Construction and Biological Characterization of ORF133-Deletion Mutant of Lumpy Skin Disease Virus.

Abstract

Lumpy skin disease virus (LSDV), agenus member, causes severe cattle disease. Thoughshare high nucleotide sequence homology indicating common ancestry, they have evolved distinct host adaptations. The LSDV genome encodes numerous proteins, with ORF133 being LSDV-specific and lacking clear homologs in other, implying potential roles in host range and virulence. To explore ORF133's function, this study generated mouse polyclonal antibodies against ORF133 and constructed the ORF133-deleted recombinant virus (LSDVΔORF133-EGFP) via homologous recombination with an EGFP reporter. Preliminary characterization showed that ORF133 deletion affects viral replication. This study provides critical tools and theoretical references for subsequent investigations into the functional mechanisms underlying ORF133 in LSDV.