Identification and characterization of a rabbit novel IFN-α unlocated in genome
The multigene family of rabbit IFN-α (RbIFN-α) is located on chromosome 1, which shows seven functional genes in type I IFN locus. A novel RbIFN-α that remains unlocated in the rabbit genome was amplified and designated as the first novel rabbit IFN-α (RbIFN-αNov1), which possesses the typical molec...
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Veröffentlicht in: | Developmental and comparative immunology 2018-01, Vol.78, p.91-99 |
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Sprache: | eng |
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Zusammenfassung: | The multigene family of rabbit IFN-α (RbIFN-α) is located on chromosome 1, which shows seven functional genes in type I IFN locus. A novel RbIFN-α that remains unlocated in the rabbit genome was amplified and designated as the first novel rabbit IFN-α (RbIFN-αNov1), which possesses the typical molecular characteristics of type I IFNs and could be induced in RK-13 cells and peripheral blood mononuclear cells. After the mature peptide of RbIFN-αNov1 was expressed, its antiviral activity, physicochemical characteristics, and cytotoxicity were determined in vitro. Results indicated that RbIFN-αNov1 exerted a high specific antiviral activity against VSV and a low cytotoxic effect on RK-13 cells. RbIFN-αNov1 showed high sensitivity to trypsin and remained relatively stable after acid, alkali, or heat treatment. RbIFN-αNov1 could induce Mx1 expression on RK-13 cells and activate the NF-κB, ISRE and BoIFN-β promoter activities on bovine testicular cells. Overall, our research on RbIFN-αNov1 not only enriches the knowledge about rabbit IFNs but also makes RbIFN-αNov1 have the potential to be used as an effective therapeutic agent for rabbit viral diseases.
•Rabbit type I interferon locus was constructed and analyzed.•An unlocated rabbit IFN-α designated as RbIFN-αNov1 was characterized.•RbIFN-αNov1 has broad antiviral activity and antiproliferative activity.•RbIFN-αNov1 can induce Mx1 expression to exert antiviral activity.•RbIFN-αNov1 can induce NF-κB, ISRE and BoIFNβ promotor activity on BT cells. |
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ISSN: | 0145-305X 1879-0089 |
DOI: | 10.1016/j.dci.2017.09.016 |