Class I HLA Allele Predicted Restricted Antigenic Coverages for Spike and Nucleocapsid Proteins Are Associated With Deaths Related to COVID-19
The world is dealing with one of the worst pandemics ever. SARS-CoV-2 is the etiological agent of COVID-19 that has already spread to more than 200 countries. However, infectivity, severity, and mortality rates do not affect all countries equally. Here we consider 140 HLA alleles and extensively inv...
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doaj-306a8eab81bc4b109ba0943cedeccae02020-12-16T04:29:54ZengFrontiers Media S.A.Frontiers in Immunology1664-32242020-12-011110.3389/fimmu.2020.565730565730Class I HLA Allele Predicted Restricted Antigenic Coverages for Spike and Nucleocapsid Proteins Are Associated With Deaths Related to COVID-19Marco Antônio M. Pretti0Marco Antônio M. Pretti1Rômulo G. Galvani2Rômulo G. Galvani3Rômulo G. Galvani4Gustavo Fioravanti Vieira5Gustavo Fioravanti Vieira6Adriana Bonomo7Adriana Bonomo8Martín H. Bonamino9Martín H. Bonamino10Mariana Boroni11Laboratory of Bioinformatics and Computational Biology, Division of Experimental and Translational Research, Brazilian National Cancer Institute (INCA), Rio de Janeiro, BrazilProgram of Immunology and Tumor Biology, Division of Experimental and Translational Research, Brazilian National Cancer Institute (INCA), Rio de Janeiro, BrazilLaboratory of Bioinformatics and Computational Biology, Division of Experimental and Translational Research, Brazilian National Cancer Institute (INCA), Rio de Janeiro, BrazilFaculdade de Biomedicina, Universidade Veiga de Almeida, Rio de Janeiro, BrazilLaboratory for Thymus Research (LPT), Oswaldo Cruz Institute, Oswaldo Cruz Foundation (FIOCRUZ), Rio de Janeiro, BrazilLaboratory of Immunoinformatics (NBLI), Department of Genetics, Institute of Biosciences, Federal University of Rio Grande do Sul, Porto Alegre, BrazilLaboratory of In Silico Human Health, Post Graduate Program in Health and Human Development, La Salle University, Canoas, BrazilLaboratory for Thymus Research (LPT), Oswaldo Cruz Institute, Oswaldo Cruz Foundation (FIOCRUZ), Rio de Janeiro, BrazilVice-Presidency of Research and Biological Collections (VPPCB), Oswaldo Cruz Foundation (FIOCRUZ), Rio de Janeiro, BrazilProgram of Immunology and Tumor Biology, Division of Experimental and Translational Research, Brazilian National Cancer Institute (INCA), Rio de Janeiro, BrazilVice-Presidency of Research and Biological Collections (VPPCB), Oswaldo Cruz Foundation (FIOCRUZ), Rio de Janeiro, BrazilLaboratory of Bioinformatics and Computational Biology, Division of Experimental and Translational Research, Brazilian National Cancer Institute (INCA), Rio de Janeiro, BrazilThe world is dealing with one of the worst pandemics ever. SARS-CoV-2 is the etiological agent of COVID-19 that has already spread to more than 200 countries. However, infectivity, severity, and mortality rates do not affect all countries equally. Here we consider 140 HLA alleles and extensively investigate the landscape of 3,723 potential HLA-I A and B restricted SARS-CoV-2-derived antigens and how 37 countries in the world are predicted to respond to those peptides considering their HLA-I distribution frequencies. The clustering of HLA-A and HLA-B allele frequencies partially separates most countries with the lowest number of deaths per million inhabitants from the other countries. We further correlated the patterns of in silico predicted population coverage and epidemiological data. The number of deaths per million inhabitants correlates to the predicted antigen coverage of S and N derived peptides and its module is influenced if a given set of frequent or rare HLA alleles are analyzed in a given population. Moreover, we highlighted a potential risk group carrying HLAs associated with an elevated number of deaths per million inhabitants. In addition, we identified three potential antigens bearing at least one amino acid of the four-length insertion that differentiates SARS-CoV-2 from previous coronavirus strains. We believe these data can contribute to the search for peptides with the potential to be used in vaccine strategies considering the role of herd immunity to hamper the spread of the disease. Importantly, to the best of our knowledge, this work is the first to use a populational approach in association with COVID-19 outcome.https://www.frontiersin.org/articles/10.3389/fimmu.2020.565730/fullCOVID-19SARS-CoV-2Betacoronavirusligandomepopulation coverage analysisherd immunity |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Marco Antônio M. Pretti Marco Antônio M. Pretti Rômulo G. Galvani Rômulo G. Galvani Rômulo G. Galvani Gustavo Fioravanti Vieira Gustavo Fioravanti Vieira Adriana Bonomo Adriana Bonomo Martín H. Bonamino Martín H. Bonamino Mariana Boroni |
