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The global population of SARS-CoV-2 is composed of six major subtypes

The World Health Organization characterized COVID-19 as a pandemic in March 2020, the second pandemic of the twenty-first century. Expanding virus populations, such as that of SARS-CoV-2, accumulate a number of narrowly shared polymorphisms, imposing a confounding effect on traditional clustering me...

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Autores principales: Morais, Ivair José, Polveiro, Richard Costa, Souza, Gabriel Medeiros, Bortolin, Daniel Inserra, Sassaki, Flávio Tetsuo, Lima, Alison Talis Martins
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588421/
https://www.ncbi.nlm.nih.gov/pubmed/33106569
http://dx.doi.org/10.1038/s41598-020-74050-8
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author Morais, Ivair José
Polveiro, Richard Costa
Souza, Gabriel Medeiros
Bortolin, Daniel Inserra
Sassaki, Flávio Tetsuo
Lima, Alison Talis Martins
author_facet Morais, Ivair José
Polveiro, Richard Costa
Souza, Gabriel Medeiros
Bortolin, Daniel Inserra
Sassaki, Flávio Tetsuo
Lima, Alison Talis Martins
author_sort Morais, Ivair José
collection PubMed
description The World Health Organization characterized COVID-19 as a pandemic in March 2020, the second pandemic of the twenty-first century. Expanding virus populations, such as that of SARS-CoV-2, accumulate a number of narrowly shared polymorphisms, imposing a confounding effect on traditional clustering methods. In this context, approaches that reduce the complexity of the sequence space occupied by the SARS-CoV-2 population are necessary for robust clustering. Here, we propose subdividing the global SARS-CoV-2 population into six well-defined subtypes and 10 poorly represented genotypes named tentative subtypes by focusing on the widely shared polymorphisms in nonstructural (nsp3, nsp4, nsp6, nsp12, nsp13 and nsp14) cistrons and structural (spike and nucleocapsid) and accessory (ORF8) genes. The six subtypes and the additional genotypes showed amino acid replacements that might have phenotypic implications. Notably, three mutations (one of them in the Spike protein) were responsible for the geographical segregation of subtypes. We hypothesize that the virus subtypes detected in this study are records of the early stages of SARS-CoV-2 diversification that were randomly sampled to compose the virus populations around the world. The genetic structure determined for the SARS-CoV-2 population provides substantial guidelines for maximizing the effectiveness of trials for testing candidate vaccines or drugs.
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spelling pubmed-75884212020-10-27 The global population of SARS-CoV-2 is composed of six major subtypes Morais, Ivair José Polveiro, Richard Costa Souza, Gabriel Medeiros Bortolin, Daniel Inserra Sassaki, Flávio Tetsuo Lima, Alison Talis Martins Sci Rep Article The World Health Organization characterized COVID-19 as a pandemic in March 2020, the second pandemic of the twenty-first century. Expanding virus populations, such as that of SARS-CoV-2, accumulate a number of narrowly shared polymorphisms, imposing a confounding effect on traditional clustering methods. In this context, approaches that reduce the complexity of the sequence space occupied by the SARS-CoV-2 population are necessary for robust clustering. Here, we propose subdividing the global SARS-CoV-2 population into six well-defined subtypes and 10 poorly represented genotypes named tentative subtypes by focusing on the widely shared polymorphisms in nonstructural (nsp3, nsp4, nsp6, nsp12, nsp13 and nsp14) cistrons and structural (spike and nucleocapsid) and accessory (ORF8) genes. The six subtypes and the additional genotypes showed amino acid replacements that might have phenotypic implications. Notably, three mutations (one of them in the Spike protein) were responsible for the geographical segregation of subtypes. We hypothesize that the virus subtypes detected in this study are records of the early stages of SARS-CoV-2 diversification that were randomly sampled to compose the virus populations around the world. The genetic structure determined for the SARS-CoV-2 population provides substantial guidelines for maximizing the effectiveness of trials for testing candidate vaccines or drugs. Nature Publishing Group UK 2020-10-26 /pmc/articles/PMC7588421/ /pubmed/33106569 http://dx.doi.org/10.1038/s41598-020-74050-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Morais, Ivair José
Polveiro, Richard Costa
Souza, Gabriel Medeiros
Bortolin, Daniel Inserra
Sassaki, Flávio Tetsuo
Lima, Alison Talis Martins
The global population of SARS-CoV-2 is composed of six major subtypes
title The global population of SARS-CoV-2 is composed of six major subtypes
title_full The global population of SARS-CoV-2 is composed of six major subtypes
title_fullStr The global population of SARS-CoV-2 is composed of six major subtypes
title_full_unstemmed The global population of SARS-CoV-2 is composed of six major subtypes
title_short The global population of SARS-CoV-2 is composed of six major subtypes
title_sort global population of sars-cov-2 is composed of six major subtypes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588421/
https://www.ncbi.nlm.nih.gov/pubmed/33106569
http://dx.doi.org/10.1038/s41598-020-74050-8
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