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Identification of immunogenic determinants of the spike protein of SARS-like coronavirus

Bat SARS-like coronavirus (SL-CoV) has a genome organization almost identical to that of SARS-CoV, but the N-terminus of the Spike (S) proteins, which interacts with host receptor and is a major target of neutralizing antibodies against CoVs, of the two viruses has only 63–64% sequence identity. Alt...

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Detalles Bibliográficos
Autores principales: Zhou, Peng, Han, Zhenggang, Wang, Lin-Fa, Shi, Zhengli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SP Wuhan Institute of Virology, CAS 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090416/
https://www.ncbi.nlm.nih.gov/pubmed/23575730
http://dx.doi.org/10.1007/s12250-013-3292-y
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author Zhou, Peng
Han, Zhenggang
Wang, Lin-Fa
Shi, Zhengli
author_facet Zhou, Peng
Han, Zhenggang
Wang, Lin-Fa
Shi, Zhengli
author_sort Zhou, Peng
collection PubMed
description Bat SARS-like coronavirus (SL-CoV) has a genome organization almost identical to that of SARS-CoV, but the N-terminus of the Spike (S) proteins, which interacts with host receptor and is a major target of neutralizing antibodies against CoVs, of the two viruses has only 63–64% sequence identity. Although there have been reports studying the overall immunogenicity of S(SL), knowledge on the precise location of immunodominant determinants for S(SL) is still lacking. In this study, using a series of truncated expressed S(SL) fragments and S(SL) specific mouse sera, we identified two immunogenic determinants for S(SL). Importantly, one of the two regions seems to be located in a region not shared by known immunogenic determinants of the S(SARS). This finding will be of potential use in future monitoring of SL-CoV infection in bats and spillover animals and in development of more effective vaccine to cover broad protection against this new group of coronaviruses.
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spelling pubmed-70904162020-03-24 Identification of immunogenic determinants of the spike protein of SARS-like coronavirus Zhou, Peng Han, Zhenggang Wang, Lin-Fa Shi, Zhengli Virol Sin Research Article Bat SARS-like coronavirus (SL-CoV) has a genome organization almost identical to that of SARS-CoV, but the N-terminus of the Spike (S) proteins, which interacts with host receptor and is a major target of neutralizing antibodies against CoVs, of the two viruses has only 63–64% sequence identity. Although there have been reports studying the overall immunogenicity of S(SL), knowledge on the precise location of immunodominant determinants for S(SL) is still lacking. In this study, using a series of truncated expressed S(SL) fragments and S(SL) specific mouse sera, we identified two immunogenic determinants for S(SL). Importantly, one of the two regions seems to be located in a region not shared by known immunogenic determinants of the S(SARS). This finding will be of potential use in future monitoring of SL-CoV infection in bats and spillover animals and in development of more effective vaccine to cover broad protection against this new group of coronaviruses. SP Wuhan Institute of Virology, CAS 2013-04-11 /pmc/articles/PMC7090416/ /pubmed/23575730 http://dx.doi.org/10.1007/s12250-013-3292-y Text en © Wuhan Institute of Virology, CAS and Springer-Verlag Berlin Heidelberg 2013
spellingShingle Research Article
Zhou, Peng
Han, Zhenggang
Wang, Lin-Fa
Shi, Zhengli
Identification of immunogenic determinants of the spike protein of SARS-like coronavirus
title Identification of immunogenic determinants of the spike protein of SARS-like coronavirus
title_full Identification of immunogenic determinants of the spike protein of SARS-like coronavirus
title_fullStr Identification of immunogenic determinants of the spike protein of SARS-like coronavirus
title_full_unstemmed Identification of immunogenic determinants of the spike protein of SARS-like coronavirus
title_short Identification of immunogenic determinants of the spike protein of SARS-like coronavirus
title_sort identification of immunogenic determinants of the spike protein of sars-like coronavirus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090416/
https://www.ncbi.nlm.nih.gov/pubmed/23575730
http://dx.doi.org/10.1007/s12250-013-3292-y
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