Rickettsia Sca4 Reduces Vinculin-Mediated Intercellular Tension to Promote Spread

Rebecca L Lamason1, Effie Bastounis2, Natasha M Kafai1

  • 1Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA.

Cell
|October 22, 2016
PubMed

Insights

Spotted fever group rickettsiae spread differently than other bacteria. Rickettsia parkeri uses a novel mechanism involving the effector Sca4 to reduce cell tension, facilitating cell-to-cell movement.

Area of Science:

  • Microbiology
  • Cell Biology
  • Pathogen-Host Interactions

Background:

  • Spotted fever group (SFG) rickettsiae are human pathogens that infect vascular cells.
  • Bacterial dissemination often relies on actin-based motility for cell-to-cell spread.
  • SFG rickettsiae spread involves protrusion formation, engulfment, and vacuolar escape.

Purpose of the Study:

  • To investigate the mechanism of cell-to-cell spread employed by SFG rickettsiae, specifically Rickettsia parkeri.
  • To identify bacterial factors involved in SFG rickettsiae dissemination.
  • To elucidate how Rickettsia parkeri manipulates host cell processes to spread through tissues.

Main Methods:

  • Transposon mutagenesis was used to identify key bacterial effectors.
  • Interaction studies were performed to map protein-protein interactions (Sca4, vinculin, α-catenin).
  • Traction and monolayer stress microscopy were employed to analyze host cell mechanics.

Main Results:

  • Rickettsia parkeri typically lacks actin tails during cell spread.
  • The secreted effector Sca4 promotes protrusion engulfment by interacting with vinculin and disrupting vinculin-α-catenin binding.
  • Sca4 reduces vinculin-dependent mechanotransduction at cell-cell junctions, lowering intercellular tension.

Conclusions:

  • SFG rickettsiae, like Rickettsia parkeri, utilize a unique strategy for dissemination that does not rely on actin-based motility.
  • The effector Sca4 plays a critical role in facilitating spread by reducing host intercellular tension.
  • This mechanism represents a novel approach to manipulating host cytoskeletal forces for pathogen spread.

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