Detection of equine arteritis virus by real-time TaqMan® reverse transcription-PCR assay

Udeni B R Balasuriya, Christian M. Leutenegger, J. B. Topol, William H. McCollum, Peter J. Timoney, Nigel J Maclachlan

Research output: Contribution to journalArticle

59 Scopus citations

Abstract

A one-tube real-time TaqMan® reverse transcription-polymerase chain reaction (RT-PCR) assay was developed for the detection of equine arteritis virus (EAV). The test was validated using the seminal plasma and nasal secretions of infected horses that were proven to contain EAV by traditional virus isolation in rabbit kidney thirteen (RK-13) cells, as well as a variety of cell culture-propagated European and North American strains of EAV. The primers and a fluorogenic TaqMan® probe were designed to amplify and detect a highly conserved region of open reading frame 7 (ORF7) of EAV. The real-time TaqMan® PCR assay detected EAV RNA in all samples that were confirmed to contain infectious EAV by virus isolation. The assay had an analytical sensitivity of 10 molecules of EAV RNA allowing the detection of EAV in clinical samples or tissue culture fluid (TCF) containing at least 200 viral RNA copies per ml. Thus, the one-tube real-time TaqMan® RT-PCR assay provides a rapid, accurate, quantitative, convenient and high sample throughput system for diagnosis of EAV infection, in a closed-tube format that minimizes the risk of cross-contamination.

Original languageEnglish (US)
Pages (from-to)21-28
Number of pages8
JournalJournal of Virological Methods
Volume101
Issue number1-2
DOIs
StatePublished - 2002

Keywords

  • Equine arteritis virus (EAV)
  • Real-time TaqMan® reverse transcription-PCR

ASJC Scopus subject areas

  • Virology

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