Rice ragged stunt virus-induced apoptosis affects virus transmission from its insect vector, the brown planthopper to the rice plant

Sci Rep. 2015 Jun 15:5:11413. doi: 10.1038/srep11413.

Abstract

Most plant viruses that seriously damage agricultural crops are transmitted by insects. However, the mechanisms enabling virus transmission by insect vectors are poorly understood. The brown planthopper (Nilaparvata lugens) is one of the most serious rice pests, causing extensive damage to rice plants by sucking the phloem sap and transmitting viruses, including Rice ragged stunt virus (RRSV). In this study, we investigated the mechanisms of RRSV transmission from its insect vector to the rice plant in vivo using the terminal deoxynucleotidyl transferase dUTP nick-end labeling assay and RNA interference technology. RRSV induced apoptosis in the salivary gland cells of its insect vector, N. lugens. The RRSV-induced apoptosis was regulated through a caspase-dependent manner, and inhibition of the expression of N. lugens caspase-1 genes significantly interfered with virus transmission. Our findings establish a link between virus-associated apoptosis and virus transmission from the insect vector to the host plant.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Apoptosis / genetics
  • Caspase 1 / genetics*
  • Caspase 1 / metabolism
  • Gene Expression Regulation
  • Hemiptera / classification
  • Hemiptera / genetics*
  • Hemiptera / virology
  • Host-Pathogen Interactions
  • In Situ Nick-End Labeling
  • Insect Proteins / genetics*
  • Insect Proteins / metabolism
  • Insect Vectors / genetics*
  • Insect Vectors / virology
  • Molecular Sequence Data
  • Oryza / parasitology*
  • Oryza / virology
  • Phloem / parasitology
  • Phloem / virology
  • Phylogeny
  • Plant Diseases / virology
  • Plant Viruses / pathogenicity
  • RNA Interference
  • Reoviridae / pathogenicity
  • Salivary Glands / metabolism
  • Salivary Glands / pathology
  • Salivary Glands / virology*
  • Sequence Alignment
  • Signal Transduction

Substances

  • Insect Proteins
  • Caspase 1