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Detection of a novel human coronavirus by real-time reverse-transcription polymerase chain reaction.

Identifieur interne : 001D37 ( Main/Exploration ); précédent : 001D36; suivant : 001D38

Detection of a novel human coronavirus by real-time reverse-transcription polymerase chain reaction.

Auteurs : V M Corman [Allemagne] ; I. Eckerle ; T. Bleicker ; A. Zaki ; O. Landt ; M. Eschbach-Bludau ; S. Van Boheemen ; R. Gopal ; M. Ballhause ; T M Bestebroer ; D. Muth ; M A Müller ; J F Drexler ; M. Zambon ; A D Osterhaus ; R M Fouchier ; C. Drosten

Source :

RBID : pubmed:23041020

Descripteurs français

English descriptors

Abstract

We present two real-time reverse-transcription polymerase chain reaction assays for a novel human coronavirus (CoV), targeting regions upstream of the E gene (upE) or within open reading frame (ORF)1b, respectively. Sensitivity for upE is 3.4 copies per reaction (95% confidence interval (CI): 2.5–6.9 copies) or 291 copies/mL of sample. No cross-reactivity was observed with coronaviruses OC43, NL63, 229E, SARS-CoV, nor with 92 clinical specimens containing common human respiratory viruses. We recommend using upE for screening and ORF1b for confirmation.

DOI: 10.2807/ese.17.39.20285-en
PubMed: 23041020


Affiliations:


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<term>Arabie saoudite</term>
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<div type="abstract" xml:lang="en">We present two real-time reverse-transcription polymerase chain reaction assays for a novel human coronavirus (CoV), targeting regions upstream of the E gene (upE) or within open reading frame (ORF)1b, respectively. Sensitivity for upE is 3.4 copies per reaction (95% confidence interval (CI): 2.5–6.9 copies) or 291 copies/mL of sample. No cross-reactivity was observed with coronaviruses OC43, NL63, 229E, SARS-CoV, nor with 92 clinical specimens containing common human respiratory viruses. We recommend using upE for screening and ORF1b for confirmation.</div>
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