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Evaluation of propidium monoazide real-time PCR for enumeration of probiotic lactobacilli microencapsulated in calcium alginate beads

机译:单叠氮化丙锭实时PCR评估微囊化藻酸钙珠粒中益生菌乳杆菌的评估

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摘要

The aim of the study was to evaluate real-time PCR coupled with propidium monoazide (PMA) treatment for enumeration of microencapsulated probiotic lactobacilli microencapsulated in calcium alginate beads. Lactobacillus gasseri K7 (CCM 7710) and Lactobacillus delbrueckii subsp. bulgaricus (CCM 7712) were analysed by plate counting and PMA real-time PCR during storage at 4 degrees C for 90 days. PMA was effective in preventing PCR amplification of the target sequences of DNA released from heat-compromised bacteria. The values obtained by real-time PCR of non-treated samples were in general higher than those obtained by real-time PCR of PMA-treated samples or by plate counting, indicating the presence of sub-lethally injured cells. This study shows that plate count could not be completely replaced by culture independent method PMA real-time PCR for enumeration of probiotics, but may rather complement the well-established plate counting, providing useful information about the ratio of compromised bacteria in the samples.
机译:这项研究的目的是评估实时PCR结合单叠氮化丙锭(PMA)处理对微囊化在藻酸钙珠粒中的微囊化益生菌乳杆菌的计数。盖氏乳杆菌K7(CCM 7710)和德氏乳杆菌亚种。在4摄氏度下储存90天期间,通过板计数和PMA实时PCR分析了保加利亚(CCM 7712)。 PMA可以有效防止PCR扩增从热受损细菌释放的DNA的靶序列。通过未处理样品的实时PCR获得的值通常高于通过PMA处理样品的实时PCR或通过平板计数获得的值,表明存在亚致死性损伤的细胞。这项研究表明,不能用培养无关的方法PMA实时PCR完全取代板计数来计数益生菌,而是可以补充已建立的板计数,从而提供有关样品中受感染细菌比率的有用信息。

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