Identification of domains of the Tomato spotted wilt virus NSm protein involved in tubule formation, movement and symptomatology

Virology. 2009 Jul 20;390(1):110-21. doi: 10.1016/j.virol.2009.04.027. Epub 2009 May 29.

Abstract

Deletion and alanine-substitution mutants of the Tomato spotted wilt virus NSm protein were generated to identify domains involved in tubule formation, movement and symptomatology using a heterologous Tobacco mosaic virus expression system. Two regions of NSm, G(19)-S(159) and G(209)-V(283), were required for both tubule formation in protoplasts and cell-to-cell movement in plants, indicating a correlation between these activities. Three amino acid groups, D(154), EYKK(205-208) and EEEEE(284-288) were linked with long-distance movement in Nicotiana benthamiana. EEEEE(284-288) was essential for NSm-mediated long-distance movement, whereas D(154) was essential for tubule formation and cell-to-cell movement; indicating separate genetic controls for cell-to-cell and long-distance movement. The region I(57)-N(100) was identified as the determinant of foliar necrosis in Nicotiana benthamiana, and mutagenesis of HH(93-94) greatly reduced necrosis. These findings are likely applicable to other tospovirus species, especially those within the 'New World' group as NSm sequences are highly conserved.

MeSH terms

  • Amino Acid Sequence
  • Amino Acid Substitution
  • Base Sequence
  • Conserved Sequence
  • DNA Primers / genetics
  • Molecular Sequence Data
  • Movement
  • Mutagenesis
  • Nicotiana / virology
  • Phylogeny
  • Plant Diseases / virology
  • Plant Viral Movement Proteins / chemistry
  • Plant Viral Movement Proteins / genetics
  • Plant Viral Movement Proteins / physiology
  • Protein Structure, Tertiary
  • Protoplasts / virology
  • Sequence Deletion
  • Sequence Homology, Amino Acid
  • Tospovirus / genetics
  • Tospovirus / pathogenicity
  • Tospovirus / physiology*
  • Viral Nonstructural Proteins / chemistry*
  • Viral Nonstructural Proteins / genetics
  • Viral Nonstructural Proteins / physiology*

Substances

  • DNA Primers
  • Plant Viral Movement Proteins
  • Viral Nonstructural Proteins