Salmon Pancreas Disease Virus, an Alphavirus Infecting Farmed Atlantic Salmon, Salmo salar L

• Published in: Virology (New York, N.Y.) N.Y.), 1999-04, Vol.256 (2), p.188-195
• Main Authors: Weston, Jonathan H., Welsh, Michael D., McLoughlin, Marian F., Todd, Daniel
• Format: Article
• Language: English
• Subjects: 3' Untranslated Regions; Alphavirus; Alphavirus - genetics; Alphavirus Infections - veterinary; Alphavirus Infections - virology; Amino Acid Sequence; Animals; Base Sequence; Cell Line; Cloning, Molecular; DNA, Viral; Fish Diseases - virology; Genome, Viral; Marine; Molecular Sequence Data; Salmo salar; Salmo salar - virology; salmon pancreas disease virus; salmon pancrease disease virus; Sequence Analysis, RNA; Sequence Homology, Nucleic Acid; Vira; Viral Envelope Proteins - genetics
• ISSN: 0042-6822; 1096-0341
• DOI: 10.1006/viro.1999.9654

A 5.2-kb region at the 3′ terminus of the salmon pancreas disease virus (SPDV) RNA genome has been cloned and sequenced. The nucleotide and predicted amino acid sequences show that SPDV shares considerable organizational and sequence identity to members of the genus alphavirus within the family Togaviridae. The SPDV structural proteins encoded by the 5.2-kb region contain a number of unique features when compared to other sequenced alphaviruses. Based on cleavage site homologies, the predicted sizes of the SPDV envelope glycoproteins E2 (438 aa) and E1 (461 aa) are larger than those of other alphaviruses, while the predicted size of the alphavirus 6K protein is 3.2 K (32 aa) in SPDV. The E2 and E1 proteins each carry one putative N-linked glycosylation site, with the site in E1 being found at a unique position. From amino acid sequence comparisons of the SPDV structural region with sequenced alphaviruses overall homology is uniform, ranging from 32 to 33%. While nucleotide sequence analysis of the 26S RNA junction region shows that SPDV is similar to other alphaviruses, analysis of the 3′-nontranslated region reveals that SPDV shows divergence in this region.