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dc.contributor.authorGanjoor, M.S.
dc.contributor.authorZorriehzahra, S.J.
dc.contributor.authorMehrabi, M.R.
dc.contributor.authorGhaedi, A.R.
dc.contributor.authorGhasemi, M.
dc.contributor.authorRastiannasab, A.
dc.coverage.spatialIranen_US
dc.coverage.spatialKohgiluyeh and Boyer-Ahmad provinceen_US
dc.coverage.spatialYasujen_US
dc.date.accessioned2018-03-12T12:57:57Z
dc.date.available2018-03-12T12:57:57Z
dc.date.issued2017
dc.identifier.issn1026-1354
dc.identifier.urihttp://hdl.handle.net/1834/12377
dc.description.abstractIHNV (Infectious Hematopoietic Necrosis Virus) is one of the most important pathogens in cultured rainbow trout (Oncorhynchus mykiss). The virus causes the disease that affects the hematopoietic tissue and blood vessels of fish, especially in larvae and fingerling stages. The disease is highly contagious and causes mass fish casualty (up to 95%). Therefore, continuous health monitoring of fish farms is necessary. The objectives of the present study were to identify and track the probable presence of the virus in fish farm in Dasht-e-Rome, Kohgiluyeh and Boyer-Ahmad province, Iran. Samples were prepared from the liver, spleen, kidney, egg, sperm and larvae of the adult fish and broodfish during four years from 2012 to 2016. About one percent of the broodstock population was used for sampling (1%×3000 broodfish×4years=120fish). In order to detect the presence of IHN-virus, samples were sent to a laboratory in frozen condition. After preparation of samples, they were inoculated with two types of cell line (BF2 and EPC) and examined by the molecular methods (Reverse Transcriptase-PCR) to detect the presence of IHN virus. The results showed that all samples were free from the IHN virus and the frequency of virus was 0% in all examined samples.en_US
dc.language.isofaen_US
dc.relation.urihttp://isfj.areo.ir/en_US
dc.subject.otherOncorhynchus mykissen_US
dc.titleContinuous health monitoring and disapproval of IHN (Infectious Hematopoietic Necrosis Virus) presence in rainbow trout (Oncorhynchus mykiss) broodstock by cell culture and molecular methods (RT-PCR) from 2012 to 2016 in the suburb of Yasuj (Iran).en_US
dc.typeJournal Contributionen_US
dc.bibliographicCitation.issue4en_US
dc.bibliographicCitation.titleIranian Scientific Fisheries Journalen_US
dc.bibliographicCitation.volume26en_US
dc.description.statusPublisheden_US
dc.format.pagerangepp.189-193en_US
dc.subject.asfaCold water fishen_US
dc.subject.asfaViral diseaseen_US
dc.subject.asfaIHNen_US
dc.subject.asfaRT-PCR molecular methoden_US
dc.type.refereedRefereeden_US
refterms.dateFOA2021-01-30T18:48:20Z


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