利用荧光d -氨基酸标记和荧光原位杂交技术对体内肠道微生物群生长进行成像和定量分析的综合方法。

Yingjun Zhou, Liyuan Lin, Wei Wang
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引用次数: 0

摘要

肠道菌群对人体健康的深远影响已得到公认;然而,我们对肠道中微生物生长和活动的高度多样化和动态过程的理解仍然存在实质性的差距。传统的方法主要依赖于DNA测序,对这些方面提供的见解有限。本文提出了一种将荧光d -氨基酸(FDAA)代谢标记与荧光原位杂交(FISH)相结合的方案,用于成像和定量分析肠道微生物群的体内生长。通过小鼠灌胃顺序给予两种FDAAs,我们标记了肠道细菌在其天然环境中的肽聚糖,使细菌细胞壁上的标记信号作为细胞增殖和分裂的标记。我们还证明了fda标记的强度与肠道细菌的代谢活性直接相关。此外,FISH通过荧光显微镜或流式细胞术来区分特定的细菌分类群。这种综合方法大大提高了我们可视化和测量各种肠道细菌体内生长和代谢状态的能力,从而阐明了肠道生态系统中以前被模糊的“暗物质”。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An integrative approach for imaging and quantitative analysis of gut microbiota growth in vivo using fluorescent D-amino acid labeling and fluorescence in situ hybridization.

The profound influence of gut microbiota on human health has been well-recognized; however, substantial gaps remain in our understanding of the highly diverse and dynamic processes of microbial growth and activities in the gut. Conventional methods, which primarily rely on DNA sequencing, provide limited insights into these aspects. This paper presents a protocol that integrates fluorescent D-amino acid (FDAA) metabolic labeling with fluorescence in situ hybridization (FISH) for imaging and quantitatively analyzing the in vivo growth of gut microbiota. By administering two FDAAs sequentially through mouse gavage, we label the peptidoglycan of gut bacteria in their native environment, allowing the labeling signals on bacterial cell walls to serve as markers of cellular proliferation and division. We have also demonstrated that the intensity of FDAA labeling directly correlates with the metabolic activity of gut bacteria. Additionally, FISH is employed to distinguish specific bacterial taxa of interest via fluorescence microscopy or flow cytometry. This integrative method greatly enhances our capacity to visualize and measure the in vivo growth and metabolic states of various gut bacteria, thereby illuminating the previously obscured "dark matter" in the gut ecosystem.

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