes Z. Variations in the fecundity and body size of digenean (Opecoelidae) species parasitizing fishes from Northern Chile. Revista de Biología Marina y Oceanografía, 2013, vol. 48, no. 3, pp. 421–429. https://doi.org/10.4067/S0718-19572013000300002

Heneberg P., Sitko J., Bizos J. Integrative taxonomy of central European parasitic flatworms of the family Prosthogonimidae Lühe, 1909 (Trematoda: Plagiorchiida). Parasitology International, 2015, vol. 64, iss. 5, pp. 264–273. https://doi.org/10.1016/j.parint.2015.02.003

Jousson O., Bartoli P. Molecules, morphology and morphometrics of Cainocreadium labracis and Cainocreadium dentecis n. sp. (Digenea: Opecoelidae) parasitic in marine fishes. International Journal for Parasitology, 2001, vol. 31, iss. 7, pp. 706–714. https://doi.org/10.1016/s0020-7519(01)00180-1

Kumar S., Stecher G., Li M., Knyaz C., Tamura K. MEGA X: Molecular Evolutionary Genetics Analysis across computing platforms. Molecular Biology and Evolution, 2018, vol. 35, pp. 1547–1549. https://doi.org/10.1093/molbev/msy096

Lagrue C., Joannes A., Poulin R., Blasco-Costa I. Genetic structure and host-parasite co-divergence: Evidence for trait-specific local adaptation. Biological Journal of the Linnean Society, 2016, vol. 118, iss. 2, pp. 344–358. https://doi.org/10.1111/bij.12722

León-Règagnon V. Evidence of new species of Haematoloechus (Platyhelminthes: Digenea) using partial cox1 sequences, mitochondrial DNA. The Journal of DNA Mapping, Sequencing, and Analysis, 2010, vol. 21, iss. s1., pp. 12–17. https://doi.org/10.3109/19401736.2010.523700

Librado P., Rozas J. DnaSP v5: A software for comprehensive analysis of DNA polymorphism data. Bioinformatics, 2009, vol. 25, iss. 11, pp. 1451–1452. https://doi.org/10.1093/bioinformatics/btp187

López Z., Cárdenas L., Runil F., González M. T. Contrasting definitive hosts as determinants of the genetic structure in a parasite with complex life cycle along the south-eastern Pacific. Molecular Ecology, 2015, vol. 24, iss. 5, pp. 1060–1073. https://doi.org/10.1111/mec.13080

Martin S. B., Huston D. C., Cutmore S. C., Cribb T. H. A new classification for deep-sea opecoelid trematodes based on the phylogenetic position of some unusual taxa from shallow-water, herbivorous fishes off south-west Australia. Zoological Journal of the Linnean Society, 2019, vol. 186, iss. 2, pp. 385–413. https://doi.org/10.1093/zoolinnean/zly081

Pérez-Ponce D. E., León G., García-Varela M., Pinacho-Pinacho C. D., Sereno-Uribe A. L., Poulin R. Species delimitation in trematodes using DNA sequences: Middle-American Clinostomum as a case study. Parasitology, 2016, vol. 143, iss. 13, pp. 1773–1789. https://doi.org/10.1017/S0031182016001517

Rosser T. G., Alberson N. R., Woodyard E. T., Cunningham F. L., Pote L. M., Griffin M. J. Clinostomum album n. sp. and Clinostomum marginatum (Rudolphi, 1819), parasites of the great egret Ardea alba L. from Mississippi, USA. Systematic Parasitology, 2017, vol. 94, iss. 1, pp. 35–49. https://doi.org/10.1007/s11230-016-9686-0

Shekhovtsov S. V., Katokhin A. V., Kolchanov N. A., Mordvinov V. A. The complete mitochondrial genomes of the liver flukes Opisthorchis felineus and Clonorchis sinensis (Trematoda). Parasitology International, 2010, vol. 59, iss. 1, pp. 100–103. https://doi.org/10.1016/j.parint.2009.10.012

Vilas R., Criscione C. D., Blouin M. S. A comparison between mitochondrial DNA and the ribosomal internal transcribed regions in prospecting for cryptic species of platyhelminth parasites. Parasitology, 2005, vol. 131, iss. 6, pp. 839–846. https://doi.org/10.1017/S0031182005008437

Wilke T., Davis G. M., Qiu D. C., Spear R. C. Extreme mitochondrial sequence diversity in the intermediate schistosomiasis host Oncomelania hupensis robertsoni: Another case of ancestral polymorphism? Malacologia, 2006, vol. 48, no. 1, pp. 43–157.

Yano A., Urabe M. Larval stages of Neoplagioporus elongatus (Goto and Ozaki, 1930) (Opecoelidae: Plagioporinae), with notes on potential second intermediate hosts. Parasitology International, 2017, vol. 66, iss. 2, pp. 181–185. https://doi.org/10.1016/j.parint.2016.12.012

Funding

The research was supported by RFBR grant No. 18-44-920027 р_а and partially carried out within the framework of IBSS government research assignment “Patterns of formation and anthropogenic transformation of biodiversity and biological resources of the Sea of Azov – Black Sea basin and other parts of the World Ocean” (No. АААА-А18-118020890074-2).

Statistics

Downloads

Download data is not yet available.