Preliminary Identification of Potential Vaccine Targets for the COVID-19 Coronavirus (SARS-CoV-2) Based on SARS-CoV Immunological Studies

The beginning of 2020 has seen the emergence of COVID-19 outbreak caused by a novel coronavirus, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). There is an imminent need to better understand this new virus and to develop ways to control its spread. In this study, we sought to gain ins...

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Published inViruses Vol. 12; no. 3; p. 254
Main Authors Ahmed, Syed Faraz, Quadeer, Ahmed A., McKay, Matthew R.
Format Journal Article
LanguageEnglish
Published Switzerland MDPI 25.02.2020
MDPI AG
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Abstract The beginning of 2020 has seen the emergence of COVID-19 outbreak caused by a novel coronavirus, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). There is an imminent need to better understand this new virus and to develop ways to control its spread. In this study, we sought to gain insights for vaccine design against SARS-CoV-2 by considering the high genetic similarity between SARS-CoV-2 and SARS-CoV, which caused the outbreak in 2003, and leveraging existing immunological studies of SARS-CoV. By screening the experimentally-determined SARS-CoV-derived B cell and T cell epitopes in the immunogenic structural proteins of SARS-CoV, we identified a set of B cell and T cell epitopes derived from the spike (S) and nucleocapsid (N) proteins that map identically to SARS-CoV-2 proteins. As no mutation has been observed in these identified epitopes among the 120 available SARS-CoV-2 sequences (as of 21 February 2020), immune targeting of these epitopes may potentially offer protection against this novel virus. For the T cell epitopes, we performed a population coverage analysis of the associated MHC alleles and proposed a set of epitopes that is estimated to provide broad coverage globally, as well as in China. Our findings provide a screened set of epitopes that can help guide experimental efforts towards the development of vaccines against SARS-CoV-2.
AbstractList The beginning of 2020 has seen the emergence of COVID-19 outbreak caused by a novel coronavirus, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). There is an imminent need to better understand this new virus and to develop ways to control its spread. In this study, we sought to gain insights for vaccine design against SARS-CoV-2 by considering the high genetic similarity between SARS-CoV-2 and SARS-CoV, which caused the outbreak in 2003, and leveraging existing immunological studies of SARS-CoV. By screening the experimentally-determined SARS-CoV-derived B cell and T cell epitopes in the immunogenic structural proteins of SARS-CoV, we identified a set of B cell and T cell epitopes derived from the spike (S) and nucleocapsid (N) proteins that map identically to SARS-CoV-2 proteins. As no mutation has been observed in these identified epitopes among the 120 available SARS-CoV-2 sequences (as of 21 February 2020), immune targeting of these epitopes may potentially offer protection against this novel virus. For the T cell epitopes, we performed a population coverage analysis of the associated MHC alleles and proposed a set of epitopes that is estimated to provide broad coverage globally, as well as in China. Our findings provide a screened set of epitopes that can help guide experimental efforts towards the development of vaccines against SARS-CoV-2.The beginning of 2020 has seen the emergence of COVID-19 outbreak caused by a novel coronavirus, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). There is an imminent need to better understand this new virus and to develop ways to control its spread. In this study, we sought to gain insights for vaccine design against SARS-CoV-2 by considering the high genetic similarity between SARS-CoV-2 and SARS-CoV, which caused the outbreak in 2003, and leveraging existing immunological studies of SARS-CoV. By screening the experimentally-determined SARS-CoV-derived B cell and T cell epitopes in the immunogenic structural proteins of SARS-CoV, we identified a set of B cell and T cell epitopes derived from the spike (S) and nucleocapsid (N) proteins that map identically to SARS-CoV-2 proteins. As no mutation has been observed in these identified epitopes among the 120 available SARS-CoV-2 sequences (as of 21 February 2020), immune targeting of these epitopes may potentially offer protection against this novel virus. For the T cell epitopes, we performed a population coverage analysis of the associated MHC alleles and proposed a set of epitopes that is estimated to provide broad coverage globally, as well as in China. Our findings provide a screened set of epitopes that can help guide experimental efforts towards the development of vaccines against SARS-CoV-2.
