Small molecule inhibitors of the response regulator ArsR exhibit bactericidal activity against Helicobacter pylori

González Rodríguez, Andrés (Universidad de Zaragoza) ; Casado, Javier ; Chueca, Eduardo ; Salillas, Sandra (Universidad de Zaragoza) ; Velázquez-Campoy, Adrián (Universidad de Zaragoza) ; Sancho, Javier (Universidad de Zaragoza) ; Lanas, Ángel (Universidad de Zaragoza)

Resumen: Helicobacter pylori is considered the most prevalent bacterial pathogen in humans. The increasing antibiotic resistance evolved by this microorganism has raised alarm bells worldwide due to the significant reduction in the eradication rates of traditional standard therapies. A major challenge in this antibiotic resistance crisis is the identification of novel microbial targets whose inhibitors can overcome the currently circulating resistome. In the present study, we have validated the use of the essential response regulator ArsR as a novel and promising therapeutic target against H. pylori infections. A high-throughput screening of a repurposing chemical library using a fluorescence-based thermal shift assay identified several ArsR binders. At least four of these low-molecular weight compounds noticeably inhibited the DNA binding activity of ArsR and showed bactericidal effects against antibiotic-resistant strains of H. pylori. Among the ArsR inhibitors, a human secondary bile acid, lithocholic acid, quickly destroyed H. pylori cells and exhibited partial synergistic action in combination with clarithromycin or levofloxacin, while the antimicrobial effect of this compound against representative members of the normal human microbiota such as Escherichia coli and Staphylococcus epidermidis appeared irrelevant. Our results enhance the battery of novel therapeutic tools against refractory infections caused by multidrug-resistant H. pylori strains.

Idioma: Inglés

DOI: 10.3390/microorganisms8040503

Año: 2020

Publicado en: Microorganisms 8, 4 (2020), 503 [16 pp.]
ISSN: 2076-2607

Factor impacto JCR: 4.128 (2020)

Categ. JCR: MICROBIOLOGY rank: 52 / 136 = 0.382 (2020) - Q2 - T2

Factor impacto SCIMAGO: 0.857 - Microbiology (Q2) - Virology (Q2) - Microbiology (medical) (Q2)

Financiación: info:eu-repo/grantAgreement/ES/DGA/B25-17R
Financiación: info:eu-repo/grantAgreement/ES/DGA/E45-17R
Financiación: info:eu-repo/grantAgreement/ES/FIS/PI11-02578
Financiación: info:eu-repo/grantAgreement/ES/MINECO/BFU2016-78232-P
Financiación: info:eu-repo/grantAgreement/ES/MINECO/FJCI-2014-20704
Financiación: info:eu-repo/grantAgreement/ES/MINECO/IJCI-2016-27419

Tipo y forma: Artículo (Versión definitiva)

Área (Departamento): Area Medicina (Dpto. Medicina, Psiqu. y Derm.)
Área (Departamento): Área Bioquímica y Biolog.Mole. (Dpto. Bioq.Biolog.Mol. Celular)