Affiliation:
1. Plum Island Animal Disease Center, Agricultural Research Service, U.S. Department of Agriculture, Greenport, New York 11944-0848
Abstract
ABSTRACT
Sequence analysis of the right variable genomic region of the pathogenic African swine fever virus (ASFV) isolate E70 revealed a novel gene,
UK
, that is immediately upstream from the previously described ASFV virulence-associated gene
NL-S
(L. Zsak, Z. Lu, G. F. Kutish, J. G. Neilan, and D. L. Rock, J. Virol. 70:8865–8871, 1996).
UK
, transcriptionally oriented toward the right end of the genome, predicts a protein of 96 amino acids with a molecular mass of 10.7 kDa. Searches of genetic databases did not find significant similarity between
UK
and other known genes. Sequence analysis of the
UK
genes from several pathogenic ASFVs from Europe, the Caribbean, and Africa demonstrated that this gene was highly conserved among diverse pathogenic isolates, including those from both tick and pig sources. Polyclonal antibodies raised against the UK protein specifically precipitated a 15-kDa protein from ASFV-infected macrophage cell cultures as early as 2 h postinfection. A recombinant
UK
gene deletion mutant, ΔUK, and its revertant, UK-R, were constructed from the E70 isolate to study gene function. Although deletion of
UK
did not affect the growth characteristics of the virus in macrophage cell cultures, ΔUK exhibited reduced virulence in infected pigs. While mortality among parental E70- or UK-R-infected animals was 100%, all ΔUK-infected pigs survived infection. Fever responses were comparable in E70-, UK-R-, and ΔUK-infected groups; however, ΔUK-infected animals exhibited significant, 100- to 1,000-fold, reductions in viremia titers. These data indicate that the highly conserved
UK
gene of ASFV, while being nonessential for growth in macrophages in vitro, is an important viral virulence determinant for domestic pigs.
Publisher
American Society for Microbiology
Subject
Virology,Insect Science,Immunology,Microbiology