Evidence map›Paper›PMID 42274602›Full record

ArticleCells2026

Multifactorial Analysis Identifies Conditions for Robust HCoV-OC43 Replication in Primary Human Bronchial Epithelial Cells Cultured at Air-Liquid Interface.

Natalie Fischhaber, Julian Vogler, Ivana Martan, Thomas Michler

Abstract read
In one paragraph

Article in Cells, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Natalie FischhaberInstitute of Laboratory Medicine, Ludwig-Maximilians-University Hospital, Ludwig-Maximilians-University Munich, 80539 Munich, Germany.ORCID 0009-0008-0755-8599
Julian VoglerInstitute of Laboratory Medicine, Ludwig-Maximilians-University Hospital, Ludwig-Maximilians-University Munich, 80539 Munich, Germany.ORCID 0000-0002-3213-6231
Ivana MartanInstitute of Laboratory Medicine, Ludwig-Maximilians-University Hospital, Ludwig-Maximilians-University Munich, 80539 Munich, Germany.
Thomas MichlerInstitute of Laboratory Medicine, Ludwig-Maximilians-University Hospital, Ludwig-Maximilians-University Munich, 80539 Munich, Germany.ORCID 0000-0002-4174-3316

Funding

Deutsche Forschungsgemeinschaft 516634310Volkswagen Stiftung 9A874
6 · The paper itself

Abstract

Air-liquid interface (ALI) cultures recapitulate key features of the airway epithelium by driving basal cell differentiation into ciliated, club, and goblet cells and by generating a functional mucus barrier, thereby representing a highly relevant model of the human respiratory tract. Using a reduced factorial Design of Experiments (DoE) methodology, we simultaneously investigated the effects of seven variables on human coronavirus OC43 (HCoV-OC43) replication in air-liquid interface (ALI)-cultured primary human bronchial epithelial cells (pHBECs) to identify robust conditions that support infection and viral replication. Epithelial differentiation was monitored by measuring transepithelial electrical resistance and determining expression levels of marker genes for basal, goblet, club, and ciliated cells using reverse transcription quantitative PCR (RT-qPCR). HCoV-OC43 replication was monitored by quantifying genomic and subgenomic RNA by RT-qPCR. Viral RNA peaked three days post-infection in cell lysates and four days post-infection in apical washes. Initiation of ALI conditions induced epithelial differentiation, which was complete after 21 days and emerged as the strongest determinant of viral replication. Differentiated pHBEC cultures showed significantly reduced viral RNA compared with undifferentiated cultures, particularly following apical infection. In contrast, basal infection resulted in lower viral RNA levels in undifferentiated cultures than apical infection but was less dependent on epithelial differentiation. However, productive infection following basal exposure was less consistent and more strongly dependent on viral inoculum size. We further demonstrate that repeated mucus washes prior to infection increased HCoV-OC43 replication in mature cultures. In summary, our findings show that epithelial differentiation negatively affects HCoV-OC43 replication and we identify conditions that maximize viral replication in fully differentiated pHBEC cultures.

Indexed as

BronchiCoronavirus OC43, HumanEpithelial CellsVirus ReplicationAirCell DifferentiationCells, CulturedHumansRNA, ViralRNA, Viralair–liquid interfacebronchial epithelial differentiationDesign of ExperimentHCOV-OC43

Identifiers

PMID42274602
PMCPMC13256164

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.