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体外条件下两歧双歧杆菌 PRL2010 的全基因组转录谱分析及定量实时 PCR 参考基因的鉴定。

Global genome transcription profiling of Bifidobacterium bifidum PRL2010 under in vitro conditions and identification of reference genes for quantitative real-time PCR.

机构信息

Laboratory of Probiogenomics, Department of Genetics, Biology of Microorganisms, Anthropology and Evolution, University of Parma, Parma, Italy.

出版信息

Appl Environ Microbiol. 2011 Dec;77(24):8578-87. doi: 10.1128/AEM.06352-11. Epub 2011 Oct 14.

Abstract

Bifidobacteria have attracted significant scientific attention due to their perceived role as health-promoting microorganisms, although the genetics of the bacterial group is still underexplored. In this study, we investigated the transcriptome of Bifidobacterium bifidum PRL2010 during in vitro growth by microarray technology. When B. bifidum PRL2010 was grown in liquid broth, 425 of the 1,644 PRL2010 genes represented on the array were expressed in at least one of the three investigated growth phases, i.e., the lag, exponential, and stationary phases. These transcriptional analyses identified a core in vitro transcriptome encompassing 150 genes that are expressed in all phases. A proportion of these genes were further investigated as potential reference genes by quantitative real-time reverse transcription-PCR (qRT-PCR) assays. Their expression stability was evaluated under different growth conditions, which included cultivation on different carbon sources, exposure to environmental stresses (thermal, acidic, and osmotic), and growth phases. Our analyses validated six reference genes suitable for normalizing mRNA expression levels in qRT-PCR experiments applied to bifidobacteria.

摘要

双歧杆菌由于被认为是具有促进健康作用的微生物,引起了科学界的极大关注,尽管该细菌群的遗传学仍未得到充分探索。在这项研究中,我们通过微阵列技术研究了双歧杆菌 PRl2010 在体外生长过程中的转录组。当 PRl2010 在液体肉汤中生长时,在微阵列上表示的 1644 个 PRl2010 基因中的 425 个在至少三个研究的生长阶段(即迟滞期、指数期和稳定期)中的一个中表达。这些转录分析确定了一个包含 150 个基因的核心体外转录组,这些基因在所有阶段都表达。这些基因中的一部分作为潜在的参考基因进一步通过定量实时逆转录 PCR(qRT-PCR) 检测进行了研究。根据不同的生长条件,评估了它们的表达稳定性,这些条件包括在不同的碳源上培养、暴露于环境压力(热、酸和渗透压)以及生长阶段。我们的分析验证了 6 个适用于双歧杆菌 qRT-PCR 实验中标准化 mRNA 表达水平的参考基因。

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