Single-cell RNA-seq methods to interrogate virus-host interactions

被引:0
作者
Kalani Ratnasiri
Aaron J. Wilk
Madeline J. Lee
Purvesh Khatri
Catherine A. Blish
机构
[1] Stanford University School of Medicine,Stanford Immunology Program
[2] Stanford University School of Medicine,Department of Medicine, Division of Infectious Diseases and Geographic Medicine
[3] Stanford University School of Medicine,Medical Scientist Training Program
[4] Stanford University School of Medicine,Institute for Immunity, Transplantation and Infection
[5] Center for Biomedical Informatics Research,Department of Medicine
[6] Inflammatix,undefined
[7] Inc.,undefined
[8] Chan Zuckerberg Biohub,undefined
来源
Seminars in Immunopathology | 2023年 / 45卷
关键词
Single-cell RNA sequencing; Antiviral immunity; Virus; Transcriptomics;
D O I
暂无
中图分类号
学科分类号
摘要
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.
引用
收藏
页码:71 / 89
页数:18
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