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PKR Binds Enterovirus IRESs, Displaces Host Translation Factors, and Impairs Viral Translation to Enable Innate Antiviral Signaling.

Publication ,  Journal Article
Dobrikov, MI; Dobrikova, EY; McKay, ZP; Kastan, JP; Brown, MC; Gromeier, M
Published in: mBio
June 28, 2022

For RNA virus families except Picornaviridae, viral RNA sensing includes Toll-like receptors and/or RIG-I. Picornavirus RNAs, whose 5' termini are shielded by a genome-linked protein, are predominately recognized by MDA5. This has important ramifications for adaptive immunity, as MDA5-specific patterns of type-I interferon (IFN) release are optimal for CD4+T cell TH1 polarization and CD8+T cell priming. We are exploiting this principle for cancer immunotherapy with recombinant poliovirus (PV), PVSRIPO, the type 1 (Sabin) PV vaccine containing a rhinovirus type 2 internal ribosomal entry site (IRES). Here we show that PVSRIPO-elicited MDA5 signaling is preceded by early sensing of the IRES by the double-stranded (ds)RNA-activated protein kinase (PKR). PKR binding to IRES stem-loop domains 5-6 led to dimerization and autoactivation, displaced host translation initiation factors, and suppressed viral protein synthesis. Early PKR-mediated antiviral responses tempered incipient viral translation and the activity of cytopathogenic viral proteinases, setting up accentuated MDA5 innate inflammation in response to PVSRIPO infection. IMPORTANCE Among the RIG-I-like pattern recognition receptors, MDA5 stands out because it senses long dsRNA duplexes independent of their 5' features (RIG-I recognizes viral [v]RNA 5'-ppp blunt ends). Uniquely among RNA viruses, the innate defense against picornaviruses is controlled by MDA5. We show that prior to engaging MDA5, recombinant PV RNA is sensed upon PKR binding to the viral IRES at a site that overlaps with the footprint for host translation factors mediating 40S subunit recruitment. Our study demonstrates that innate antiviral type-I IFN responses orchestrated by MDA5 involve separate innate modules that recognize distinct vRNA features and interfere with viral functions at multiple levels.

Duke Scholars

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Published In

mBio

DOI

EISSN

2150-7511

Publication Date

June 28, 2022

Volume

13

Issue

3

Start / End Page

e0085422

Location

United States

Related Subject Headings

  • Receptors, Pattern Recognition
  • RNA, Viral
  • RNA, Double-Stranded
  • RNA Viruses
  • Poliovirus
  • Internal Ribosome Entry Sites
  • Immunity, Innate
  • Enterovirus
  • Antiviral Agents
  • 3207 Medical microbiology
 

Citation

APA
Chicago
ICMJE
MLA
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Dobrikov, M. I., Dobrikova, E. Y., McKay, Z. P., Kastan, J. P., Brown, M. C., & Gromeier, M. (2022). PKR Binds Enterovirus IRESs, Displaces Host Translation Factors, and Impairs Viral Translation to Enable Innate Antiviral Signaling. MBio, 13(3), e0085422. https://doi.org/10.1128/mbio.00854-22
Dobrikov, Mikhail I., Elena Y. Dobrikova, Zachary P. McKay, Jonathan P. Kastan, Michael C. Brown, and Matthias Gromeier. “PKR Binds Enterovirus IRESs, Displaces Host Translation Factors, and Impairs Viral Translation to Enable Innate Antiviral Signaling.MBio 13, no. 3 (June 28, 2022): e0085422. https://doi.org/10.1128/mbio.00854-22.
Dobrikov MI, Dobrikova EY, McKay ZP, Kastan JP, Brown MC, Gromeier M. PKR Binds Enterovirus IRESs, Displaces Host Translation Factors, and Impairs Viral Translation to Enable Innate Antiviral Signaling. mBio. 2022 Jun 28;13(3):e0085422.
Dobrikov, Mikhail I., et al. “PKR Binds Enterovirus IRESs, Displaces Host Translation Factors, and Impairs Viral Translation to Enable Innate Antiviral Signaling.MBio, vol. 13, no. 3, June 2022, p. e0085422. Pubmed, doi:10.1128/mbio.00854-22.
Dobrikov MI, Dobrikova EY, McKay ZP, Kastan JP, Brown MC, Gromeier M. PKR Binds Enterovirus IRESs, Displaces Host Translation Factors, and Impairs Viral Translation to Enable Innate Antiviral Signaling. mBio. 2022 Jun 28;13(3):e0085422.

Published In

mBio

DOI

EISSN

2150-7511

Publication Date

June 28, 2022

Volume

13

Issue

3

Start / End Page

e0085422

Location

United States

Related Subject Headings

  • Receptors, Pattern Recognition
  • RNA, Viral
  • RNA, Double-Stranded
  • RNA Viruses
  • Poliovirus
  • Internal Ribosome Entry Sites
  • Immunity, Innate
  • Enterovirus
  • Antiviral Agents
  • 3207 Medical microbiology