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Single-cell RNA-seq methods to interrogate virus-host interactions
The twenty-first century has seen the emergence of many epidemic and pandemic viruses, with the most recent being the SARS-CoV-2-driven COVID-19 pandemic. As obligate intracellular parasites, viruses rely on host cells to replicate and produce progeny, resulting in complex virus and host dynamics du...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684776/ https://www.ncbi.nlm.nih.gov/pubmed/36414692 http://dx.doi.org/10.1007/s00281-022-00972-2 |
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author | Ratnasiri, Kalani Wilk, Aaron J. Lee, Madeline J. Khatri, Purvesh Blish, Catherine A. |
author_facet | Ratnasiri, Kalani Wilk, Aaron J. Lee, Madeline J. Khatri, Purvesh Blish, Catherine A. |
author_sort | Ratnasiri, Kalani |
collection | PubMed |
description | The twenty-first century has seen the emergence of many epidemic and pandemic viruses, with the most recent being the SARS-CoV-2-driven COVID-19 pandemic. As obligate intracellular parasites, viruses rely on host cells to replicate and produce progeny, resulting in complex virus and host dynamics during an infection. Single-cell RNA sequencing (scRNA-seq), by enabling broad and simultaneous profiling of both host and virus transcripts, represents a powerful technology to unravel the delicate balance between host and virus. In this review, we summarize technological and methodological advances in scRNA-seq and their applications to antiviral immunity. We highlight key scRNA-seq applications that have enabled the understanding of viral genomic and host response heterogeneity, differential responses of infected versus bystander cells, and intercellular communication networks. We expect further development of scRNA-seq technologies and analytical methods, combined with measurements of additional multi-omic modalities and increased availability of publicly accessible scRNA-seq datasets, to enable a better understanding of viral pathogenesis and enhance the development of antiviral therapeutics strategies. |
format | Online Article Text |
id | pubmed-9684776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-96847762022-11-28 Single-cell RNA-seq methods to interrogate virus-host interactions Ratnasiri, Kalani Wilk, Aaron J. Lee, Madeline J. Khatri, Purvesh Blish, Catherine A. Semin Immunopathol Review The twenty-first century has seen the emergence of many epidemic and pandemic viruses, with the most recent being the SARS-CoV-2-driven COVID-19 pandemic. As obligate intracellular parasites, viruses rely on host cells to replicate and produce progeny, resulting in complex virus and host dynamics during an infection. Single-cell RNA sequencing (scRNA-seq), by enabling broad and simultaneous profiling of both host and virus transcripts, represents a powerful technology to unravel the delicate balance between host and virus. In this review, we summarize technological and methodological advances in scRNA-seq and their applications to antiviral immunity. We highlight key scRNA-seq applications that have enabled the understanding of viral genomic and host response heterogeneity, differential responses of infected versus bystander cells, and intercellular communication networks. We expect further development of scRNA-seq technologies and analytical methods, combined with measurements of additional multi-omic modalities and increased availability of publicly accessible scRNA-seq datasets, to enable a better understanding of viral pathogenesis and enhance the development of antiviral therapeutics strategies. Springer Berlin Heidelberg 2022-11-21 2023 /pmc/articles/PMC9684776/ /pubmed/36414692 http://dx.doi.org/10.1007/s00281-022-00972-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Ratnasiri, Kalani Wilk, Aaron J. Lee, Madeline J. Khatri, Purvesh Blish, Catherine A. Single-cell RNA-seq methods to interrogate virus-host interactions |
title | Single-cell RNA-seq methods to interrogate virus-host interactions |
title_full | Single-cell RNA-seq methods to interrogate virus-host interactions |
title_fullStr | Single-cell RNA-seq methods to interrogate virus-host interactions |
title_full_unstemmed | Single-cell RNA-seq methods to interrogate virus-host interactions |
title_short | Single-cell RNA-seq methods to interrogate virus-host interactions |
title_sort | single-cell rna-seq methods to interrogate virus-host interactions |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684776/ https://www.ncbi.nlm.nih.gov/pubmed/36414692 http://dx.doi.org/10.1007/s00281-022-00972-2 |
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