| Literature DB >> 29484596 |
Janine Habier1, Patrick May1, Anna Heintz-Buschart1,2,3, Anubrata Ghosal4, Anke K Wienecke-Baldacchino5, Esther N M Nolte-'t Hoen6, Paul Wilmes1, Joëlle V Fritz7,8.
Abstract
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.Keywords: Analysis; Bacteria; Density gradient; Extraction; Gram-negative; Outer membrane vesicle (OMV); RNA; Sequencing; Ultracentrifugation; Ultrafiltration
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Year: 2018 PMID: 29484596 DOI: 10.1007/978-1-4939-7634-8_13
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745