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Journal of Clinical Microbiology, January 2000, p. 18-21, Vol. 38, No. 1
Department of Clinical
Pathology1 and Central Clinical
Laboratory,2 Bouseidai, Isehara, and
Roche Diagnostics K. K., Tokyo,3
Japan, and Roche Molecular Systems, Inc., Pleasanton,
California 94588-27224
Received 29 March 1999/Returned for modification 21 July
1999/Accepted 22 September 1999
We developed and evaluated a prototype automated specimen
preparation instrument for the specific capture of hepatitis C virus (HCV) RNA with probes and magnetic bead-fluid separation. HCV RNA was
isolated from serum by lysis of virus particles with a chaotropic
agent, followed by hybridization of the RNA with biotinylated probes
and capture of the hybridized RNA with streptavidin-coated paramagnetic
particles. After washing of the hybrid-particle complexes to remove
nonspecifically bound materials, the particles were resuspended in a
specimen diluent and were then ready for amplification and detection
with a fully automated PCR system (COBAS AMPLICOR; Roche Diagnostic
Systems). The analytical sensitivity in the dilution series was 33 copies per ml or greater. Comparison of the test results with those
obtained by a manual method based on organic extraction and
precipitation of RNA (SepaGene RV-R; Sanko Junyaku Co., Ltd.) showed
93% (49 of 53 samples) sensitivity and 100% (12 of 12 samples)
specificity. There was 94% overall agreement between results. When RNA
was extracted by the manual method from serum containing
103 or 105 copies of HCV per ml in the presence
of heparin, there was an inhibitory effect on detection of both HCV RNA
and the internal control. In contrast, when RNA was extracted from the
serum by the automated method, there was no inhibitory effect. This
inhibitory effect of heparin on the manual method was also observed for
a series of serum specimens from a hemodialysis patient, but the inhibitory effect was eliminated by the automated specimen preparation method. In summary, a fully automated RNA extraction system for PCR
detection of HCV RNA by use of specific capture with probes and
magnetic bead-fluid separation was shown to have performance similar to
that of the conventional manual method. In addition, it successfully
eliminated the inhibitory effect of the heparin in the serum and
permitted the detection of HCV RNA in serum samples from a hemodialysis
patient. The prototype automated RNA extraction system is suitable as a
totally automated system, starting with RNA extraction to detection of
HCV, if it was combined with the fully automated COBAS AMPLICOR PCR system.
0095-1137/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Automated Specific Capture of Hepatitis C Virus RNA
with Probes and Paramagnetic Particle Separation
*
Corresponding author. Mailing address: Department of
Clinical Pathology, Bouseidai, Isehara, Kanagawa 259-1193 Japan. Phone: 81-463 (93) 1121. Fax: 81-463(93)8607. E-mail:
miyachi{at}is.icc.u-tokai.ac.jp.
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