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Naturally occurring SARS-CoV-2 gene deletions close to the spike S1/S2 cleavage site in the viral quasispecies of COVID19 patients

Authors :
Andrés, Cristina
Garcia-Cehic, D.
Gregori, Josep
Piñana, Maria
Rodriguez-Frias, Francisco
Guerrero-Murillo, Mercedes
Esperalba, Juliana
Rando, Adriana
Goterris, Lidia
Codina, Gema
Quer, Susanna
Martín, Maria Carmen
Campins Martí, Magda
Ferrer, Ricard
Almirante, Benito
Esteban Mur, Juan Ignacio
Pumarola, Tomás
Antón, Andrés
Quer, Josep
Andrés, Cristina
Garcia-Cehic, D.
Gregori, Josep
Piñana, Maria
Rodriguez-Frias, Francisco
Guerrero-Murillo, Mercedes
Esperalba, Juliana
Rando, Adriana
Goterris, Lidia
Codina, Gema
Quer, Susanna
Martín, Maria Carmen
Campins Martí, Magda
Ferrer, Ricard
Almirante, Benito
Esteban Mur, Juan Ignacio
Pumarola, Tomás
Antón, Andrés
Quer, Josep
Publication Year :
2020

Abstract

The SARS-CoV-2 spike (S) protein, the viral mediator for binding and entry into the host cell, has sparked great interest as a target for vaccine development and treatments with neutralizing antibodies. Initial data suggest that the virus has low mutation rates, but its large genome could facilitate recombination, insertions, and deletions, as has been described in other coronaviruses. Here, we deep-sequenced the complete SARS-CoV-2 S gene from 18 patients (10 with mild and 8 with severe COVID-19), and found that the virus accumulates deletions upstream and very close to the S1/S2 cleavage site (PRRAR/S), generating a frameshift with appearance of a stop codon. These deletions were found in a small percentage of the viral quasispecies (2.2%) in samples from all the mild and only half the severe COVID-19 patients. Our results suggest that the virus may generate free S1 protein released to the circulation. We suggest that natural selection has favoured a "Don't burn down the house" strategy, in which free S1 protein may compete with viral particles for the ACE2 receptor, thus reducing the severity of the infection and tissue damage without losing transmission capability.

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1312226993
Document Type :
Electronic Resource