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

机译:肠道菌群测定:一种高通量qPCR方法,可与下一代测序相结合,以研究肠道微生物多样性

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Background The 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. Results The 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. Conclusion The 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:背景技术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,人们越来越重视肠道细菌的重要性。可以采用几种分子方法来描述微生物群的组成。这项研究使用了一种新方法,即肠道微生物菌群测定法:将24个引物对组装成一个针对肠道菌群的主要菌群和与分类学相关的亚组的方法,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的小肠和大肠成分中提取的DNA进行测试。从AA48.48收获2304个反应室的PCR扩增子,纯化,并使用454技术测序。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上的显着差异。 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。结论肠道微生物菌群测定法可对许多样品中的细菌成分进行快速且可负担的高通量定量分析,如果与454测序结合使用,则可以获得进一步的描述性分类信息。

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