Functional Microbiology, Institute of Microbiology, Department of Pathobiology, University of Veterinary Medicine Vienna, 1210 Vienna, Austria.
Chair of Food Chemistry and Molecular Sensory Science, Technical University of Munich, Lise-Meitner-Straße 34, 85354 Freising, Germany.
Toxins (Basel). 2021 Feb 4;13(2):115. doi: 10.3390/toxins13020115.
The emetic toxin cereulide is a 1.2 kDa dodecadepsipeptide produced by the food pathogen . As cereulide poses a serious health risk to humans, sensitive and specific detection, as well as toxin purification and quantification, methods are of utmost importance. Recently, a stable isotope dilution assay tandem mass spectrometry (SIDA-MS/MS)-based method has been described, and an method for the quantitation of cereulide in foods was established by the International Organization for Standardization (ISO). However, although this SIDA-MS/MS method is highly accurate, the sophisticated high-end MS equipment required for such measurements limits the method's suitability for microbiological and molecular research. Thus, we aimed to develop a method for cereulide toxin detection and isolation using equipment commonly available in microbiological and biochemical research laboratories. Reproducible detection and relative quantification of cereulide was achieved, employing reversed phase chromatography (RPC). Chromatographic signals were cross validated by ultraperformance liquid chromatography-mass spectrometry (UPLC-MS/MS). The specificity of the RPC method was tested using a test panel of strains that included non-emetic representatives of the group, emetic strains, and cereulide-deficient isogenic mutants. In summary, the new method represents a robust, economical, and easily accessible research tool that complements existing diagnostics for the detection and quantification of cereulide.
呕吐毒素 cereulide 是一种 1.2 kDa 的十二肽,由食源性病原体产生。由于 cereulide 对人类健康构成严重威胁,因此敏感、特异的检测以及毒素的纯化和定量方法至关重要。最近,描述了一种基于稳定同位素稀释分析串联质谱(SIDA-MS/MS)的方法,并由国际标准化组织(ISO)建立了一种定量检测食品中 cereulide 的方法。然而,尽管这种 SIDA-MS/MS 方法非常准确,但这种测量所需的复杂高端 MS 设备限制了该方法在微生物学和分子研究中的适用性。因此,我们旨在开发一种使用微生物学和生化研究实验室常用设备检测和分离 cereulide 毒素的方法。采用反相色谱(RPC)实现了 cereulide 的可重复检测和相对定量。通过超高效液相色谱-质谱联用(UPLC-MS/MS)对色谱信号进行了交叉验证。使用包括非呕吐型 代表菌株、呕吐型菌株和 cereulide 缺陷同基因突变体的测试面板测试了 RPC 方法的特异性。总之,该新方法代表了一种强大、经济且易于获取的研究工具,可补充现有用于检测和定量 cereulide 的诊断方法。