Microbial pathogenesis · 2023
In vitro and in silico evidences about the inhibition of MepA efflux pump by coumarin derivatives.
СтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Martin Ana Luíza A R, Pereira Raimundo Luiz Silva, Rocha Janaína Esmeraldo, Farias Pablo A M, Freitas Thiago S, de Lemos Caldas Francisco Rodrigo, Figueredo Fernando G, Sampaio Nadghia Figueiredo Leite, Ribeiro-Filho Jaime, Menezes Irwin Rose de Alencar, Brancaglion Guilherme Andrade, de Paulo Daniela Carvalho, Carvalho Diogo T, Lima Micheline Azevedo, Coutinho Henrique D M, Fonteles Marta M F
Аннотация
The discovery of antibiotics has significantly transformed the outcomes of bacterial infections in the last decades. However, the development of antibiotic resistance mechanisms has allowed an increasing number of bacterial strains to overcome the action of antibiotics, decreasing their effectiveness against infections they were developed to treat. This study aimed to evaluate the antibacterial activity of synthetic coumarins Staphylococcus aureus in vitro and analyze their interaction with the MepA efflux pump in silico. The Minimum Inhibitory Concentration (MIC) determination showed that none of the test compounds have antibacterial activity. However, all coumarin derivatives decreased the MIC of the standard efflux inhibitor ethidium bromide, indicating antibacterial synergism. On the other hand, the C14 derivative potentiated the antibacterial activity of ciprofloxacin against the resistant strain. In silico analysis showed that C9, C11, and C13 coumarins showed the most favorable interaction with the MepA efflux pump. Nevertheless, due to the present in silico and in vitro investigation limitations, further experimental research is required to confirm the therapeutic potential of these compounds in vivo.