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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

Authors :
Felipe Gomes Naveca
Valdinete Nascimento
Victor Souza
André de Lima Corado
Fernanda Nascimento
George Silva
Matilde Contreras Mejía
Maria Júlia Brandão
Ágatha Costa
Débora Duarte
Karina Pessoa
Michele Jesus
Luciana Gonçalves
Cristiano Fernandes
Tirza Mattos
Ligia Abdalla
João Hugo Santos
Alex Martins
Fabiola Mendonça Chui
Fernando Fonseca Val
Gisely Cardoso de Melo
Mariana Simão Xavier
Vanderson de Souza Sampaio
Maria Paula Mourão
Marcus Vinícius Lacerda
Érika Lopes Rocha Batista
Alessandro Leonardo Álvares Magalhães
Nathânia Dábilla
Lucas Carlos Gomes Pereira
Fernando Vinhal
Fabio Miyajima
Fernando Braga Stehling Dias
Eduardo Ruback dos Santos
Danilo Coêlho
Matheus Ferraz
Roberto Lins
Gabriel Luz Wallau
Edson Delatorre
Tiago Gräf
Marilda Mendonça Siqueira
Paola Cristina Resende
Gonzalo Bello
Source :
Microbiology Spectrum, Vol 10, Iss 1 (2022)
Publication Year :
2022
Publisher :
American Society for Microbiology, 2022.

Abstract

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 Pango Lineages P.1.3 to P.1.6, harboring two types of additional Spike changes: deletions in the N-terminal (NTD) domain (particularly Δ144 or Δ141-144) 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

Details

Language :
English
ISSN :
21650497
Volume :
10
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Microbiology Spectrum
Publication Type :
Academic Journal
Accession number :
edsdoj.21aca3daf8e48c892530e26b736507b
Document Type :
article
Full Text :
https://doi.org/10.1128/spectrum.02366-21