The Molecular Mechanism of Herpes Simplex Virus 1 UL31 in Antagonizing the Activity of IFN-β

Microbiol Spectr. 2022 Feb 23;10(1):e0188321. doi: 10.1128/spectrum.01883-21. Epub 2022 Feb 23.

Abstract

Virus infection triggers intricate signal cascade reactions to activate the host innate immunity, which leads to the production of type I interferon (IFN-I). Herpes simplex virus 1 (HSV-1), a human-restricted pathogen, is capable of encoding over 80 viral proteins, and several of them are involved in immune evasion to resist the host antiviral response through the IFN-I signaling pathway. Here, we determined that HSV-1 UL31, which is associated with nuclear matrix and is essential for the formation of viral nuclear egress complex, could inhibit retinoic acid-inducible gene I (RIG-I)-like receptor pathway-mediated interferon beta (IFN-β)-luciferase (Luc) and (PRDIII-I)4-Luc (an expression plasmid of IFN-β positive regulatory elements III and I) promoter activation, as well as the mRNA transcription of IFN-β and downstream interferon-stimulated genes (ISGs), such as ISG15, ISG54, ISG56, etc., to promote viral infection. UL31 was shown to restrain IFN-β activation at the interferon regulatory factor 3 (IRF3)/IRF7 level. Mechanically, UL31 was demonstrated to interact with TANK binding kinase 1 (TBK1), inducible IκB kinase (IKKi), and IRF3 to impede the formation of the IKKi-IRF3 complex but not the formation of the IRF7-related complex. UL31 could constrain the dimerization and nuclear translocation of IRF3. Although UL31 was associated with the CREB binding protein (CBP)/p300 coactivators, it could not efficiently hamper the formation of the CBP/p300-IRF3 complex. In addition, UL31 could facilitate the degradation of IKKi and IRF3 by mediating their K48-linked polyubiquitination. Taken together, these results illustrated that UL31 was able to suppress IFN-β activity by inhibiting the activation of IKKi and IRF3, which may contribute to the knowledge of a new immune evasion mechanism during HSV-1 infection. IMPORTANCE The innate immune system is the first line of host defense against the invasion of pathogens. Among its mechanisms, IFN-I is an essential cytokine in the antiviral response, which can help the host eliminate a virus. HSV-1 is a double-stranded DNA virus that can cause herpes and establish a lifelong latent infection, due to its possession of multiple mechanisms to escape host innate immunity. In this study, we illustrate for the first time that the HSV-1-encoded UL31 protein has a negative regulatory effect on IFN-β production by blocking the dimerization and nuclear translocation of IRF3, as well as promoting the K48-linked polyubiquitination and degradation of both IKKi and IRF3. This study may be helpful for fully understanding the pathogenesis of HSV-1.

Keywords: HSV-1; IFN-β; RLR; UL31; innate immunity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chlorocebus aethiops
  • Cytokines
  • DEAD Box Protein 58
  • HEK293 Cells
  • HeLa Cells
  • Herpes Simplex
  • Herpesvirus 1, Human / genetics*
  • Herpesvirus 1, Human / immunology*
  • Host-Pathogen Interactions
  • Humans
  • Immune Evasion
  • Immunity, Innate
  • Interferon Regulatory Factor-3 / genetics
  • Interferon Regulatory Factor-3 / immunology
  • Interferon Regulatory Factor-3 / metabolism
  • Interferon Regulatory Factor-7
  • Interferon Type I
  • Interferon-beta / genetics*
  • Interferon-beta / immunology*
  • Interferon-beta / metabolism
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / immunology*
  • Nuclear Proteins / metabolism
  • Protein Serine-Threonine Kinases
  • Receptors, Immunologic
  • Signal Transduction
  • Vero Cells
  • Viral Proteins / genetics*
  • Viral Proteins / immunology*
  • Viral Proteins / metabolism

Substances

  • Cytokines
  • IRF3 protein, human
  • IRF7 protein, human
  • Interferon Regulatory Factor-3
  • Interferon Regulatory Factor-7
  • Interferon Type I
  • Nuclear Proteins
  • Receptors, Immunologic
  • UL31 protein, Human herpesvirus 1
  • Viral Proteins
  • Interferon-beta
  • Protein Serine-Threonine Kinases
  • TBK1 protein, human
  • RIGI protein, human
  • DEAD Box Protein 58