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Journal of Clinical Microbiology, January 1998, p. 286-289, Vol. 36, No. 1
Laboratory for Viral Hepatitis, Bureau of
Microbiology, Laboratory Centre for Disease Control, Health Canada,
Ottawa, Ontario, Canada
Received 16 May 1997/Returned for modification 19 August
1997/Accepted 10 October 1997
Forty-four clinical samples positive for GB virus C
(GBV-C)/hepatitis G virus (HGV) were tested with six primer sets, four from the 5' untranslated region (5'-UTR) and two from the NS5a genomic
region. Two of the 5'-UTR primer sets, when used in a single-round
60-cycle PCR, detected between 86.4 and 97.7% of the positive samples,
while two different sets from the same area, when used in a nested PCR,
amplified between 97.7 and 100% of the positive specimens. Both sets
from the NS5a region, when used in a single-round PCR, detected 95.5%
of the GBV-C/HGV-positive samples. Parallel testing with two PCR sets,
one from the 5'-UTR and a second from NS5a, may eliminate
false-negative results attributable to the genetic heterogeneity of the
virus.
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Comparison of Six Sets of PCR Primers from Two
Different Genomic Regions for Amplification of GB Virus
C/Hepatitis G Virus RNA
*
Corresponding author. Mailing address: Laboratory for
Viral Hepatitis, Bureau of Microbiology, Laboratory Centre for Disease Control, Virus Bldg. 10, Rm. B-7, Postal Locator 1000E1, Tunney's Pasture, Ottawa, Ontario K1A 0L2, Canada. Phone: (613) 957-0175. Fax:
(613) 954-0207. E-mail: Anton_Andonov{at}inet.hwc.ca.
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