Re-analysis of SARS-CoV-2-infected host cell proteomics time-course data by impact pathway analysis and network analysis: a potential link with inflammatory response

Aging (Albany NY). 2020 Jun 23;12(12):11277-11286. doi: 10.18632/aging.103524. Epub 2020 Jun 23.

Abstract

Coronavirus disease 2019 (COVID-19), caused by an outbreak of the severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) in Wuhan, China, has led to an unprecedented health and economic crisis worldwide. To develop treatments that can stop or lessen the symptoms and severity of SARS-CoV-2 infection, it is critical to understand how the virus behaves inside human cells, and so far studies in this area remain scarce. A recent study investigated translatome and proteome host cell changes induced in vitro by SARS-CoV-2. Here, we use the publicly available proteomics data from this study to re-analyze the in vitro cellular consequences of SARS-CoV-2 infection by impact pathways analysis and network analysis. Notably, proteins linked to the inflammatory response, but also proteins related to chromosome segregation during mitosis, were found to be altered in response to viral infection. Upregulation of inflammatory response proteins is in line with the propagation of inflammatory reaction and lung injury that is observed in advanced stages of COVID-19 patients and which worsens with age.

Keywords: COVID-19; SARS-CoV-2; inflammatory response; proteomics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging
  • Angiotensin-Converting Enzyme 2
  • Betacoronavirus / physiology*
  • COVID-19
  • Coronavirus Infections / virology*
  • Gene Expression Regulation
  • Gene Regulatory Networks
  • Humans
  • Inflammation
  • Pandemics
  • Peptidyl-Dipeptidase A / metabolism
  • Pneumonia, Viral / virology*
  • Proteomics*
  • SARS-CoV-2
  • Virus Replication

Substances

  • Peptidyl-Dipeptidase A
  • ACE2 protein, human
  • Angiotensin-Converting Enzyme 2