DExD/H Box Helicases DDX24 and DDX49 Inhibit Reactivation of Kaposi's Sarcoma Associated Herpesvirus by Interacting with Viral mRNAs

Viruses. 2022 Sep 20;14(10):2083. doi: 10.3390/v14102083.

Abstract

Kaposi's sarcoma-associated herpesvirus (KSHV) is an oncogenic gammaherpesvirus that is the causative agent of primary effusion lymphoma and Kaposi's sarcoma. In healthy carriers, KSHV remains latent, but a compromised immune system can lead to lytic viral replication that increases the probability of tumorigenesis. RIG-I-like receptors (RLRs) are members of the DExD/H box helicase family of RNA binding proteins that recognize KSHV to stimulate the immune system and prevent reactivation from latency. To determine if other DExD/H box helicases can affect KSHV lytic reactivation, we performed a knock-down screen that revealed DHX29-dependent activities appear to support viral replication but, in contrast, DDX24 and DDX49 have antiviral activity. When DDX24 or DDX49 are overexpressed in BCBL-1 cells, transcription of all lytic viral genes and genome replication were significantly reduced. RNA immunoprecipitation of tagged DDX24 and DDX49 followed by next-generation sequencing revealed that the helicases bind to mostly immediate-early and early KSHV mRNAs. Transfection of expression plasmids of candidate KSHV transcripts, identified from RNA pull-down, demonstrated that KSHV mRNAs stimulate type I interferon (alpha/beta) production and affect the expression of multiple interferon-stimulated genes. Our findings reveal that host DExD/H box helicases DDX24 and DDX49 recognize gammaherpesvirus transcripts and convey an antiviral effect in the context of lytic reactivation.

Keywords: KSHV; deadbox helicases; innate immunity; pattern recognition receptor; type I interferon.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Antiviral Agents / metabolism
  • DEAD-box RNA Helicases / genetics
  • DEAD-box RNA Helicases / metabolism
  • DNA Helicases / genetics
  • Gene Expression Regulation, Viral
  • Herpesvirus 8, Human* / physiology
  • Humans
  • Interferon Type I* / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Sarcoma, Kaposi*
  • Virus Activation / genetics
  • Virus Latency / genetics
  • Virus Replication / genetics

Substances

  • Antiviral Agents
  • DDX24 protein, human
  • DEAD-box RNA Helicases
  • DNA Helicases
  • Interferon Type I
  • RNA, Messenger
  • DDX49 protein, human