Hostname: page-component-cd9895bd7-8ctnn Total loading time: 0 Render date: 2024-12-28T01:23:06.526Z Has data issue: false hasContentIssue false
  • English
  • Français

Bivalvulidan (Myxozoa: Myxosporea) parasites of damselfishes with description of twelve novel species from Australia's Great Barrier Reef

Published online by Cambridge University Press:  05 September 2008

N. L. GUNTER  and
R. D. ADLARD
N. L. GUNTER
Affiliation:
Biodiversity Program, Queensland Museum, PO Box 3300, South Brisbane, Queensland 4101, Australia School of Molecular and Microbial Sciences, The University of Queensland, Brisbane, Queensland 4072, Australia
R. D. ADLARD*
Affiliation:
Biodiversity Program, Queensland Museum, PO Box 3300, South Brisbane, Queensland 4101, Australia School of Molecular and Microbial Sciences, The University of Queensland, Brisbane, Queensland 4072, Australia
*
*Corresponding author: Biodiversity Program, Queensland Museum, PO Box 3300, South Brisbane, Queensland 4101, Australia. Tel: +617 3840 7723. Fax: +617 3846 1226. E-mail: robert.adlard@qm.qld.gov.au
Get access Rights & Permissions [Opens in a new window]

Summary

Bivalvulidan parasites from the gall bladder of 31 species of damselfishes (family Pomacentridae) were examined for their taxonomic identity and their relatedness to other species of myxozoans. This paper describes 11 novel ceratomyxid species and a novel Myxidium sp. Each species is characterized morphologically and small subunit (SSU) rDNA sequences were used in molecular phylogenetic analyses. Five pomacentrid species were found to harbour multiple infections of bivalvulidan species. One species of Ceratomyxa and Myxidium were found to infect more than a single species of damselfish. Phylogenetic analyses revealed there has been no radiation of ceratomyxids that can be associated with the fish host taxon and that Myxidium queenslandicus n.sp. was more closely related to Zschokkella mugilis and Ellipsomyxa gobii than other members of the genus Myxidium.

