Quantitative proteomics study of host response to virulent and attenuated pseudorabies virus infection in mouse brain

Biochim Biophys Acta Proteins Proteom. 2018 Feb;1866(2):307-315. doi: 10.1016/j.bbapap.2017.11.010. Epub 2017 Nov 23.

Abstract

Bartha, the pseudorabies virus (PRV) vaccine strain, is widely used in studies of neuronal circuit-tracing, due to its attenuated virulence and retrograde spreading. However, we know little regarding the molecular mechanisms of PRV infection and spreading between structurally connected neurons. In this study, we systematically analyzed the host brain proteomes after acute infection with PRV, attempting to identified the proteins involved in the processes. Mice were injected with PRV-Bartha and PRV-Becker (PRV-Bartha's wild-type parent strain) in the olfactory system, the proteomes of the brain and synaptosome were analyzed and compared at various infection intervals using mass spectrometry-based proteomics techniques. In all, we identified >100 PRV-infection regulated proteins at the whole-tissue level and the synaptosome level. While at whole-tissue level, bioinformatics analyses mapped most of the regulations to the inflammation pathways, at the synaptosome level, most of those to synaptic transmission, cargo transport and cytoskeleton organization. We established regulated protein networks demonstrating distinct cellular regulation pattern between the global and the synaptosome levels. Moreover, we identified a series of potentially PRV-strain-specific regulated proteins with diverse biological functions. This study may provide new clues for molecular mechanisms for PRV infection and spread.

Keywords: Nervous system; Pseudorabies virus; Quantitative proteomics; Synaptosome; Virus trafficking.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / metabolism*
  • Brain / pathology
  • Brain / virology
  • Herpesvirus 1, Suid / metabolism*
  • Male
  • Mice
  • Nerve Tissue Proteins / metabolism*
  • Proteomics*
  • Pseudorabies / metabolism*
  • Pseudorabies / pathology
  • Synaptosomes / metabolism*
  • Synaptosomes / pathology
  • Synaptosomes / virology

Substances

  • Nerve Tissue Proteins