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- Publisher Website: 10.1128/JVI.02389-06
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- PMID: 17314167
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Article: Natural mutations in the receptor binding domain of spike glycoprotein determine the reactivity of cross-neutralization between palm civet coronavirus and severe acute respiratory syndrome coronavirus
Title | Natural mutations in the receptor binding domain of spike glycoprotein determine the reactivity of cross-neutralization between palm civet coronavirus and severe acute respiratory syndrome coronavirus |
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Authors | |
Issue Date | 2007 |
Publisher | American Society for Microbiology. The Journal's web site is located at http://jvi.asm.org/ |
Citation | Journal Of Virology, 2007, v. 81 n. 9, p. 4694-4700 How to Cite? |
Abstract | The severe acute respiratory syndrome (SARS) outbreak of 2002 and 2003 occurred as a result of zoonotic transmission. Coronavirus (CoV) found in naturally infected palm civet (civet-CoV) represents the closest genetic relative to SARS-CoV, but the degree and the determinants of cross-neutralization among these viruses remain to be investigated. Studies indicate that the receptor binding domain (RBD) of the SARS-CoV spike (S) glycoprotein contains major determinants for viral entry and neutralization. We aim to characterize the impact of natural mutations within the RBDs of civet-CoVs on viral entry and cross-neutralization. In this study, the S glycoprotein genes were recovered from naturally infected civets in central China (Hubei province), extending the geographic distribution of civet-CoV beyond the southeastern province of Guangdong. Moreover, pseudoviruses generated in our laboratory with four civet S genes, each with a distinct RBD, infected cells expressing human receptor angiotensin-converting enzyme 2, but with 90 to 95% less efficiency compared to that of SARS-CoV. These four civet S genes were also constructed as DNA vaccines to immunize mice. Immunized sera elicited against most civet S glycoproteins displayed potent neutralizing activities against autologous viruses but were much less efficient (50% inhibitory concentration, 20- to 40-fold) at neutralizing SARS-CoV and vice versa. Convalescence-phase sera from humans were similarly ineffective against the dominant civet pseudovirus. Our findings suggest that the design of SARS vaccine should consider not only preventing the reemergence of SARS-CoV but also providing cross-protection, thus interrupting zoonotic transmission of a group of genetically divergent civet CoVs of broad geographic origin. Copyright © 2007, American Society for Microbiology. All Rights Reserved. |
Persistent Identifier | http://hdl.handle.net/10722/157479 |
ISSN | 2023 Impact Factor: 4.0 2023 SCImago Journal Rankings: 1.378 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Liu, L | en_US |
dc.contributor.author | Fang, Q | en_US |
dc.contributor.author | Deng, F | en_US |
dc.contributor.author | Wang, H | en_US |
dc.contributor.author | Yi, CE | en_US |
dc.contributor.author | Ba, L | en_US |
dc.contributor.author | Yu, W | en_US |
dc.contributor.author | Lin, RD | en_US |
dc.contributor.author | Li, T | en_US |
dc.contributor.author | Hu, Z | en_US |
dc.contributor.author | Ho, DD | en_US |
dc.contributor.author | Zhang, L | en_US |
dc.contributor.author | Chen, Z | en_US |
dc.date.accessioned | 2012-08-08T08:50:22Z | - |
dc.date.available | 2012-08-08T08:50:22Z | - |
dc.date.issued | 2007 | en_US |
dc.identifier.citation | Journal Of Virology, 2007, v. 81 n. 9, p. 4694-4700 | en_US |
dc.identifier.issn | 0022-538X | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/157479 | - |
