From the right-hand end of the ectromelia virus (strain Moscow) genome, 323
18 bps have been sequenced, and characterized to include a total of 18 open
reading frames (ORFs) and six regions which apparently no longer code for
functional proteins. At least six of the ORFs appear to be involved in bloc
king the inflammatory/immune host response to infection, and therefore prob
ably contribute significantly to the virulence of this virus in its natural
host, the mouse. One of these genes encoded an isolog of the poxvirus chem
okine binding protein, and was shown to be the most abundant protein secret
ed from ectromelia virus infected cells. Two regions were found to have sig
nificant similarity to poxvirus genes encoding tumor necrosis factor (TNF)
binding proteins. Both are distinct from cytokine response modifier (crm)B
and crmC but only one is predicted to encode a functional TNF binding prote
in. A novel similarity between the C-terminal domain of poxvirus TNF bindin
g proteins and several other poxvirus proteins is also presented. The resul
ts are discussed in the context of ectromelia virus pathogenesis of mice. (
C) 2000 Elsevier Science B.V. All rights reserved.