Journal
NATURE COMMUNICATIONS
Volume 12, Issue 1, Pages -Publisher
NATURE PORTFOLIO
DOI: 10.1038/s41467-021-25551-1
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Funding
- Deutsche Forschungsgemeinscha.t (DFG, German Research Foundation) [KR1143/9-2, ZI618/6-2, KFO309, 2842373453, TRR81/3, 109546710, SFB1213/2, 268555672, SFB1021/2, 197785619, SFBTR84, GRK 2573, 416910386]
- INST [160/708-1 FUGB]
- German Ministry for Education and Research (RAPID, COVINET) [DZIF TTU 01.806]
- LOEWE program of the state of Hesse (DRUID)
- IMPRS program of the Max Planck Society
- Excellence Cluster CardioPulmonary Institute (EXC 2026: Cardio-Pulmonary Institute (CPI) [390649896]
- DZL/UGMLC/ILH program
- Von-Behring-Roentgen-Stiftung
- Pandemics Network Hesse
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The study demonstrates that the ER stress inducer thapsigargin can efficiently inhibit coronavirus replication, partially reverse virus-induced translational shut-down, and improve cell viability. Thapsigargin affects various mechanisms crucial for CoV replication and could potentially be developed into broad-spectrum anti-CoV drugs.
Here, Shaban et al. show that coronaviruses modulate ER stress and the unfolded protein response. The ER stress inducer thapsigargin exerts potent antiviral effects, partially reverses the virus-induced translational shut-down, reprograms the host proteome and suppresses autophagic flux, thereby inhibiting coronavirus replication at multiple levels. Coronaviruses (CoVs) are important human pathogens for which no specific treatment is available. Here, we provide evidence that pharmacological reprogramming of ER stress pathways can be exploited to suppress CoV replication. The ER stress inducer thapsigargin efficiently inhibits coronavirus (HCoV-229E, MERS-CoV, SARS-CoV-2) replication in different cell types including primary differentiated human bronchial epithelial cells, (partially) reverses the virus-induced translational shut-down, improves viability of infected cells and counteracts the CoV-mediated downregulation of IRE1 alpha and the ER chaperone BiP. Proteome-wide analyses revealed specific pathways, protein networks and components that likely mediate the thapsigargin-induced antiviral state, including essential (HERPUD1) or novel (UBA6 and ZNF622) factors of ER quality control, and ER-associated protein degradation complexes. Additionally, thapsigargin blocks the CoV-induced selective autophagic flux involving p62/SQSTM1. The data show that thapsigargin hits several central mechanisms required for CoV replication, suggesting that this compound (or derivatives thereof) may be developed into broad-spectrum anti-CoV drugs.
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