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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Main Authors: Marco Antônio M. Pretti, Rômulo G. Galvani, Gustavo Fioravanti Vieira, Adriana Bonomo, Martín H. Bonamino, Mariana Boroni
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-12-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2020.565730/full
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spelling 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
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