Skip to content
Licensed Unlicensed Requires Authentication Published by De Gruyter April 13, 2018

Morphological, histological and molecular characterization of Myxobolus kingchowensis and Thelohanellus cf. sinensis infecting gibel carp Carassius auratus gibelio (Bloch, 1782)

  • Bo Zhang , Yanhua Zhai , Zemao Gu and Yang Liu EMAIL logo
From the journal Acta Parasitologica

Abstract

A Myxobolus species and a Thelohanellus species infecting Carassius auratus gibelio (Bloch, 1782) were redescribed by their morphological, histological and molecular characterization. In the present study, the Myxobolus species infecting the muscle was identified as Myxobolus kingchowensisChen et Ma, 1998 by the morphological and molecular data. Histologically, mature spores of M. kingchowensis were observed in the intercellular and connective tissue of muscle, though the plasmodia were not found. In addition, scattered spores also occurred in the intercellular of haematopoietic cells, intraepithelial of the renal tubules and interior of the melano-macrophage centres. Phylogenetic analysis showed that M. kingchowensis clustered in the clade of muscle-infecting Myxobolus species, further supporting muscle as the infection site of M. kingchowensis. The present Thelohanellus species infecting the gills was identified conspecific as Thelohanellus sinensis reported in Sun (2006) (mark it as T. sinensis-Sun)based on spore morphology, biological traits (host specificity and organ specificity), and molecular data. However, compared with the original description of T. sinensisChen et Hsieh, 1960, the present Thelohanellus species and T. sinensis-Sun both infecting the gills of gibel carp are distinguishable from the original description in the host and infection site, which made the validity of T. sinensis-Sun dubious. Due to the absence of molecular data in the original description of T. sinensis, we suggest marking the present species and T. sinensis-Sun as T. cf. sinensis to avoid the confusion until T. sinensis is obtained from the type host and type infection site.

Acknowledgement

We would like to thank Zizhen Wu for samples collection. This study was supported by the Nature Science Foundation of China (Project Number 31501848, 31572233), China Agriculture Research System (CARS-46) and Demonstration of Key Techniques for High Quality Aquatic Products (Project Number 2016620000001046).

References

Atkinson S.D., Bartošová-Sojková P., Whipps C.M., Bartholomew J.L. 2015. Approaches for characterising myxozoan species. (Eds B. Okamura, A. Gruhl, J. L. Bartholomew) Myxozoan Evolution, Ecology and Development, Cham, Springer. pp. 111–123. https://doi.org/10.1007/978-3-319-14753-6_610.1007/978-3-319-14753-6_6Search in Google Scholar

Chen C.L. 1973. An illustrated guide to the fish diseases and causative pathogenic fauna and flora in the Hubei Province. Inst. Hydrobiol., Publishing House Science, Beijing, China. (In Chinese)Search in Google Scholar

Chen C.L., Hsieh S.R. 1960. Studies on sporozoa from the freshwater fishes Ophiocephalus maculatus and O. argus of China. Actc Hydrobiologica Sinica, 2, 171–196Search in Google Scholar

Chen Q.L., Ma C.L. 1998. Myxozoa: Myxosporea. Science Press, Beijing. (In Chinese)Search in Google Scholar

Darriba D., Taboada G.L., Doallo R., Posada D. 2012. jModelTest 2: more models, new heuristics and parallel computing. Nature Methods, 9, 772–772. 10.1038/nmeth.2109Search in Google Scholar PubMed PubMed Central

Dereeper A., Audic S., Claverie J.-M., Blanc G. 2010. BLAST-EXPLORER helps you building datasets for phylogenetic analysis. BMC Evolutionary Biology, 10, 8. https://doi.org/10.1186/1471-2148-10-810.1186/1471-2148-10-8Search in Google Scholar PubMed PubMed Central

Dereeper A., Guignon V., Blanc G., Audic S., Buffet S., Chevenet F., et al. 2008. Phylogeny. fr: robust phylogenetic analysis for the non-specialist. Nucleic Acids Research, 36, W465-W469. https://doi.org/10.1093/nar/gkn18010.1093/nar/gkn180Search in Google Scholar PubMed PubMed Central

Drummond A.J., Rambaut A. 2007. BEAST: Bayesian evolutionary analysis by sampling trees. BMC Evolutionary Biology, 7, 214. https://doi.org/10.1186/1471-2148-7-21410.1186/1471-2148-7-214Search in Google Scholar PubMed PubMed Central

Eiras J.C., Molnár K., Lu Y.S. 2005. Synopsis of the species of Myxobolus Bütschli, 1882 (Myxozoa: Myxosporea: Myxobolidae). Systematic Parasitology, 61, 1–46. 10.1007/s11230-004-6343-9Search in Google Scholar PubMed

Fiala I., Bartošová-Sojková P., Whipps C.M. 2015. Classification and phylogenetics of Myxozoa. (Eds B. Okamura, A. Gruhl, J. L. Bartholomew) Myxozoan Evolution, Ecology and Development, Cham, Springer. pp. 85–110. https://doi.org/10.1007/978-3-319-14753-6_510.1007/978-3-319-14753-6_5Search in Google Scholar

Guindon S., Dufayard J.F., Lefort V., Anisimova M., Hordijk W., Gascuel O. 2010. New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. Systematic Biology, 59, 307–321. 10.1093/sysbio/syq010Search in Google Scholar PubMed

Guindon S., Gascuel O. 2003. A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Systematic Biology, 52, 696–704. 10.1080/10635150390235520Search in Google Scholar PubMed

