Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024:2808:121-127.
doi: 10.1007/978-1-0716-3870-5_9.

Dual RNA-seq Analysis of Patients' Cells and Viral Genome After Measles Infection

Affiliations

Dual RNA-seq Analysis of Patients' Cells and Viral Genome After Measles Infection

Vasiliki Pogka et al. Methods Mol Biol. 2024.

Abstract

During the infection of a host cell by an infectious agent, a series of gene expression changes occurs as a consequence of host-pathogen interactions. Unraveling this complex interplay is the key for understanding of microbial virulence and host response pathways, thus providing the basis for new molecular insights into the mechanisms of pathogenesis and the corresponding immune response. Dual RNA sequencing (dual RNA-seq) has been developed to simultaneously determine pathogen and host transcriptomes enabling both differential and coexpression analyses between the two partners as well as genome characterization in the case of RNA viruses. Here, we provide a detailed laboratory protocol and bioinformatics analysis guidelines for dual RNA-seq experiments focusing on - but not restricted to - measles virus (MeV) as a pathogen of interest. The application of dual RNA-seq technologies in MeV-infected patients can potentially provide valuable information on the structure of the viral RNA genome and on cellular innate immune responses and drive the discovery of new targets for antiviral therapy.

Keywords: Dual RNA-seq; Host response; Measles virus; Poly(A) enrichment; RNA viral genome; Ribodepletion.

PubMed Disclaimer

References

    1. Garcıa-Sastre A, Sansonetti PJ (2010) Host–pathogen interactions. Curr Opin Immunol 2010(22):425–427. https://doi.org/10.1016/j.coi.2010.06.005 - DOI
    1. Westermann AJ, Barquist L, Vogel J (2017) Resolving host–pathogen interactions by dual RNA-seq. PLoS Pathog 13(2):e1006033. https://doi.org/10.1371/journal.ppat.1006033 - DOI - PubMed - PMC
    1. Saliba A-E, Santos SC, Vogel J (2017) New RNA-seq approaches for the study of bacterial pathogens. Curr Opin Microbiol 35:78–87. https://doi.org/10.1016/j.mib.2017.01.001
    1. Karamitros T, Pogka V, Papadopoulou G, Tsitsilonis O, Evangelidou M, Sympardi S, Mentis A (2021) Dual RNA-Seq Enables Full-Genome Assembly of Measles Virus and Characterization of Host-Pathogen Interactions. Microorganisms 9(7):1538. https://doi.org/10.3390/microorganisms9071538
    1. Langmead B, Salzberg S (2012) Fast gapped-read alignment with Bowtie2. Nat Methods 9:357–359. https://doi.org/10.1038/nmeth.1923

LinkOut - more resources