Capripoxviruses : Exploring the genetic relatedness between field and vaccine strains from Egypt

• Published in: Veterinary World 2019-12, Vol.12 (12), p.1924-1930
• Main Authors: Rouby, Sherin Reda, Bazid, Abdel-Hamid, Wasfy, Momtaz, El-Sayed, Magdy
• Format: Article
• Language: English
• Subjects: Amino acids; Analysis; Capripoxvirus; Cell culture; Characterization; Chromatin; Culture; Deoxyribonucleic acid; Diseases; DNA; Farms; Fetuses; G protein-coupled receptors; g protein-coupled receptors gene; G proteins; Genes; Genetic diversity; Homology; Identity; Isolation; Kidneys; Lumpy skin disease; Lysergide; Oligonucleotides; phylogenetic; Phylogenetics; Phylogeny; Polymerase chain reaction; romanian; Sheep; Skin; Skin diseases; Skin lesions; Strains (organisms); Vaccination; Vaccines; Virulence (Microbiology); Viruses
• ISSN: 0972-8988; 2231-0916
• DOI: 10.14202/vetworld.2019.1924-1930

Lumpy skin disease (LSD) and sheep pox are economically important -induced diseases of cattle and sheep, respectively. Despite the extensive vaccination program adopted by Egyptian veterinary authorities, LSD and sheep pox are still prevalent and spread throughout the whole country. The current study was designed for molecular characterization and phylogenetic analysis of LSD virus (LSDV) and (SPPV) recovered from field cases in Egypt along with vaccinal strains to assess their genetic relatedness. Skin biopsies were collected from naturally infected cases of LSD in Ismailia (n=3 farms) and Beni-Suef (n=2 farms) Governorates and sheep pox in Beni-Suef (n=1 flock). Virus isolation was carried out on primary ovine fetal kidney and heart cell cultures. DNA was extracted from infected materials (skin lesions, infected cell cultures) as well as LSDV Neethling vaccine strain and Romanian SPPV vaccine strain. Polymerase chain reaction was performed using oligonucleotide primers targeting the entire open reading frame of G protein-coupled receptors (GPCR) gene and gene sequences were analyzed. Virus isolation on primary ovine fetal kidney and heart cell culture revealed a cytopathic effect at the third passage characterized by rounding of infected cells and margination of nuclear chromatin. Comparative sequence analysis of GPCR gene revealed that Egyptian LSDV isolated from Ismailia and Beni-Suef shared 99:100% nucleotide and amino acid (AA) identities with each other. In comparison to the vaccinal strains, Egyptian LSDV isolates shared 98:99 nucleotide and AA identities with LSDV Neethling vaccine strain and 93:94% with SPPV Romanian vaccine strain. No differences at the nucleotide or AAs were observed between the SPPV vaccine and virulent strains (100% identity). Phylogenetic analyses revealed that LSDV Neethling vaccine strain is more related to field Egyptian LSDV and clustered within the LSDV group while Romanian SPPV vaccine strain clustered in a separate clade with SPPV field isolates. Comparative sequencing and phylogenetic analyses of the GPCR gene reveal a minimal genetic variation between LSDV field isolates from different locations and a close relationship between virulent field strains and homologous vaccines.