Evidence map›Paper›PMID 33114247›Full record

ArticleViruses2020

The Cell Tropism of Porcine Respiratory Coronavirus for Airway Epithelial Cells Is Determined by the Expression of Porcine Aminopeptidase N.

Ju-Yi Peng, Darsaniya Punyadarsaniya, Dai-Lun Shin, Suvarin Pavasutthipaisit, Andreas Beineke, Guangxing Li, Nai-Huei Wu, Georg Herrler

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.2field-weighted citation impact, top 33% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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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

8 authors at 4 institutions in 4 countries.

Ju-Yi PengInstitute of Virology, University of Veterinary Medicine Hannover, 30559 Hannover, Germany.
Darsaniya PunyadarsaniyaVirology and Immunology Department, Faculty of Veterinary Medicine, Mahanakorn University of Technology, Bangkok 10100, Thailand.
Dai-Lun ShinInstitute of Virology, University of Veterinary Medicine Hannover, 30559 Hannover, Germany.
Suvarin PavasutthipaisitDepartment of Pathology, University of Veterinary Medicine Hannover, 30559 Hannover, Germany.
Andreas BeinekeDepartment of Pathology, University of Veterinary Medicine Hannover, 30559 Hannover, Germany.
Guangxing LiCollege of Veterinary Medicine, Northeast Agricultural University, 59 Mucai Street, Xiangfang District, Harbin 150000, China.
Nai-Huei WuInstitute of Virology, University of Veterinary Medicine Hannover, 30559 Hannover, Germany.
Georg HerrlerInstitute of Virology, University of Veterinary Medicine Hannover, 30559 Hannover, Germany.
University of Veterinary Medicine Hannover, Foundation · DEMahanakorn University of Technology · THNational Taiwan University · TWNortheast Agricultural University · CN

Funding

Deutsche Forschungsgemeinschaft HE 1168/19-1Deutsche Forschungsgemeinschaft WU 929/1-1
6 · The paper itself

Abstract

Porcine respiratory coronavirus (PRCoV) infects the epithelial cells in the respiratory tract of pigs, causing a mild respiratory disease. We applied air-liquid interface (ALI) cultures of well-differentiated porcine airway cells to mimic the respiratory tract epithelium in vitro and use it for analyzing the infection by PRCoV. As reported for most coronaviruses, virus entry and virus release occurred mainly via the apical membrane domain. A novel finding was that PRCoV preferentially targets non-ciliated and among them the non-mucus-producing cells. Aminopeptidase N (APN), the cellular receptor for PRCoV was also more abundantly expressed on this type of cell suggesting that APN is a determinant of the cell tropism. Interestingly, differentiation-dependent differences were found both in the expression of pAPN and the susceptibility to PRCoV infection. Cells in an early differentiation stage express higher levels of pAPN and are more susceptible to infection by PRCoV than are well-differentiated cells. A difference in the susceptibility to infection was also detected when tracheal and bronchial cells were compared. The increased susceptibility to infection of bronchial epithelial cells was, however, not due to an increased abundance of APN on the cell surface. Our data reveal a complex pattern of infection in porcine differentiated airway epithelial cells that could not be elucidated with immortalized cell lines. The results are expected to have relevance also for the analysis of other respiratory viruses.

Indexed as

Viral TropismAnimalsBronchiCD13 AntigensCell DifferentiationCells, CulturedEpithelial CellsPorcine Respiratory CoronavirusReceptors, VirusRespiratory MucosaSwineTracheaVirus InternalizationVirus ReleaseVirus ReplicationCD13 AntigensReceptors, Virusair–liquid interface cultureporcine aminopeptidase Nporcine respiratory coronavirustropism

Identifiers

PMID33114247
PMCPMC7690903
OpenAlexW3094476322

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.