Abstract

SummaryInterferon-stimulated genes (ISGs) act in concert to provide a tight barrier against viruses. Recent studies have shed light on the contribution of individual ISG effectors to the antiviral state, but most have examined those acting on early, intracellular stages of the viral life cycle. Here, we applied an image-based screen to identify ISGs inhibiting late stages of influenza A virus (IAV) infection. We unraveled a directly antiviral function for the gene SERPINE1, encoding plasminogen activator inhibitor 1 (PAI-1). By targeting extracellular airway proteases, PAI-1 inhibits IAV glycoprotein cleavage, thereby reducing infectivity of progeny viruses. This was biologically relevant for IAV restriction in vivo. Further, partial PAI-1 deficiency, attributable to a polymorphism in human SERPINE1, conferred increased susceptibility to IAV in vitro. Together, our findings reveal that manipulating the extracellular environment to inhibit the last step in a virus life cycle is an important mechanism of the antiviral response.

Highlights

  • RESULTSAs obligate intracellular parasites, the fate of viruses is intricately linked to the metabolism of their host cells

  • We demonstrate that plasminogen activator inhibitor 1 (PAI-1) inhibits influenza A virus (IAV) maturation by targeting host proteases needed for viral glycoprotein cleavage and that this is physiologically relevant in natural proteolytic landscapes both in vitro and in vivo

  • We identified a number of IFN-stimulated genes (ISGs) with previously uncharacterized antiviral activities: MAP3K14, ELF1, PMM2, FAM46C, TBX3, SCO2, CRY1, TNFSF10 (TRAIL), XAF1, MAFF, and SERPINE1

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Summary

Graphical Abstract

Plasminogen activator inhibitor (PAI-1) blocks surface glycoprotein maturation of influenza A virus, reducing virus spread in the airways and revealing that the innate immune system, driven by type I IFN, uses modulation of the extracellular environment to inhibit viruses.

SUMMARY
RESULTS
DISCUSSION
Findings
IAV fibroblasts
EXPERIMENTAL PROCEDURES

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