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Dual RNA-Sequencing of Mycobacterium tuberculosis-Infected Cells from a Murine Infection Model

Dual RNA-sequencing is a powerful technique to assess both bacterial and host transcriptomes in an unbiased way. We developed a protocol to perform Dual RNA-seq on in vivo-derived macrophage populations infected with Mycobacterium tuberculosis. Here, we provide a practical step-by-step guide to exec...

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Detalles Bibliográficos
Autores principales: Pisu, Davide, Huang, Lu, Rin Lee, Bom Nae, Grenier, Jennifer K., Russell, David G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756974/
https://www.ncbi.nlm.nih.gov/pubmed/33377017
http://dx.doi.org/10.1016/j.xpro.2020.100123
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author Pisu, Davide
Huang, Lu
Rin Lee, Bom Nae
Grenier, Jennifer K.
Russell, David G.
author_facet Pisu, Davide
Huang, Lu
Rin Lee, Bom Nae
Grenier, Jennifer K.
Russell, David G.
author_sort Pisu, Davide
collection PubMed
description Dual RNA-sequencing is a powerful technique to assess both bacterial and host transcriptomes in an unbiased way. We developed a protocol to perform Dual RNA-seq on in vivo-derived macrophage populations infected with Mycobacterium tuberculosis. Here, we provide a practical step-by-step guide to execute the protocol on Mtb-infected cells from a murine infection model. Our protocol can also be easily applied to perform Dual RNA-seq on in vitro-derived cells as well as different Mtb-infected host cell types. For complete details on the use and execution of this protocol, please refer to Pisu et al. (2020)
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spelling pubmed-77569742020-12-28 Dual RNA-Sequencing of Mycobacterium tuberculosis-Infected Cells from a Murine Infection Model Pisu, Davide Huang, Lu Rin Lee, Bom Nae Grenier, Jennifer K. Russell, David G. STAR Protoc Protocol Dual RNA-sequencing is a powerful technique to assess both bacterial and host transcriptomes in an unbiased way. We developed a protocol to perform Dual RNA-seq on in vivo-derived macrophage populations infected with Mycobacterium tuberculosis. Here, we provide a practical step-by-step guide to execute the protocol on Mtb-infected cells from a murine infection model. Our protocol can also be easily applied to perform Dual RNA-seq on in vitro-derived cells as well as different Mtb-infected host cell types. For complete details on the use and execution of this protocol, please refer to Pisu et al. (2020) Elsevier 2020-10-06 /pmc/articles/PMC7756974/ /pubmed/33377017 http://dx.doi.org/10.1016/j.xpro.2020.100123 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Pisu, Davide
Huang, Lu
Rin Lee, Bom Nae
Grenier, Jennifer K.
Russell, David G.
Dual RNA-Sequencing of Mycobacterium tuberculosis-Infected Cells from a Murine Infection Model
title Dual RNA-Sequencing of Mycobacterium tuberculosis-Infected Cells from a Murine Infection Model
title_full Dual RNA-Sequencing of Mycobacterium tuberculosis-Infected Cells from a Murine Infection Model
title_fullStr Dual RNA-Sequencing of Mycobacterium tuberculosis-Infected Cells from a Murine Infection Model
title_full_unstemmed Dual RNA-Sequencing of Mycobacterium tuberculosis-Infected Cells from a Murine Infection Model
title_short Dual RNA-Sequencing of Mycobacterium tuberculosis-Infected Cells from a Murine Infection Model
title_sort dual rna-sequencing of mycobacterium tuberculosis-infected cells from a murine infection model
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756974/
https://www.ncbi.nlm.nih.gov/pubmed/33377017
http://dx.doi.org/10.1016/j.xpro.2020.100123
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