This article has been reviewed according to Science X's editorial process and policies. Editors have highlighted the following attributes while ensuring the content's credibility:

fact-checked

proofread

A unique pathogenic mechanism of SARS-CoV-2 omicron variant: Selective induction of cellular senescence

A unique pathogenic mechanism of SARS-CoV-2 omicron variant: Selective induction of cellular senescence
Graphical abstract of known differences of SARS-CoV-2 delta and omicron variant entry and findings of our study obtained from mRNA sequence data of 24 h post infection. Credit: 2023 Hornung et al.

SARS-CoV-2 variants are constantly emerging with a variety of changes in the conformation of the spike protein, resulting in alterations of virus entry mechanisms. Solely omicron variants use the endosomal clathrin-mediated entry.

In a new study, researchers investigate the influence of defined altered spike formations to study their impact on premature .

Their research paper was published on the cover of Aging, titled, "Uncovering a unique pathogenic mechanism of SARS-CoV-2 omicron variant: selective induction of cellular senescence."

"In our study, in vitro infections of SARS-CoV-2 variants delta (B.1.617.2) and omicron (B.1.1.529) were analyzed by using human primary small alveolar epithelial cells and human ex vivo lung slices. We confirmed cellular senescence in human lungs of COVID-19 patients. Hence, global gene expression patterns of infected human primary alveolar epithelial cells were identified via mRNA sequencing," the researchers write.

Solely omicron variants of SARS-CoV-2 influenced the expression of cell cycle genes, highlighted by an increased p21 expression in human primary lung cells and human ex vivo lungs. Additionally, an upregulated senescence-associated secretory phenotype (SASP) was detected.

Credit: Impact Journals LLC

Transcriptomic data indicate an increased gene expression of p16, and p38 in omicron-infected lung cells. Significant changes due to different SARS-CoV-2 infections in human primary alveolar epithelial cells with an overall impact on premature aging could be identified.

A substantially different cellular response with an upregulation of cell cycle, inflammation- and integrin-associated pathways in omicron infected cells indicates premature cellular senescence.

"This difference may be attributed to the distinct endocytic cell entry and intracellular pathways of the when compared to the delta variant. The induction of cellular senescence in lung tissue following acute SARS-CoV-2 infection could potentially contribute to the reported cytokine storm and the development of long-COVID," the authors conclude.

More information: Franziska Hornung et al, Uncovering a unique pathogenic mechanism of SARS-CoV-2 omicron variant: selective induction of cellular senescence, Aging (2023). DOI: 10.18632/aging.205297

Provided by Impact Journals LLC
Citation: A unique pathogenic mechanism of SARS-CoV-2 omicron variant: Selective induction of cellular senescence (2023, December 18) retrieved 13 April 2024 from https://medicalxpress.com/news/2023-12-unique-pathogenic-mechanism-sars-cov-omicron.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Explore further

Study: Gene expression signatures of human senescent corneal and conjunctival epithelial cells

2 shares

Feedback to editors