Pseudorabies virus (PRV)
infection could cause severe histopathological damage via releasing multiple factors, including
cytokines,
peptides, etc. Here, peptidomic results showed that 129
peptides were identified in PRV-infected mouse lungs and were highly involved in the process of PRV
infection. The role of one down-regulated biological
peptide (designated as AGDP) during PRV
infection was investigated. To verify the expression profiles of AGDP in response to PRV
infection, the expression level of the precursor
protein of AGDP
mRNA was significantly decreased in PRV-infected mouse lungs and cells. The synthesized AGDP-treating cells were less susceptible to PRV challenges than the controls, as demonstrated by the decreased virus production and gE expression. AGDP not only inhibited the expression of TNF-α and
IL-8 but also appeared to suppress the extracellular release of high-mobility group box 1 (
HMGB1) by inhibiting the output of nuclear
HMGB1 in cells. AGDP could also inhibit the degradation of IκBα and the phosphorylation levels of P65 after PRV
infection. In total, our results revealed many meaningful
peptides involved in PRV
infection, thereby enhancing the current understanding of the host response to PRV
infection, and how AGDP may serve as a promising candidate for developing novel anti-PRV drugs.