Serveur d'exploration SRAS

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Characterizing 56 complete SARS-CoV S-gene sequences from Hong Kong.

Identifieur interne : 001F82 ( PubMed/Curation ); précédent : 001F81; suivant : 001F83

Characterizing 56 complete SARS-CoV S-gene sequences from Hong Kong.

Auteurs : Julian W. Tang [République populaire de Chine] ; Jo L K. Cheung ; Ida M T. Chu ; Margaret Ip ; Mamie Hui ; Malik Peiris ; Paul K S. Chan

Source :

RBID : pubmed:17112780

Descripteurs français

English descriptors

Abstract

The spike glycoprotein (S) gene of the severe acute respiratory syndrome-associated coronavirus (SARS-CoV) has been useful in analyzing the molecular epidemiology of the 2003 SARS outbreaks.

DOI: 10.1016/j.jcv.2006.10.001
PubMed: 17112780

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pubmed:17112780

Le document en format XML

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<term>Hong Kong (epidemiology)</term>
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<term>Femelle</term>
<term>Flambées de maladies</term>
<term>Glycoprotéine de spicule des coronavirus</term>
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<div type="abstract" xml:lang="en">The spike glycoprotein (S) gene of the severe acute respiratory syndrome-associated coronavirus (SARS-CoV) has been useful in analyzing the molecular epidemiology of the 2003 SARS outbreaks.</div>
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<Month>03</Month>
<Day>01</Day>
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<DateRevised>
<Year>2020</Year>
<Month>04</Month>
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<Title>Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology</Title>
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<ArticleTitle>Characterizing 56 complete SARS-CoV S-gene sequences from Hong Kong.</ArticleTitle>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">The spike glycoprotein (S) gene of the severe acute respiratory syndrome-associated coronavirus (SARS-CoV) has been useful in analyzing the molecular epidemiology of the 2003 SARS outbreaks.</AbstractText>
<AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">To characterize complete SARS-CoV S-gene sequences from Hong Kong.</AbstractText>
<AbstractText Label="STUDY DESIGN" NlmCategory="METHODS">Fifty-six SARS-CoV S-gene sequences, obtained from patients who presented with SARS to the Prince of Wales Hospital during March-May 2003, were analysed using a maximum likelihood (ML) approach, together with 138 other (both human and animal) S-gene sequences downloaded from GenBank.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The maximum-likelihood (ML) trees showed little evolution occurring within these 56 sequences. Analysis with the other sequences, showed three distinct SARS clusters, closely correlated to previously defined early, middle and late phases of the 2003 international SARS outbreaks. In addition, two new single nucleotide variations (SNVs), T21615A and T21901A, were discovered, not previously reported elsewhere.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">The ML approach to the reconstruction of tree phylogenies is known to be superior to the more popular, less computationally and time-demanding neighbour-joining (NJ) approach. The ML analysis in this study confirms the previously reported SARS epidemiology analysed mostly using the NJ approach. The two new SNVs reported here are most likely due to the tissue-culture passaging of the clinical samples.</AbstractText>
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