National Food Institute, Technical University of Denmark, Søborg, Denmark.
FEMS Microbiol Lett. 2012 Dec;337(1):38-47. doi: 10.1111/1574-6968.12004. Epub 2012 Oct 3.
Alterations in the human gut microbiota caused, for example, by diet, functional foods, antibiotics, or occurring as a function of age are now known to be of relevance for host health. Therefore, there is a strong need for methods to detect such alterations in a rapid and comprehensive manner. In the present study, we developed and validated a high-throughput real-time quantitative PCR-based analysis platform, termed 'GUt Low-Density Array' (GULDA). The platform was designed for simultaneous analysis of the change in the abundance of 31 different microbial 16S rRNA gene targets in fecal samples obtained from individuals at various points in time. The target genes represent important phyla, genera, species, or other taxonomic groups within the five predominant bacterial phyla of the gut, Firmicutes, Bacteroidetes, Actinobacteria, Proteobacteria, and Verrucomicrobia and also Euryarchaeota. To demonstrate the applicability of GULDA, analysis of fecal samples obtained from six healthy infants at both 9 and 18 months of age was performed and showed a significant increase over time of the relative abundance of bacteria belonging to Clostridial cluster IV (Clostridia leptum group) and Bifidobacterium bifidum and concurrent decrease in the abundance of Clostridium butyricum and a tendency for decrease in Enterobacteriaceae over the 9-month period.
例如,饮食、功能性食品、抗生素引起的人类肠道微生物群的改变,或者随着年龄的增长而发生的改变,现在被认为与宿主健康有关。因此,非常需要一种快速、全面的方法来检测这些改变。在本研究中,我们开发并验证了一种高通量实时定量 PCR 分析平台,称为“GUt 低通量阵列”(GULDA)。该平台旨在同时分析来自不同时间点个体的粪便样本中 31 种不同微生物 16S rRNA 基因靶标的丰度变化。靶基因代表了肠道中五个主要细菌门(厚壁菌门、拟杆菌门、放线菌门、变形菌门和疣微菌门)以及古菌门内的重要门、属、种或其他分类群。为了证明 GULDA 的适用性,对 6 名健康婴儿在 9 个月和 18 个月时获得的粪便样本进行了分析,结果表明,属于梭菌簇 IV(Clostridia leptum 组)和双歧杆菌的细菌相对丰度随着时间的推移显著增加,而丁酸梭菌的丰度同时下降,肠杆菌科的数量有减少的趋势。