Potentiation of Antibiotic Activity by a Meldrum’s Acid Arylamino Methylene Derivative against Multidrug-Resistant Bacterial Strains

被引:0
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作者
Maria M. C. da Silva
José B. de Araújo-Neto
Ana C. J. de Araújo
Priscilla R. Freitas
Cícera D. de M. Oliveira-Tintino
Iêda M. Begnini
Ricardo A. Rebelo
Luiz E. da Silva
Sandro L. Mireski
Michele C. Nasato
Maria I. L. Krautler
Jaime Ribeiro-Filho
Henrique D. M. Coutinho
Saulo R. Tintino
机构
[1] Regional University of Cariri—URCA,Laboratory of Microbiology and Molecular Biology (LMBM), Department of Biological Chemistry
[2] Federal University of Paraná—UFPR,Postgraduate Program in Sustainable Territorial Development—Coastal Sector
[3] Regional University of Blumenau—FURB,Department of Chemistry
[4] Oswaldo Cruz Foundation—IGM-FIOCRUZ/BA,Laboratory of Investigation in Genetics and Translational Hematology, Gonçalo Moniz Institute
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关键词
Antibiotic resistance; Fluoroquinolones; Meldrum’s acid; Arylamino derivatives;
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摘要
This study aimed to evaluate the intrinsic antibacterial activity and antibiotic-enhancing effect of an arylamino methylene derivative (MAD) in association with fluoroquinolones. The antibacterial activity against multiresistant Pseudomonas aeruginosa, Staphylococcus aureus and Escherichia coli was analyzed by determining the minimum inhibitory concentration (MIC) using the broth micro dilution method. A reduction in the MIC of the fluoroquinolones against strains treated simultaneously with the MAD was interpreted as an enhanced antibiotic activity. While the MAD exhibited no clinically effective action (MIC ≥ 1.024 µg/mL), it was found to significantly potentiate the activity of norfloxacin, ofloxacin and lomefloxacin against all the strains, which may be related to structural similarities between the MAD and quinolones. Our findings suggest that Meldrum’s acid arylamino derivatives may represent promising molecules in the elaboration of new drugs to reverse resistance to fluoroquinolones.
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页码:100 / 103
页数:3
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