Molecular Co-Chaperone SGT1 Is Critical for Cell-to-Cell Movement and Systemic Infection of Tomato Spotted Wild Virus in Nicotiana benthamiana

Viruses. 2018 Nov 17;10(11):647. doi: 10.3390/v10110647.

Abstract

Tospovirus is a tripartite negative stranded RNA virus and is considered as one of the most devastating plant viruses. Successful virus infection in plant requires many host factors. To date, very few host factors have been identified as important in Tospovirus infection in plants. We reported earlier that NSm protein encoded by Tomato spotted wilt virus (TSWV), a type species of the genus Orthotospovirus, plays critical roles in viral cell-to-cell and long-distance movement. In this study, we determined that molecular co-chaperone NbSGT1 interacted with TSWV NSm in Nicotianabenthamiana. TSWV infection significantly upregulated the expression of NbSGT1 gene and transient overexpression of NbSGT1 in N.benthamiana leaves accelerated TSWV infection. In contrast, silencing the NbSGT1 gene expression using a virus-induced gene silencing (VIGS) approach strongly inhibited TSWV NSm cell-to-cell movement, as well as TSWV local and systemic infection in N.benthamiana plants. Furthermore, NbSGT1 was found to regulate the infection of both American and Euro/Asia type tospoviruses in N.benthamiana plant. Collectively, our findings presented in this paper and the results published previously indicated that molecular co-chaperone NbSGT1 plays important roles in modulating both positive stranded and tripartite negative stranded RNA virus infection in plants.

Keywords: SGT1; TSWV NSm; Tomato spotted wilt virus; molecular co-chaperone; tripartite negative stranded RNA virus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Glucosyltransferases / metabolism*
  • Host-Pathogen Interactions*
  • Molecular Chaperones / metabolism*
  • Nicotiana / enzymology*
  • Nicotiana / virology
  • Plant Viral Movement Proteins / metabolism
  • Protein Binding
  • Tospovirus / physiology*
  • Virus Internalization*
  • Virus Release*

Substances

  • Molecular Chaperones
  • Plant Viral Movement Proteins
  • Glucosyltransferases