Evidence map›Paper›PMID 38679164›Full record

ArticleJournal of virological methods2024

Establishment of Swine Primary Nasal, Tracheal, and Bronchial Epithelial Cell Culture Models for the Study of Influenza Virus Infection.

Madelyn Krunkosky, Thomas M Krunkosky, Victoria Meliopoulos, Constantinos S Kyriakis, Stacey Schultz-Cherry, S Mark Tompkins

Abstract read
In one paragraph

Article in Journal of virological methods, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Animal organoids as models for integrated One Health research.One health (Amsterdam, Netherlands) · 2026
    Review
  2. Microbiology spectrum · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Interplay between respiratory viruses and cilia in the airways.European respiratory review : an official journal of the European Respiratory Society · 2025
    Review
  8. Article
  9. The Mucus-Binding Factor MediatesMicroorganisms · 2024
    Article
  10. 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.

Madelyn KrunkoskyCenter for Vaccines and Immunology, University of Georgia, Athens, GA, United States; Department of Infectious Diseases, University of Georgia, Athens, GA, United States; Emory-UGA Centers of Excellence for Influenza Research and Surveillance (CEIRS), Athens, GA, United States.
Thomas M KrunkoskyDepartment of Biomedical Sciences, University of Georgia, Athens, GA, United States.
Victoria MeliopoulosDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, United States.
Constantinos S KyriakisEmory-UGA Centers of Excellence for Influenza Research and Surveillance (CEIRS), Athens, GA, United States; Department of Pathobiology, Auburn University, Auburn, AL, United States.
Stacey Schultz-CherryDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, United States.
S Mark TompkinsCenter for Vaccines and Immunology, University of Georgia, Athens, GA, United States; Department of Infectious Diseases, University of Georgia, Athens, GA, United States; Emory-UGA Centers of Excellence for Influenza Research and Surveillance (CEIRS), Athens, GA, United States. Electronic address: smt@uga.edu.

Funding

NIAID NIH HHS HHSN272201400004C
6 · The paper itself

Abstract

We established primary porcine nasal, tracheal, and bronchial epithelial cells that recapitulate the physical and functional properties of the respiratory tract and have the ability to fully differentiate. Trans-well cultures demonstrated increased transepithelial electrical resistance over time the presence of tight junctions as demonstrated by immunohistochemistry. The nasal, tracheal, and bronchial epithelial cells developed cilia, secreted mucus, and expressed sialic acids on surface glycoproteins, the latter which are required for influenza A virus infection. Swine influenza viruses were shown to replicate efficiently in the primary epithelial cell cultures, supporting the use of these culture models to assess swine influenza and other virus infection. Primary porcine nasal, tracheal, and bronchial epithelial cell culture models enable assessment of emerging and novel influenza viruses for pandemic potential as well as mechanistic studies to understand mechanisms of infection, reassortment, and generation of novel virus. As swine are susceptible to infection with multiple viral and bacterial respiratory pathogens, these primary airway cell models may enable study of the cellular response to infection by pathogens associated with Porcine Respiratory Disease Complex.

Indexed as

Epithelial CellsAnimalsBronchiCell Culture TechniquesCells, CulturedInfluenza A virusSwineTracheaVirus ReplicationEpithelial cellsInfluenza A virusModelsN-Acetylneuraminic acidSwine

Identifiers

PMID38679164
PMCPMC11129919

What OpenQuestion holds

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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.