Literature DB >> 33322639

Ketone- and Cyano-Selenoesters to Overcome Efflux Pump, Quorum-Sensing, and Biofilm-Mediated Resistance.

Nikoletta Szemerédi1, Annamária Kincses1, Katerina Rehorova2, Lan Hoang2, Noemi Salardón-Jiménez3, Clotilde Sevilla-Hernández3, Jitka Viktorová2, Enrique Domínguez-Álvarez3, Gabriella Spengler1.   

Abstract

The emergence of drug-resistant pathogens leads to a gradual decline in the efficacy of many antibacterial agents, which poses a serious problem for proper therapy. Multidrug resistance (MDR) mechanisms allow resistant bacteria to have limited uptake of drugs, modification of their target molecules, drug inactivation, or release of the drug into the extracellular space by efflux pumps (EPs). In previous studies, selenoesters have proved to be promising derivatives with a noteworthy antimicrobial activity. On the basis of these results, two series of novel selenoesters were synthesized to achieve more potent antibacterial activity on Gram-positive and Gram-negative bacteria. Fifteen selenoesters (eight ketone-selenoesters and seven cyano-selenoesters) were investigated with regards to their efflux pump-inhibiting, anti-quorum-sensing (QS), and anti-biofilm effects in vitro. According to the results of the antibacterial activity, the ketone-selenoesters proved to be more potent antibacterial compounds than the cyano-selenoesters. With regard to efflux pump inhibition, one cyano-selenoester on methicillin-resistant S. aureus and one ketone-selenoester on Salmonella Typhimurium were potent inhibitors. The biofilm inhibitory capacity and the ability of the derivatives to disrupt mature biofilms were noteworthy in all the experimental systems applied. Regarding QS inhibition, four ketone-selenoesters and three cyano-selenoesters exerted a noteworthy effect on Vibrio campbellii strains.

Entities:  

Keywords:  Pseudomonas aeruginosa; Salmonella species; Staphylococcus aureus; antibacterial activity; biofilm; multidrug resistance; quorum sensing; selenoesters

Year:  2020        PMID: 33322639      PMCID: PMC7763688          DOI: 10.3390/antibiotics9120896

Source DB:  PubMed          Journal:  Antibiotics (Basel)        ISSN: 2079-6382


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