Coronavirus Spike Protein and Tropism Changes
Identifieur interne : 001060 ( Main/Exploration ); précédent : 001059; suivant : 001061Coronavirus Spike Protein and Tropism Changes
Auteurs : R. J. G. Hulswit ; C. A. M. De Haan ; B.-J. BoschSource :
- Advances in Virus Research [ 0065-3527 ] ; 2016.
Descripteurs français
- KwdFr :
- Animaux, Conformation des protéines, Coronavirus du syndrome respiratoire du Moyen-Orient (génétique), Coronavirus du syndrome respiratoire du Moyen-Orient (métabolisme), Coronavirus du syndrome respiratoire du Moyen-Orient (ultrastructure), Domaines protéiques, Expression des gènes, Glycoprotéine de spicule des coronavirus (), Glycoprotéine de spicule des coronavirus (génétique), Glycoprotéine de spicule des coronavirus (ultrastructure), Humains, Modèles moléculaires, Protéolyse, Pénétration virale, Récepteurs viraux (), Récepteurs viraux (génétique), Récepteurs viraux (ultrastructure), Sous-unités de protéines (), Sous-unités de protéines (génétique), Tropisme viral, Variation génétique, Virion (génétique), Virion (métabolisme), Virion (ultrastructure), Virus du SRAS (génétique), Virus du SRAS (métabolisme), Virus du SRAS (ultrastructure).
- MESH :
- génétique : Coronavirus du syndrome respiratoire du Moyen-Orient, Glycoprotéine de spicule des coronavirus, Récepteurs viraux, Sous-unités de protéines, Virion, Virus du SRAS.
- métabolisme : Coronavirus du syndrome respiratoire du Moyen-Orient, Virion, Virus du SRAS.
- Animaux, Conformation des protéines, Coronavirus du syndrome respiratoire du Moyen-Orient, Domaines protéiques, Expression des gènes, Glycoprotéine de spicule des coronavirus, Humains, Modèles moléculaires, Protéolyse, Pénétration virale, Récepteurs viraux, Sous-unités de protéines, Tropisme viral, Variation génétique, Virion, Virus du SRAS.
English descriptors
- KwdEn :
- Animals, Gene Expression, Genetic Variation, Humans, Middle East Respiratory Syndrome Coronavirus (genetics), Middle East Respiratory Syndrome Coronavirus (metabolism), Middle East Respiratory Syndrome Coronavirus (ultrastructure), Models, Molecular, Protein Conformation, Protein Domains, Protein Subunits (chemistry), Protein Subunits (genetics), Proteolysis, Receptors, Virus (chemistry), Receptors, Virus (genetics), Receptors, Virus (ultrastructure), SARS Virus (genetics), SARS Virus (metabolism), SARS Virus (ultrastructure), Spike Glycoprotein, Coronavirus (chemistry), Spike Glycoprotein, Coronavirus (genetics), Spike Glycoprotein, Coronavirus (ultrastructure), Viral Tropism, Virion (genetics), Virion (metabolism), Virion (ultrastructure), Virus Internalization.
- MESH :
- chemical , chemistry : Protein Subunits, Receptors, Virus, Spike Glycoprotein, Coronavirus.
- genetics : Middle East Respiratory Syndrome Coronavirus, Protein Subunits, Receptors, Virus, SARS Virus, Spike Glycoprotein, Coronavirus, Virion.
- metabolism : Middle East Respiratory Syndrome Coronavirus, SARS Virus, Virion.
- ultrastructure : Middle East Respiratory Syndrome Coronavirus, Receptors, Virus, SARS Virus, Spike Glycoprotein, Coronavirus, Virion.
- Animals, Gene Expression, Genetic Variation, Humans, Models, Molecular, Protein Conformation, Protein Domains, Proteolysis, Viral Tropism, Virus Internalization.
