| Literature DB >> 25080482 |
Jun Zou1, Bartolomeo Gorgoglione2, Nicholas G H Taylor3, Thitiya Summathed4, Po-Tsang Lee4, Akshaya Panigrahi4, Carine Genet5, Young-Mao Chen6, Tzong-Yueh Chen6, Mahmood Ul Hassan7, Sharif M Mughal8, Pierre Boudinot9, Christopher J Secombes1.
Abstract
Fish type I IFNs are classified into two groups with two (group I) or four (group II) cysteines in the mature peptide and can be further divided into four subgroups, termed IFN-a, -b, -c, and -d. Salmonids possess all four subgroups, whereas other teleost species have one or more but not all groups. In this study, we have discovered two further subgroups (IFN-e and -f) in rainbow trout Oncorhynchus mykiss and analyzed the expression of all six subgroups in rainbow trout and brown trout Salmo trutta. In rainbow trout RTG-2 and RTS-11 cells, polyinosinic-polycytidylic acid stimulation resulted in early activation of IFN-d, whereas the IFN-e subgroup containing the highest number of members showed weak induction. In contrast with the cell lines, remarkable induction of IFN-a, -b, and -c was detected in primary head kidney leukocytes after polyinosinic-polycytidylic acid treatment, whereas a moderate increase of IFNs was observed after stimulation with resiquimod. Infection of brown trout with hemorrhagic septicemia virus resulted in early induction of IFN-d, -e, and -f and a marked increase of IFN-b and IFN-c expression in kidney and spleen. IFN transcripts were found to be strongly correlated with the viral burden and with marker genes of the IFN antiviral cascade. The results demonstrate that the IFN system of salmonids is far more complex than previously realized, and in-depth research is required to fully understand its regulation and function.Entities:
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Year: 2014 PMID: 25080482 DOI: 10.4049/jimmunol.1301796
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422