Receptor recognition and cross-species infections of SARS coronavirus.
Identifieur interne : 001115 ( PubMed/Checkpoint ); précédent : 001114; suivant : 001116Receptor recognition and cross-species infections of SARS coronavirus.
Auteurs : Fang Li [États-Unis]Source :
- Antiviral research [ 1872-9096 ] ; 2013.
Descripteurs français
- KwdFr :
- Animaux, Glycoprotéine de spicule des coronavirus (), Glycoprotéine de spicule des coronavirus (génétique), Glycoprotéine de spicule des coronavirus (métabolisme), Humains, Infection croisée (génétique), Infection croisée (métabolisme), Infection croisée (virologie), Peptidyl-Dipeptidase A (génétique), Peptidyl-Dipeptidase A (métabolisme), Récepteurs viraux (génétique), Récepteurs viraux (métabolisme), Spécificité d'espèce, Syndrome respiratoire aigu sévère (métabolisme), Syndrome respiratoire aigu sévère (virologie), Virus du SRAS (), Virus du SRAS (génétique), Virus du SRAS (métabolisme).
- MESH :
- génétique : Glycoprotéine de spicule des coronavirus, Infection croisée, Peptidyl-Dipeptidase A, Récepteurs viraux, Virus du SRAS.
- métabolisme : Glycoprotéine de spicule des coronavirus, Infection croisée, Peptidyl-Dipeptidase A, Récepteurs viraux, Syndrome respiratoire aigu sévère, Virus du SRAS.
- virologie : Infection croisée, Syndrome respiratoire aigu sévère.
- Animaux, Glycoprotéine de spicule des coronavirus, Humains, Spécificité d'espèce, Virus du SRAS.
English descriptors
- KwdEn :
- Animals, Cross Infection (genetics), Cross Infection (metabolism), Cross Infection (virology), Humans, Peptidyl-Dipeptidase A (genetics), Peptidyl-Dipeptidase A (metabolism), Receptors, Virus (genetics), Receptors, Virus (metabolism), SARS Virus (chemistry), SARS Virus (classification), SARS Virus (genetics), SARS Virus (metabolism), Severe Acute Respiratory Syndrome (metabolism), Severe Acute Respiratory Syndrome (virology), Species Specificity, Spike Glycoprotein, Coronavirus (chemistry), Spike Glycoprotein, Coronavirus (genetics), Spike Glycoprotein, Coronavirus (metabolism).
- MESH :
- chemical , chemistry : Spike Glycoprotein, Coronavirus.
- chemical , genetics : Peptidyl-Dipeptidase A, Receptors, Virus, Spike Glycoprotein, Coronavirus.
- chemistry : SARS Virus.
- classification : SARS Virus.
- genetics : Cross Infection, SARS Virus.
- metabolism : Cross Infection, Peptidyl-Dipeptidase A, Receptors, Virus, SARS Virus, Severe Acute Respiratory Syndrome, Spike Glycoprotein, Coronavirus.
- virology : Cross Infection, Severe Acute Respiratory Syndrome.
- Animals, Humans, Species Specificity.
Abstract
Receptor recognition is a major determinant of the host range, cross-species infections, and pathogenesis of the severe acute respiratory syndrome coronavirus (SARS-CoV). A defined receptor-binding domain (RBD) in the SARS-CoV spike protein specifically recognizes its host receptor, angiotensin-converting enzyme 2 (ACE2). This article reviews the latest knowledge about how RBDs from different SARS-CoV strains interact with ACE2 from several animal species. Detailed research on these RBD/ACE2 interactions has established important principles on host receptor adaptations, cross-species infections, and future evolution of SARS-CoV. These principles may apply to other emerging animal viruses, including the recently emerged Middle East respiratory syndrome coronavirus (MERS-CoV). This paper forms part of a series of invited articles in Antiviral Research on "From SARS to MERS: 10years of research on highly pathogenic human coronaviruses".
DOI: 10.1016/j.antiviral.2013.08.014
PubMed: 23994189
Affiliations:
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A defined receptor-binding domain (RBD) in the SARS-CoV spike protein specifically recognizes its host receptor, angiotensin-converting enzyme 2 (ACE2). This article reviews the latest knowledge about how RBDs from different SARS-CoV strains interact with ACE2 from several animal species. Detailed research on these RBD/ACE2 interactions has established important principles on host receptor adaptations, cross-species infections, and future evolution of SARS-CoV. These principles may apply to other emerging animal viruses, including the recently emerged Middle East respiratory syndrome coronavirus (MERS-CoV). This paper forms part of a series of invited articles in Antiviral Research on "From SARS to MERS: 10years of research on highly pathogenic human coronaviruses". </div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">23994189</PMID><DateCompleted><Year>2014</Year><Month>07</Month><Day>02</Day></DateCompleted><DateRevised><Year>2020</Year><Month>04</Month><Day>07</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1872-9096</ISSN><JournalIssue CitedMedium="Internet"><Volume>100</Volume><Issue>1</Issue><PubDate><Year>2013</Year><Month>Oct</Month></PubDate></JournalIssue><Title>Antiviral research</Title><ISOAbbreviation>Antiviral Res.</ISOAbbreviation></Journal><ArticleTitle>Receptor recognition and cross-species infections of SARS coronavirus.</ArticleTitle><Pagination><MedlinePgn>246-54</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1016/j.antiviral.2013.08.014</ELocationID><ELocationID EIdType="pii" ValidYN="Y">S0166-3542(13)00222-2</ELocationID><Abstract><AbstractText>Receptor recognition is a major determinant of the host range, cross-species infections, and pathogenesis of the severe acute respiratory syndrome coronavirus (SARS-CoV). A defined receptor-binding domain (RBD) in the SARS-CoV spike protein specifically recognizes its host receptor, angiotensin-converting enzyme 2 (ACE2). This article reviews the latest knowledge about how RBDs from different SARS-CoV strains interact with ACE2 from several animal species. Detailed research on these RBD/ACE2 interactions has established important principles on host receptor adaptations, cross-species infections, and future evolution of SARS-CoV. These principles may apply to other emerging animal viruses, including the recently emerged Middle East respiratory syndrome coronavirus (MERS-CoV). This paper forms part of a series of invited articles in Antiviral Research on "From SARS to MERS: 10years of research on highly pathogenic human coronaviruses". </AbstractText><CopyrightInformation>Copyright © 2013 Elsevier B.V. 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