The beginning of 2020 has seen the emergence of COVID-19 outbreak caused by a novel coronavirus, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). There is an imminent need to better understand this new virus and to develop ways to control its spread. In this study, we sought to gain insights for vaccine design against SARS-CoV-2 by considering the high genetic similarity between SARS-CoV-2 and SARS-CoV, which caused the outbreak in 2003, and leveraging existing immunological studies of SARS-CoV. By screening the experimentally-determined SARS-CoV-derived B cell and T cell epitopes in the immunogenic structural proteins of SARS-CoV, we identified a set of B cell and T cell epitopes derived from the spike (S) and nucleocapsid (N) proteins that map identically to SARS-CoV-2 proteins. As no mutation has been observed in these identified epitopes among the 120 available SARS-CoV-2 sequences (as of 21 February 2020), immune targeting of these epitopes may potentially offer protection against this novel virus. For the T cell epitopes, we performed a population coverage analysis of the associated MHC alleles and proposed a set of epitopes that is estimated to provide broad coverage globally, as well as in China. Our findings provide a screened set of epitopes that can help guide experimental efforts towards the development of vaccines against SARS-CoV-2.
Author Ahmed, Syed Faraz
Quadeer, Ahmed A.
McKay, Matthew R.
AuthorAffiliation 1 Department of Electronic and Computer Engineering, The Hong Kong University of Science and Technology, Hong Kong, China; sfahmed@connect.ust.hk
2 Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Hong Kong, China
AuthorAffiliation_xml – name: 2 Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Hong Kong, China
– name: 1 Department of Electronic and Computer Engineering, The Hong Kong University of Science and Technology, Hong Kong, China; sfahmed@connect.ust.hk
Author_xml – sequence: 1
  givenname: Syed Faraz
  orcidid: 0000-0002-6086-0307
  surname: Ahmed
  fullname: Ahmed, Syed Faraz
– sequence: 2
  givenname: Ahmed A.
  orcidid: 0000-0002-5295-9067
  surname: Quadeer
  fullname: Quadeer, Ahmed A.
– sequence: 3
  givenname: Matthew R.
  surname: McKay
  fullname: McKay, Matthew R.
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32106567$$D View this record in MEDLINE/PubMed
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Issue 3
Keywords B cell epitopes
COVID-19
SARS-CoV-2
vaccine
Coronavirus
T cell epitopes
2019 novel coronavirus
SARS-CoV
MERS-CoV
2019-nCoV
Language English
License https://creativecommons.org/licenses/by/4.0
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These authors contributed equally to this work.
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SubjectTerms 2019 novel coronavirus
2019-ncov
b cell epitopes
Betacoronavirus - genetics
Betacoronavirus - immunology
coronavirus
Coronavirus Infections - prevention & control
Coronavirus Nucleocapsid Proteins
COVID-19
COVID-19 Vaccines
Epitope Mapping
Epitopes, B-Lymphocyte - genetics
Epitopes, B-Lymphocyte - immunology
Epitopes, T-Lymphocyte - genetics
Epitopes, T-Lymphocyte - immunology
Genome, Viral
Humans
mers-cov
Nucleocapsid Proteins - genetics
Nucleocapsid Proteins - immunology
Phosphoproteins
Phylogeny
Pneumonia, Viral - prevention & control
Protein Structure, Tertiary
sars-cov
SARS-CoV-2
Severe acute respiratory syndrome-related coronavirus - genetics
Severe acute respiratory syndrome-related coronavirus - immunology
Spike Glycoprotein, Coronavirus - genetics
Spike Glycoprotein, Coronavirus - immunology
t cell epitopes
vaccine
Viral Vaccines - immunology
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Title Preliminary Identification of Potential Vaccine Targets for the COVID-19 Coronavirus (SARS-CoV-2) Based on SARS-CoV Immunological Studies
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