Comparative sequence and structural analysis of the ORF095 gene, a vaccinia virus A4L homolog of capripoxvirus in sheep and goats.
Animals
Capripoxvirus
/ genetics
DNA, Viral
/ genetics
Genes, Viral
Goat Diseases
/ virology
Goats
/ virology
India
Open Reading Frames
Phylogeny
Polymerase Chain Reaction
Poxviridae Infections
/ veterinary
Sequence Alignment
Sequence Analysis, DNA
Sheep
/ virology
Sheep Diseases
/ virology
Species Specificity
Journal
Archives of virology
ISSN: 1432-8798
Titre abrégé: Arch Virol
Pays: Austria
ID NLM: 7506870
Informations de publication
Date de publication:
Jun 2020
Jun 2020
Historique:
received:
03
11
2019
accepted:
23
03
2020
pubmed:
21
4
2020
medline:
28
5
2020
entrez:
21
4
2020
Statut:
ppublish
Résumé
Sheeppox and goatpox are important transboundary animal viral diseases of sheep and goats caused by sheeppox virus (SPPV) and goatpox virus (GTPV), respectively, of the genus Capripoxvirus, family Poxviridae. Among the proteins encoded by the capripoxvirus (CaPV) genome, ORF095 (vaccinia virus A4L homolog) is an immunodominant virion core protein that plays a pivotal role in virus assembly and morphogenesis. In the present study, sequence analysis of the ORF095 genes of 27 SPPV and GTPV isolates or field samples from different geographical regions of India was performed, and structure was prediction was done by homology modeling. A multiple sequence alignment of different CaPV isolates revealed that CaPV-A4L is highly conserved, with several species-specific signature residues, namely A93, A216, A315, G136 and G146 in GTPV, G47, A63, A168 and A276 in SPPV, and G48 and C98 in lumpy skin disease virus (LSDV). Phylogenetically, the CaPV isolates were separated into three major clusters, GTPV, SPPV and LSDV, based on the complete coding sequence of the CaPV-A4L gene. Genus-specific clustering of poxviruses was observed in phylogenetic analysis based on A4L protein homologs of chordopoxviruses. A secondary structure prediction showed the presence of six α-helices and one β-sheet as well as some coils. The signature residues identified here are potentially useful for genotyping, and the predicted characteristics of the CaPV-A4L protein make it an ideal candidate for use as an immunogenic or diagnostic antigen for the development of immunoassays in the sero-evaluation of CaPV in target hosts.
Identifiants
pubmed: 32307603
doi: 10.1007/s00705-020-04623-5
pii: 10.1007/s00705-020-04623-5
doi:
Substances chimiques
DNA, Viral
0
Types de publication
Comparative Study
Journal Article
Langues
eng
Sous-ensembles de citation
IM