Dissection of Influenza Infection In Vivo by Single-Cell RNA Sequencing

Summary

The influenza virus is a major cause of morbidity and mortality worldwide. Yet, both the impact of intracellular viral replication and the variation in host response across different cell types remain uncharacterized. Here we used single-cell RNA sequencing to investigate the heterogeneity in the response of lung tissue cells to in vivo influenza infection. Analysis of viral and host transcriptomes in the same single cell enabled us to resolve the cellular heterogeneity of bystander (exposed but uninfected) as compared with infected cells. We reveal that all major immune and non-immune cell types manifest substantial fractions of infected cells, albeit at low viral transcriptome loads relative to epithelial cells. We show that all cell types respond primarily with a robust generic transcriptional response, and we demonstrate novel markers specific for influenza-infected as opposed to bystander cells. These findings open new avenues for targeted therapy aimed exclusively at infected cells.

Graphical Abstract

Highlights

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  Combined measurements of host-viral scRNA-seq during in vivo influenza infection

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  High prevalence of infection in a variety of immune and non-immune cell types

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  Extensive cellular heterogeneity exists within infected and bystander cells

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  Generic and cell-type-specific differences between infected and bystander cells

Abstract

Simultaneous mapping of host and viral transcriptomes at the same single cell provides a framework to study host-viral interactions. Analysis of cells derived from lungs of in vivo influenza infection reveals both generic and cell-type-specific infection response. By analyzing the cellular heterogeneity of both bystander (exposed but uninfected) and infected cells, we characterize novel markers specific for influenza-infected as opposed to bystanders. These findings open new avenues for targeted therapy aimed exclusively at infected cells.