Identification of antiviral roles for the exon–junction complex and nonsense-mediated decay in flaviviral infection

Minghua Li, Jeffrey R. Johnson, Billy Truong, Grace Kim, Nathan Weinbren, Mark Dittmar, Priya S. Shah, John Von Dollen, Billy W. Newton, Gwendolyn M. Jang, Nevan J. Krogan, Sara Cherry, Holly Ramage

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

Abstract

West Nile virus (WNV) is an emerging mosquito-borne flavivirus, related to dengue virus and Zika virus. To gain insight into host pathways involved in WNV infection, we performed a systematic affinity-tag purification mass spectrometry (APMS) study to identify 259 WNV-interacting human proteins. RNA interference screening revealed 26 genes that both interact with WNV proteins and influence WNV infection. We found that WNV, dengue and Zika virus capsids interact with a conserved subset of proteins that impact infection. These include the exon–junction complex (EJC) recycling factor PYM1, which is antiviral against all three viruses. The EJC has roles in nonsense-mediated decay (NMD), and we found that both the EJC and NMD are antiviral and the EJC protein RBM8A directly binds WNV RNA. To counteract this, flavivirus infection inhibits NMD and the capsid–PYM1 interaction interferes with EJC protein function and localization. Depletion of PYM1 attenuates RBM8A binding to viral RNA, suggesting that WNV sequesters PYM1 to protect viral RNA from decay. Together, these data suggest a complex interplay between the virus and host in regulating NMD and the EJC.

Original languageEnglish (US)
Pages (from-to)985-995
Number of pages11
JournalNature Microbiology
Volume4
Issue number6
DOIs
StatePublished - Jun 1 2019
Externally publishedYes

ASJC Scopus subject areas

  • Microbiology
  • Immunology
  • Applied Microbiology and Biotechnology
  • Genetics
  • Microbiology (medical)
  • Cell Biology

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