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Spread of Gamma (P.1) sub-lineages carrying Spike mutations close to the furin cleavage site and deletions in the N-terminal domain drives ongoing transmission of SARS-CoV-2 in Amazonas, Brazil

Naveca, F. G.; Nascimento, V.; Souza, V.; Corado, A. L.; Nascimento, F.; Silva, G.; Mejia, M. C.; Brandao, M. J.; Costa, A.; Duarte, D.; Pessoa, K.; Jesus, M.; Goncalves, L.; Fernandes, C.; Mattos, T.; Abdalla, L.; Santos, J. H.; Martins, A.; Chui, F. M.; Val, F. F.; Melo, G. C. d.; Simao, M. X.; Sampaio, V. d. S.; Mourao, M. P.; Lacerda, M. V.; Batista, E. L.; Magalhaes, A. L.; Dabilla, N.; Pereira, L. C. G.; Vinhal, F.; Miyajima, F.; Dias, F. S.; dos Santos, E. R.; Coelho, D.; Ferraz, M.; Lins, R.; Wallau, G. L.; Delatorre, E.; Gräf, T.; Siqueira, M. M.; Resende, P. C.; Bello, G.

2021-09-15 infectious diseases
10.1101/2021.09.12.21263453
Show abstract

The Amazonas was one of the most heavily affected Brazilian states by the COVID-19 epidemic. Despite a large number of infected people, particularly during the second wave associated with the spread of the Variant of Concern (VOC) Gamma (lineage P.1), SARS-CoV-2 continues to circulate in the Amazonas. To understand how SARS-CoV-2 persisted in a human population with a high immunity barrier, we generated 1,188 SARS-CoV-2 whole-genome sequences from individuals diagnosed in the Amazonas state from 1st January to 6th July 2021, of which 38 were vaccine breakthrough infections. Our study reveals a sharp increase in the relative prevalence of Gamma plus (P.1+) variants, designated as Pango Lineages P.1.3 to P.1.6, harboring two types of additional Spike changes: deletions in the N-terminal (NTD) domain (particularly{Delta} 144 or{Delta} 141-144) associated with resistance to anti-NTD neutralizing antibodies or mutations at the S1/S2 junction (N679K or P681H) that probably enhance the binding affinity to the furin cleavage site, as suggested by our molecular dynamics simulations. As lineages P.1.4 (S:N679K) and P.1.6 (S:P681H) expanded (Re > 1) from March to July 2021, the lineage P.1 declined (Re < 1) and the median Ct value of SARS-CoV-2 positive cases in Amazonas significantly decreases. Still, we found no overrepresentation of P.1+ variants among breakthrough cases of fully vaccinated patients (71%) in comparison to unvaccinated individuals (93%). This evidence supports that the ongoing endemic transmission of SARS-CoV-2 in the Amazonas is driven by the spread of new local Gamma/P.1 sub-lineages that are more transmissible, although not more efficient to evade vaccine-elicited immunity than the parental VOC. Finally, as SARS-CoV-2 continues to spread in human populations with a declining density of susceptible hosts, the risk of selecting new variants with higher infectivity are expected to increase.

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