<I>Gyrodactylus salaris</I> Malmberg, 1957, a monogenean parasite of salmonid fish, has caused the death of up to 95% of salmon parr in 37 Norwegian rivers. In order to prevent further spread of this parasite, a reliable method of identifying <I>G. salaris</I> and distinguishing it from other closely related species is required. This study, the first investigation of <I>Gyrodactylus</I> genetics, has demonstrated that DNA technology can provide methods of gyrodactylid species identification suitable for routine use. DNA was extracted from <I>G. salaris</I> and two other species common on salmonid fish; <I>G. derjavini</I> and <I>G. truttae</I>. The small subunit ribosomal RNA (srRNA) gene was amplified from this DNA by polymerase chain reaction (PCR). The complete nucleotide sequence of the srRNA gene from <I>G. salaris</I> was determined. This was used to predict a secondary structure for gyrodactylid srRNA and to construct molecular phylogenies of platyhelminths including <I>Gyrodactylus. </I>Fragments of the srRNA gene from each species were compared by Denaturing Gradient Gel Electrophoresis. Mobility differences in <I>G. truttae</I> fragments were found and one fragment showed variation between and within species. The V4 region of srRNA was amplified from single specimens of gyrodactylids using a combined lysis and PCR reaction and sequenced. Examination of these sequences enabled prediction of Restriction Fragment Length Polymorphisms (RFLPs) between species and the design of oligonucleotide probes specific for each species. Digestion of the srRNA gene V4 region with two restriction enzymes produced restriction fragment polymorphisms that can be used to discriminate between <I>G. salaris</I>, <I>G. derjavini</I> and <I>G. truttae</I>. The digoxigenin labelled oligonucleotides GsV4, GdV4 and GdV4 are specific for <I>G. salaris, G. derjavini</I> and <I>G. truttae</I> respectively and can detect PCR amplified DNA from single specimens in dot blots. Both RFLP and probe methods of identifying <I>Gyrodactylus </I>species are suitable for use in diagnostic laboratories.
| Identifer | oai:union.ndltd.org:bl.uk/oai:ethos.bl.uk:239923 |
| Date | January 1995 |
| Creators | Cunningham, Carey O. |
| Publisher | University of Aberdeen |
| Source Sets | Ethos UK |
| Detected Language | English |
| Type | Electronic Thesis or Dissertation |
| Source | http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU068351 |
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