Respiratory long COVID in aged hamsters features impaired lung function post-exercise with bronchiolization and fibrosis

Long-term consequences of SARS-CoV-2 infection affect millions of people and strain public health systems. The underlying pathomechanisms remain unclear, necessitating further research in appropriate animal models. This study aimed to characterize the trajectory of lung regeneration over 112 days in the male hamster model by combining morphological, transcriptomic and functional readouts. We demonstrate that in the acute phase, SARS-CoV-2 Delta-infected, male, aged hamsters show a severe impairment of lung function at rest. In the chronic phase, similar impairments persisted up to 7 weeks post-infection but were only evident after exercise on a rodent treadmill. The male hamster model recapitulates chronic pulmonary fibrotic changes observed in many patients with respiratory long COVID, but lacks extra-pulmonary long-term lesions. We show that sub-pleural and interstitial pulmonary fibrosis as well as alveolar bronchiolization persist until 112 dpi. Interestingly, CK8<sup>+</sup> alveolar differentiation intermediate (ADI) cells are becoming less prominent in the alveolar proliferation areas from 28 dpi on. Instead, CK14<sup>+</sup> airway basal cells and SCGB1A1<sup>+</sup> club cells, expressing cell proliferation markers, mainly populate alveolar bronchiolization areas at later time-points. We postulate that pulmonary fibrosis and SCGB1A1<sup>+</sup> club cell-rich areas of alveolar bronchiolization represent potential risk factors for other diseases in long-COVID survivors.

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Publication Details

Journal
Nature Communications
Published
2025-02-28
DOI
https://doi.org/10.1038/s41467-025-57267-x
Citations
12
Primary Topic
Long-Term Effects of COVID-19
Type
article
Field-Weighted Citation Impact
16.67

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article

Respiratory long COVID in aged hamsters features impaired lung function post-exercise with bronchiolization and fibrosis

L. Heydemann, Federico Armando, Carina Gross, Dirk Schaudien et al.
12 citations
Nature Communications
Long-Term Effects of COVID-19
16.67
article

Respiratory long COVID in aged hamsters features impaired lung function post-exercise with bronchiolization and fibrosis

L. Heydemann, Federico Armando, Carina Gross, Dirk Schaudien, Sabrina Clever, Maren von Köckritz‐Blickwede, Georg Beythien, Georgios Amanakis, Lukas Mathias Michaely, Tom Schreiner, Klaus Schughart, Christian Meyer zu Natrup, Wolfgang Baumgärtner, Wencke Reineking, Asisa Volz, Kirsten Hülskötter, Katharina M. Gregor, Mika K. Kaneko, Yukinari Kato, Robert Geffers, Theresa Störk, Andreas Pavlou, Isabel Zdora, Tamara Tuchel, Małgorzata Ciurkiewicz, Timo Henneck, Karl Röhn, Lisa-Marie Schünemann
article en
12 citations

Abstract

Long-term consequences of SARS-CoV-2 infection affect millions of people and strain public health systems. The underlying pathomechanisms remain unclear, necessitating further research in appropriate animal models. This study aimed to characterize the trajectory of lung regeneration over 112 days in the male hamster model by combining morphological, transcriptomic and functional readouts. We demonstrate that in the acute phase, SARS-CoV-2 Delta-infected, male, aged hamsters show a severe impairment of lung function at rest. In the chronic phase, similar impairments persisted up to 7 weeks post-infection but were only evident after exercise on a rodent treadmill. The male hamster model recapitulates chronic pulmonary fibrotic changes observed in many patients with respiratory long COVID, but lacks extra-pulmonary long-term lesions. We show that sub-pleural and interstitial pulmonary fibrosis as well as alveolar bronchiolization persist until 112 dpi. Interestingly, CK8<sup>+</sup> alveolar differentiation intermediate (ADI) cells are becoming less prominent in the alveolar proliferation areas from 28 dpi on. Instead, CK14<sup>+</sup> airway basal cells and SCGB1A1<sup>+</sup> club cells, expressing cell proliferation markers, mainly populate alveolar bronchiolization areas at later time-points. We postulate that pulmonary fibrosis and SCGB1A1<sup>+</sup> club cell-rich areas of alveolar bronchiolization represent potential risk factors for other diseases in long-COVID survivors.

Nature CommunicationsVol. 16(1)
University of Parma (IT), University of Tennessee Health Science Center (US), University of Veterinary Medicine Hannover, Foundation (DE), Tohoku University (JP), University of Münster (DE), Medizinische Hochschule Hannover (DE), Zimmer Biomet (Germany) (DE), Fraunhofer Institute for Toxicology and Experimental Medicine (DE), Helmholtz Centre for Infection Research (DE), Center for Experimental and Clinical Infection Research (DE)
Niedersächsische Ministerium für Wissenschaft und Kultur
Openalex Percentile: Top 1%
Long-Term Effects of COVID-19
16.67
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