OPEN bioRxiv : the preprint server for biology | 6 Jan 2021
E Andreano, G Piccini, D Licastro, L Casalino, NV Johnson, I Paciello, SD Monego, E Pantano, N Manganaro, A Manenti, R Manna, E Casa, I Hyseni, L Benincasa, E Montomoli, RE Amaro, JS McLellan and R Rappuoli
To investigate the evolution of SARS-CoV-2 in the immune population, we co-incubated authentic virus with a highly neutralizing plasma from a COVID-19 convalescent patient. The plasma fully neutralized the virus for 7 passages, but after 45 days, the deletion of F140 in the spike N-terminal domain (NTD) N3 loop led to partial breakthrough. At day 73, an E484K substitution in the receptor-binding domain (RBD) occurred, followed at day 80 by an insertion in the NTD N5 loop containing a new glycan sequon, which generated a variant completely resistant to plasma neutralization. Computational modeling predicts that the deletion and insertion in loops N3 and N5 prevent binding of neutralizing antibodies. The recent emergence in the United Kingdom and South Africa of natural variants with similar changes suggests that SARS-CoV-2 has the potential to escape an effective immune response and that vaccines and antibodies able to control emerging variants should be developed.
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