dc.description.abstract | The severe acute respiratory syndrome (SARS) outbreak of 2002 and 2003 occurred as a result of zoonotic transmission. Coronavirus (CoV) found in naturally infected palm civet (civet-CoV) represents the closest genetic relative to SARS-CoV, but the degree and the determinants of cross-neutralization among these viruses remain to be investigated. Studies indicate that the receptor binding domain (RBD) of the SARS-CoV spike (S) glycoprotein contains major determinants for viral entry and neutralization. We aim to characterize the impact of natural mutations within the RBDs of civet-CoVs on viral entry and cross-neutralization. In this study, the S glycoprotein genes were recovered from naturally infected civets in central China (Hubei province), extending the geographic distribution of civet-CoV beyond the southeastern province of Guangdong. Moreover, pseudoviruses generated in our laboratory with four civet S genes, each with a distinct RBD, infected cells expressing human receptor angiotensin-converting enzyme 2, but with 90 to 95% less efficiency compared to that of SARS-CoV. These four civet S genes were also constructed as DNA vaccines to immunize mice. Immunized sera elicited against most civet S glycoproteins displayed potent neutralizing activities against autologous viruses but were much less efficient (50% inhibitory concentration, 20- to 40-fold) at neutralizing SARS-CoV and vice versa. Convalescence-phase sera from humans were similarly ineffective against the dominant civet pseudovirus. Our findings suggest that the design of SARS vaccine should consider not only preventing the reemergence of SARS-CoV but also providing cross-protection, thus interrupting zoonotic transmission of a group of genetically divergent civet CoVs of broad geographic origin. Copyright © 2007, American Society for Microbiology. All Rights Reserved. | en_US |
dc.language | eng | en_US |
dc.publisher | American Society for Microbiology. The Journal's web site is located at http://jvi.asm.org/ | en_US |
dc.relation.ispartof | Journal of Virology | en_US |
dc.subject.mesh | Base Sequence | en_US |
dc.subject.mesh | China | en_US |
dc.subject.mesh | Cluster Analysis | en_US |
dc.subject.mesh | Cross Reactions - Genetics - Immunology | en_US |
dc.subject.mesh | Membrane Glycoproteins - Genetics - Metabolism | en_US |
dc.subject.mesh | Molecular Sequence Data | en_US |
dc.subject.mesh | Mutation - Genetics | en_US |
dc.subject.mesh | Neutralization Tests | en_US |
dc.subject.mesh | Phylogeny | en_US |
dc.subject.mesh | Protein Structure, Tertiary | en_US |
dc.subject.mesh | Reverse Transcriptase Polymerase Chain Reaction | en_US |
dc.subject.mesh | Sars Virus - Genetics | en_US |
dc.subject.mesh | Sequence Analysis, Dna | en_US |
dc.subject.mesh | Viral Envelope Proteins - Genetics - Metabolism | en_US |
dc.title | Natural mutations in the receptor binding domain of spike glycoprotein determine the reactivity of cross-neutralization between palm civet coronavirus and severe acute respiratory syndrome coronavirus | en_US |
dc.type | Article | en_US |
dc.identifier.email | Chen, Z:zchenai@hkucc.hku.hk | en_US |
dc.identifier.authority | Chen, Z=rp00243 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1128/JVI.02389-06 | en_US |
dc.identifier.pmid | 17314167 | - |
dc.identifier.scopus | eid_2-s2.0-34247647376 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-34247647376&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 81 | en_US |
dc.identifier.issue | 9 | en_US |
dc.identifier.spage | 4694 | en_US |
dc.identifier.epage | 4700 | en_US |
dc.identifier.eissn | 1098-5514 | - |
dc.identifier.isi | WOS:000246501900032 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Liu, L=36068379000 | en_US |
dc.identifier.scopusauthorid | Fang, Q=55248545600 | en_US |
dc.identifier.scopusauthorid | Deng, F=35847541100 | en_US |
dc.identifier.scopusauthorid | Wang, H=22942629300 | en_US |
dc.identifier.scopusauthorid | Yi, CE=8557032800 | en_US |
dc.identifier.scopusauthorid | Ba, L=8557032300 | en_US |
dc.identifier.scopusauthorid | Yu, W=7403914045 | en_US |
dc.identifier.scopusauthorid | Lin, RD=35074462700 | en_US |
dc.identifier.scopusauthorid | Li, T=8876653800 | en_US |
dc.identifier.scopusauthorid | Hu, Z=7404210963 | en_US |
dc.identifier.scopusauthorid | Ho, DD=7402971998 | en_US |
dc.identifier.scopusauthorid | Zhang, L=8783285300 | en_US |
dc.identifier.scopusauthorid | Chen, Z=35271180800 | en_US |
dc.identifier.issnl | 0022-538X | - |