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dc.contributor.authorMortensen, Stein
dc.contributor.authorSælemyr, Lisbeth
dc.contributor.authorSkår, Cecilie K.
dc.contributor.authorBodvin, Torjan
dc.contributor.authorJelmert, Anders
dc.date.accessioned2016-09-21T06:46:16Z
dc.date.available2016-09-21T06:46:16Z
dc.date.issued2016-02
dc.identifier.issn1893-4536
dc.identifier.urihttp://hdl.handle.net/11250/2409000
dc.description.abstractNorwegian populations of European flat oysters, Ostrea edulis, have been considered free from notifiable diseases. In 2006, microcells resembling the oyster parasite Bonamia sp. were observed during histopathological examination of tissue specimens of flat oysters, Ostrea edulis from the Arendal area, southern Norway. In 2008, the EU reference laboratory received samples from the Norwegian Veterinary Institute, and reported one Bonamia sp. in a haemocyte from one oyster. By real-time PCR, positive results were obtained from two oysters in one triplicate sample. Sequencing of the PCR products gave 100% identity with B. ostreae. After this diagnose, both the Norwegian Veterinary Institute and The Institute of Marine Research have monitored the population. The observed microcells have been observed since the sampling at the site was initiated, always at a low prevalence and intensity. No inflammation, pathology or reductions of the oyster's condition have been associated with the observation. The population appears healthy, with a normal reproductive cycle pattern. Several cohorts have been present throughout the study period. Since 2009, more than 2 200 oysters have been examined by histology, and samples from 581 of the oysters have been analyzed by PCR, all with negative results. The situation has thus been stable since 2006. A 10 years long sub-clinical Bonamia infection seems unlikely. If the diagnosis from 2009 is correct, Bonamia must be present at a very low prevalence, escaping PCR detection due to the sample sizes in the present study and living in co-existence with the oysters, thus not killing its host. One possible explanation is that the observed cells are not closely related to Bonamia ostreae, but another organism not detected by the assays used. We will perform a new extraction of DNA from haemocytes during spring and summer 2016, when the microcells are presumably present. As the situation has been unchanged for 10 years, there is no need to sample 150 oysters every six months. The sample size may be reduced to 60. We recommend however restrictions on the movement of bivalve into, and out of, this area, until results from the sampling in spring 2016 has been analyzed and reported.nb_NO
dc.publisherHavforskningsinstituttetnb_NO
dc.relation.ispartofseriesRapport fra Havforskningen;11-2016
dc.titleHealth surveillance of the flat oyster populations in Aust-Agder County, southern Norway in the period 2009 – 2015nb_NO
dc.typeWorking papernb_NO
dc.subject.nsiVDP::Mathematics and natural science: 400::Zoology and botany: 480::Marine biology: 497nb_NO
dc.source.pagenumber11 s.nb_NO


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