PilG and PilH antagonistically control flagellum-dependent and pili-dependent motility in the phytopathogen Xanthomonas campestris pv. campestris

BMC Microbiol. 2020 Feb 18;20(1):37. doi: 10.1186/s12866-020-1712-3.

Abstract

Background: The virulence of the plant pathogen Xanthomonas campestris pv. campestris (Xcc) involves the coordinate expression of many virulence factors, including surface appendages flagellum and type IV pili, which are required for pathogenesis and the colonization of host tissues. Despite many insights gained on the structure and functions played by flagellum and pili in motility, biofilm formation, surface attachment and interactions with bacteriophages, we know little about how these appendages are regulated in Xcc.

Results: Here we present evidence demonstrating the role of two single domain response regulators PilG and PilH in the antagonistic control of flagellum-dependent (swimming) and pili-dependent (swarming) motility. Using informative mutagenesis, we reveal PilG positively regulates swimming motility while and negatively regulating swarming motility. Conversely, PilH negatively regulates swimming behaviour while and positively regulating swarming motility. By transcriptome analyses (RNA-seq and RT-PCR) we confirm these observations as PilG is shown to upregulate many genes involved chemotaxis and flagellar biosynthesis but these similar genes were downregulated by PilH. Co-immunoprecipitation, bacterial two-hybrid and pull-down analyses showed that PilH and PilG were able to interact with district subsets of proteins that potentially account for their regulatory impact. Additionally, we present evidence, using mutagenesis that PilG and PilH are involved in other cellular processes, including chemotaxis and virulence.

Conclusions: Taken together, we demonstrate that for the conditions tested PilG and PilH have inverse regulatory effects on flagellum-dependent and pili-dependent motility in Xcc and that this regulatory impact depends on these proteins influences on genes/proteins involved in flagellar biosynthesis and pilus assembly.

Keywords: Antagonistic control; Motility; PilG and PilH; Virulence factors; Xanthomonas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chemotaxis
  • Fimbriae Proteins / genetics*
  • Fimbriae Proteins / metabolism
  • Fimbriae, Bacterial / genetics*
  • Fimbriae, Bacterial / metabolism
  • Flagella / genetics*
  • Flagella / metabolism
  • Gene Expression Profiling
  • Gene Expression Regulation, Bacterial
  • Mutagenesis
  • Real-Time Polymerase Chain Reaction
  • Sequence Analysis, RNA
  • Xanthomonas campestris / pathogenicity
  • Xanthomonas campestris / physiology*

Substances

  • Fimbriae Proteins