Ribosomal protein L18 is an essential factor that promote rice stripe virus accumulation in small brown planthopper

Virus Res. 2018 Mar 2:247:15-20. doi: 10.1016/j.virusres.2018.01.011. Epub 2018 Jan 31.

Abstract

Rice stripe virus (RSV) transmitted by the vector, small brown planthopper (SBPH), can cause a severe rice disease. The nucleocapsid (N) protein is the major component of RSV ribonucleoprotein particles (RNPs), and it plays important roles in viral persistent-propagative transmission by SBPH. To gain further insights into the vector components enabling RSV transmission, a GAL4-based yeast two-hybrid system was utilized to find unknown vector factors that interact with the N protein. Thirteen different proteins were identified as factors that interact with the N protein. The interaction between 60S ribosomal protein L18 (RPL18) and the N protein was further studied. Although the expression of RPL18 was not altered in insects during RSV infection, RPL18 was validated to bind directly to RSV RNPs and interact with RSV N protein. Knockdown of RPL18 dramatically reduced viral RNA and protein levels, especially viral protein expression, indicating a requirement for RPL18 in RSV translation and replication. Our results provide evidence that RPL18 is a critical factor required for RSV accumulation in SBPH, which suggests that the vector factor RPL18 may be as a potential target to develop for controlling the transmission of rice virus.

Keywords: Ribosomal protein L18; Rice stripe virus; Small brown planthopper; Viral interaction factors; Virus accumulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Gene Expression Regulation, Viral*
  • Genes, Reporter
  • Hemiptera / genetics*
  • Hemiptera / metabolism
  • Hemiptera / virology
  • Insect Vectors / genetics*
  • Insect Vectors / metabolism
  • Insect Vectors / virology
  • Nucleocapsid Proteins / genetics*
  • Nucleocapsid Proteins / metabolism
  • Oryza / virology
  • Plant Diseases / virology
  • Protein Binding
  • RNA, Viral / genetics*
  • RNA, Viral / metabolism
  • Ribosomal Proteins / genetics*
  • Ribosomal Proteins / metabolism
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism
  • Tenuivirus / genetics*
  • Tenuivirus / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Two-Hybrid System Techniques
  • Virus Replication

Substances

  • DNA-Binding Proteins
  • GAL4 protein, S cerevisiae
  • Nucleocapsid Proteins
  • RNA, Viral
  • Ribosomal Proteins
  • Saccharomyces cerevisiae Proteins
  • Transcription Factors
  • ribosomal protein L18