spellingShingle |
Marco Antônio M. Pretti Marco Antônio M. Pretti Rômulo G. Galvani Rômulo G. Galvani Rômulo G. Galvani Gustavo Fioravanti Vieira Gustavo Fioravanti Vieira Adriana Bonomo Adriana Bonomo Martín H. Bonamino Martín H. Bonamino Mariana Boroni Class I HLA Allele Predicted Restricted Antigenic Coverages for Spike and Nucleocapsid Proteins Are Associated With Deaths Related to COVID-19 Frontiers in Immunology COVID-19 SARS-CoV-2 Betacoronavirus ligandome population coverage analysis herd immunity |
author_facet |
Marco Antônio M. Pretti Marco Antônio M. Pretti Rômulo G. Galvani Rômulo G. Galvani Rômulo G. Galvani Gustavo Fioravanti Vieira Gustavo Fioravanti Vieira Adriana Bonomo Adriana Bonomo Martín H. Bonamino Martín H. Bonamino Mariana Boroni |
author_sort |
Marco Antônio M. Pretti |
title |
Class I HLA Allele Predicted Restricted Antigenic Coverages for Spike and Nucleocapsid Proteins Are Associated With Deaths Related to COVID-19 |
title_short |
Class I HLA Allele Predicted Restricted Antigenic Coverages for Spike and Nucleocapsid Proteins Are Associated With Deaths Related to COVID-19 |
title_full |
Class I HLA Allele Predicted Restricted Antigenic Coverages for Spike and Nucleocapsid Proteins Are Associated With Deaths Related to COVID-19 |
title_fullStr |
Class I HLA Allele Predicted Restricted Antigenic Coverages for Spike and Nucleocapsid Proteins Are Associated With Deaths Related to COVID-19 |
title_full_unstemmed |
Class I HLA Allele Predicted Restricted Antigenic Coverages for Spike and Nucleocapsid Proteins Are Associated With Deaths Related to COVID-19 |
title_sort |
class i hla allele predicted restricted antigenic coverages for spike and nucleocapsid proteins are associated with deaths related to covid-19 |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Immunology |
issn |
1664-3224 |
publishDate |
2020-12-01 |
description |
The world is dealing with one of the worst pandemics ever. SARS-CoV-2 is the etiological agent of COVID-19 that has already spread to more than 200 countries. However, infectivity, severity, and mortality rates do not affect all countries equally. Here we consider 140 HLA alleles and extensively investigate the landscape of 3,723 potential HLA-I A and B restricted SARS-CoV-2-derived antigens and how 37 countries in the world are predicted to respond to those peptides considering their HLA-I distribution frequencies. The clustering of HLA-A and HLA-B allele frequencies partially separates most countries with the lowest number of deaths per million inhabitants from the other countries. We further correlated the patterns of in silico predicted population coverage and epidemiological data. The number of deaths per million inhabitants correlates to the predicted antigen coverage of S and N derived peptides and its module is influenced if a given set of frequent or rare HLA alleles are analyzed in a given population. Moreover, we highlighted a potential risk group carrying HLAs associated with an elevated number of deaths per million inhabitants. In addition, we identified three potential antigens bearing at least one amino acid of the four-length insertion that differentiates SARS-CoV-2 from previous coronavirus strains. We believe these data can contribute to the search for peptides with the potential to be used in vaccine strategies considering the role of herd immunity to hamper the spread of the disease. Importantly, to the best of our knowledge, this work is the first to use a populational approach in association with COVID-19 outcome. |
topic |
COVID-19 SARS-CoV-2 Betacoronavirus ligandome population coverage analysis herd immunity |
url |
https://www.frontiersin.org/articles/10.3389/fimmu.2020.565730/full |
work_keys_str_mv |
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