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Clinical and Diagnostic Laboratory Immunology, January 2001, p. 123-128, Vol. 8, No. 1
Institute of Virology1
and Department of Internal Veterinary
Medicine,2 University of Zurich, and
Institute of Animal Science, Swiss Federal Institute of
Technology,3 Zurich, Switzerland
Received 13 July 2000/Returned for modification 25 September
2000/Accepted 11 October 2000
A fluorogenic PCR specific for ovine herpesvirus 2 (OvHV-2)
DNA was developed and compared to a previously established
conventional seminested PCR. Testing of a total of 152 blood samples
from both positive and negative animals revealed that the results of
both assays corresponded to each other in 100% of the cases. A
second fluorogenic PCR for genomic sheep DNA was required to
normalize the quantity of viral DNA in the sample.
Separate standard curves had to be constructed for each PCR. The
analytical sensitivity of the new PCRs ranged between at least 10 copies and sometimes even 1 copy of target DNA per reaction mixture. In
dilution series of the target DNAs, linear decreases of the signals
were observed over 7 orders of magnitude. Thus, it was possible to
calculate the amounts of viral DNA in relation to the amounts of
cellular DNA by normalizing the absolute quantity of OvHV-2 DNA with
the amount of genomic sheep DNA. By this technique, it was possible for
the first time to quantitatively characterize the course of OvHV-2
replication in naturally infected sheep.
1071-412X/01/$04.00+0 DOI: 10.1128/CDLI.8.1.123-128.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Quantitative Fluorogenic PCR Assay for Measuring
Ovine Herpesvirus 2 Replication in Sheep
*
Corresponding author. Mailing address: Institute of
Virology, Veterinary Medical Faculty, University of Zurich,
Winterthurerstrasse 266a, CH-8057 Zurich, Switzerland. Phone: 41 1 635 87 01. Fax: 41 1 635 89 11. E-mail: ma{at}vetvir.unizh.ch.
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