Antibiofilm activity of promethazine against ESBL-producing strains of Escherichia coli in urinary catheters

大肠杆菌 微生物学 异丙嗪 泌尿系统 肠杆菌科 生物 医学 化学 药理学 内科学 生物化学 基因
作者
Cecília Rocha da Silva,Vitória Pessoa de Farias Cabral,Daniel Sampaio Rodrigues,Sarah Alves Barbosa,Amanda Dias Barbosa,Sarah Alves Barbosa,Sarah Alves Barbosa,Lara Elloyse Almeida Moreira,Sarah Alves Barbosa,Marisa Vieira de Queiroz,Sarah Alves Barbosa,Sarah Alves Barbosa,Sarah Alves Barbosa,Lívia Gurgel do Amaral Valente Sá
出处
期刊:Microbial Pathogenesis [Elsevier]
卷期号:193: 106769-106769
标识
DOI:10.1016/j.micpath.2024.106769
摘要

The bacterium Escherichia coli is one of the main causes of urinary tract infections. The formation of bacterial biofilms, especially associated with the use of urinary catheters, contributes to the establishment of recurrent infections and the development of resistance to treatment. Strains of E. coli that produce extended-spectrum beta-lactamases (ESBL) have a greater ability to form biofilms. In addition, there is a lack of drugs available in the market with antibiofilm activity. Promethazine (PMZ) is an antihistamine known to have antimicrobial activity against different pathogens, including in the form of biofilms, but there are still few studies of its activity against ESBL E. coli biofilms. The aim of this study was to evaluate the antimicrobial activity of PMZ against ESBL E. coli biofilms, as well as to assess the application of this drug as a biofilm prevention agent in urinary catheters. To this end, the minimum inhibitory concentration and minimum bactericidal concentration of PMZ in ESBL E. coli strains were determined using the broth microdilution assay and tolerance level measurement. The activity of PMZ against the cell viability of the in vitro biofilm formation of ESBL E. coli was analyzed by the MTT colorimetric assay and its ability to prevent biofilm formation when impregnated in a urinary catheter was investigated by counting colony-forming units (CFU) and confirmed by scanning electron microscopy (SEM). PMZ showed bactericidal activity and significantly reduced (p < 0.05) the viability of the biofilm being formed by ESBL E. coli at concentrations of 256 and 512 μg/ml, as well as preventing the formation of biofilm on urinary catheters at concentrations starting at 512 μg/ml by reducing the number of CFUs, as also observed by SEM. Thus, PMZ is a promising candidate to prevent the formation of ESBL E. coli biofilms on abiotic surfaces.
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