Evidence map›Paper›PMID 25888408›Full record

ArticleBMC genomics2015

The transcriptome of a complete episode of acute otitis media.

Michelle Hernandez, Anke Leichtle, Kwang Pak, Nicholas J Webster, Stephen I Wasserman, Allen F Ryan

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

36 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Immunomodulation as a Protective Strategy in Chronic Otitis Media.Frontiers in cellular and infection microbiology · 2022
    Article
  5. Article
  6. Article
  7. The role of CDHR3 in susceptibility to otitis media.Journal of molecular medicine (Berlin, Germany) · 2021
    Article
  8. Article
  9. Article
  10. TheFrontiers in cellular and infection microbiology · 2021
    Article
  11. Article
  12. Leukotriene B4 Is a Major Determinant of Leukocyte Recruitment During Otitis Media.Frontiers in cellular and infection microbiology · 2021
    Article
  13. Innate Immunity in the Middle Ear Mucosa.Frontiers in cellular and infection microbiology · 2021
    Review
  14. Learning from -omics strategies applied to uncoverComputational and structural biotechnology journal · 2021
    Review
  15. Article
  16. Panel 8: Vaccines and immunology.International journal of pediatric otorhinolaryngology · 2020
    Review
  17. Panel 2- recent advance in otitis media bioinformatics.International journal of pediatric otorhinolaryngology · 2020
    Review
  18. A Bacterial Epigenetic Switch in Non-typeableFrontiers in cellular and infection microbiology · 2020
    Article
  19. Article
  20. Article
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

6 authors at 2 institutions in 2 countries.

Michelle HernandezDivisions of Surgery / Otolaryngology, University of California, San Diego, La Jolla, CA, USA. michelle_hernandez@med.unc.edu.
Anke LeichtleDivisions of Surgery / Otolaryngology, University of California, San Diego, La Jolla, CA, USA. ankeleichtle@yahoo.de.
Kwang PakDivisions of Surgery / Otolaryngology, University of California, San Diego, La Jolla, CA, USA. kpak@ucsd.edu.
Nicholas J WebsterMedicine / Endocrinology, University of California, San Diego, La Jolla, CA, USA. nwebster@ucsd.edu.
Stephen I WassermanRheumatology, Allergy and Immunology, University of California, San Diego, La Jolla, CA, USA. swasserman@ucsd.edu.
Allen F RyanDivisions of Surgery / Otolaryngology, University of California, San Diego, La Jolla, CA, USA. afryan@ucsd.edu.
University of California San Diego · USUniversity of North Carolina at Chapel Hill · US

Funding

Middle ear responses in Otitis MediaR01DC000129 · NIDCD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RYAN, ALLEN F. · 1989 to 2021
$6.8M
Innovative therapy for diseases of the middle earR01DC012595 · NIDCD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RYAN, ALLEN F. · 2012 to 2023
$3.3M
Mechanisms of Persistence and Recovery in Otitis MediaR01DC006279 · NIDCD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WASSERMAN, STEPHEN I · 2003 to 2014
$3.1M
Basic Mechanisms on Hearing Loss of Cochlear OriginI01BX001205 · VA · VA SAN DIEGO HEALTHCARE SYSTEM · PI RYAN, ALLEN F. · 2013 to 2024
–
A Biological Interface for Auditory Rehabilitation with a Cochlear ImplantI01RX000977 · VA · VA SAN DIEGO HEALTHCARE SYSTEM · PI RYAN, ALLEN F. · 2014 to 2016
–
BLRD VA I01 BX001205NIDCD NIH HHS DC000129NIDCD NIH HHS DC006279NIDCD NIH HHS DC012595NIDCD NIH HHS R01 DC000129NIDCD NIH HHS R01 DC006279NIDCD NIH HHS R01 DC012595RRD VA I01 RX000977
6 · The paper itself

Abstract

backgroundOtitis media is the most common disease of childhood, and represents an important health challenge to the 10-15% of children who experience chronic/recurrent middle ear infections. The middle ear undergoes extensive modifications during otitis media, potentially involving changes in the expression of many genes. Expression profiling offers an opportunity to discover novel genes and pathways involved in this common childhood disease. The middle ears of 320 WBxB6 F1 hybrid mice were inoculated with non-typeable Haemophilus influenzae (NTHi) or PBS (sham control). Two independent samples were generated for each time point and condition, from initiation of infection to resolution. RNA was profiled on Affymetrix mouse 430 2.0 whole-genome microarrays.

resultsApproximately 8% of the sampled transcripts defined the signature of acute NTHi-induced otitis media across time. Hierarchical clustering of signal intensities revealed several temporal gene clusters. Network and pathway enrichment analysis of these clusters identified sets of genes involved in activation of the innate immune response, negative regulation of immune response, changes in epithelial and stromal cell markers, and the recruitment/function of neutrophils and macrophages. We also identified key transcriptional regulators related to events in otitis media, which likely determine the expression of these gene clusters. A list of otitis media susceptibility genes, derived from genome-wide association and candidate gene studies, was significantly enriched during the early induction phase and the middle re-modeling phase of otitis but not in the resolution phase. Our results further indicate that positive versus negative regulation of inflammatory processes occur with highly similar kinetics during otitis media, underscoring the importance of anti-inflammatory responses in controlling pathogenesis.

conclusionsThe results characterize the global gene response during otitis media and identify key signaling and transcription factor networks that control the defense of the middle ear against infection. These networks deserve further attention, as dysregulated immune defense and inflammatory responses may contribute to recurrent or chronic otitis in children.

Indexed as

TranscriptomeAcute DiseaseAnimalsDisease Models, AnimalEar, MiddleHaemophilus InfectionsHaemophilus influenzaeHumansImmunity, InnateInflammationMiceOtitis MediaSignal Transduction

Identifiers

PMID25888408
PMCPMC4394589
OpenAlexW2010314221

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.