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Human airway cells prevent SARS-CoV-2 multibasic cleavage site cell culture adaptation.

eLife (2021-04-10)
Mart M Lamers, Anna Z Mykytyn, Tim I Breugem, Yiquan Wang, Douglas C Wu, Samra Riesebosch, Petra B van den Doel, Debby Schipper, Theo Bestebroer, Nicholas C Wu, Bart L Haagmans
ZUSAMMENFASSUNG

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.

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Sigma-Aldrich
Fetales Kälberserum, non-USA origin, sterile-filtered, suitable for cell culture
Sigma-Aldrich
Camostat -mesylat, ≥98% (HPLC)