Host-induced bacterial cell wall decomposition mediates pattern-triggered immunity in Arabidopsis

Elife. 2014 Jun 23:3:e01990. doi: 10.7554/eLife.01990.

Abstract

Peptidoglycans (PGNs) are immunogenic bacterial surface patterns that trigger immune activation in metazoans and plants. It is generally unknown how complex bacterial structures such as PGNs are perceived by plant pattern recognition receptors (PRRs) and whether host hydrolytic activities facilitate decomposition of bacterial matrices and generation of soluble PRR ligands. Here we show that Arabidopsis thaliana, upon bacterial infection or exposure to microbial patterns, produces a metazoan lysozyme-like hydrolase (lysozyme 1, LYS1). LYS1 activity releases soluble PGN fragments from insoluble bacterial cell walls and cleavage products are able to trigger responses typically associated with plant immunity. Importantly, LYS1 mutant genotypes exhibit super-susceptibility to bacterial infections similar to that observed on PGN receptor mutants. We propose that plants employ hydrolytic activities for the decomposition of complex bacterial structures, and that soluble pattern generation might aid PRR-mediated immune activation in cell layers adjacent to infection sites.

Keywords: arabidopsis; glycan hydrolase; innate immunity; pattern-triggered immunity; peptidoglycan; plant biology; plant lysozyme.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis / genetics
  • Arabidopsis / immunology*
  • Arabidopsis / microbiology*
  • Bacteria / metabolism*
  • Base Sequence
  • Cell Wall / metabolism*
  • Gene Expression Regulation, Plant
  • Hydrolysis
  • Ligands
  • Molecular Sequence Data
  • Muramidase / chemistry
  • Nicotiana / genetics
  • Nicotiana / microbiology
  • Peptides / chemistry
  • Peptidoglycan / chemistry
  • Plant Immunity*
  • Plants, Genetically Modified / immunology
  • Plants, Genetically Modified / microbiology
  • Sequence Homology, Nucleic Acid

Substances

  • Ligands
  • Peptides
  • Peptidoglycan
  • Muramidase

Grants and funding

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.