A new species of microphallid (Trematoda: Digenea) infecting a novel host family, the Muraenidae, on the northern Great Barrier Reef, Australia
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A new species of microphallid, Longiductotrema tethepae n. sp., is reported from a muraenid eel Gymnothorax pseudothyrsoideus (Bleeker) on the northern Great Barrier Reef. The new species is described based on adults from Gy. pseudothyrsoideus and metacercariae from a grapsid crab, Grapsus albolineatus Latreille in Milbert, collected from off Lizard Island, Queensland, Australia. The new species is assigned to Longiductotrema Deblock & Heard, 1969 based on morphological characters (presence of a cirrus-sac; a long metraterm, intensively ensheathed by gland-cells; an entirely postcaecal uterus; vitellarium composed of two lateral clusters each of about ten follicles, situated in the testicular and post-testicular areas). Longiductotrema tethepae n. sp. is the third species assigned to the genus, differing from its congeners in having a distinctly larger body dimensions, a smaller pharynx in relation to oral sucker, the anterior limits of the vitelline fields at the level of the testes (vs at the level of the ovary) and in its parasitism of a muraenid fish (vs birds). Additionally, the new species differs from L. floridense Deblock & Heard, 1969 in having a shorter metraterm and from L. scandolensis Deblock & Bartoli, 1988 in having a less elongate forebody in relation to body length, shorter caeca and prepharynx, and slightly larger eggs. Phylogenetic analyses, based on partial 28S rRNA gene sequences, showed that the present species is sister to all other microphallids for which sequence data are available. This is the fourth report of a microphallid from a marine eel, the first from the Muraenidae Rafinesque and the first from a marine fish in the Indo-west Pacific. A summary of all species of the Microphallidae parasitising fish is provided.
KeywordsVentral Sucker Oral Sucker Maximum Likelihood Analysis Bayesian Inference Analysis Intestinal Bifurcation
The authors would like to thank Dr Nathan Bott, Storm Martin, Dan Huston and Russell Yong for their assistance in the collection of hosts and the staff of the Lizard Island Research Station (Australian Museum). The authors thank the Australian Biological Resources Study (ABRS) for their ongoing support to THC and SCC. This study was supported in part by the Czech Science Foundation (project ECIP P505/12/G112) to OK.
Compliance with ethical standards
Conflict of interest
The authors declare that they have no conflict of interest.
All applicable institutional, national and international guidelines for the care and use of animals were followed.
- Bray, R. A. (2008). Introduction and Key to Superfamilies. In Bray, R. A., Gibson, D. I. & Jones, A. (Eds.), Keys to the Trematoda, Volume 3. Wallingford: CAB International and The Natural History Museum, pp. 1–5.Google Scholar
- Belopol’skaya, M. M. (1952). Family Microphallidae. Osnovy Trematodologii, 6, 619–756. (In Russian).Google Scholar
- Belopol’skaya, M. M. (1963). Family Microphallidae. Osnovy Trematodologii, 21, 260–502. (In Russian).Google Scholar
- Deblock, S. (2008). Family Microphallidae Ward, 1901. In R. A. Bray, D. I. Gibson, & A. Jones (Eds.), Keys to the Trematoda, Volume 3. Wallingford: CAB International and The Natural History Museum, pp. 451–492.Google Scholar
- Deblock, S., & Heard, R. W. (1969). Contribution à l’étude des Microphallidae Travassos, 1920 (Trematoda). XIX. Description de Maritrema prosthometra n. sp. et de Longiductotrema nov. gen. parasites d’Oiseaux Ralliformes d’Amerique du Nord. Annales de Parasitologie Humaine et Comparée, 44, 415–424.PubMedGoogle Scholar
- Davie, P. (2011). Wild guide to Moreton Bay and adjacent coasts, Volume 2. Brisbane: Queensland Museum, 322 pp.Google Scholar
- Díaz, M., Gómez, E., Kashem, A., & Guillarte, D. V. (2015). Levinseniella (Levinseniella) gavilanicola sp. nov. (Trematoda: Microphallidae) in the common black hawk Buteogallus anthracinus from Venezuela, and notes on its life cycle. Revista Científica, 25, 260–265.Google Scholar
- Galaktionov, K. V., Blasco-Costa, I., & Olson, P. D. (2012). Life cycles, molecular phylogeny and historical biogeography of the ‘pygmaeus’ microphallids (Digenea: Microphallidae): widespread parasites of marine and coastal birds in the Holarctic. Parasitology, 139, 1346–1360.CrossRefPubMedGoogle Scholar
- Gibson, D. I. (1996). Trematoda. In: Margolis, L., & Kabata, Z. (Eds) Guide to the Parasites of Fishes of Canada, Part IV. Ottawa: NRC Press, 373 pp.Google Scholar
- Kakui, K. (2014). A novel transmission pathway: first report of a larval trematode in a tanaidacean crustacean. Fauna Ryukyuana, 17, 13–22.Google Scholar
- Kudlai, O., Cutmore, S. C., & Cribb, T. H. (2015). Morphological and molecular data for three species of the Microphallidae (Trematoda: Digenea) in Australia, including the first descriptions of the cercariae of Maritrema brevisacciferum Shimazu et Pearson, 1991 and Microphallus minutus Johnston, 1948. Folia Parasitologica, 62, 053.Google Scholar
- Maddison, W. P., & Maddison, D. R. (2015). Mesquite: a modular system for evolutionary analysis. Version 3.01 http://mesquiteproject.org.
- Miller, M. A., Pfeiffer, W., & Schwartz, T. (2010). Creating the CIPRES Science Gateway for inference of large phylogenetic trees. In Proceedings of the Gateway Computing Environments Workshop (GCE), 14 Nov. 2010, New Orleans, LA, pp. 1–8.Google Scholar
- Overstreet, R. M., Cook, J. O., & Heard, R. W. (2009). Trematoda (Platyhelminthes) of the Gulf of Mexico. In Tunnell, J. W., Felder, D. L., & Earle, S. A. (Eds.), Gulf of Mexico origin, waters, and biota: Volume 1, Biodiversity. Texas A&M University Press, Austin, pp. 419–486.Google Scholar
- Reimer, L. F., & Szuks, H. (1973). Zum Auftreten von Microphallidae bei Meeresfischen. Zoologischer Anzeiger, 190, 127–132.Google Scholar
- West, J., Mitchell, A., & Pung, O. J. (2014). Optimization of conditions for in vitro culture of the microphallid digenean Gynaecotyla adunca. Journal of Parasitology Research, 382153.Google Scholar