Evidence map›Paper›PMID 28103897›Full record

ArticleGenome biology2017

Dual RNA-seq reveals viral infections in asthmatic children without respiratory illness which are associated with changes in the airway transcriptome.

Agata Wesolowska-Andersen, Jamie L Everman, Rebecca Davidson, Cydney Rios, Rachelle Herrin, Celeste Eng, William J Janssen, Andrew H Liu, Sam S Oh, Rajesh Kumar and 4 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Genome biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

38 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
  2. Article
  3. The PRIMERO birth cohort: Design and baseline characteristics.The journal of allergy and clinical immunology. Global · 2025
    Article
  4. Article
  5. Type 1 Immune Responses Related to Viral Infection Influence Corticosteroid Response in Asthma.American journal of respiratory and critical care medicine · 2025
    Article
  6. Viral Determinants of Childhood Asthma Exacerbation Severity and Treatment Response.The journal of allergy and clinical immunology. In practice · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. RNA-Seq Data Processing in Plant-Pathogen Interaction System: A Case Study.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  12. Age-related Differences in the Nasal Mucosal Immune Response to SARS-CoV-2.American journal of respiratory cell and molecular biology · 2022
    Article
  13. Article
  14. Article
  15. Heterogeneous associations of polyomaviruses and herpesviruses with allergy-related phenotypes in childhood.Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. Immune response to SARS-CoV-2 in the nasal mucosa in children and adults.medRxiv : the preprint server for health sciences · 2021
    Article
  20. Frontiers in immunology · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 2 countries.

Agata Wesolowska-AndersenCenter for Genes, Environment, and Health, National Jewish Health, Denver, CO, USA.
Jamie L EvermanCenter for Genes, Environment, and Health, National Jewish Health, Denver, CO, USA.
Rebecca DavidsonCenter for Genes, Environment, and Health, National Jewish Health, Denver, CO, USA.
Cydney RiosCenter for Genes, Environment, and Health, National Jewish Health, Denver, CO, USA.
Rachelle HerrinCenter for Genes, Environment, and Health, National Jewish Health, Denver, CO, USA.
Celeste EngDepartment of Medicine, University of California, San Francisco, CA, USA.
William J JanssenDepartment of Medicine, National Jewish Health, Denver, CO, USA.
Andrew H LiuDepartment of Pediatrics, National Jewish Health, 1400 Jackson St, Denver, CO, 80206, USA.
Sam S OhDepartment of Medicine, University of California, San Francisco, CA, USA.
Rajesh KumarDepartment of Pediatrics, The Ann and Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Tasha E FingerlinCenter for Genes, Environment, and Health, National Jewish Health, Denver, CO, USA.
Jose Rodriguez-SantanaCentro de Neumologia Pediatrica, San Juan, Puerto Rico.
Esteban G BurchardDepartment of Medicine, University of California, San Francisco, CA, USA.
Max A SeiboldCenter for Genes, Environment, and Health, National Jewish Health, Denver, CO, USA. seiboldm@njhealth.org.
National Jewish Health · USUniversity of Colorado Denver · USUniversity of California, San Francisco · USCentro de Neumologia Pediatrica · PRNorthwestern University · US

Funding

Integrative Program in Complex Biological System (ipCBS)T32EB009383 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MARSHALL, WALLACE, WEINER, ORION D · 2009 to 2022
$3.2M
Genetic Control of Airway Epithelium Gene Expression in Childhood AsthmaticsR01HL128439 · NHLBI · NATIONAL JEWISH HEALTH · PI SEIBOLD, MAX A · 2015 to 2019
$3.1M
NHLBI NIH HHS R01 HL128439NIBIB NIH HHS T32 EB009383
6 · The paper itself

Abstract

backgroundRespiratory illness caused by viral infection is associated with the development and exacerbation of childhood asthma. Little is known about the effects of respiratory viral infections in the absence of illness. Using quantitative PCR (qPCR) for common respiratory viruses and for two genes known to be highly upregulated in viral infections (CCL8/CXCL11), we screened 92 asthmatic and 69 healthy children without illness for respiratory virus infections.

resultsWe found 21 viral qPCR-positive and 2 suspected virus-infected subjects with high expression of CCL8/CXCL11. We applied a dual RNA-seq workflow to these subjects, together with 25 viral qPCR-negative subjects, to compare qPCR with sequencing-based virus detection and to generate the airway transcriptome for analysis. RNA-seq virus detection achieved 86% sensitivity when compared to qPCR-based screening. We detected additional respiratory viruses in the two CCL8/CXCL11-high subjects and in two of the qPCR-negative subjects. Viral read counts varied widely and were used to stratify subjects into Virus-High and Virus-Low groups. Examination of the host airway transcriptome found that the Virus-High group was characterized by immune cell airway infiltration, downregulation of cilia genes, and dampening of type 2 inflammation. Even the Virus-Low group was differentiated from the No-Virus group by 100 genes, some involved in eIF2 signaling.

conclusionsRespiratory virus infection without illness is not innocuous but may determine the airway function of these subjects by driving immune cell airway infiltration, cellular remodeling, and alteration of asthmogenic gene expression.

Indexed as

RNA VirusesTranscriptomeAsthmaCase-Control StudiesChildGene Expression ProfilingGene Expression Regulation, ViralHigh-Throughput Nucleotide SequencingHost-Pathogen InteractionsHumansRespiratory MucosaRespiratory Tract InfectionsRNA Virus InfectionsSequence Analysis, RNAAirway epitheliumAsthmaAsymptomaticChildrenHost responseHost-virus interactionsInfectionRNA-seqTranscriptomeVirus

Identifiers

PMID28103897
PMCPMC5244706
OpenAlexW2579339833

What OpenQuestion holds

Textmetadata
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Registered trials

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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.