Ebola virus VP35 has novel NTPase and helicase-like activities

Nucleic Acids Res. 2019 Jun 20;47(11):5837-5851. doi: 10.1093/nar/gkz340.

Abstract

Ebola virus (EBOV) is a non-segmented, negative-sense RNA virus (NNSV) in the family Filoviridae, and is recognized as one of the most lethal pathogens in the planet. For RNA viruses, cellular or virus-encoded RNA helicases play pivotal roles in viral life cycles by remodelling viral RNA structures and/or unwinding viral dsRNA produced during replication. However, no helicase or helicase-like activity has ever been found to associate with any NNSV-encoded proteins, and it is unknown whether the replication of NNSVs requires the participation of any viral or cellular helicase. Here, we show that despite of containing no conserved NTPase/helicase motifs, EBOV VP35 possesses the NTPase and helicase-like activities that can hydrolyse all types of NTPs and unwind RNA helices in an NTP-dependent manner, respectively. Moreover, guanidine hydrochloride, an FDA-approved compound and inhibitor of certain viral helicases, inhibited the NTPase and helicase-like activities of VP35 as well as the replication/transcription of an EBOV minigenome replicon in cells, highlighting the importance of VP35 helicase-like activity during EBOV life cycle. Together, our findings provide the first demonstration of the NTPase/helicase-like activity encoded by EBOV, and would foster our understanding of EBOV and NNSVs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / chemistry
  • Amino Acid Motifs
  • Cells, Cultured
  • DNA Helicases / metabolism
  • Ebolavirus / genetics*
  • Ebolavirus / metabolism*
  • Hemorrhagic Fever, Ebola / virology*
  • Humans
  • Nucleocapsid Proteins
  • Nucleoproteins / genetics
  • Nucleoproteins / metabolism
  • Nucleoproteins / physiology*
  • Nucleoside-Triphosphatase / genetics
  • Protein Binding
  • RNA Helicases / metabolism
  • RNA, Double-Stranded / chemistry*
  • RNA, Viral / metabolism
  • Viral Core Proteins / genetics
  • Viral Core Proteins / metabolism
  • Viral Core Proteins / physiology*
  • Viral Nonstructural Proteins / metabolism
  • Virus Replication

Substances

  • Nucleocapsid Proteins
  • Nucleoproteins
  • RNA, Double-Stranded
  • RNA, Viral
  • Viral Core Proteins
  • Viral Nonstructural Proteins
  • nucleoprotein VP35, Ebola virus
  • Adenosine Triphosphate
  • Nucleoside-Triphosphatase
  • DNA Helicases
  • RNA Helicases