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Adenylate cyclase toxin of Bordetella parapertussis disrupts the epithelial barrier granting the bacterial access to the intracellular space of epithelial cells.

Juan Pablo GorgojoMariela Del Carmen CarricaCarlos Manuel BaroliHugo Alberto ValdezJimena Alvarez HayesMaria Eugenia Rodriguez
Published in: PloS one (2023)
B. parapertussis is one of the etiological agents of whooping cough. Once inhaled, the bacteria bind to the respiratory epithelium and start the infection. Little is known about this first step of host colonization and the role of the human airway epithelial barrier on B. parapertussis infection. We here investigated the outcome of the interaction of B. parapertussis with a polarized monolayer of respiratory epithelial cells. Our results show that B. parapertussis preferentially attaches to the intercellular boundaries, and causes the disruption of the tight junction integrity through the action of adenylate cyclase toxin (CyaA). We further found evidence indicating that this disruption enables the bacterial access to components of the basolateral membrane of epithelial cells to which B. parapertussis efficiently attaches and gains access to the intracellular location, where it can survive and eventually spread back into the extracellular environment. Altogether, these results suggest that the adenylate cyclase toxin enables B. parapertussis to overcome the epithelial barrier and eventually establish a niche of persistence within the respiratory epithelial cells.
Keyphrases
  • escherichia coli
  • endothelial cells
  • blood brain barrier
  • respiratory tract
  • cystic fibrosis
  • reactive oxygen species
  • high resolution
  • mass spectrometry
  • atomic force microscopy
  • prefrontal cortex
  • high speed