Synergistic inhibition of pseudorabies virus replication by porcine alpha/beta interferon and gamma interferon in vitro

Eur Cytokine Netw. 2007 Jun;18(2):71-7. doi: 10.1684/ecn.2007.0088. Epub 2007 Jun 26.

Abstract

Interferon (IFN) is crucial for initiating the innate immune response and for the generation of the adaptive response. IFN, in most species, comprises IFN-alpha (IFN-alpha), IFN-beta (IFN-beta) and IFN-gamma (IFN-gamma). In this study, we compared the capacity of porcine IFN-alpha, -beta and -gamma, or a combination of them, to protect IBRS-2 cells (porcine kidney cells) from infection with pseudorabies virus (PRV). The results demonstrated that porcine IFN-beta (PoIFN-beta) was the most efficient of the three IFNs in conferring resistance PRV infection; 100 U/mL PoIFN-beta inhibited PRV plaque formation 5.3-fold. Compared with PoIFN-beta, porcine IFN-gamma (PoIFN-gamma) was less capable of inhibiting PRV plaque formation (3.3-fold inhibition). Porcine IFN-alpha (PoIFN-alpha) had the least capability of the three PoIFNs, and inhibited PRV plaque formation only 1.26-fold. The inhibitory capacity increased to only 2.3-fold with a treatment of 12,800 U/mL PoIFN-alpha. A combination of PoIFN-gamma and PoIFN-alpha or PoIFN-beta inhibited PRV plaque formation 12.8-fold or 100-fold, respectively. Treatment of IBRS-2 cells with PoIFN-alpha/beta and PoIFN-gamma inhibited PRV replication 29- or 146-fold. Additionally, real-time PCR analyses of the PRV immediate early (IE) gene revealed that IE mRNA expression was profoundly decreased in cells stimulated with PoIFN-alpha/beta and PoIFN-gamma (23.8-133.0-fold) compared with vehicle-treated cells. All the findings indicate that PoIFN-gamma acts synergistically with other PoIFNs (PoIFN-alpha and -beta) to potently inhibit PRV replication in vitro.

MeSH terms

  • Adsorption
  • Animals
  • Antiviral Agents / pharmacology*
  • Cattle
  • Cell Line
  • Gene Expression Regulation, Viral*
  • Herpesvirus 1, Suid / metabolism*
  • In Vitro Techniques
  • Interferon-alpha / metabolism*
  • Interferon-beta / metabolism*
  • Interferon-gamma / metabolism*
  • Pseudorabies / drug therapy
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Swine
  • Virus Replication*

Substances

  • Antiviral Agents
  • Interferon-alpha
  • RNA, Messenger
  • Interferon-beta
  • Interferon-gamma