Evidence map›Paper›PMID 29976658›Full record

ArticleJournal of virology2018

Strand-Specific Dual RNA Sequencing of Bronchial Epithelial Cells Infected with Influenza A/H3N2 Viruses Reveals Splicing of Gene Segment 6 and Novel Host-Virus Interactions.

Giulia Fabozzi, Andrew J Oler, Poching Liu, Yong Chen, Samuel Mindaye, Michael A Dolan, Heather Kenney, Marjan Gucek, Jun Zhu, Ronald L Rabin and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

33 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Biosafety and health · 2026
    Article
  3. Viral Modulation of Host Splicing.Annual review of virology · 2025
    Review
  4. Article
  5. Human long noncoding RNAJournal of virology · 2025
    Article
  6. Article
  7. Human long noncoding RNA,bioRxiv : the preprint server for biology · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
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  15. Review
  16. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Giulia Fabozzi *Laboratory of Immunobiochemistry, Division of Bacterial, Parasitic and Allergenic Products, Office of Vaccines Research and Review, Center for Biologics Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, Maryland, USA.
Andrew J Oler *Bioinformatics and Computational Biosciences Branch, Office of Cyber Infrastructure and Computational Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Poching LiuSystems Biology Center, National Heart Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
Yong ChenProteomics Core, National Heart Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
Samuel MindayeLaboratory of Immunobiochemistry, Division of Bacterial, Parasitic and Allergenic Products, Office of Vaccines Research and Review, Center for Biologics Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, Maryland, USA.
Michael A DolanBioinformatics and Computational Biosciences Branch, Office of Cyber Infrastructure and Computational Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Heather KenneyEmerging Respiratory Viruses Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Marjan GucekProteomics Core, National Heart Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
Jun ZhuSystems Biology Center, National Heart Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
Ronald L RabinLaboratory of Immunobiochemistry, Division of Bacterial, Parasitic and Allergenic Products, Office of Vaccines Research and Review, Center for Biologics Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, Maryland, USA ronald.rabin@fda.hhs.gov KSUBBARAO@niaid.nih.gov.ORCID https://orcid.org/0000-0003-3496-0504
Kanta SubbaraoEmerging Respiratory Viruses Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA ronald.rabin@fda.hhs.gov KSUBBARAO@niaid.nih.gov.ORCID https://orcid.org/0000-0003-1713-3056
National Institutes of Health · USCenter for Biologics Evaluation and Research · US

Funding

Clinical Studies of Vaccines for Pandemic InfluenzaZIAAI000997 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI COHEN, JEFFREY · 2009 to 2021
$29.9M
Proteomics CoreZICHL005903 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI GUCEK, MARJAN · 2009 to 2022
$23.3M
RNA systems biologyZIAHL006230 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI ZHU, JUN · 2017 to 2018
$1.0M
6 · The paper itself

Abstract

Host-influenza virus interplay at the transcript level has been extensively characterized in epithelial cells. Yet, there are no studies that simultaneously characterize human host and influenza A virus (IAV) genomes. We infected human bronchial epithelial BEAS-2B cells with two seasonal IAV/H3N2 strains, Brisbane/10/07 and Perth/16/09 (reference strains for past vaccine seasons) and the well-characterized laboratory strain Udorn/307/72. Strand-specific RNA sequencing (RNA-seq) of the infected BEAS-2B cells allowed for simultaneous analysis of host and viral transcriptomes, in addition to pathogen genomes, to reveal changes in mRNA expression and alternative splicing (AS). In general, patterns of global and immune gene expression induced by the three IAVs were mostly shared. However, AS of host transcripts and small nuclear RNAs differed between the seasonal and laboratory strains. Analysis of viral transcriptomes showed deletions of the polymerase components (defective interfering-like RNAs) within the genome. Surprisingly, we found that the neuraminidase gene undergoes AS and that the splicing event differs between seasonal and laboratory strains. Our findings reveal novel elements of the host-virus interaction and highlight the importance of RNA-seq in identifying molecular changes at the genome level that may contribute to shaping RNA-based innate immunity.

Indexed as

BronchiEpithelial CellsGene Expression ProfilingGenome, HumanGenome, ViralHemagglutinin Glycoproteins, Influenza VirusHost-Pathogen InteractionsHumansImmunity, InnateInfluenza A Virus, H3N2 SubtypeInfluenza, HumanNeuraminidaseRNA SplicingSeasonsSequence Analysis, RNAHemagglutinin Glycoproteins, Influenza VirusNeuraminidasealternative splicingbronchial epithelial cellsdual RNA-seqhost-virus interactioninfluenza A virus H3N2neuraminidaseseasonal H3N2 strainsstrand-specific RNA seqUdorn/72 strainviral transcriptome

Identifiers

PMID29976658
PMCPMC6096831
OpenAlexW2810957255

What OpenQuestion holds

Textmetadata
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.