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采用新型基于 PCR 的定量方法测定的紫锥菊内总细菌负荷与 LPS 水平和体外巨噬细胞活性相关。

Total bacterial load within Echinacea purpurea, determined using a new PCR-based quantification method, is correlated with LPS levels and in vitro macrophage activity.

机构信息

National Center for Natural Products Research, University of Mississippi, University, MS 38677-1848, USA.

出版信息

Planta Med. 2013 Jan;79(1):9-14. doi: 10.1055/s-0032-1328023. Epub 2012 Dec 4.

Abstract

Our previous studies indicate that the majority of in vitro monocyte/macrophage activation exhibited by extracts of Echinacea depends on bacterial components. In the present study, total bacterial load was determined within E. purpurea samples and ranged from 6.4 × 10(6) to 3.3 × 10(8) bacteria/g of dry plant material. To estimate total bacterial load, we developed a PCR-based quantification method that circumvents the problems associated with nonviable/nonculturable cells (which precludes using plate counts) or the coamplification of mitochondrial or chloroplast DNA with the use of universal bacterial primers (which precludes the use of qPCR). Differences in total bacterial load within Echinacea samples were strongly correlated with the activity (NF-κB activation in THP-1 cells) and content of bacterial lipopolysaccharides within extracts of this plant material. These results add to the growing body of evidence that bacteria within Echinacea are the main source of components responsible for enhancing innate immune function.

摘要

我们之前的研究表明,紫锥菊提取物中体外单核细胞/巨噬细胞激活多数依赖于细菌成分。在本研究中,我们测定了紫锥菊样品中的总细菌负荷,范围为每克干植物材料 6.4×10(6)至 3.3×10(8)个细菌。为了估计总细菌负荷,我们开发了一种基于 PCR 的定量方法,该方法规避了与非存活/不可培养细胞相关的问题(这排除了使用平板计数),或使用通用细菌引物时线粒体或叶绿体 DNA 的共扩增(这排除了 qPCR 的使用)。紫锥菊样品中的总细菌负荷差异与该植物材料提取物中的细菌脂多糖的活性(THP-1 细胞中的 NF-κB 激活)和含量强烈相关。这些结果增加了越来越多的证据,即紫锥菊中的细菌是增强固有免疫功能的成分的主要来源。

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