Berlec Aleš, Janež Nika, Sterniša Meta, Klančnik Anja, Sabotič Jerica
Department of Biotechnology, Jožef Stefan Institute, Ljubljana, Slovenia.
Faculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.
Bio Protoc. 2022 Feb 5;12(3):e4308. doi: 10.21769/BioProtoc.4308.
Biofilms serve as a bacterial survival strategy, allowing bacteria to persist under adverse environmental conditions. The non-pathogenic Listeria innocua is used as a surrogate organism for the foodborne pathogen Listeria monocytogenes, because they share genetic and physiological similarities and can be used in a Biosafety Level 1 laboratory. Several methods are used to evaluate biofilms, including different approaches to determine biofilm biomass or culturability, viability, metabolic activity, or other microbial community properties. Routinely used methods for biofilm assay include the classical culture-based plate counting method, biomass staining methods (e.g., crystal violet and safranin red), DNA staining methods (e.g., Syto 9), methods that use metabolic substrates to detect live bacteria (e.g., tetrazolium salts or resazurin), and PCR-based methods to quantify bacterial DNA. The NanoLuc (Nluc) luciferase biofilm assay is a viable alternative or complement to existing methods. Functional Nluc was expressed in L. innocua using the nisin-inducible expression system and bacterial detection was performed using furimazine as substrate. Concentration dependent bioluminescence signals were obtained over a concentration range greater than three log units. The Nluc bioluminescence method allows absolute quantification of bacterial cells, has high sensitivity, broad range, good day-to-day repeatability, and good precision with acceptable accuracy. The advantages of Nluc bioluminescence also include direct detection, absolute cell quantification, and rapid execution. Graphic abstract: Engineering to express NanoLuc and its application in bioluminescence assay.
生物膜是细菌的一种生存策略,使细菌能够在不利的环境条件下持续存在。无害李斯特菌作为食源性病原体单核细胞增生李斯特菌的替代生物体,因为它们具有遗传和生理上的相似性,并且可以在生物安全1级实验室中使用。有几种方法用于评估生物膜,包括确定生物膜生物量或可培养性、活力、代谢活性或其他微生物群落特性的不同方法。生物膜检测常用的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(如Syto 9)、使用代谢底物检测活细菌的方法(如四唑盐或刃天青)以及基于PCR的方法来定量细菌DNA。纳米荧光素酶(Nluc)生物膜检测是现有方法的可行替代或补充。使用乳链菌肽诱导表达系统在无害李斯特菌中表达功能性Nluc,并使用呋喃嗪作为底物进行细菌检测。在大于三个对数单位的浓度范围内获得了浓度依赖性生物发光信号。Nluc生物发光方法能够对细菌细胞进行绝对定量,具有高灵敏度、宽范围、良好的日常重复性以及在可接受准确性下的良好精密度。Nluc生物发光的优点还包括直接检测、绝对细胞定量和快速执行。图形摘要:工程改造以表达纳米荧光素酶及其在生物发光检测中的应用。