Evidence map›Paper›PMID 29155483›Full record

ArticleCellular microbiology2018

Modelling persistent Mycoplasma pneumoniae infection of human airway epithelium.

Oliver A Prince, Thomas M Krunkosky, Edward S Sheppard, Duncan C Krause

Abstract read
In one paragraph

Article in Cellular microbiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Modeling chronic infection withInfection and immunity · 2026
    Article
  4. Review
  5. Immune dysregulation inFrontiers in immunology · 2026
    Review
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  8. Advances in adhesion-related pathogenesis inFrontiers in microbiology · 2025
    Review
  9. Review
  10. Transboundary and emerging diseases · 2024
    Article
  11. Article
  12. Clinical features and "early" corticosteroid treatment outcome of pediatricFrontiers in cellular and infection microbiology · 2023
    Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. 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

4 authors at 1 institution in 1 country.

Oliver A PrinceDepartment of Microbiology, University of Georgia, Athens, GA, USA.
Thomas M KrunkoskyDepartment of Veterinary Biosciences and Diagnostic Imaging, University of Georgia, Athens, GA, USA.
Edward S SheppardDepartment of Microbiology, University of Georgia, Athens, GA, USA.
Duncan C KrauseDepartment of Microbiology, University of Georgia, Athens, GA, USA.ORCID 0000-0003-3548-0422
University of Georgia · US

Funding

Mycoplasma pneumoniae Gliding MotilityR01AI049194 · NIAID · UNIVERSITY OF GEORGIA (UGA) · PI JENSEN, GRANT J, KRAUSE, DUNCAN C · 2002 to 2012
$2.7M
Human Airway Colonization by Mycoplasma pneumoniaeR01AI110098 · NIAID · UNIVERSITY OF GEORGIA · PI KRAUSE, DUNCAN C · 2014 to 2018
$1.9M
NIAID NIH HHS R01 AI049194NIAID NIH HHS R01 AI110098
6 · The paper itself

Abstract

Mycoplasma pneumoniae is a human respiratory tract pathogen causing acute and chronic airway disease states that can include long-term carriage and extrapulmonary spread. The mechanisms of persistence and migration beyond the conducting airways, however, remain poorly understood. We previously described an acute exposure model using normal human bronchial epithelium (NHBE) in air-liquid interface culture, showing that M. pneumoniae gliding motility is essential for initial colonisation and subsequent spread, including localisation to epithelial cell junctions. We extended those observations here, characterizing M. pneumoniae infection of NHBE for up to 4 weeks. Colonisation of the apical surface was followed by pericellular invasion of the basolateral compartment and migration across the underlying transwell membrane. Despite fluctuations in transepithelial electrical resistance and increased NHBE cell desquamation, barrier function remained largely intact. Desquamation was accompanied by epithelial remodelling that included cytoskeletal reorganisation and development of deep furrows in the epithelium. Finally, M. pneumoniae strains S1 and M129 differed with respect to invasion and histopathology, consistent with contrasting virulence in experimentally infected mice. In summary, this study reports pericellular invasion, NHBE cytoskeletal reorganisation, and tissue remodelling with persistent infection in a human airway epithelium model, providing clear insight into the likely route for extrapulmonary spread.

Indexed as

BronchiCells, CulturedEpithelial CellsHumansMycoplasma pneumoniaePneumonia, MycoplasmaRespiratory SystemAirway epitheliumin vitro modellingMycoplasma pneumoniaepersistent infectionrespiratory disease

Identifiers

PMID29155483
PMCPMC5807195
OpenAlexW2769986083

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.