| Literature DB >> 25733388 |
Qian Chen1, Jie Ma2, Yuding Fan2, Yan Meng2, Jin Xu2, Yong Zhou2, Wenzhi Liu2, Xianhui Zeng2, Lingbing Zeng3.
Abstract
The type I IFNs play a major role in the first line of defense against virus infections. In this study, the type I IFN gene designated gsIFN was identified and characterized in the Chinese giant salamander (Andrias davidianus). The genomic DNA of gsIFN contains 5 exons and 4 introns and has a total length of 5622 bp. The full-length cDNA sequence of gsIFN is 1113 bp and encodes a putative protein of 186 amino acids that has a 43% identity to type I IFN of Xenopus tropicalis. The deduced amino acid sequence has the C-terminal CAWE motif, that is mostly conserved in the higher vertebrate type I IFNs. Real-time fluorescence quantitative RT-PCR analysis revealed broad expression of gsIFN in vivo and the highest level expression in blood, kidney and spleen. Additionally, the expression of gsIFN at the mRNA level was significantly induced in peripheral blood leucocytes after stimulation with poly I:C and after infection with the Chinese giant salamander iridovirus (GSIV). A plasmid expressing gsIFN was constructed and transfected into the Chinese giant salamander muscle cell line. Expression of the IFN-inducible gene Mx was up-regulated in the gsIFN-overexpressing cells after GSIV infection. The virus load and titer were significantly reduced compared with that in control cells. Additionally, a lower level of virus major capsid protein synthesis was confirmed by immunofluorescence assay compared to the control cells. These results suggest that the gsIFN gene plays an important role in the antiviral innate immune response.Entities:
Keywords: Andrias davidianus; Antiviral activity; Chinese giant salamander; Innate immunity; Type I IFN
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Year: 2015 PMID: 25733388 DOI: 10.1016/j.molimm.2015.02.015
Source DB: PubMed Journal: Mol Immunol ISSN: 0161-5890 Impact factor: 4.407