Abstract
Coronaviruses (CoVs) have a remarkable potential to change tropism. This is particularly illustrated over the last 15 years by the emergence of two zoonotic CoVs, the severe acute respiratory syndrome (SARS)- and Middle East respiratory syndrome (MERS)-CoV. Due to their inherent genetic variability, it is inevitable that new cross-species transmission events of these enveloped, positive-stranded RNA viruses will occur. Research into these medical and veterinary important pathogens—sparked by the SARS and MERS outbreaks—revealed important principles of inter- and intraspecies tropism changes. The primary determinant of CoV tropism is the viral spike (S) entry protein. Trimers of the S glycoproteins on the virion surface accommodate binding to a cell surface receptor and fusion of the viral and cellular membrane. Recently, high-resolution structures of two CoV S proteins have been elucidated by single-particle cryo-electron microscopy. Using this new structural insight, we review the changes in the S protein that relate to changes in virus tropism. Different concepts underlie these tropism changes at the cellular, tissue, and host species level, including the promiscuity or adaptability of S proteins to orthologous receptors, alterations in the proteolytic cleavage activation as well as changes in the S protein metastability. A thorough understanding of the key role of the S protein in CoV entry is critical to further our understanding of virus cross-species transmission and pathogenesis and for development of intervention strategies.
Url:
DOI: 10.1016/bs.aivir.2016.08.004
PubMed: 27712627
PubMed Central: 7112277
Affiliations:
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Le document en format XML
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<term>Middle East Respiratory Syndrome Coronavirus (metabolism)</term>
<term>Middle East Respiratory Syndrome Coronavirus (ultrastructure)</term>
<term>Models, Molecular</term>
<term>Protein Conformation</term>
<term>Protein Domains</term>
<term>Protein Subunits (chemistry)</term>
<term>Protein Subunits (genetics)</term>
<term>Proteolysis</term>
<term>Receptors, Virus (chemistry)</term>
<term>Receptors, Virus (genetics)</term>
<term>Receptors, Virus (ultrastructure)</term>
<term>SARS Virus (genetics)</term>
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<term>Spike Glycoprotein, Coronavirus (genetics)</term>
<term>Spike Glycoprotein, Coronavirus (ultrastructure)</term>
<term>Viral Tropism</term>
<term>Virion (genetics)</term>
<term>Virion (metabolism)</term>
<term>Virion (ultrastructure)</term>
<term>Virus Internalization</term>
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<term>Coronavirus du syndrome respiratoire du Moyen-Orient (métabolisme)</term>
<term>Coronavirus du syndrome respiratoire du Moyen-Orient (ultrastructure)</term>
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<term>Expression des gènes</term>
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<term>Glycoprotéine de spicule des coronavirus (génétique)</term>
<term>Glycoprotéine de spicule des coronavirus (ultrastructure)</term>
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<front><div type="abstract" xml:lang="en"><p>Coronaviruses (CoVs) have a remarkable potential to change tropism. This is particularly illustrated over the last 15 years by the emergence of two zoonotic CoVs, the severe acute respiratory syndrome (SARS)- and Middle East respiratory syndrome (MERS)-CoV. Due to their inherent genetic variability, it is inevitable that new cross-species transmission events of these enveloped, positive-stranded RNA viruses will occur. Research into these medical and veterinary important pathogens—sparked by the SARS and MERS outbreaks—revealed important principles of inter- and intraspecies tropism changes. The primary determinant of CoV tropism is the viral spike (S) entry protein. Trimers of the S glycoproteins on the virion surface accommodate binding to a cell surface receptor and fusion of the viral and cellular membrane. Recently, high-resolution structures of two CoV S proteins have been elucidated by single-particle cryo-electron microscopy. Using this new structural insight, we review the changes in the S protein that relate to changes in virus tropism. Different concepts underlie these tropism changes at the cellular, tissue, and host species level, including the promiscuity or adaptability of S proteins to orthologous receptors, alterations in the proteolytic cleavage activation as well as changes in the S protein metastability. A thorough understanding of the key role of the S protein in CoV entry is critical to further our understanding of virus cross-species transmission and pathogenesis and for development of intervention strategies.</p>
</div>
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