Janež Nika, Ladányi Márta, Zaveršek Nika, Čotar Petra, Sebastijanović Aleksandar, Štrancar Janez, Sabotič Jerica, Pajk Stane
Department of Biotechnology, Jožef Stefan Institute, Ljubljana, Slovenia.
Department of Applied Statistics, Institute of Mathematics and Basic Science, Hungarian University of Agriculture and Life Sciences (MATE), Budapest, Hungary.
J Microbiol Methods. 2025 Sep;236:107206. doi: 10.1016/j.mimet.2025.107206. Epub 2025 Jul 29.
Imaging bacterial biofilms using confocal fluorescence microscopy is used to study their structures, but its wider application is constrained by the limited availability of effective labelling tools. Small chemical fluorescent probes offer a versatile alternative to heterologous expression of fusion or reporter proteins, but data on their effects on biofilm formation are lacking. In this study, we synthesized a series of new lipophilic fluorescent probes based on Nile blue, Nile red and coumarin scaffold. We investigated them for the labelling of Listeria biofilms and determined their effects on the growth and biofilm biomass formation. The Nile red probe SP-AM 7 and the coumarin probe PAG 31 inhibited biofilm development and showed a strong bactericidal effect. The Nile blue probe PAG 19 had the least effect on the tested parameters, but labelled slowly, while the fast-labelling Nile red probe SP-AM 8 promoted biofilm formation. Both are suitable for use during biofilm growth, resulting in less variation in biomass-related measurements than probes added prior to imaging. In the 3D imaging-based measurements for selected probes, we found no difference in the total biomass formed compared to the control dye, but a redistribution of biomass in the 3D layers was observed. Other probes were found to be slow to label, leave traces of unused probes or interfere with attachment to the surface. Our results show that fluorescent probe labelling should be evaluated from chemical, physical and biological points of view to understand their reliability and credibility.
使用共聚焦荧光显微镜对细菌生物膜进行成像可用于研究其结构,但其更广泛的应用受到有效标记工具可用性有限的限制。小型化学荧光探针为融合蛋白或报告蛋白的异源表达提供了一种通用的替代方法,但关于它们对生物膜形成影响的数据却很缺乏。在本研究中,我们基于尼罗蓝、尼罗红和香豆素支架合成了一系列新型亲脂性荧光探针。我们研究了它们对李斯特菌生物膜的标记作用,并确定了它们对生长和生物膜生物量形成的影响。尼罗红探针SP-AM 7和香豆素探针PAG 31抑制生物膜发育,并显示出很强的杀菌作用。尼罗蓝探针PAG 19对测试参数的影响最小,但标记速度较慢,而快速标记的尼罗红探针SP-AM 8促进生物膜形成。两者都适用于生物膜生长过程中使用,与成像前添加的探针相比,在与生物量相关的测量中产生的变化更小。在对选定探针进行的基于三维成像的测量中,我们发现与对照染料相比,形成的总生物量没有差异,但观察到生物量在三维层中的重新分布。发现其他探针标记速度慢、会留下未使用探针的痕迹或干扰与表面的附着。我们的结果表明,应从化学、物理和生物学角度评估荧光探针标记,以了解其可靠性和可信度。