The presence and absence of periplasmic rings in bacterial flagellar motors correlates with stator type

Elife. 2019 Jan 16:8:e43487. doi: 10.7554/eLife.43487.

Abstract

The bacterial flagellar motor, a cell-envelope-embedded macromolecular machine that functions as a cellular propeller, exhibits significant structural variability between species. Different torque-generating stator modules allow motors to operate in different pH, salt or viscosity levels. How such diversity evolved is unknown. Here, we use electron cryo-tomography to determine the in situ macromolecular structures of three Gammaproteobacteria motors: Legionella pneumophila, Pseudomonas aeruginosa, and Shewanella oneidensis, providing the first views of intact motors with dual stator systems. Complementing our imaging with bioinformatics analysis, we find a correlation between the motor's stator system and its structural elaboration. Motors with a single H+-driven stator have only the core periplasmic P- and L-rings; those with dual H+-driven stators have an elaborated P-ring; and motors with Na+ or Na+/H+-driven stators have both their P- and L-rings embellished. Our results suggest an evolution of structural elaboration that may have enabled pathogenic bacteria to colonize higher-viscosity environments in animal hosts.

Keywords: Legionella pneumophila; Pseudomonas aeruginosa; Shewanella oneidensis MR-1; bacterial flagellar motor; electron cryo-tomography; evolution; evolutionary biology; infectious disease; microbiology.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Flagella / metabolism*
  • Flagella / ultrastructure
  • Gammaproteobacteria / metabolism*
  • Gammaproteobacteria / ultrastructure
  • Molecular Motor Proteins / chemistry*
  • Periplasm / metabolism*
  • Periplasm / ultrastructure
  • Phylogeny
  • Sodium / metabolism

Substances

  • Molecular Motor Proteins
  • Sodium