Litcius/Paper detail

Crippling life support for SARS-CoV-2 and other viruses through synthetic lethality

Fred D. Mast, Arti T. Navare, Almer M. van der Sloot, Jasmin Coulombe‐Huntington, Michael P. Rout, Nitin S. Baliga, Alexis Kaushansky, Brian T. Chait, Alan Aderem, Charles M. Rice, Andrej Šali, Mike Tyers, John D. Aitchison

2020The Journal of Cell Biology28 citationsDOIOpen Access PDF

Abstract

With the rapid global spread of SARS-CoV-2, we have become acutely aware of the inadequacies of our ability to respond to viral epidemics. Although disrupting the viral life cycle is critical for limiting viral spread and disease, it has proven challenging to develop targeted and selective therapeutics. Synthetic lethality offers a promising but largely unexploited strategy against infectious viral disease; as viruses infect cells, they abnormally alter the cell state, unwittingly exposing new vulnerabilities in the infected cell. Therefore, we propose that effective therapies can be developed to selectively target the virally reconfigured host cell networks that accompany altered cellular states to cripple the host cell that has been converted into a virus factory, thus disrupting the viral life cycle.

Topics & Concepts

CrippleViral life cycleLethalityVirologyLimitingVirusBiologySevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)Coronavirus disease 2019 (COVID-19)DiseaseHost (biology)Infectious disease (medical specialty)Viral replicationMedicineGeneticsNursingPathologyEngineeringMechanical engineeringSARS-CoV-2 and COVID-19 ResearchCRISPR and Genetic EngineeringViral Infections and Outbreaks Research