Li H, Xiao J, Zhou Y, Wang Q, Zhang Y
State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, China.
Shanghai Engineering Research Center of Maricultured Animal Vaccines, Shanghai, China.
Lett Appl Microbiol. 2017 Sep;65(3):206-212. doi: 10.1111/lam.12763. Epub 2017 Jul 25.
Vibrio harveyi is an opportunistic pathogen in seawater and can cause severe vibriosis. It is prevalent in hatcheries worldwide and can lead to severe economic losses. Therefore, there is an urgent need to develop a rapid detection method for monitoring this pathogen. In this study, to increase the detection sensitivity of our assay with monoclonal antibodies (Mabs) against V. harveyi, the conditions of the dot blot assay were optimized, and enhanced chemiluminescent (ECL) substrate replaced the traditional tetramethylbenzidine (TMB) substrate. Based on the optimization results, an ECL-based novel dot blot assay was developed for the rapid and sensitive detection of V. harveyi. Compared with the traditional dot blot assay, the incubation time was shortened from 8 to 2 h. The limit of detection (LOD) for V. harveyi was 2 × 10 CFU per ml (10 CFU per spot) in pure bacterial suspension, which was 50-fold more sensitive than the traditional dot blot assay (1 × 10 CFU per ml). Furthermore, when compared with indirect ELISA, the dot blot assay showed approximately 1000-fold higher sensitivity (CFU/CFU). After the test sample was pre-enriched in turbot homogenates for 6 h before the dot blot analysis, the LOD for V. harveyi was 10 CFU per ml.
Vibrio harveyi is one of the most opportunistic pathogens that can cause high mortality in hatcheries worldwide. To detect this pathogen, a novel dot blot based on enhanced chemiluminescent (ECL) has been established. This ECL-based dot blot was found to be more sensitive and rapid for V. harveyi detection than traditional dot blot, and this technology is recommended as an applied protocol for monitoring V. harveyi in seawater to reduce economic losses.
哈维氏弧菌是海水中的一种机会致病菌,可导致严重的弧菌病。它在世界各地的孵化场中普遍存在,并可能导致严重的经济损失。因此,迫切需要开发一种快速检测方法来监测这种病原体。在本研究中,为了提高我们使用抗哈维氏弧菌单克隆抗体(Mabs)的检测方法的灵敏度,对斑点印迹法的条件进行了优化,并用增强化学发光(ECL)底物取代了传统的四甲基联苯胺(TMB)底物。基于优化结果,开发了一种基于ECL的新型斑点印迹法,用于快速灵敏地检测哈维氏弧菌。与传统的斑点印迹法相比,孵育时间从8小时缩短至2小时。在纯细菌悬液中,哈维氏弧菌的检测限(LOD)为每毫升2×10 CFU(每点10 CFU),比传统的斑点印迹法(每毫升1×10 CFU)灵敏50倍。此外,与间接ELISA相比,斑点印迹法的灵敏度高出约1000倍(CFU/CFU)。在斑点印迹分析前,将测试样品在大菱鲆匀浆中预富集6小时后,哈维氏弧菌的LOD为每毫升10 CFU。
哈维氏弧菌是最具机会致病性的病原体之一,可在世界各地的孵化场中导致高死亡率。为了检测这种病原体,建立了一种基于增强化学发光(ECL)的新型斑点印迹法。发现这种基于ECL的斑点印迹法在检测哈维氏弧菌方面比传统的斑点印迹法更灵敏、快速,该技术被推荐作为监测海水中哈维氏弧菌以减少经济损失的应用方案。