Human airway cells prevent SARS-CoV-2 multibasic cleavage site cell culture adaptation.
Mart M LamersAnna Z MykytynTim I BreugemYiquan WangDouglas C WuSamra RieseboschPetra B van den DoelDebby SchipperTheo BestebroerNicholas C WuBart L HaagmansPublished in: eLife (2021)
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.
Keyphrases
- sars cov
- endothelial cells
- induced apoptosis
- respiratory syndrome coronavirus
- induced pluripotent stem cells
- cell cycle arrest
- pluripotent stem cells
- healthcare
- oxidative stress
- endoplasmic reticulum stress
- signaling pathway
- cell proliferation
- transcription factor
- binding protein
- dna binding
- high intensity
- protein protein