Human airway cells prevent SARS-CoV-2 multibasic cleavage site cell culture adaptation.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 33835028.
- Also identified by DOI 10.7554/eLife.66815 and PMC identifier 8131099.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Virus propagation methods generally use transformed cell lines to grow viruses from clinical specimens, which may force viruses to rapidly adapt to cell culture conditions, a process facilitated by high viral mutation rates. Upon propagation in VeroE6 cells, SARS-CoV-2 may mutate or delete the multibasic cleavage site (MBCS) in the spike protein. Previously, we showed that the MBCS facilitates serine protease-mediated entry into human airway cells (Mykytyn et al., 2021). Here, we report that propagating SARS-CoV-2 on the human airway cell line Calu-3 - that expresses serine proteases - prevents cell culture adaptations in the MBCS and directly adjacent to the MBCS (S686G). Similar results were obtained using a human airway organoid-based culture system for SARS-CoV-2 propagation. Thus, in-depth knowledge on the biology of a virus can be used to establish methods to prevent cell culture adaptation.
Medical subject headings
- Epithelial Cells
- SARS-CoV-2
- Spike Glycoprotein, Coronavirus
- Virus Cultivation
- Virus Internalization