Glycosylation regulates specific induction of rice immune responses by Acidovorax avenae flagellin

J Biol Chem. 2011 Jul 22;286(29):25519-30. doi: 10.1074/jbc.M111.254029. Epub 2011 May 31.

Abstract

Plants have a sensitive system that detects various pathogen-derived molecules to protect against infection. Flagellin, a main component of the bacterial flagellum, from the rice avirulent N1141 strain of the Gram-negative phytopathogenic bacterium Acidovorax avenae induces plant immune responses including H₂O generation, whereas flagellin from the rice virulent K1 strain of A. avenae does not induce these immune responses. To clarify the molecular mechanism that leads to these differing responses between the K1 and N1141 flagellins, recombinant K1 and N1141 flagellins were generated using an Escherichia coli expression system. When cultured rice cells were treated with recombinant K1 or N1141 flagellin, both flagellins equally induced H₂O₂ generation, suggesting that post-translational modifications of the flagellins are involved in the specific induction of immune responses. Mass spectrometry analyses using glycosyltransferase-deficient mutants showed that 1,600- and 2,150-Da glycans were present on the flagellins from N1141 and K1, respectively. A deglycosylated K1 flagellin induced immune responses in the same manner as N1141 flagellin. Site-directed mutagenesis revealed that glycans were attached to four amino acid residues (Ser¹⁷⁸, Ser¹⁸³, Ser²¹², and Thr³⁵¹) in K1 flagellin. Among mutant K1 flagellins in which each glycan-attached amino acid residue was changed to alanine, S178A and S183A, K1 flagellin induced a strong immune response in cultured rice cells, indicating that the glycans at Ser¹⁷⁸ and Ser¹⁸³ in K1 flagellin prevent epitope recognition in rice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Binding Sites
  • Cells, Cultured
  • Comamonadaceae / genetics
  • Comamonadaceae / immunology*
  • Epitopes / immunology
  • Escherichia coli / genetics
  • Flagellin / chemistry
  • Flagellin / genetics
  • Flagellin / immunology*
  • Flagellin / metabolism*
  • Glycosylation
  • Molecular Sequence Data
  • Oryza / immunology*
  • Oryza / microbiology*
  • Polysaccharides / metabolism
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / immunology
  • Recombinant Proteins / metabolism
  • Sequence Deletion

Substances

  • Epitopes
  • Polysaccharides
  • Recombinant Proteins
  • Flagellin