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Proteolytic activity of surface‐exposed HtrA determines its expression level and is needed to survive acidic conditions in Clostridioides difficile
Open accessPublished 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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Highly accurate protein structure prediction with AlphaFold
Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O., Tunyasuvunakool, K., Bates, R., Žídek, A., Potapenko, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03819-2 · Cited by 43,764
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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
- ORCID
- 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
- hybrid
- doi.org
- Licence
- 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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