An Intrinsically Disordered Region of the DNA Repair Protein Nbs1 Is a Species-Specific Barrier to Herpes Simplex Virus 1 in Primates

Cell Host Microbe. 2016 Aug 10;20(2):178-88. doi: 10.1016/j.chom.2016.07.003.

Abstract

Humans occasionally transmit herpes simplex virus 1 (HSV-1) to captive primates, who reciprocally harbor alphaherpesviruses poised for zoonotic transmission to humans. To understand the basis for the species-specific restriction of HSV-1 in primates, we simulated what might happen during the cross-species transmission of HSV-1 and found that the DNA repair protein Nbs1 from only some primate species is able to promote HSV-1 infection. The Nbs1 homologs that promote HSV-1 infection also interact with the HSV-1 ICP0 protein. ICP0 interaction mapped to a region of structural disorder in the Nbs1 protein. Chimeras reversing patterns of disorder in Nbs1 reversed titers of HSV-1 produced in the cell. By extending this analysis to 1,237 virus-interacting mammalian proteins, we show that proteins that interact with viruses are highly enriched in disorder, suggesting that viruses commonly interact with host proteins through intrinsically disordered domains.

MeSH terms

  • Animals
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism*
  • Cell Line
  • DNA Repair Enzymes / genetics
  • DNA Repair Enzymes / metabolism*
  • Herpesvirus 1, Human / immunology*
  • Herpesvirus 1, Human / physiology*
  • Host-Pathogen Interactions*
  • Humans
  • Immediate-Early Proteins / metabolism*
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Primates
  • Protein Binding
  • Protein Interaction Domains and Motifs
  • Protein Interaction Mapping
  • Sequence Homology, Amino Acid
  • Ubiquitin-Protein Ligases / metabolism*
  • Viral Load
  • Virus Replication*

Substances

  • Cell Cycle Proteins
  • Immediate-Early Proteins
  • NBN protein, human
  • Nuclear Proteins
  • Ubiquitin-Protein Ligases
  • Vmw110 protein, Human herpesvirus 1
  • DNA Repair Enzymes