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SARS-CoV and emergent coronaviruses: viral determinants of interspecies transmission

Identifieur interne : 001729 ( Pmc/Curation ); précédent : 001728; suivant : 001730

SARS-CoV and emergent coronaviruses: viral determinants of interspecies transmission

Auteurs : Meagan Bolles [États-Unis] ; Eric Donaldson [États-Unis] ; Ralph Baric [États-Unis]

Source :

RBID : PMC:3237677

Abstract

Highlights

► Coronaviruses maintain a diverse phylogeny by distinct molecular mechanisms. ► BatCoV phylogenetics and receptor use may suggest a direct emergence of SARS-CoV. ► SARS Spike–receptor binding is the minimum determinant of cross-species transmission. ► Mutation and recombination-driven changes to Spike drive CoV host range expansion. ► Novel structural modeling tools allow assessment of receptor-binding determinants.


Url:
DOI: 10.1016/j.coviro.2011.10.012
PubMed: 22180768
PubMed Central: 3237677

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PMC:3237677

Le document en format XML

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</TEI>
<pmc article-type="review-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Curr Opin Virol</journal-id>
<journal-id journal-id-type="iso-abbrev">Curr Opin Virol</journal-id>
<journal-title-group>
<journal-title>Current Opinion in Virology</journal-title>
</journal-title-group>
<issn pub-type="ppub">1879-6257</issn>
<issn pub-type="epub">1879-6265</issn>
<publisher>
<publisher-name>Elsevier B.V.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">22180768</article-id>
<article-id pub-id-type="pmc">3237677</article-id>
<article-id pub-id-type="publisher-id">S1879-6257(11)00131-3</article-id>
<article-id pub-id-type="doi">10.1016/j.coviro.2011.10.012</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Article</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>SARS-CoV and emergent coronaviruses: viral determinants of interspecies transmission</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Bolles</surname>
<given-names>Meagan</given-names>
</name>
<xref rid="aff0005" ref-type="aff">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Donaldson</surname>
<given-names>Eric</given-names>
</name>
<xref rid="aff0010" ref-type="aff">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Baric</surname>
<given-names>Ralph</given-names>
</name>
<email>rbaric@email.unc.edu</email>
<xref rid="aff0005" ref-type="aff">1</xref>
<xref rid="aff0010" ref-type="aff">2</xref>
</contrib>
</contrib-group>
<aff id="aff0005">
<label>1</label>
Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, United States</aff>
<aff id="aff0010">
<label>2</label>
Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, United States</aff>
<pub-date pub-type="pmc-release">
<day>12</day>
<month>11</month>
<year>2011</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="ppub">
<month>12</month>
<year>2011</year>
</pub-date>
<pub-date pub-type="epub">
<day>12</day>
<month>11</month>
<year>2011</year>
</pub-date>
<volume>1</volume>
<issue>6</issue>
<fpage>624</fpage>
<lpage>634</lpage>
<permissions>
<copyright-statement>Copyright © 2011 Elsevier B.V. All rights reserved.</copyright-statement>
<copyright-year>2011</copyright-year>
<copyright-holder>Elsevier B.V.</copyright-holder>
<license>
<license-p>Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.</license-p>
</license>
</permissions>
<abstract abstract-type="graphical">
<title>Highlights</title>
<p>► Coronaviruses maintain a diverse phylogeny by distinct molecular mechanisms. ► BatCoV phylogenetics and receptor use may suggest a direct emergence of SARS-CoV. ► SARS Spike–receptor binding is the minimum determinant of cross-species transmission. ► Mutation and recombination-driven changes to Spike drive CoV host range expansion. ► Novel structural modeling tools allow assessment of receptor-binding determinants.</p>
</abstract>
<abstract>
<p>Most new emerging viruses are derived from strains circulating in zoonotic reservoirs. Coronaviruses, which had an established potential for cross-species transmission within domesticated animals, suddenly became relevant with the unexpected emergence of the highly pathogenic human SARS-CoV strain from zoonotic reservoirs in 2002. SARS-CoV infected approximately 8000 people worldwide before public health measures halted the epidemic. Supported by robust time-ordered sequence variation, structural biology, well-characterized patient pools, and biological data, the emergence of SARS-CoV represents one of the best-studied natural models of viral disease emergence from zoonotic sources. This review article summarizes previous and more recent advances into the molecular and structural characteristics, with particular emphasis on host–receptor interactions, that drove this remarkable virus disease outbreak in human populations.</p>
</abstract>
</article-meta>
</front>
</pmc>
</record>

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