The symbiotic biofilm of Sinorhizobium fredii SMH12, necessary for successful colonization and symbiosis of Glycine max cv Osumi, is regulated by Quorum Sensing systems and inducing flavonoids via NodD1

PLoS One. 2014 Aug 28;9(8):e105901. doi: 10.1371/journal.pone.0105901. eCollection 2014.

Abstract

Bacterial surface components, especially exopolysaccharides, in combination with bacterial Quorum Sensing signals are crucial for the formation of biofilms in most species studied so far. Biofilm formation allows soil bacteria to colonize their surrounding habitat and survive common environmental stresses such as desiccation and nutrient limitation. This mode of life is often essential for survival in bacteria of the genera Mesorhizobium, Sinorhizobium, Bradyrhizobium, and Rhizobium. The role of biofilm formation in symbiosis has been investigated in detail for Sinorhizobium meliloti and Bradyrhizobium japonicum. However, for S. fredii this process has not been studied. In this work we have demonstrated that biofilm formation is crucial for an optimal root colonization and symbiosis between S. fredii SMH12 and Glycine max cv Osumi. In this bacterium, nod-gene inducing flavonoids and the NodD1 protein are required for the transition of the biofilm structure from monolayer to microcolony. Quorum Sensing systems are also required for the full development of both types of biofilms. In fact, both the nodD1 mutant and the lactonase strain (the lactonase enzyme prevents AHL accumulation) are defective in soybean root colonization. The impairment of the lactonase strain in its colonization ability leads to a decrease in the symbiotic parameters. Interestingly, NodD1 together with flavonoids activates certain quorum sensing systems implicit in the development of the symbiotic biofilm. Thus, S. fredii SMH12 by means of a unique key molecule, the flavonoid, efficiently forms biofilm, colonizes the legume roots and activates the synthesis of Nod factors, required for successfully symbiosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Biofilms*
  • Flavonoids / biosynthesis*
  • Gene Expression Regulation, Bacterial
  • Glycine max / microbiology*
  • Mutation
  • Quorum Sensing
  • Sinorhizobium fredii / physiology*
  • Symbiosis

Substances

  • Bacterial Proteins
  • Flavonoids

Grants and funding

This work was supported by the following grants: AGL2012-38831 from the Spanish Ministerio de Economía y Competitividad, http://www.idi.mineco.gob.es/portal/site/MICINN/ P10-AGR-5821 and P11-CVI-7050 from the Junta de Andalucía, Consejería de Innovación, Ciencia y Empresas. http://www.juntadeandalucia.es/organismos/economiainnovacioncienciayempleo.html. Dr. Pérez-Montaño’s work was supported by an FPU fellowship from the Spanish Ministerio de Ciencia y Tecnología and a contract from the University of Seville. http://www.idi.mineco.gob.es/portal/site/MICINN/http://www.us.es/. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.