The Catabolite Repressor/Activator Cra Is a Bridge Connecting Carbon Metabolism and Host Colonization in the Plant Drought Resistance-Promoting Bacterium Pantoea alhagi LTYR-11Z

Appl Environ Microbiol. 2018 Jun 18;84(13):e00054-18. doi: 10.1128/AEM.00054-18. Print 2018 Jul 1.

Abstract

Efficient root colonization is a prerequisite for application of plant growth-promoting (PGP) bacteria in improving health and yield of agricultural crops. We have recently identified an endophytic bacterium, Pantoea alhagi LTYR-11Z, with multiple PGP properties that effectively colonizes the root system of wheat and improves its growth and drought tolerance. To identify novel regulatory genes required for wheat colonization, we screened an LTYR-11Z transposon (Tn) insertion library and found cra to be a colonization-related gene. By using transcriptome (RNA-seq) analysis, we found that transcriptional levels of an eps operon, the ydiV gene encoding an anti-FlhD4C2 factor, and the yedQ gene encoding an enzyme for synthesis of cyclic dimeric GMP (c-di-GMP) were significantly downregulated in the Δcra mutant. Further studies demonstrated that Cra directly binds to the promoters of the eps operon, ydiV, and yedQ and activates their expression, thus inhibiting motility and promoting exopolysaccharide (EPS) production and biofilm formation. Consistent with previous findings that Cra plays a role in transcriptional regulation in response to carbon source availability, the activating effects of Cra were much more pronounced when LTYR-11Z was grown within a gluconeogenic environment than when it was grown within a glycolytic environment. We further demonstrate that the ability of LTYR-11Z to colonize wheat roots is modulated by the availability of carbon sources. Altogether, these results uncover a novel strategy utilized by LTYR-11Z to achieve host colonization in response to carbon nutrition in the environment, in which Cra bridges a connection between carbon metabolism and colonization capacity of LTYR-11Z.IMPORTANCE Rapid and appropriate response to environmental signals is crucial for bacteria to adapt to competitive environments and to establish interactions with their hosts. Efficient colonization and persistence within the host are controlled by various regulatory factors that respond to specific environmental cues. The most common is nutrient availability. In this work, we unraveled the pivotal role of Cra in regulation of colonization ability of Pantoea alhagi LTYR-11Z in response to carbon source availability. Moreover, we identified three novel members of the Cra regulon involved in EPS synthesis, regulation of flagellar biosynthesis, and synthesis of c-di-GMP and propose a working model to explain the Cra-mediated regulatory mechanism that links carbon metabolism to host colonization. This study elucidates the regulatory role of Cra in bacterial attachment and colonization of plants, which raises the possibility of extending our studies to other bacteria associated with plant and human health.

Keywords: Cra; biofilm; c-di-GMP; carbon metabolism; colonization; exopolysaccharides; motility.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Biofilms
  • Carbon / metabolism*
  • Carrier Proteins
  • Cyclic GMP / metabolism
  • Droughts*
  • Endophytes / metabolism
  • Gene Expression Regulation, Bacterial
  • Host Microbial Interactions / genetics
  • Host Microbial Interactions / physiology
  • Operon
  • Pantoea / genetics
  • Pantoea / metabolism*
  • Plant Roots / microbiology
  • Polysaccharides, Bacterial
  • Promoter Regions, Genetic
  • Regulon
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism*
  • Transcriptome
  • Triticum / metabolism*
  • Triticum / microbiology*

Substances

  • Bacterial Proteins
  • Carrier Proteins
  • Polysaccharides, Bacterial
  • Repressor Proteins
  • exopolysaccharide, Bacillus
  • FruR protein, Bacteria
  • Carbon
  • Cyclic GMP