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Journal of Clinical Microbiology, November 1999, p. 3672-3675, Vol. 37, No. 11
Department of Microbiology and
Immunology,1 Department of Pediatric
Infectious Diseases,2 Department of
Medicine,3 and University of Rochester
Cancer Center,4 University of Rochester
Medical Center, Rochester, New York 14642
Received 11 June 1999/Returned for modification 13 July
1999/Accepted 4 August 1999
The role of human herpesvirus 6 (HHV-6) in disease beyond primary
infection remains unclear. We have developed and validated a new
reverse transcription-PCR (RT-PCR) assay for HHV-6 that can determine
the presence of HHV-6 in clinical specimens and differentiate between
latent and replicating virus. Peripheral blood mononuclear cells from
109 children were evaluated for HHV-6 by RT-PCR, DNA PCR, and viral
culture. Of these samples, 106 were suitable for analysis. A total of
20 samples were positive for HHV-6 by culture and DNA PCR, of which 19 were positive by RT-PCR (sensitivity, 95%). All 28 samples from
children that were negative by viral culture, but positive by DNA PCR,
were negative for viral transcripts by our RT-PCR assay. One positive
RT-PCR result was observed in 56 samples that were negative by tissue
culture and DNA PCR. This indicates a low rate of false-positive
results (1.2%) and a specificity of 98.8%. This RT-PCR assay can
reliably differentiate between latent and actively replicating HHV-6
and should allow insight into the pathogenesis of this ubiquitous virus.
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Detection of Human Herpesvirus 6 by Reverse
Transcription-PCR
*
Corresponding author. Mailing address: University of
Rochester Medical Center, Box 689, 601 Elmwood Ave., Rochester, NY
14642. Phone: (716) 275-7989. Fax: (716) 273-1104. E-mail:
Renee_Norton{at}urmc.rochester.edu.
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