Comparative sequence and structural analysis of the ORF095 gene, a vaccinia virus A4L homolog of capripoxvirus in sheep and goats.


Journal

Archives of virology
ISSN: 1432-8798
Titre abrégé: Arch Virol
Pays: Austria
ID NLM: 7506870

Informations de publication

Date de publication:
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

Pagination

1419-1431

Auteurs

Aparna Madhavan (A)

Division of Virology, ICAR-Indian Veterinary Research Institute, Mukteswar 263 138, Nainital District, Uttarakhand, India.

Gnanavel Venkatesan (G)

Division of Virology, ICAR-Indian Veterinary Research Institute, Mukteswar 263 138, Nainital District, Uttarakhand, India. gnanamvirol@gmail.com.

Amit Kumar (A)

Division of Virology, ICAR-Indian Veterinary Research Institute, Mukteswar 263 138, Nainital District, Uttarakhand, India.

Sargam Arya (S)

Division of Virology, ICAR-Indian Veterinary Research Institute, Mukteswar 263 138, Nainital District, Uttarakhand, India.

A B Pandey (AB)

Division of Virology, ICAR-Indian Veterinary Research Institute, Mukteswar 263 138, Nainital District, Uttarakhand, India.

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