Nod Factor-Independent Nodulation in Aeschynomene evenia Required the Common Plant-Microbe Symbiotic Toolkit

Plant Physiol. 2015 Dec;169(4):2654-64. doi: 10.1104/pp.15.01134. Epub 2015 Oct 7.

Abstract

Nitrogen fixation in the legume-rhizobium symbiosis is a crucial area of research for more sustainable agriculture. Our knowledge of the plant cascade in response to the perception of bacterial Nod factors has increased in recent years. However, the discovery that Nod factors are not involved in the Aeschynomene-Bradyrhizobium spp. interaction suggests that alternative molecular dialogues may exist in the legume family. We evaluated the conservation of the signaling pathway common to other endosymbioses using three candidate genes: Ca(2+)/Calmodulin-Dependent Kinase (CCaMK), which plays a central role in cross signaling between nodule organogenesis and infection processes; and Symbiosis Receptor Kinase (SYMRK) and Histidine Kinase1 (HK1), which act upstream and downstream of CCaMK, respectively. We showed that CCaMK, SYMRK, and HK1 are required for efficient nodulation in Aeschynomene evenia. Our results demonstrate that CCaMK and SYMRK are recruited in Nod factor-independent symbiosis and, hence, may be conserved in all vascular plant endosymbioses described so far.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Bradyrhizobium / metabolism
  • Bradyrhizobium / physiology*
  • Calcium-Calmodulin-Dependent Protein Kinases / classification
  • Calcium-Calmodulin-Dependent Protein Kinases / genetics
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism
  • Fabaceae / genetics
  • Fabaceae / microbiology*
  • Fabaceae / physiology*
  • Gene Expression Regulation, Plant
  • Histidine Kinase
  • Host-Pathogen Interactions
  • Lipopolysaccharides / metabolism
  • Microscopy, Confocal
  • Molecular Sequence Data
  • Phylogeny
  • Plant Proteins / classification
  • Plant Proteins / genetics
  • Plant Proteins / metabolism
  • Plant Root Nodulation / genetics
  • Plant Root Nodulation / physiology*
  • Plants, Genetically Modified
  • Protein Kinases / classification
  • Protein Kinases / genetics
  • Protein Kinases / metabolism
  • Receptor Protein-Tyrosine Kinases / genetics
  • Receptor Protein-Tyrosine Kinases / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Homology, Amino Acid
  • Symbiosis / physiology*

Substances

  • Lipopolysaccharides
  • Nod factor, Rhizobium leguminosarum
  • Plant Proteins
  • Protein Kinases
  • Receptor Protein-Tyrosine Kinases
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Histidine Kinase