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Translocation of Yersinia enterocolitica through an endothelial monolayer by polymorphonuclear leukocytes

H Rüssmann1, K Ruckdeschel, J Heesemann

  • 1Institute for Hygiene and Microbiology, University of Würzburg, Germany.

Insights

Human polymorphonuclear leukocytes (PMNs) infected with Yersinia bacteria can move through endothelial cell layers. This bacterial translocation may aid Yersinia dissemination in hosts.

Area of Science:

  • Microbiology
  • Immunology
  • Cell Biology

Background:

  • Yersinia bacteria are pathogenic microorganisms that can cause severe infections.
  • Polymorphonuclear leukocytes (PMNs) are crucial immune cells involved in combating bacterial infections.
  • Understanding pathogen-host interactions at the cellular level is vital for developing effective treatments.

Purpose of the Study:

  • To investigate the ability of Yersinia-infected human polymorphonuclear leukocytes (PMNs) to translocate across an endothelial cell monolayer.
  • To determine if Yersinia bacteria can be transported by PMNs through a biological barrier.

Main Methods:

  • Cultured human endothelial cells on a basement membrane-coated microporous membrane.
  • Infected PMNs with varying concentrations of Yersinia bacteria (1-8 bacteria per PMN).
  • Assessed the translocation of infected PMNs and viable Yersinia from an upper chamber to a chemoattractant-containing lower chamber.

Main Results:

  • PMNs infected with Yersinia were capable of translocating across the endothelial cell monolayer.
  • Viable Yersinia bacteria were successfully transported from the upper to the lower chamber by the translocating PMNs.
  • The study demonstrated PMN-mediated translocation of Yersinia in vitro.

Conclusions:

  • Yersinia-infected PMNs can facilitate the movement of bacteria across endothelial barriers.
  • This PMN-mediated translocation process may represent a mechanism for Yersinia extravasation and dissemination within the host.
  • The findings highlight a novel aspect of Yersinia pathogenesis involving immune cell participation.

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