Falco Natalie, Griffin Matthew E
Department of Pharmaceutical Sciences, University of California, Irvine, Irvine, CA 92697, USA.
Department of Pharmaceutical Sciences, University of California, Irvine, Irvine, CA 92697, USA; Department of Molecular Biology & Biochemistry, University of California, Irvine, Irvine, CA 92697, USA; Department of Chemistry, University of California, Irvine, Irvine, CA 92697, USA.
Curr Opin Chem Biol. 2025 Feb;84:102551. doi: 10.1016/j.cbpa.2024.102551. Epub 2024 Nov 30.
Our microbiota plays crucial roles in immune development and homeostasis and has been implicated in virtually all major diseases of the 21st century. Nevertheless, our understanding of the exact microbial functions that underlie these correlations remains extremely limited, due in large part to the difficulty of profiling cellular activities within non-model organisms and complex communities. Over the past decade, new flow cytometric approaches have been developed to distinguish specific microbial populations based on their interactions with metabolite analogs, modified biomolecules, and reactive compounds. By selecting and separating active microbes via fluorescence-activated cell sorting, PRobe INcorporation for Targeted sequencing (PRINT-seq) has inspired innovative approaches to identify and characterize functional members of our microbiota. Here, we provide a broad overview of this evolving technology and summarize how this method has been recently employed as a diagnostic fingerprint for diverse microbial activities.
我们的微生物群在免疫发育和体内平衡中发挥着关键作用,并且几乎与21世纪的所有主要疾病都有关联。然而,我们对这些关联背后确切的微生物功能的理解仍然极为有限,这在很大程度上是由于在非模式生物和复杂群落中分析细胞活动存在困难。在过去十年中,已经开发出了新的流式细胞术方法,用于根据微生物与代谢物类似物、修饰的生物分子和反应性化合物的相互作用来区分特定的微生物群体。通过荧光激活细胞分选来选择和分离活性微生物,靶向测序的探针掺入法(PRINT-seq)激发了识别和表征我们微生物群功能成员的创新方法。在这里,我们对这项不断发展的技术进行了广泛概述,并总结了该方法最近是如何被用作各种微生物活动的诊断指纹的。