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Journal of Clinical Microbiology, February 2000, p. 712-715, Vol. 38, No. 2
Departments of
Virology1 and
Haematology,2 University Hospital
Rotterdam, Rotterdam, The Netherlands
Received 21 July 1999/Returned for modification 20 September
1999/Accepted 23 November 1999
With the use of real-time PCR, we developed and evaluated a rapid,
sensitive, specific, and reproducible method for the detection of
Epstein-Barr virus (EBV) DNA in plasma samples. This method allowed us
to screen plasma and serum samples over a range between 100 and
107 copies of DNA per ml using two sample preparation
methods based on absorption. A precision study yielded an average
coefficient of variation for both methods of less than 12%, with a
coefficient of regression for the standard curve of a minimum of 0.98. We detected EBV DNA in 19.2% of plasma samples from immunosuppressed solid-organ transplant patients without symptoms of EBV infections with
a mean load of 440 copies per ml. EBV DNA could be detected in all
transplant patients diagnosed with posttransplant lymphoproliferative disorder, with a mean load of 544,570 copies per ml. No EBV DNA could
be detected in healthy individuals in nonimmunosuppressed control
groups and a mean of 6,400 copies per ml could be detected in patients
with infectious mononucleosis. Further studies revealed that the
inhibitory effect of heparinized plasma could be efficiently removed by
use of an extraction method with Celite as the absorbent.
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Development of a Real-Time Quantitative Assay for
Detection of Epstein-Barr Virus
*
Corresponding author. Mailing address: Department of
Virology, University Hospital Rotterdam, Dr. Molewaterplein 40, 3015 GD
Rotterdam, The Netherlands. Phone: 31-10-463.3431. Fax: 31-10-463.3441. E-mail: niesters{at}viro.fgg.eur.nl.
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