Time-resolved proteomics of adenovirus infected cells

PLoS One. 2018 Sep 25;13(9):e0204522. doi: 10.1371/journal.pone.0204522. eCollection 2018.

Abstract

Viral infections cause large problems in the world and deeper understanding of the disease mechanisms is needed. Here we present an analytical strategy to investigate the host cell protein changes during human adenovirus type 2 (HAdV-C2 or Ad2) infection of lung fibroblasts by stable isotope labelling of amino acids in cell culture (SILAC) and nanoLC-MS/MS. This work focuses on early phase of infection (6 and 12 h post-infection (hpi)) but the data is combined with previously published late phase (24 and 36 hpi) proteomics data to produce a time series covering the complete infection. As many as 2169 proteins were quantitatively monitored from 6 to 36 hpi, while some proteins were time-specific. After applying different filter criteria, 2027 and 2150 proteins were quantified at 6 and 12 hpi and among them, 431 and 544 were significantly altered at the two time points. Pathway analysis showed that the De novo purine and pyrimidine biosynthesis, Glycolysis and Cytoskeletal regulation by Rho GTPase pathways were activated early during infection while inactivation of the Integrin signalling pathway started between 6 and 12 hpi. Moreover, upstream regulator analysis predicted MYC to be activated with time of infection and protein and RNA data for genes controlled by this transcription factor showed good correlation, which validated the use of protein data for this prediction. Among the identified phosphorylation sites, a group related to glycolysis and cytoskeletal reorganization were up-regulated during infection. The results show specific aspects on how the host cell proteins, the final products in the genetic information flow, are influenced by Ad2 infection, which would be overlooked if only knowledge derived from mRNA data is considered.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae Infections / genetics
  • Adenoviridae Infections / metabolism*
  • Adenoviridae Infections / virology
  • Adenoviruses, Human / genetics
  • Adenoviruses, Human / metabolism*
  • Amino Acids / metabolism
  • Cell Line
  • Host Microbial Interactions / genetics
  • Host Microbial Interactions / physiology
  • Humans
  • Kinetics
  • Metabolic Networks and Pathways / genetics
  • Phosphopeptides / genetics
  • Phosphopeptides / metabolism
  • Proteome / genetics
  • Proteome / metabolism
  • Proteomics / methods
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Tandem Mass Spectrometry
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • Amino Acids
  • Phosphopeptides
  • Proteome
  • RNA, Messenger
  • Transcription Factors

Grants and funding

This work was supported by Åke Wiberg Foundation (SBL, M14-0127), Magnus Bergvall Foundation (SBL, 2015-01200, 2016-01675), Carl Trygger Foundation (SBL, CST 15:57), Clas Groschinsky memory foundation (SBL, M1603, M1742) and Kjell and Märta Beijer Foundation (UP). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.