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Background  Serine protease HtrA exhibits both proteolytic and chaperone activities, which are involved in cellular protein quality control. Moreover, HtrA is an important virulence factor in many pathogens including  Helicobacter pylori , for which the crucial stage of infection is the cleavage of E-cadherin and other cell-to-cell junction proteins.    Methods  The in vitro study of  H. pylori  HtrA (HtrA  Hp  ) chaperone activity was carried out using light scattering assays and investigation of lysozyme protein aggregates. We produced  H. pylori  ∆ htrA  deletion and HtrA  Hp   point mutants without proteolytic activity in strain N6 and investigated the survival of the bacteria under thermal, osmotic, acidic and general stress conditions as well as the presence of puromycin or metronidazole using serial dilution tests and disk diffusion method. The levels of cellular and secreted proteins were examined using biochemical fraction and Western blotting. We also studied the proteolytic activity of secreted HtrA  Hp   using zymography and the enzymatic digestion of β-casein. Finally, the consequences of E-cadherin cleavage were determined by immunofluorescence microscopy.    Results  We demonstrate that HtrA  Hp   displays chaperone activity that inhibits the aggregation of lysozyme and is stable under various pH and temperature conditions. Next, we could show that N6 expressing only HtrA chaperone activity grow well under thermal, pH and osmotic stress conditions, and in the presence of puromycin or metronidazole. In contrast, in the absence of the entire  htrA  gene the bacterium was more sensitive to a number of stresses. Analysing the level of cellular and secreted proteins, we noted that  H. pylori  lacking the proteolytic activity of HtrA display reduced levels of secreted HtrA. Moreover, we compared the amounts of secreted HtrA from several clinical  H. pylori  strains and digestion of β-casein. We also demonstrated a significant effect of the HtrA  Hp   variants during infection of human epithelial cells and for E-cadherin cleavage.    Conclusion  Here we identified the chaperone activity of the HtrA  Hp   protein and have proven that this activity is important and sufficient for the survival of  H. pylori  under multiple stress conditions. We also pinpointed the importance of HtrA  Hp   chaperone activity for E- cadherin degradation and therefore for the virulence of this eminent pathogen.

Chaperone activity of serine protease HtrA of Helicobacter pylori as a crucial survival factor under stress conditions