Mr protein is one of several antiviral proteins that are induced by the typ
e I interferons (IFN), IFN alpha and beta, in mammals. In this work inducti
on of a 76 kDa Mr protein by double-stranded RNA (dsRNA) or type I IFN-like
activity in Atlantic salmon macrophages, Atlantic salmon fibroblast cells
(AS cells) and in Chinook salmon embryo cells (CHSE-214) is reported. Type
I IFN-like activity was produced by the stimulation of Atlantic salmon macr
ophages with the synthetic dsRNA polyinosinic polycytidylic acid (poly I:C)
. A correlation appeared to exist between Mr protein expression and protect
ion against infectious pancreatic necrosis virus (IPNV) induced by IFN in C
HSE-214 cells. Several observations in the present work suggest that, as in
mammals, the induction of Mr protein by dsRNA in fish cells primarily occu
rs via induction of type I IFN. First, type I IFN-like activity but not pol
y I:C, induced Mx protein expression in CHSE-214 cells. These cells apparen
tly lack the ability to produce IFN in response to poly I:C. Second, the pu
tative IFN induced maximal Mr protein expression 48 h earlier than poly I:C
in AS cells. Third, the peak expression of Mr protein in macrophages induc
ed by poly I:C occurred after 48 h whereas peak in IFN-like activity was ob
served by 24 h after addition of poly I:C. The present work supports the no
tion of using Mr protein as a molecular marker for the production of putati
ve type I IFN in fish. (C) 2000 Academic Press.