Evidence map›Paper›PMID 29451492›Full record

ArticleeLife2018

Extreme heterogeneity of influenza virus infection in single cells.

Alistair B Russell, Cole Trapnell, Jesse D Bloom

Open access · goldAbstract read
In one paragraph

Article in eLife, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 182 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
182citing papers in PubMed, 1 pooled it
29.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

182 citing papers in PubMed, 1 synthesis or guideline pooled it, 317 citations in OpenAlex.

  1. Single-cell RNA sequencing offers novel perspectives in viral infection research.Frontiers in cellular and infection microbiology · 2026
    Pooled it
  2. Article
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  6. Review
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  14. Intrinsic OASL expression governs heterogeneity in interferon induction during influenza A virus infection.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  15. Article
  16. The HIV-1 Vpr R77Q mutant alters host apoptotic gene regulation in CD4+ T cells.Frontiers in cellular and infection microbiology · 2026
    Article
  17. Cellular sensor DAP5 decodesFrontiers in immunology · 2026
    Article
  18. Article
  19. Article
  20. Human Assembloid Model of Emergent Neurotropic Enteroviruses.bioRxiv : the preprint server for biology · 2025
    Article

122 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Alistair B RussellBasic Sciences Division and Computational Biology Program, Fred Hutchinson Cancer Research Center, Seattle, United States.ORCID http://orcid.org/0000-0002-5342-2309
Cole TrapnellDepartment of Genome Sciences, University of Washington, Seattle, United States.
Jesse D BloomBasic Sciences Division and Computational Biology Program, Fred Hutchinson Cancer Research Center, Seattle, United States.ORCID http://orcid.org/0000-0003-1267-3408
University of Washington · USFred Hutch Cancer Center · US

Funding

High-throughput experiments to guide influenza vaccine strain selectionR01AI127893 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BLOOM, JESSE D · 2016 to 2020
$2.1M
Mapping epistasis in molecular evolution: the influenza nucleoproteinR01GM102198 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BLOOM, JESSE D · 2012 to 2016
$1.6M
Damon Runyon Cancer Research Foundation DRG-2227-15Damon Runyon Cancer Research Foundation Postdoctoral FellowshipHoward Hughes Medical Institute Faculty Scholar AwardNIAID NIH HHS AI127897NIAID NIH HHS R01 AI127893NICHD NIH HHS DP2OD020868NIGMS NIH HHS R01 GM102198NIGMS NIH HHS R01GM102198
6 · The paper itself

Abstract

Viral infection can dramatically alter a cell's transcriptome. However, these changes have mostly been studied by bulk measurements on many cells. Here we use single-cell mRNA sequencing to examine the transcriptional consequences of influenza virus infection. We find extremely wide cell-to-cell variation in the productivity of viral transcription - viral transcripts comprise less than a percent of total mRNA in many infected cells, but a few cells derive over half their mRNA from virus. Some infected cells fail to express at least one viral gene, but this gene absence only partially explains variation in viral transcriptional load. Despite variation in viral load, the relative abundances of viral mRNAs are fairly consistent across infected cells. Activation of innate immune pathways is rare, but some cellular genes co-vary in abundance with the amount of viral mRNA. Overall, our results highlight the complexity of viral infection at the level of single cells.

Indexed as

Single-Cell AnalysisA549 CellsAnimalsDogsGene Expression ProfilingHEK293 CellsHost-Pathogen InteractionsHumansMadin Darby Canine Kidney CellsOrthomyxoviridaeRNA, MessengerRNA, ViralSequence Analysis, RNATranscription, GeneticViral LoadRNA, MessengerRNA, Viraldefective particleevolutionary biologygenomicshumaninfectious diseaseinfluenza virusinterferonsmicrobiologysingle-cell RNAseqstochasiticityvirus

Identifiers

PMID29451492
PMCPMC5826275
OpenAlexW2759082725

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.