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The Gut Microbiotassay: a high-throughput qPCR approach combinable with next generation sequencing to study gut microbial diversity

机译:肠道微生物测定:高通量qpCR方法与下一代测序相结合,可研究肠道微生物多样性

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摘要

BackgroundThe intestinal microbiota is a complex and diverse ecosystem that plays a significant role in maintaining the health and well-being of the mammalian host. During the last decade focus has increased on the importance of intestinal bacteria. Several molecular methods can be applied to describe the composition of the microbiota. This study used a new approach, the Gut Microbiotassay: an assembly of 24 primer sets targeting the main phyla and taxonomically related subgroups of the intestinal microbiota, to be used with the high-throughput qPCR chip ‘Access Array 48.48′, AA48.48, (Fluidigm®) followed by next generation sequencing. Primers were designed if necessary and all primer sets were screened against DNA extracted from pure cultures of 15 representative bacterial species. Subsequently the setup was tested on DNA extracted from small and large intestinal content from piglets with and without diarrhoea. The PCR amplicons from the 2304 reaction chambers were harvested from the AA48.48, purified, and sequenced using 454-technology.ResultsThe Gut Microbiotassay was able to detect significant differences in the quantity and composition of the microbiota according to gut sections and diarrhoeic status. 454-sequencing confirmed the specificity of the primer sets. Diarrhoea was associated with a reduced number of members from the genus Streptococcus, and in particular S. alactolyticus.ConclusionThe Gut Microbiotassay provides fast and affordable high-throughput quantification of the bacterial composition in many samples and enables further descriptive taxonomic information if combined with 454-sequencing.
机译:背景肠道菌群是一个复杂多样的生态系统,在维持哺乳动物宿主的健康和福祉方面发挥着重要作用。在过去的十年中,重点已经放在肠道细菌的重要性上。可以采用几种分子方法来描述微生物群的组成。这项研究采用了一种新方法,即肠道微生物菌群测定法:将24个引物组组装成针对肠道菌群的主要菌群和与分类学相关的亚组,并与高通量qPCR芯片'Access Array 48.48',AA48.48, (Fluidigm®),然后进行下一代测序。如果需要,设计引物,并针对从15种代表性细菌物种的纯培养物中提取的DNA筛选所有引物。随后,对从有和没有腹泻的仔猪小肠和大肠中提取的DNA进行测试。来自2304个反应室的PCR扩增子是从AA48.48收获的,并使用454技术进行了测序和测序。结果肠道菌群分析能够根据肠道切片和腹泻状况检测出菌群的数量和组成之间的显着差异。 454测序证实了引物组的特异性。腹泻与链球菌属,尤其是解乳链球菌的成员数量减少有关。结论肠道菌群分析可对许多样品中的细菌成分进行快速,可负担的高通量定量分析,如果与454-结合使用可提供进一步的描述性分类学信息排序。

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