Different activation of STAT1 and STAT2 phosphorylation by IFNc, IFNd, and IFNh in tilapia.

Type I IFNs are a subset of cytokines exerting their antiviral effects mainly through the JAK-STAT signalling. Immunogenetic studies have shown that fish possess key components of IFN-JAK-STAT cascade, but the information about the distinct responses of STAT1 and STAT2 to different IFNs is rather limited in fish. Here, we identified and cloned STAT1 and STAT2 genes (named as On-STAT1 and On-STAT2) from tilapia, Oreochromis niloticus. On-STAT1 and On-STAT2 genes were detected in all orangs/tissues examined, and were rapidly induced in spleen, head kidney, and liver following the stimulation of poly(I:C). In addition, the stimulation of poly(I:C), poly(A:T), and different subgroups of recombinant IFNs could induce the expression of On-STAT1 and On-STAT2 in TA-02 cells with distinct induction levels. Importantly, On-STAT2 was rapidly phosphorylated by all three subgroups of IFNs, but the phosphorylation of On-STAT1 was only observed in IFNc- and IFNh-treated TA-02 cells, reflecting the distinct activation of STAT by different subgroups of fish IFNs. The present results thus contribute to better understanding of the JAK-STAT signalling mediated by different subgroups of IFNs in fish. • STAT1 and STAT2 genes were identified and characterized in tilapia. • STAT1 and STAT2 genes were ubiquitously expressed in all tested tissues and up-regulated after poly(I:C) stimulation in vivo. • Poly(I:C) and poly(A:T) differently induced the expression of STAT1 and STAT2 in TA-02 cells. • Recombinant IFNc, IFNd, and IFNh markedly induced the expression of STAT1 and STAT2 in TA-02 cells. • Recombinant IFNc, IFNd, and IFNh differently induced the tyrosine phosphorylation of STAT1 and STAT2 in TA-02 cells. [ABSTRACT FROM AUTHOR]