Niño-Padilla Esmeralda Ivonne, Espitia Clara, Velazquez Carlos, Alday Efrain, Silva-Campa Erika, Burgara-Estrella Alexel, Enciso-Moreno José Antonio, Valenzuela Olivia, Astiazarán-García Humberto, Garibay-Escobar Adriana
Departamento de Ciencias Químico Biológicas, Universidad de Sonora, Rosales y Luis Encinas s/n, Hermosillo 83000, Sonora, México.
Departamento de Inmunología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad Universitaria, Coyoacán 04510, Ciudad de México, México.
ACS Omega. 2023 Oct 20;8(43):40665-40676. doi: 10.1021/acsomega.3c05703. eCollection 2023 Oct 31.
The aim of this study was to evaluate the potential antibiofilm activity of () compounds over BCG ( BCG) as a model for (). We evaluated the antibiofilm activity as the ability to both inhibit biofilm formation and disrupt preformed biofilms (bactericidal) of compounds, which have been previously described as being antimycobacterials against . BCG developed air-liquid interface biofilms with surface attachment ability and drug tolerance. Of the extracts and compounds that were tested, precatorin A (PreA) displayed the best biofilm inhibitory activity, as evaluated by biofilm biomass quantification, viable cell count, and confocal and atomic force microscopy procedures. Furthermore, its combination with isoniazid at subinhibitory concentrations inhibited BCG biofilm formation. Nonetheless, neither PreA nor the extract showed bactericidal effects. PreA is the compound responsible for biofilm inhibitory activity against BCG.
本研究的目的是评估()化合物对卡介苗(BCG)作为()模型的潜在抗生物膜活性。我们将抗生物膜活性评估为抑制生物膜形成和破坏已形成生物膜(杀菌)的能力,这些化合物先前已被描述为抗分枝杆菌药物。卡介苗形成了具有表面附着能力和耐药性的气液界面生物膜。在所测试的提取物和化合物中,通过生物膜生物量定量、活菌计数以及共聚焦和原子力显微镜程序评估,前胡素A(PreA)表现出最佳的生物膜抑制活性。此外,其与亚抑制浓度的异烟肼联合使用可抑制卡介苗生物膜的形成。尽管如此,PreA和提取物均未显示出杀菌作用。PreA是对卡介苗具有生物膜抑制活性的()化合物。