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A sensitive quantification of HHV-6B by real-time PCR

Biological Procedures Online volume 4, pages 88–93 (2002)Cite this article

Abstract

Human herpesvirus (HHV)-6B is a pathogen causing latent infection in virtually all humans. Nevertheless, the interaction of HHV-6B with its host cells is poorly understood. Although HHV-6B is approximately 90% homologous to HHV-6A, it expresses certain B-specific genes. In order to quantify the amount of expressed viral mRNA we have developed a method using real-time PCR on a LightCycler instrument. Here we describe an assay for the detection of the HHV-6B B6 mRNA, but our approach can easily be extended to involve other mRNAs. This method is useful during the study of HHV-6B biology and offers reliable and reproducible, quantitative detection of viral mRNA below the attomol range.

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Authors and Affiliations

  1. Department of Medical Microbiology and Immunology, University of Aarhus, Bartholin Building, DK-8000, Aarhus C, Denmark

    Bodil Øster & Per Höllsberg M.D.

Authors
  1. Bodil Øster
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  2. Per Höllsberg M.D.
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Correspondence to Per Höllsberg M.D..

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Published: December 9, 2002

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Øster, B., Höllsberg, P. A sensitive quantification of HHV-6B by real-time PCR. Biol Proced Online 4, 88–93 (2002). https://doi.org/10.1251/bpo38

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  • DOI: https://doi.org/10.1251/bpo38

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Biological Procedures Online

ISSN: 1480-9222

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