Habier Janine, May Patrick, Heintz-Buschart Anna, Ghosal Anubrata, Wienecke-Baldacchino Anke K, Nolte-'t Hoen Esther N M, Wilmes Paul, Fritz Joëlle V
Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Belvaux, Luxembourg.
German Centre for Integrative Biodiversity Research (iDiv) Leipzig-Halle-Jena, Leipzig, Germany.
Methods Mol Biol. 2018;1737:213-230. doi: 10.1007/978-1-4939-7634-8_13.
Outer membrane vesicles (OMVs) are released by commensal as well as pathogenic Gram-negative bacteria. These vesicles contain numerous bacterial components, such as proteins, peptidoglycans, lipopolysaccharides, DNA, and RNA. To examine if OMV-associated RNA molecules are bacterial degradation products and/or are functionally active, it is necessary to extract RNA from pure OMVs for subsequent analysis. Therefore, we describe here an isolation method of ultrapure OMVs and the subsequent extraction of RNA and basic steps of RNA-Seq analysis. Bacterial culture, extracellular supernatant concentration, OMV purification, and the subsequent RNA extraction out of OMVs are described. Specific pitfalls within the protocol and RNA contamination sources are highlighted.
外膜囊泡(OMV)由共生菌和致病性革兰氏阴性菌释放。这些囊泡含有多种细菌成分,如蛋白质、肽聚糖、脂多糖、DNA和RNA。为了检测与OMV相关的RNA分子是细菌降解产物和/或具有功能活性,有必要从纯OMV中提取RNA用于后续分析。因此,我们在此描述一种超纯OMV的分离方法以及随后的RNA提取和RNA测序分析的基本步骤。描述了细菌培养、细胞外上清液浓缩、OMV纯化以及随后从OMV中提取RNA的过程。强调了该方案中的特定陷阱和RNA污染来源。