Single-Cell Profiling of the Differential In Vivo Impact of Severe Acute Respiratory Syndrome Coronavirus 2 Infection Among Lung Tissue Cell Subtypes at the Protein Level.
Leila Fotooh AbadiMadhav B SharmaTheodoros KelesidisPublished in: The Journal of infectious diseases (2024)
The complexity of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and its variants in lung cells can truly be characterized only at the tissue and protein levels among unique cell subtypes. However, in vivo data are limited due to lack of accessible human tissues. Using a transgenic mouse model of SARS-CoV-2 infection and flow cytometry, we provide in vivo novel insight at the protein level that the differential impact of SARS-CoV-2 (Wuhan strain) and its B.1.617.2 (Delta) and BA.1 (Omicron) variants on lung may be attributed to differential patterns of viral protein levels among ciliated airway cells, alveolar types 1 and 2 cells, immune cells, and endothelial lung cells.
Keyphrases
- respiratory syndrome coronavirus
- sars cov
- induced apoptosis
- single cell
- cell cycle arrest
- coronavirus disease
- endothelial cells
- mouse model
- flow cytometry
- endoplasmic reticulum stress
- cell death
- protein protein
- cell therapy
- machine learning
- signaling pathway
- small molecule
- dna methylation
- copy number
- artificial intelligence
- mesenchymal stem cells
- bone marrow