Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/28532
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dc.contributor.advisorWeidmann, Manfred-
dc.contributor.advisorMacKenzie, Simon-
dc.contributor.authorMcGowan, Michael John-
dc.date.accessioned2019-01-17T15:09:58Z-
dc.date.available2019-01-17T15:09:58Z-
dc.date.issued2018-04-
dc.identifier.urihttp://hdl.handle.net/1893/28532-
dc.description.abstractAccurate smoltification and disease management in Atlantic salmon (Salmo salar) are key issues for the aquaculture industry. Due to their anadromous lifecycle the transfer of salmon from fresh water (FW) to seawater (SW) is crucial to their survival; too early can cause mortality, too late can cause desmoltification and long-term health problems. Both scenarios can increase susceptibility to four viral diseases: Salmon alphavirus (SAV), Infectious salmon anemia virus (ISAV), orthoreovirus (PRV), and Piscine myocarditis virus (PMCV). They all show similar clinical and histopathological symptoms and can easily spread throughout farms. Understanding the initial innate immune response to these viruses may provide biomarkers that could help identify and monitor infections. An in house and onsite Na+/K+ ATPase (NKA) qRT-PCR assay was developed for the salmon biomarker ATPase to test smoltification readiness in salmon smolts. Tested against NKA enzymatic assays it showed a similar success rate over 3 years: NKA qRT-PCR (57%), NKA activity assay (60%). Onsite tests confirmed that the ATPase mRNA transcript is a useful biomarker for smoltification detection. An in-lab and mobile multiplex qRT-PCR assay was developed for detection of SAV, PRV and PMCV. The analytical sensitivity of the SAV (86.5% SE 0.11), PRV (90.94%, SE 0.09) and PMCV (100.46%, SE 0.19) assays was 102 copies for PMCV and 103 for SAV and PRV. Initial results suggest individual assays could be run on site at farms. Addition of an internal control, probit analysis and viral positive tests are still required for multiplex assay integration. Salmon erythrocytes were infected with ISAV, SAV and Poly I:C to investigate whether they induce and up-regulate innate immune response genes. All genes were expressed at low levels in all parameters investigated including non-infected control erythrocytes. These findings suggest erythrocytes act as an initial buffer to viral infections and may help stimulate the innate immune response.en_GB
dc.language.isoenen_GB
dc.publisherUniversity of Stirlingen_GB
dc.subjectSalmonen_GB
dc.subjectsmoltificationen_GB
dc.subjectATPaseen_GB
dc.subjectPMCVen_GB
dc.subjectinnate immunityen_GB
dc.subjecterythrocytesen_GB
dc.subjectSAVen_GB
dc.subjectPRVen_GB
dc.subjectMultiplexen_GB
dc.subjectMobile diagnosticsen_GB
dc.subjectqRT-PCRen_GB
dc.subjectqPCRen_GB
dc.subjectPCRen_GB
dc.subject.lcshSalmonen_GB
dc.subject.lcshErythrocytesen_GB
dc.subject.lcshAnadromous fishesen_GB
dc.subject.lcshSalmon Infections.en_GB
dc.titleMolecular regulators of smoltification and viral infection management tools for salmon aquacultureen_GB
dc.typeThesis or Dissertationen_GB
dc.type.qualificationlevelDoctoralen_GB
dc.type.qualificationnameDoctor of Philosophyen_GB
dc.contributor.funderEuropharma, Innovate UK, SAICen_GB
dc.author.emailmikel2564@gmail.comen_GB
dc.contributor.affiliationAquacultureen_GB
Appears in Collections:Aquaculture eTheses



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