4.6 Article

The Two Groups of Zebrafish Virus-Induced Interferons Signal via Distinct Receptors with Specific and Shared Chains

Journal

JOURNAL OF IMMUNOLOGY
Volume 183, Issue 6, Pages 3924-3931

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.0901495

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Funding

  1. Agence Nationale pour la Recherche [MIME2007]
  2. Institut Pasteur, and Institut National de la Recherche Agronomique [PTR231]
  3. The Danish Cancer Society [95095721]
  4. Novo Nordisk Foundation
  5. The Danish Medical Research Council [22-04-0704]
  6. The Carlsberg Foundation
  7. Ame Hansen stipend
  8. U.S. Public Health Services
  9. National Institute of Allergy and Infectious Diseases [R01 AI057468]

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Because the availability of fish genomic data, the number of reported sequences for fish type II helical cytokines is rapidly growing, featuring different IFNs including virus-induced IFNs (IFN phi) and IFN-gamma, and IL-10 with its related cytokines (IL-20, IL-22, and IL-26). Many candidate receptors exist for these cytokines and various authors have postulated which receptor chain would be involved in which functional receptor in fish. To date, only the receptor for zebrafish IFN phi 1 has been identified functionally. Three genes encoding virus-induced IFN phi s have been reported in zebrafish. In addition to these genes clustered on chromosome 3, we have identified a fourth IFN phi gene on chromosome 12. All these genes possess the intron-exon organization of mammalian lambda IFNs. In the zebrafish larva, all induce the expression of reporter antiviral genes; protection in a viral challenge assay was observed for IFN phi 1 and IFN phi 2. Using a combination of gain- and loss-of-function experiments, we also show that all zebrafish IFN phi s do not bind to the same receptor. Two subgroups of fish virus-induced IFNs have been defined based on conserved cysteines, and we find that this subdivision correlates with receptor usage. Both receptor complexes include a common short chain receptor (CRFB5) and a specific long chain receptor (CRFB1 or CRFB2). The Journal of Immunology, 2009, 183: 3924-3931.

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