Abstract:[Background] Pseudorabies virus (PRV) has been mutating since 2011 and the classical vaccine strain can no longer completely resist the infections of PRV variants. There have been outbreaks of pseudorabies in many domestic pig farms and the PRV variants have become prevalent in China. [Objective] To isolate a PRV variant, analyze its genetic evolution and pathogenicity, and provide experimental data for the epidemiological investigation and vaccine development of PRV. [Methods] The brain tissue samples infected with PRV were collected from a pig farm in Heilongjiang province. The primers were designed according to gE and gB conserved sequences of PRV in GenBank for PCR identification. The gE and gC genes were sequenced for phylogenetic analysis. The virus was isolated from BHK-21 cells by plaque purification method and further identified by electron microscopy and indirect immunofluorescence. The growth curve was established and the pathogenicity was studied. [Results] The isolate was identified as a PRV epidemic strain by PCR and sequencing and named HLJ-01. The phylogenetic tree showed that the isolate was in the same clade with the epidemic variants isolated in recent years in China. The results of amino acid sequence analysis showed that gE and gC of the isolate had the characteristic sequences of domestic epidemic variants, indicating that the isolate was an epidemic variant. The growth curve showed that the titer of HLJ-01 was the highest (108.5 TCID50/mL) 48 h after infection. The virus particle of HLJ-01 had the diameter of about 150 nm, and it was a sphere with envelope and radial spikes outside, presenting typical characteristics of PRV. The animal infection experiments showed that the mortality rates of 107.0, 106.0, and 105.0 TCID50 infection groups were 100%, 80%, and 60%, respectively. After inoculation of HLJ-01, all the piglets showed typical symptoms and pathological changes of PRV infection, which confirmed that HLJ-01 had strong pathogenicity to piglets. [Conclusion] An epidemic variant of PRV with strong pathogenicity was isolated and identified, which laid a foundation for the epidemiological analysis of PRV and the screening of candidate vaccine strains.