Keywords

CeratomyxaMyxidiumMyxosporeaBivalvulidaPomacentridaediversityparasitephylogeny
Type
Original Articles
Information
Parasitology , Volume 135 , Issue 10 , September 2008 , pp. 1165 - 1178
Copyright
Copyright © 2008 Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Adlard, R. D. and Lester, R. G. (1994). Dynamics of the interaction between the parasitic isopod, Anilocra pomacentri, and the coral reef fish, Chromis nitida. Parasitology 109, 311–324.Google Scholar
Adlard, R. D. and O'Donoghue, P. J. (1998). Perspectives on the biodiversity of parasitic protozoa in Australia. International Journal for Parasitology 28, 887–897.Google Scholar
Allen, G. R. (1991). Damselfishes of the World. Mergus Publishers, Melle, Germany.Google Scholar
Australian Faunal Directory (2008). Australian Faunal Directory Checklist for SUPERCLASS: PISCES http://www.environment.gov.au/biodiversity/abrs/online-resources/fauna/afd/PISCES3/tree.htmlGoogle Scholar
Barker, S. C., Cribb, T. H., Bray, R. A. and Adlard, R. D. (1994). Host-parasite associations on a coral reef: pomacentrid fishes and digenean trematodes. International Journal for Parasitology 24, 643–647.Google Scholar
Bray, R. A., Cribb, T. H. and Barker, S. C. (1993). The Hemiuroidea (Digenea) of pomacentrid fishes (Perciformes) from Heron Island, Queensland, Australia. Systematic Parasitology 24,159–184.Google Scholar
Burger, M. A. A., Barnes, A. C. and Adlard, R. D. (2008). Wildlife as reservoirs for parasites infecting commercial species: host specificity and a redescription of Kudoa amamiensis from teleost fish in Australia. Journal of Fish Diseases (in the Press).CrossRefGoogle Scholar
Burger, M. A. A., Cribb, T. H. and Adlard, R. D. (2007). Patterns of relatedness in the Kudoidae with descriptions of Kudoa chaetodoni n. sp. and K. lethrini n. sp. (Myxosporea: Multivalvulida). Parasitology 134, 669–681.Google Scholar
Chambers, C. B., Cribb, T. H. and Jones, M. K. (2000). Tetraphyllidean metacestodes of teleosts of the Great Barrier Reef, and the use of in vitro cultivation to identify them. Folia Parasitologica 47, 285–292.CrossRefGoogle Scholar
Eiras, J. C. (2006). Synopsis of the species of Ceratomyxa Thelohan, 1892 (Myxozoa: Myxosporea; Ceratomyxidae). Systematic Parasitology 65, 49–71.Google Scholar
Egusa, S. and Nakajima, K. (1980). Kudoa amamiensis n. sp. (Myxosporea, Multivalvulida) found in cultured yellowtails and wild damselfishes from Amami-Ohshima and Okinawa, Japan. Bulletin of the Japanese Society of Scientific Fisheries 46, 1193–1198.Google Scholar
Fiala, I. (2006). The phylogeny of the Myxosporea (Myxozoa) based on small subunit ribosomal RNA gene analysis. International Journal for Parasitology 36, 1521–1534.Google Scholar
Hall, B. G. (2001). Phylogenetic Trees Made Easy: a How-To Manual for Molecular Biologists. Sinauer Assosiates Inc., Sunderland, MA, USA.Google Scholar
Hall, T. A. (1999). BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symposium Series 41, 95–98.Google Scholar
Hammer, Ø., Harper, D. A. T. and Ryan, P. D. (2001). PAST: Paleontological Statistics Software Package for Education and Data Analysis. Palaeontology Electronica 4, 9http://palaeo-electronica.org/2001_1/past/issue1_01.htmGoogle Scholar
Heiniger, H., Gunter, N. L. and Adlard, R. D. (2008). Relationships between four novel ceratomyxid parasites from the gall bladders of labrid fishes from Heron Island, Australia. Parasitology International 57, 158–165.Google Scholar
Heulsenbeck, J. P. and Ronquist, F. (2001). Bayesian inference of phylogeny. Biometrics 17, 754–755.Google Scholar
Jones, C. M., Nagel, L., Hughes, G. L., Cribb, T. H. and Grutter, A. S. (2007). Host specificity of two species of Gnathia (Isopoda) determined by DNA sequencing blood meals. International Journal for Parasitology 37, 927–935.Google Scholar
Lo, C. M. (1999). Mating rendezvous in monogenean gill parasites of the humbug Dascyllus aruanus (Pisces: Pomacentridae) Journal of Parasitology 85, 1178–1180.Google Scholar
Lom, J. and Arthur, J. R. (1989). A guideline for the preparation of species descriptions in Myxosporea. Journal of Fish Diseases 12, 151–156.Google Scholar
Lom, J. and Dyková, I. (1992). Protozoan Parasites of Fishes. Elsevier Science Publishers, Amsterdam, The Netherlands.Google Scholar
Lubat, J., Radujkovic, B., Marques, A. and Bouix, G. (1989). Parasites des poisons marins du Montenegro. Acta Adriatica 30, 31–50.Google Scholar
Moser, M., Kent, M. L. and Dennis, D. (1989). Gall bladder Myxosporea in coral reef fishes from Heron Island, Australia. Australian Journal of Zoology 37, 1–13.Google Scholar
Posada, D. and Crandall, K. A. (1998). Modeltest: testing the model of DNA substitution. Bioinformatics 14, 817–818.Google Scholar
Reimschuessel, R., Bennet, R. O., May, E. B. and Lipsky, M. M. (1987). Eosinophilic antigranulocytes-cell response to a microsporidian infection in a sergeant major fish, Abudefduf saxatilis (L). Journal of Fish Diseases 10, 319–322.Google Scholar
Swofford, D. L. (2002). PAUP*. Phylogenetic Analysis using Parsimony (*and otherMethods). Massachusetts, Sinauer Associates, Sunderland.Google Scholar
Thompson, J. D., Higgins, D. G. and Gibson, T. J. (1994). Clustal-W – Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Research 22, 4673–4680.CrossRefGoogle ScholarPubMed
Williams, E. H., Williams, L. B., Waldner, R. E. and Kimmel, J. J. (1982). Predisposition of a pomacentrid fish, Chromis multilinatus (Guichenot) to parasitism by a cymathoid isopod, Anilocra chromis (Williams and Williams). Journal of Parasitology 68, 942–945.Google Scholar
Whipps, C. M., Adlard, R. D., Bryant, M. S., Lester, R. J. G., Findlay, V. and Kent, M. L. (2003). The first report of three Kudoa species from Easter Australia: Kudoa thyrsites from Mahi mahi (Coryphaena hippurus), Kudoa amamiensis and Kudoa minthyrsites n. sp. from Sweeper (Pempheris ypsilychnus). Journal of Eukaryotic Microbiology 50, 215–219.Google Scholar
Yokoyama, H. and Shirakashi, S. (2007). Evaluation of hyposalinity treatment on infection with Enteromyxum leei (Myxozoa) using anemonefish Amphiprion spp. as experimental host. Bulletin of the European Association of Fish Pathology 27, 74–78.Google Scholar