2-(2-Methyl-2-nitrovinyl)furan but Not Furvina Interfere with Staphylococcus aureus Agr Quorum-Sensing System and Potentiate the Action of Fusidic Acid against Biofilms
Autor: | Simona Distinto, Reinaldo Molina Ruiz, Fernanda Borges, Zenaida Rodríguez Negrín, Diana Oliveira, Manuel Simões, Anabela Borges |
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Přispěvatelé: | Faculdade de Engenharia, Faculdade de Ciências |
Rok vydání: | 2021 |
Předmět: |
2-nitrovinylfuran derivatives
0301 basic medicine medicine.drug_class Fusidic acid 030106 microbiology Antibiotics Staphylococcus aureus Virulence Furvina medicine.disease_cause Catalysis Microbiology lcsh:Chemistry Inorganic Chemistry 03 medical and health sciences Antibiotic resistance medicine antimicrobial resistance Physical and Theoretical Chemistry lcsh:QH301-705.5 Molecular Biology Spectroscopy antimicrobial combination Chemistry Organic Chemistry Biofilm General Medicine Computer Science Applications Quorum sensing 030104 developmental biology lcsh:Biology (General) lcsh:QD1-999 Bioreporter biofilms quorum-sensing inhibition medicine.drug |
Zdroj: | International Journal of Molecular Sciences, Vol 22, Iss 613, p 613 (2021) International Journal of Molecular Sciences Volume 22 Issue 2 |
ISSN: | 1422-0067 |
DOI: | 10.3390/ijms22020613 |
Popis: | Quorum sensing (QS) plays an essential role in the production of virulence factors, in biofilm formation and antimicrobial resistance. Consequently, inhibiting QS is being considered a promising target for antipathogenic/anti-virulence therapies. This study aims to screen 2-nitrovinylfuran derivatives structurally related to Furvina (a broad-spectrum antibiotic already used for therapeutic purposes) for their effects on QS and in biofilm prevention/control. Furvina and four 2-nitrovinylfuran derivatives (compounds 1&ndash 4) were tested to assess the ability to interfere with QS of Staphylococcus aureus using bioreporter strains (S. aureus ALC1742 and ALC1743). The activity of Furvina and the most promising quorum-sensing inhibitor (QSI) was evaluated in biofilm prevention and in biofilm control (combined with fusidic acid). The biofilms were further characterized in terms of biofilm mass, viability and membrane integrity. Compound 2 caused the most significant QS inhibition with reductions between 60% and 80%. Molecular docking simulations indicate that this compound interacts preferentially with the protein hydrophobic cleft in the LytTR domain of AgrA pocket. Metabolic inactivations of 40% for S. aureus ALC1742 and 20% for S. aureus ALC1743 were reached. A 24 h-old biofilm formed in the presence of the QSI increased the metabolic inactivation by fusidic acid to 80%, for both strains. The overall results highlight the effects of compound 2 as well as the potential of combining QSI with in-use antibiotics for the management of skin and soft tissues infections. |
Databáze: | OpenAIRE |
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