Serveur d'exploration SRAS

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

Identifieur interne : 002430 ( Ncbi/Merge ); précédent : 002429; suivant : 002431

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

Descripteurs français

English descriptors

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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Links to Exploration step

PMC:3237677

Le document en format XML

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<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>
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<title level="j">Current Opinion in Virology</title>
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<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>
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<term>Disease Outbreaks</term>
<term>Disease Reservoirs (virology)</term>
<term>Humans</term>
<term>Membrane Glycoproteins (genetics)</term>
<term>Molecular Sequence Data</term>
<term>Phylogeny</term>
<term>Public Health</term>
<term>SARS Virus (genetics)</term>
<term>SARS Virus (growth & development)</term>
<term>Severe Acute Respiratory Syndrome (epidemiology)</term>
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<term>Spike Glycoprotein, Coronavirus</term>
<term>Viral Envelope Proteins (genetics)</term>
<term>Zoonoses (epidemiology)</term>
<term>Zoonoses (transmission)</term>
<term>Zoonoses (virology)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Animaux</term>
<term>Chiroptera (virologie)</term>
<term>Données de séquences moléculaires</term>
<term>Flambées de maladies</term>
<term>Glycoprotéine de spicule des coronavirus</term>
<term>Glycoprotéines membranaires (génétique)</term>
<term>Humains</term>
<term>Phylogénie</term>
<term>Protéines de l'enveloppe virale (génétique)</term>
<term>Réservoirs d'agents pathogènes (virologie)</term>
<term>Santé publique</term>
<term>Syndrome respiratoire aigu sévère (transmission)</term>
<term>Syndrome respiratoire aigu sévère (virologie)</term>
<term>Syndrome respiratoire aigu sévère (épidémiologie)</term>
<term>Séquence nucléotidique</term>
<term>Virus du SRAS (croissance et développement)</term>
<term>Virus du SRAS (génétique)</term>
<term>Zoonoses (transmission)</term>
<term>Zoonoses (virologie)</term>
<term>Zoonoses (épidémiologie)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>Membrane Glycoproteins</term>
<term>Viral Envelope Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="croissance et développement" xml:lang="fr">
<term>Virus du SRAS</term>
</keywords>
<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en">
<term>Severe Acute Respiratory Syndrome</term>
<term>Zoonoses</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>SARS Virus</term>
</keywords>
<keywords scheme="MESH" qualifier="growth & development" xml:lang="en">
<term>SARS Virus</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Glycoprotéines membranaires</term>
<term>Protéines de l'enveloppe virale</term>
<term>Virus du SRAS</term>
</keywords>
<keywords scheme="MESH" qualifier="transmission" xml:lang="en">
<term>Severe Acute Respiratory Syndrome</term>
<term>Zoonoses</term>
</keywords>
<keywords scheme="MESH" qualifier="virologie" xml:lang="fr">
<term>Chiroptera</term>
<term>Réservoirs d'agents pathogènes</term>
<term>Syndrome respiratoire aigu sévère</term>
<term>Zoonoses</term>
</keywords>
<keywords scheme="MESH" qualifier="virology" xml:lang="en">
<term>Chiroptera</term>
<term>Disease Reservoirs</term>
<term>Severe Acute Respiratory Syndrome</term>
<term>Zoonoses</term>
</keywords>
<keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr">
<term>Syndrome respiratoire aigu sévère</term>
<term>Zoonoses</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Base Sequence</term>
<term>Disease Outbreaks</term>
<term>Humans</term>
<term>Molecular Sequence Data</term>
<term>Phylogeny</term>
<term>Public Health</term>
<term>Spike Glycoprotein, Coronavirus</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Animaux</term>
<term>Données de séquences moléculaires</term>
<term>Flambées de maladies</term>
<term>Glycoprotéine de spicule des coronavirus</term>
<term>Humains</term>
<term>Phylogénie</term>
<term>Santé publique</term>
<term>Séquence nucléotidique</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">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.</div>
</front>
</TEI>
</pubmed>
</double>
</record>

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