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Physiol. Genomics (September 5, 2007). doi:10.1152/physiolgenomics.00064.2007
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Submitted on March 19, 2007
Accepted on August 24, 2007

Interferon type I and type II responses in an Atlantic salmon (Salmo salar) SHK-1 cell line using the salmon TRAITS/SGP microarray

Sam A M Martin1*, John B Taggart2, Paul J Seear3, James E Bron2, Richard Talbot4, Alan J Teale2, Glen E Sweeney3, Bjorn Hoyheim5, Dominic F. Houlihan6, Douglas R Tocher2, Jun Zou7, and Chris J Secombes1

1 School of Biological Sciences, University of Aberdeen, United Kingdom
2 Inst Aquaculture, University of Stirling, United Kingdom
3 School of Biosciences, Cardiff University, United Kingdom
4 ARK Genomics, Roslin Institute, United Kingdom
5 Norweign School of Veterinary Sciences, Norway
6 Research and Commercialisation, Univ Aberdeen, ABERDEEN, United Kingdom
7 School of Biological Sciences, University of Aberdeen, Aberdeen, aberdeen, United Kingdom

* To whom correspondence should be addressed. E-mail: sam.martin{at}abdn.ac.uk.

Interferons (IFN) are cytokines that have proinflammatory, antiviral and immunomodulatory effects, and play a central role during a host response to pathogens. The IFN family contains both type I and type II molecules. Whilst there are a number of class I IFNs, there is only one class II IFN. Recently both type I and type II IFN genes have been cloned in salmonid fish and recombinant proteins produced showing IFN activity. We have stimulated an Atlantic salmon cell line (SHK-1) with both type I and type II recombinant salmonid IFNs and analysed the transcriptional response by microarray analysis. Cells were exposed to recombinant IFNs for 6 or 24 h or left unexposed as controls. RNA was hybridised to an Atlantic salmon cDNA microarray (salmon 17K feature TRAITS/SGP array) in order to assess differential gene expression in response to IFN exposure. For IFN I and II, 47 and 72 genes were stimulated respectively, most genes were stimulated by a single interferon type, however, some were affected by both IFNs indicating co-regulation of the IFN response in fish. Real-time PCR analysis was employed to confirm the microarray results for selected differentially expressed genes in both a cell line and primary leukocyte cultures.







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