Alignment of virus-host protein-protein interaction networks by integer linear programming: SARS-CoV-2

PLoS One. 2020 Dec 7;15(12):e0236304. doi: 10.1371/journal.pone.0236304. eCollection 2020.

Abstract

Motivation: Beside socio-economic issues, coronavirus pandemic COVID-19, the infectious disease caused by the newly discovered coronavirus SARS-CoV-2, has caused a deep impact in the scientific community, that has considerably increased its effort to discover the infection strategies of the new virus. Among the extensive and crucial research that has been carried out in the last months, the analysis of the virus-host relationship plays an important role in drug discovery. Virus-host protein-protein interactions are the active agents in virus replication, and the analysis of virus-host protein-protein interaction networks is fundamental to the study of the virus-host relationship.

Results: We have adapted and implemented a recent integer linear programming model for protein-protein interaction network alignment to virus-host networks, and obtained a consensus alignment of the SARS-CoV-1 and SARS-CoV-2 virus-host protein-protein interaction networks. Despite the lack of shared human proteins in these virus-host networks, and the low number of preserved virus-host interactions, the consensus alignment revealed aligned human proteins that share a function related to viral infection, as well as human proteins of high functional similarity that interact with SARS-CoV-1 and SARS-CoV-2 proteins, whose alignment would preserve these virus-host interactions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • COVID-19 / virology
  • Coronavirus / metabolism
  • Coronavirus Infections / virology
  • Host Microbial Interactions / physiology*
  • Humans
  • Models, Theoretical
  • Pandemics
  • Pneumonia, Viral / virology
  • Programming, Linear
  • Protein Binding / physiology
  • Protein Interaction Maps / physiology*
  • Proteins / metabolism
  • SARS-CoV-2 / metabolism*
  • Spike Glycoprotein, Coronavirus / metabolism
  • Virus Replication / physiology

Substances

  • Proteins
  • Spike Glycoprotein, Coronavirus

Grants and funding

This work has been supported by the Spanish Ministry of Science, Innovation and Universities and the European Regional Development Fund through project PGC2018-096956-B-C43 (FEDER/MICINN/AEI). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.