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Toxicon ; 243: 107713, 2024 May 28.
Article in English | MEDLINE | ID: mdl-38615997

ABSTRACT

Multidrug resistance in bacteria is a major challenge worldwide, increasing both mortality by infections and costs for the health systems. Therefore, it is of utmost importance to find new drugs against resistant bacteria. Beauvericin (BEA) is a mycotoxin produced by entomopathogenic and other fungi of the genus Fusarium. Our work determines the effect of BEA combined with antibiotics, which has not been previously explored. The combination analysis included different antibiotics against non-methicillin-resistant Staphylococcus aureus (NT-MRSA), methicillin-resistant Staphylococcus aureus (MRSA), and Salmonella typhimurium. BEA showed a synergy effect with oxacillin with a fractional inhibitory concentration index (FICI) = 0.373 and an additive effect in combination with lincomycin (FICI = 0.507) against MRSA. In contrast, it was an antagonist when combined with ciprofloxacin against S. typhimurium. We propose BEA as a molecule with the potential for the development of new therapies in combination with current antibiotics against multidrug-resistant bacteria.


Subject(s)
Anti-Bacterial Agents , Depsipeptides , Methicillin-Resistant Staphylococcus aureus , Microbial Sensitivity Tests , Salmonella typhimurium , Methicillin-Resistant Staphylococcus aureus/drug effects , Anti-Bacterial Agents/pharmacology , Salmonella typhimurium/drug effects , Depsipeptides/pharmacology , Drug Synergism , Drug Resistance, Multiple, Bacterial
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