Cited by 4Clostridium difficile and Clostridium perfringens researchHeat shock proteins researchBacterial Genetics and Biotechnology

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Proteolytic activity of surface‐exposed HtrA determines its expression level and is needed to survive acidic conditions in Clostridioides difficile

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Published version of a preprint

Abstract

To survive in the host, pathogenic bacteria need to be able to react to the unfavorable conditions that they encounter, like low pH, elevated temperatures, antimicrobial peptides and many more. These conditions may lead to unfolding of envelope proteins and this may be lethal. One of the mechanisms through which bacteria are able to survive these conditions is through the protease/foldase activity of the high temperature requirement A (HtrA) protein. The gut pathogen Clostridioides difficile encodes one HtrA homolog that is predicted to contain a membrane anchor and a single PDZ domain. The function of HtrA in C. difficile is hitherto unknown but previous work has shown that an insertional mutant of htrA displayed elevated toxin levels, less sporulation and decreased binding to target cells. Here, we show that HtrA is membrane associated and localized on the surface of C. difficile and characterize the requirements for proteolytic activity of recombinant soluble HtrA. In addition, we show that the level of HtrA in the bacteria heavily depends on its proteolytic activity. Finally, we show that proteolytic activity of HtrA is required for survival under acidic conditions.

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Metadata

Authors
Corver, J., Claushuis, B., Shamorkina, T. M., de Ru, A. H., van Leeuwen, M. M., Hensbergen, P. J., & Smits, W. K.
Affiliations
  • Leiden University (NL)
  • Leiden University Medical Center (NL)
Corresponding author
Corver, Jeroen
Venue
Molecular Microbiology
Publisher
Wiley
Published
2024-07-30
Volume
122
Issue
4
Pages
413-428
ISSN
  • 0950-382X (ISSN-L)
  • 1365-2958
OpenAlex
W4401192998
Cited by
4
References
2
Citations by year
2026: 1 · 2025: 2 · 2024: 1
FWCI
1.38
Type
journal article
Language
en
Open access
Locations
  • Molecular Microbiology (publishedVersion, cc-by)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • Leiden Repository (Leiden University) (submittedVersion, cc-by)
Topics
  • Health Sciences › Medicine › Infectious Diseases › Clostridium difficile and Clostridium perfringens research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Heat shock proteins research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
Keywords
HtrA, Clostridium difficile, proteolytic activity, PDZ domain, membrane-associated protease, toxin expression, sporulation
MeSH terms
Bacterial Proteins, Hydrogen-Ion Concentration, Gene Expression Regulation, Bacterial, Clostridioides difficile, Proteolysis

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