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The UPR sensor IRE1α and the adenovirus E3-19K glycoprotein sustain persistent and lytic infections

Author

Listed:
  • Vibhu Prasad

    (University of Zurich)

  • Maarit Suomalainen

    (University of Zurich)

  • Yllza Jasiqi

    (University of Zurich)

  • Silvio Hemmi

    (University of Zurich)

  • Patrick Hearing

    (Stony Brook University)

  • Louise Hosie

    (University of Warwick, School of Life Sciences
    The Francis Crick Institute)

  • Hans-Gerhard Burgert

    (University of Warwick, School of Life Sciences
    Institute of Virology, University Medical Center Freiburg)

  • Urs F. Greber

    (University of Zurich)

Abstract

Persistent viruses cause chronic disease, and threaten the lives of immunosuppressed individuals. Here, we elucidate a mechanism supporting the persistence of human adenovirus (AdV), a virus that can kill immunosuppressed patients. Cell biological analyses, genetics and chemical interference demonstrate that one of five AdV membrane proteins, the E3-19K glycoprotein specifically triggers the unfolded protein response (UPR) sensor IRE1α in the endoplasmic reticulum (ER), but not other UPR sensors, such as protein kinase R-like ER kinase (PERK) and activating transcription factor 6 (ATF6). The E3-19K lumenal domain activates the IRE1α nuclease, which initiates mRNA splicing of X-box binding protein-1 (XBP1). XBP1s binds to the viral E1A-enhancer/promoter sequence, and boosts E1A transcription, E3-19K levels and lytic infection. Inhibition of IRE1α nuclease interrupts the five components feedforward loop, E1A, E3-19K, IRE1α, XBP1s, E1A enhancer/promoter. This loop sustains persistent infection in the presence of the immune activator interferon, and lytic infection in the absence of interferon.

Suggested Citation

  • Vibhu Prasad & Maarit Suomalainen & Yllza Jasiqi & Silvio Hemmi & Patrick Hearing & Louise Hosie & Hans-Gerhard Burgert & Urs F. Greber, 2020. "The UPR sensor IRE1α and the adenovirus E3-19K glycoprotein sustain persistent and lytic infections," Nature Communications, Nature, vol. 11(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-15844-2
    DOI: 10.1038/s41467-020-15844-2
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