Growth conditions determine the DNF2 requirement for symbiosis

PLoS One. 2014 Mar 14;9(3):e91866. doi: 10.1371/journal.pone.0091866. eCollection 2014.

Abstract

Rhizobia and legumes are able to interact in a symbiotic way leading to the development of root nodules. Within nodules, rhizobia fix nitrogen for the benefit of the plant. These interactions are efficient because spectacularly high densities of nitrogen fixing rhizobia are maintained in the plant cells. DNF2, a Medicago truncatula gene has been described as required for nitrogen fixation, bacteroid's persistence and to prevent defense-like reactions in the nodules. This manuscript shows that a Rhizobium mutant unable to differentiate is not sufficient to trigger defense-like reactions in this organ. Furthermore, we show that the requirement of DNF2 for effective symbiosis can be overcome by permissive growth conditions. The dnf2 knockout mutants grown in vitro on agarose or Phytagel as gelling agents are able to produce nodules fixing nitrogen with the same efficiency as the wild-type. However, when agarose medium is supplemented with the plant defense elicitor ulvan, the dnf2 mutant recovers the fix- phenotype. Together, our data show that plant growth conditions impact the gene requirement for symbiotic nitrogen fixation and suggest that they influence the symbiotic suppression of defense reactions in nodules.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Gene Knockout Techniques
  • Medicago truncatula / drug effects
  • Medicago truncatula / growth & development*
  • Medicago truncatula / metabolism
  • Medicago truncatula / microbiology*
  • Mutation
  • Nitrogen Fixation / drug effects
  • Phenotype
  • Plant Proteins / genetics
  • Plant Proteins / metabolism*
  • Polysaccharides / pharmacology
  • Rhizobium / physiology
  • Symbiosis* / drug effects

Substances

  • Plant Proteins
  • Polysaccharides
  • ulvan

Grants and funding

This work has benefited from a French State grant (reference ANR-10-LABX-0040-SPS) managed by the French National Research Agency under an Investments for the Future program (reference n°ANR-11-IDEX-0003-02). This work was supported by the Centre National de la Recherche Scientifique (CNRS) and the grant Agence Nationale de la Recherche (ANR) Blanc International SVSE 6.2010.1 (LEGUMICS) to PR. MB was supported by a PhD fellowship from the French Ministry of Research. This work has benefited from the facilities and expertise of the Imagif Cell Biology Unit of the Gif campus (www.imagif.cnrs.fr) which is supported by the Conseil Général de l’Essonne. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.