Cricket paralysis virus antagonizes Argonaute 2 to modulate antiviral defense in Drosophila

Nat Struct Mol Biol. 2010 May;17(5):547-54. doi: 10.1038/nsmb.1810. Epub 2010 Apr 18.

Abstract

Insect viruses have evolved strategies to control the host RNAi antiviral defense mechanism. In nature, Drosophila melanogaster C virus (DCV) infection causes low mortality and persistent infection, whereas the closely related cricket paralysis virus (CrPV) causes a lethal infection. We show that these viruses use different strategies to modulate the host RNAi defense machinery. The DCV RNAi suppressor (DCV-1A) binds to long double-stranded RNA and prevents processing by Dicer2. In contrast, the CrPV suppressor (CrPV-1A) interacts with the endonuclease Argonaute 2 (Ago2) and inhibits its activity without affecting the microRNA (miRNA)-Ago1-mediated silencing. We examined the link between viral RNAi suppressors and the outcome of infection using recombinant Sindbis viruses encoding either CrPV-1A or DCV-1A. Flies infected with Sindbis virus expressing CrPV-1A showed a marked increase in virus production, spread and mortality. In contrast, Sindbis pathogenesis was only modestly increased by expression of DCV- 1A. We conclude that RNAi suppressors function as virulence factors in insects and can target the Drosophila RNAi pathway at different points.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Argonaute Proteins
  • Cell Line
  • Drosophila / genetics
  • Drosophila / metabolism
  • Drosophila / virology*
  • Drosophila Proteins / antagonists & inhibitors
  • Drosophila Proteins / metabolism*
  • Host-Pathogen Interactions*
  • Insect Viruses / pathogenicity*
  • MicroRNAs / metabolism
  • Molecular Sequence Data
  • RNA Interference*
  • RNA-Induced Silencing Complex / antagonists & inhibitors
  • RNA-Induced Silencing Complex / metabolism*
  • Sequence Alignment
  • Viral Proteins / chemistry
  • Viral Proteins / metabolism*

Substances

  • AGO2 protein, Drosophila
  • Argonaute Proteins
  • Drosophila Proteins
  • MicroRNAs
  • RNA-Induced Silencing Complex
  • Viral Proteins