Hartigan A., Wilkinson M., Gower D.J., Streicher J.W., Holzer A.S., Okamura B. 2016. Myxozoan infections of caecilians demonstrate broad host specificity and indicate a link with human activity. International Journal for Parasitology, 46, 375–381. https://doi.org/10.1016/jijpara.2016.02.00110.1016/j.ijpara.2016.02.001Search in Google Scholar PubMed

Hillis D.M., Dixon M.T. 1991. Ribosomal DNA: molecular evolution and phylogenetic inference. The Quarterly Review of Biology, 66, 411–453. https://doi.org/10.1086/41733810.1086/417338Search in Google Scholar PubMed

Katoh K., Standley D.M. 2013. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Molecular Biology and Evolution, 30, 772–780. 10.1093/molbev/mst010Search in Google Scholar PubMed PubMed Central

Kent M.L., Bagshaw J.W., Nener J., Raymond B. 1996. Myxobolus cyprini Doflein, 1898, in Peamouth: First Report of This Myxosporean in the Western Hemisphere. Journal of Aquatic Animal Health, 8, 159–162. 10.1577/1548-8667 (1996) 008< 0159: MCDIPF>2.3.CO;2Search in Google Scholar

Liu Y., Zhai Y.H., Gu Z.M. 2016b. Morphological and molecular characterization of Thelohanellus macrovacuolaris n. sp. Myxosporea: Bivalvulida infecting the palate in the mouth of common carp Cyprinus carpio L. in China. Parasitology International, 65, 303–307. https://doi.org/10.1016/j.parint.2016.02.01310.1016/j.parint.2016.02.013Search in Google Scholar PubMed

Lom J., Arthur J. 1989. A guideline for the preparation of species descriptions in Myxosporea. Journal of Fish Diseases, 12, 151–156. 10.1111/j.1365-2761.1989.tb00287.xSearch in Google Scholar

Maciel P.O., Affonso E.G., Boijink C.D.L., Tavaresdias M., Inoue L.A.K.A. 2011. Myxobolus sp. (Myxozoa) in the circulating blood of Colossoma macropomum (Osteichthyes, Characidae). Revista Brasileira De Parasitologia Veterinaria, 20, 82–84. 10.1590/S1984-29612011000100018Search in Google Scholar

Molnár K. 1994. Comments on the host, organ and tissue specificity of fish myxosporeans and on the types of their intrapiscine development. Parasitology Hung, 27, 5–20Search in Google Scholar

Molnár K. 2011. Remarks to the validity of Genbank sequences of Myxobolus spp. Myxozoa, Myxosporidae infecting Eurasian fishes. Acta Parasitologica, 56, 263. https://doi.org/10.2478/s11686-011-0054-610.2478/s11686-011-0054-6Search in Google Scholar

Molnár K., Eszterbauer E. 2015. Specificity of infection sites in vertebrate hosts. In: (Eds B. Okamura, A. Gruhl, J. L. Bartholomew) Myxozoan Evolution, Ecology and Development, Cham, Springer. pp. 295–313. https://doi.org/10.1007/978-3-319-14753-6_1610.1007/978-3-319-14753-6_16Search in Google Scholar

Molnár K., Kovács-Gayer É. 1985. The pathogenicity and development within the host fish of Myxobolus cyprini Doflein, 1898. Parasitology, 90, 549–555. 10.1017/S0031182000055530Search in Google Scholar

Ronquist F., Teslenko M., Van Der Mark P., Ayres D.L., Darling A., Höhna S., et al. 2012. MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Systematic Biology, 61, 539–542. https://doi.org/10.1093/sysbio/sys02910.1093/sysbio/sys029Search in Google Scholar PubMed PubMed Central

Sun C.Y. 2006. Morphological and molecular comparison of myxosporeans. Master Thesis, Chong Qing Normal University, Chongqing, China. (In Chinese)Search in Google Scholar

Whipps C.M., Adlard R.D., Bryant M.S., Lester R.J., Findlay V., Kent M.L. 2003. First report of three Kudoa species from eastern Australia: Kudoa thyrsites from mahi mahi Coryphaena hippurus, Kudoa amamiensis and Kudoa minithyrsites n. sp. from sweeper Pempheris ypsilychnus. Journal of Eukaryotic Microbiology, 50, 215–219. 10.1111/j.1550-7408.2003.tb00120.xSearch in Google Scholar PubMed

Yuan S., Xi B., Wang J., Xie J., Zhang J. 2015. Thelohanellus wangi n. sp. Myxozoa, Myxosporea, a new gill parasite of allogynogenetic gibel carp Carassius auratus gibelio Bloch in China, causing severe gill myxosporidiosis. Parasitology Research, 114, 37–45. https://doi.org/10.1007/s00436-014-4157-510.1007/s00436-014-4157-5Search in Google Scholar PubMed

Zhang J.Y., Gu Z.M., Kalavati C., Eiras J.C., Liu Y., Guo Q.Y., et al. 2013. Synopsis of the species of Thelohanellus Kudo, 1933 (Myxozoa: Myxosporea: Bivalvulida). Systematic Parasitology, 86, 235–256. 10.1007/s11230-013-9449-0Search in Google Scholar PubMed

Received: 2017-11-13
Revised: 2018-1-11
Accepted: 2018-1-12
Published Online: 2018-4-13
Published in Print: 2018-6-26

© 2018 W. Stefański Institute of Parasitology, PAS

Downloaded on 25.4.2024 from https://www.degruyter.com/document/doi/10.1515/ap-2018-0026/html
Scroll to top button