Čukajne Tjaša, Štravs Petra, Sahin Orhan, Zhang Qijing, Berlec Aleš, Klančnik Anja
Department of Food Science and Technology, Biotechnical Faculty, University of Ljubljana, Ljubljana, Slovenia.
Department of Biotechnology, Jožef Stefan Institute, Ljubljana, Slovenia.
Bio Protoc. 2025 Feb 20;15(4):e5192. doi: 10.21769/BioProtoc.5192.
, a widespread pathogen found in birds and mammals, poses a significant risk for zoonosis worldwide despite its susceptibility to environmental and food-processing stressors. One of its main survival mechanisms is the formation of biofilms that can withstand various food-processing stressors, which is why efficient methods for assessing biofilms are crucial. Existing methods, including the classical culture-based plate counting method, biomass-staining methods (e.g., crystal violet and safranin), DNA-staining methods, those that use metabolic substrates to detect live bacteria (e.g., tetrazolium salts and resazurin), immunofluorescence with flow cytometry or fluorescence microscopy, and PCR-based methods for quantification of bacterial DNA, are diverse but often lack specificity, sensitivity, and suitability. In response to these limitations, we propose an innovative approach using NanoLuc as a reporter protein. The established protocol involves growing biofilms in microtiter plates, washing unattached cells, adding Nano-Glo luciferase substrate, and measuring bioluminescence. The bacterial concentrations in the biofilms are calculated by linear regression based on the calibration curve generated with known cell concentrations. The NanoLuc protein offers a number of advantages, such as its small size, temperature stability, and highly efficient bioluminescence, enabling rapid, non-invasive, and comprehensive assessment of biofilms together with quantification of a wide range of cell states. Although this method is limited to laboratory use due to the involvement of genetically modified organisms, it provides valuable insights into biofilm dynamics that could indirectly help in the development of improved food safety measures. Key features • Quantification of using NanoLuc luciferase. • The assay is linear in the range of 1.9 × 10 to 1.5 × 10 CFU/mL. • Following biofilm growth, less than 1 h is required for detection. • The assay requires genetically modified bacterial strains.
是一种在鸟类和哺乳动物中广泛存在的病原体,尽管它对环境和食品加工应激源敏感,但在全球范围内仍构成重大的人畜共患病风险。其主要生存机制之一是形成能够抵御各种食品加工应激源的生物膜,这就是为什么评估生物膜的有效方法至关重要。现有方法包括基于经典培养的平板计数法、生物量染色法(如结晶紫和番红)、DNA染色法、使用代谢底物检测活细菌的方法(如四氮唑盐和刃天青)、流式细胞术或荧光显微镜免疫荧光法以及基于PCR的细菌DNA定量方法,这些方法多种多样,但往往缺乏特异性、敏感性和适用性。针对这些局限性,我们提出了一种使用纳米荧光素酶(NanoLuc)作为报告蛋白的创新方法。既定方案包括在微量滴定板中培养生物膜、洗涤未附着的细胞、添加纳米荧光素酶底物并测量生物发光。根据已知细胞浓度生成的校准曲线,通过线性回归计算生物膜中的细菌浓度。纳米荧光素酶蛋白具有许多优点,例如其尺寸小、温度稳定性好和生物发光效率高,能够对生物膜进行快速、非侵入性和全面的评估,并对广泛的细胞状态进行定量。尽管由于涉及转基因生物,该方法仅限于实验室使用,但它为生物膜动态提供了有价值的见解,这可能间接有助于制定改进的食品安全措施。关键特性• 使用纳米荧光素酶对进行定量。• 该测定在1.9×10至1.5×10 CFU/mL范围内呈线性。• 生物膜生长后,检测所需时间少于1小时。• 该测定需要转基因细菌菌株。