Motility control through an anti-activation mechanism in Agrobacterium tumefaciens

Mol Microbiol. 2021 Nov;116(5):1281-1297. doi: 10.1111/mmi.14823. Epub 2021 Oct 19.

Abstract

Many bacteria can migrate from a free-living, planktonic state to an attached, biofilm existence. One factor regulating this transition in the facultative plant pathogen Agrobacterium tumefaciens is the ExoR-ChvG-ChvI system. Periplasmic ExoR regulates the activity of the ChvG-ChvI two-component system in response to environmental stress, most notably low pH. ChvI impacts hundreds of genes, including those required for type VI secretion, virulence, biofilm formation, and flagellar motility. Previous studies revealed that activated ChvG-ChvI represses expression of most of class II and class III flagellar biogenesis genes, but not the master motility regulator genes visN, visR, and rem. In this study, we characterized the integration of the ExoR-ChvG-ChvI and VisNR-Rem pathways. We isolated motile suppressors of the non-motile ΔexoR mutant and thereby identified the previously unannotated mirA gene encoding a 76 amino acid protein. We report that the MirA protein interacts directly with the Rem DNA-binding domain, sequestering Rem and preventing motility gene activation. The ChvG-ChvI pathway activates mirA expression and elevated mirA is sufficient to block motility. This study reveals how the ExoR-ChvG-ChvI pathway prevents flagellar motility in A. tumefaciens. MirA is also conserved among other members of the Rhizobiales suggesting similar mechanisms of motility regulation.

Keywords: acid stress; flagella; gene regulation; overlapping regulons; protein-protein interaction.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Agrobacterium tumefaciens / physiology*
  • Amino Acid Sequence
  • Bacterial Outer Membrane Proteins / physiology*
  • Bacterial Proteins / physiology*
  • Gene Expression Regulation, Bacterial*
  • Genes, Bacterial
  • Protein Binding
  • Protein Kinases / physiology*
  • Stress, Physiological*
  • Transcription Factors / physiology*
  • Virulence

Substances

  • Bacterial Outer Membrane Proteins
  • Bacterial Proteins
  • Transcription Factors
  • chvI protein, Bacteria
  • Protein Kinases
  • chvG protein, Bacteria