Hansen Sarah J Z, Morovic Wesley, DeMeules Martha, Stahl Buffy, Sindelar Connie W
Probiotic Development, DuPont Nutrition & Health, Madison, WI, United States.
Genomics and Microbiome Sciences, DuPont Nutrition & Health, Madison, WI, United States.
Front Microbiol. 2018 Apr 11;9:704. doi: 10.3389/fmicb.2018.00704. eCollection 2018.
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 subsp. Bl-04 and 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.
获得结果的时间长、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输送及其相关健康益处非常重要。本文描述了一种使用基于芯片的数字PCR(cdPCR)对嗜酸乳杆菌亚种Bl-04和嗜热栖热放线菌NCFM进行计数的方法,这两种菌既可以单独计数,也可以联合计数。设计了引物和探针,利用已知的单拷贝基因差异,将目标菌株与同一物种的其他菌株区分开来。该检测方法经过优化,包括单叠氮丙锭预处理,以防止与死亡益生菌细胞相关的DNA扩增,以及使用珠磨法从完整细胞膜的细胞中释放DNA。最终的检测方法能够成功地对每种菌株进行单独或多重计数。对于Bl-04和NCFM,cdPCR方法的相对标准偏差(RSD)分别为4%和5%,这使其比行业公认RSD为15%的平板计数法更精确。由于其精确性、菌株特异性以及能够在数小时内获得结果,cdPCR有潜力取代传统的平板计数法。