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Absolute Enumeration of Probiotic Strains Lactobacillus acidophilus NCFM® and Bifidobacterium animalis subsp. lactis Bl-04® via Chip-Based Digital PCR

机译:益生菌嗜酸乳杆菌NCFM®和动物双歧杆菌亚种的绝对计数。 lactisBl-04®通过基于芯片的数字PCR

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摘要

The current standard for enumeration of probiotics to obtain colony forming units by plate counts has several drawbacks: long time to results, high variability and the inability to discern between bacterial strains. Accurate probiotic cell counts are important to confirm the delivery of a clinically documented dose for its associated health benefits. A method is described using chip-based digital PCR (cdPCR) to enumerate Bifidobacterium animalis subsp. lactis Bl-04 and Lactobacillus acidophilus NCFM both as single strains and in combination. Primers and probes were designed to differentiate the target strains against other strains of the same species using known single copy, genetic differences. The assay was optimized to include propidium monoazide pre-treatment to prevent amplification of DNA associated with dead probiotic cells as well as liberation of DNA from cells with intact membranes using bead beating. The resulting assay was able to successfully enumerate each strain whether alone or in multiplex. The cdPCR method had a 4 and 5% relative standard deviation (RSD) for Bl-04 and NCFM, respectively, making it more precise than plate counts with an industry accepted RSD of 15%. cdPCR has the potential to replace traditional plate counts because of its precision, strain specificity and the ability to obtain results in a matter of hours.
机译:当前通过板计数计数益生菌以获得菌落形成单位的标准存在以下缺陷:产生时间长,变异性高以及无法区分细菌菌株。准确的益生菌细胞计数对于确认临床记录剂量的相关健康益处非常重要。描述了一种使用基于芯片的数字PCR(cdPCR)枚举动物双歧杆菌亚种的方法。乳酸菌Bl-04和嗜酸乳杆菌NCFM既可以作为单一菌株,也可以组合使用。使用已知的单拷贝,遗传差异设计引物和探针,以区分目标菌株与相同物种的其他菌株。该测定经过优化,包括预处理单叠氮化丙锭,以防止与死益生菌细胞相关的DNA扩增以及使用珠子敲打从具有完整膜的细胞中释放DNA。所得的测定能够成功地枚举每个菌株,无论是单独还是多重。 cdPCR方法对Bl-04和NCFM的相对标准偏差(RSD)分别为4%和5%,使其比板数更精确,业界认可的RSD为15%。由于cdPCR的精确度,菌株特异性以及在数小时内即可获得结果的能力,因此有可能取代传统的板数。

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