Wang Ping, Liang Lijiao, Peng Xinkai, Qu Tianming, Zhao Xiaomei, Ji Qinglong, Chen Ying
Chinese Academy of Inspection and Quarantine, Beijing 100176, China.
College of Biosystems Engineering and Food Science, Zhejiang University, Hangzhou 310058, China.
Microorganisms. 2024 Jul 23;12(8):1504. doi: 10.3390/microorganisms12081504.
As a famous probiotic, HN001 is widely added to probiotic products. Different strains have different probiotic effects, and the active HN001 strain is the key to exerting probiotic effects, so it is of great practical significance for realising the detection of HN001 at the strain level in probiotic products. In this study, strain-specific primer pairs and probes were designed. A combined treatment of sodium deoxycholate (SD) and propidium monoazide (PMA) inhibited the amplification of dead bacterial DNA, establishing a SD-PMA-ddPCR system and conditions for detecting live HN001 in probiotic powders. Specificity was confirmed using type strains and commercial strains. Sensitivity tests with spiked samples showed a detection limit of 10⁵ CFU/g and a linear quantification range of 1.42 × 10⁵-1.42 × 10⁹ CFU/g. Actual sample testing demonstrated the method's efficiency in quantifying HN001 in compound probiotic products. This method offers a reliable tool for the rapid and precise quantification of viable HN001, crucial for the quality monitoring of probiotic products.
作为一种著名的益生菌,HN001被广泛添加到益生菌产品中。不同菌株具有不同的益生菌作用,而活性HN001菌株是发挥益生菌作用的关键,因此实现益生菌产品中HN001菌株水平的检测具有重要的现实意义。在本研究中,设计了菌株特异性引物对和探针。脱氧胆酸钠(SD)和单叠氮碘化丙啶(PMA)的联合处理抑制了死细菌DNA的扩增,建立了用于检测益生菌粉中活HN001的SD-PMA-ddPCR系统和条件。使用模式菌株和商业菌株确认了特异性。加标样品的灵敏度测试显示检测限为10⁵ CFU/g,线性定量范围为1.42×10⁵-1.42×10⁹ CFU/g。实际样品测试证明了该方法在定量复合益生菌产品中HN001方面的有效性。该方法为快速、精确地定量活HN001提供了可靠工具,这对益生菌产品的质量监测至关重要。