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Comparative Study
. 2007 Jan;152(1):41-58.
doi: 10.1007/s00705-006-0840-x. Epub 2006 Aug 28.

SYBR Green real-time reverse transcription-polymerase chain reaction assay for the generic detection of coronaviruses

Affiliations
Comparative Study

SYBR Green real-time reverse transcription-polymerase chain reaction assay for the generic detection of coronaviruses

S Escutenaire et al. Arch Virol. 2007 Jan.

Abstract

Coronaviruses are etiologic agents of respiratory and enteric diseases in humans and in animals. In this study, a one-step real-time reverse transcription-polymerase chain reaction (RT-PCR) assay based on SYBR Green chemistry and degenerate primers was developed for the generic detection of coronaviruses. The primers, designed in the open reading frame 1b, enabled the detection of 32 animal coronaviruses including strains of canine coronavirus, feline coronavirus, transmissible gastroenteritis virus (TGEV), bovine coronavirus (BCoV), murine hepatitis virus (MHV) and infectious bronchitis virus (IBV). A specific amplification was also observed with the human coronaviruses (HCoV) HCoV-NL63, HCoV-OC43, HCoV-229E and severe acute respiratory syndrome coronavirus (SARS-CoV). The real-time RT-PCR detected down to 10 cRNA copies from TGEV, BCoV, SARS-CoV and IBV. In addition, the assay exhibited a high sensitivity and specificity on clinical samples from different animal species. The developed assay represents a potential tool for laboratory diagnostics and for detecting still uncharacterized coronaviruses.

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References

    1. Brian DA, Baric RS. Coronavirus genome structure and replication. Curr Top Microbiol Immunol. 2005;287:1–30. doi: 10.1007/3-540-26765-4_1. - DOI - PMC - PubMed
    1. Callison SA, Hilt DA, Jackwood MW. Rapid differentiation of avian infectious bronchitis virus isolates by sample to residual ratio quantitation using real-time reverse transcriptase-polymerase chain reaction. J Virol Methods. 2005;124:183–190. doi: 10.1016/j.jviromet.2004.11.022. - DOI - PMC - PubMed
    1. Chen R, Huang W, Lin Z, Zhou Z, Yu H, Zhu D. Development of a novel real-time RT-PCR assay with LUX primer for the detection of swine transmissible gastroenteritis virus. J Virol Methods. 2004;122:57–61. doi: 10.1016/j.jviromet.2004.08.003. - DOI - PMC - PubMed
    1. Chui L, Drebot M, Andonov A, Petrich A, Glushek M, Mahony J. Comparison of 9 different PCR primers for the rapid detection of severe acute respiratory syndrome coronavirus using 2 RNA extraction methods. Diagn Microbiol Infect Dis. 2005;53:47–55. doi: 10.1016/j.diagmicrobio.2005.03.007. - DOI - PMC - PubMed
    1. Drosten C, Chiu LL, Panning M, Leong HN, Preiser W, Tam JS, Gunther S, Kramme S, Emmerich P, Ng WL, Schmitz H, Koay ES. Evaluation of advanced reverse transcription-PCR assays and an alternative PCR target region for detection of severe acute respiratory syndrome-associated coronavirus. J Clin Microbiol. 2004;42:2043–2047. doi: 10.1128/JCM.42.5.2043-2047.2004. - DOI - PMC - PubMed

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