Expression of RcrB confers resistance to hypochlorous acid in uropathogenic


Journal

bioRxiv : the preprint server for biology
Titre abrégé: bioRxiv
Pays: United States
ID NLM: 101680187

Informations de publication

Date de publication:
01 Jun 2023
Historique:
medline: 3 7 2023
pubmed: 3 7 2023
entrez: 3 7 2023
Statut: epublish

Résumé

To eradicate bacterial pathogens, neutrophils are recruited to the sites of infection, where they engulf and kill microbes through the production of reactive oxygen and chlorine species (ROS/RCS). The most prominent RCS is antimicrobial oxidant hypochlorous acid (HOCl), which rapidly reacts with various amino acids side chains, including those containing sulfur and primary/tertiary amines, causing significant macromolecular damage. Pathogens like uropathogenic Bacterial infections pose an increasing threat to human health exacerbating the demand for alternative treatment options. UPEC, the most common etiological agent of urinary tract infections (UTIs), are confronted by neutrophilic attacks in the bladder, and must therefore be well equipped with powerful defense systems to fend off the toxic effects of RCS. How UPEC deal with the negative consequences of the oxidative burst in the neutrophil phagosome remains unclear. Our study sheds light on the requirements for the expression and protective effects of RcrB, which we recently identified as UPEC's most potent defense system towards HOCl-stress and phagocytosis. Thus, this novel HOCl-stress defense system could potentially serve as an attractive drug target to increase the body's own capacity to fight UTIs.

Identifiants

pubmed: 37398214
doi: 10.1101/2023.06.01.543251
pmc: PMC10312555
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIAID NIH HHS
ID : R15 AI164585
Pays : United States

Commentaires et corrections

Type : UpdateIn

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Auteurs

Mary E Crompton (ME)

School of Biological Sciences, Illinois State University, Microbiology, Normal, IL, USA.

Luca F Gaessler (LF)

School of Biological Sciences, Illinois State University, Microbiology, Normal, IL, USA.

Patrick O Tawiah (PO)

School of Biological Sciences, Illinois State University, Microbiology, Normal, IL, USA.

Lisa Pfirsching (L)

School of Biological Sciences, Illinois State University, Microbiology, Normal, IL, USA.

Sydney K Camfield (SK)

School of Biological Sciences, Illinois State University, Microbiology, Normal, IL, USA.

Colton Johnson (C)

School of Biological Sciences, Illinois State University, Microbiology, Normal, IL, USA.

Kennadi Meurer (K)

School of Biological Sciences, Illinois State University, Microbiology, Normal, IL, USA.

Mehdi Bennis (M)

School of Biological Sciences, Illinois State University, Microbiology, Normal, IL, USA.

Brendan Roseberry (B)

School of Biological Sciences, Illinois State University, Microbiology, Normal, IL, USA.

Sadia Sultana (S)

School of Biological Sciences, Illinois State University, Microbiology, Normal, IL, USA.

Jan-Ulrik Dahl (JU)

School of Biological Sciences, Illinois State University, Microbiology, Normal, IL, USA.

Classifications MeSH