Illumina, Inc, Madison, WI, 53719, USA.
Diversigen, Inc, New Brighton, MN, 55112, USA.
BMC Microbiol. 2023 Oct 20;23(1):299. doi: 10.1186/s12866-023-03037-y.
The microbiota that colonize the human gut and other tissues are dynamic, varying both in composition and functional state between individuals and over time. Gene expression measurements can provide insights into microbiome composition and function. However, efficient and unbiased removal of microbial ribosomal RNA (rRNA) presents a barrier to acquiring metatranscriptomic data. Here we describe a probe set that achieves efficient enzymatic rRNA removal of complex human-associated microbial communities. We demonstrate that the custom probe set can be further refined through an iterative design process to efficiently deplete rRNA from a range of human microbiome samples. Using synthetic nucleic acid spike-ins, we show that the rRNA depletion process does not introduce substantial quantitative error in gene expression profiles. Successful rRNA depletion allows for efficient characterization of taxonomic and functional profiles, including during the development of the human gut microbiome. The pan-human microbiome enzymatic rRNA depletion probes described here provide a powerful tool for studying the transcriptional dynamics and function of the human microbiome.
定植于人体肠道和其他组织的微生物群落是动态的,其组成和功能状态在个体之间以及随时间而变化。基因表达测量可以提供有关微生物组组成和功能的深入了解。然而,有效地、无偏地去除微生物核糖体 RNA(rRNA)是获取宏转录组数据的障碍。在这里,我们描述了一种探针组,可有效地通过酶促方法去除复杂的与人相关的微生物群落中的 rRNA。我们证明,通过迭代设计过程,可以进一步优化该定制探针组,以有效地从一系列人类微生物组样本中耗尽 rRNA。使用合成核酸 Spike-ins,我们表明 rRNA 耗尽过程不会在基因表达谱中引入大量定量误差。成功的 rRNA 耗尽允许对分类和功能谱进行有效的表征,包括在人类肠道微生物组的发展过程中。这里描述的泛人类微生物组酶促 rRNA 耗尽探针为研究人类微生物组的转录动态和功能提供了强大的工具。