Quantitative detection of hepatitis B virus DNA in two international reference plasma preparations

被引:115
作者
Heermann, KH
Gerlich, WH
Chudy, M
Schaefer, S
Thomssen, R
机构
[1] Univ Giessen, Inst Med Virol, D-35392 Giessen, Germany
[2] Univ Gottingen, Div Med Microbiol, D-37075 Gottingen, Germany
[3] Univ Gottingen, Natl Reference Lab Viral Hepatitis, D-37075 Gottingen, Germany
[4] Paul Ehrlich Inst, D-63225 Langen, Germany
关键词
D O I
10.1128/JCM.37.1.68-73.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Quantitative detection of hepatitis B virus (HBV) in serum or plasma is of significance for monitoring of therapy and establishment of the prognosis of the disease, as well as for infectivity assessment and quality control of the diagnosis. Unfortunately, various commercially available test kits for HBV DNA yielded conflicting quantitative results, with differences of up to a factor of 120, The Eurohep Pathobiology Group has established two reference samples of plasma from HBV carriers and determined as accurately as possible the number of HBV DNA molecules in these samples. Plasma donations from two single highly viremic carriers of HBV genotype A (HBV surface antigen subtype adw2) and genotype D (ayw2/3), respectively, were collected, and coded dilutions of these samples were analyzed by members of the Eurohep Pathobiology Group. Quantitative results from the seven laboratories reporting consistent results were initially divergent. Limiting dilution and nested PCR assays suffered from incomplete DNA extraction. Hybridization assays used inaccurately quantitated cloned DNA as a reference. Two hybridization assays could not be calibrated directly with cloned HBV DNA, because virion-derived DNA reacted much less efficiently. After identification and elimination of these problems, limiting-dilution assays from three laboratories and hybridization assays from two producers generated consistent and concordant results: 2.7 x 10(9) HBV DNA molecules/ml (range, 2.1 x 10(9) to 3.4 x 10(9) HBV DNA molecules/ml) in the plasma from the carrier of genotype A and 2.6 X 10(9) HBV DNA molecules/ml (range, 2.1 x 10(9) to 3.0 x 10(9) HBV DNA molecules/ml) in the plasma from the carrier of genotype D. The two Eurohep reference plasma samples have already been used for the standardization of test kits and in quality control trials, and the plasma from the carrier of genotype A will probably be the basis of a World Health Organisation reference sample.
引用
收藏
页码:68 / 73
页数:6
相关论文
共 29 条
[1]   AN ASSAY FOR THE DETECTION OF THE DNA GENOME OF HEPATITIS-B VIRUS IN SERUM [J].
BERNINGER, M ;
HAMMER, M ;
HOYER, B ;
GERIN, JL .
JOURNAL OF MEDICAL VIROLOGY, 1982, 9 (01) :57-68
[2]  
BISWAS R, 1976, ZBL BAKT-INT J MED M, V235, P310
[3]   Comparison of four methods for quantitative measurement of hepatitis B viral DNA [J].
Butterworth, LA ;
Prior, SL ;
Buda, PJ ;
Faoagali, JL ;
Cooksley, WGE .
JOURNAL OF HEPATOLOGY, 1996, 24 (06) :686-691
[4]   Mandatory hepatitis B virus testing for doctors [J].
Caspari, G ;
Gerlich, WH .
LANCET, 1998, 352 (9132) :991-991
[5]  
CHUDY M, 1995, HAMOSTASEOLOGIE, V15, P215
[6]  
DAVIS BD, 1980, MICROBIOLOGY INCLUDI, P880
[7]   Quantitative assay of PCR-amplified hepatitis B virus DNA using a peroxidase-labelled DNA probe and enhanced chemiluminescence [J].
Erhardt, A ;
Schaefer, S ;
Athanassiou, N ;
Kann, M ;
Gerlich, WF .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (08) :1885-1891
[8]  
GERLICH W, UNPUB
[9]   HEPATITIS-B VIRUS CONTAINS PROTEIN ATTACHED TO THE 5' TERMINUS OF ITS COMPLETE DNA STRAND [J].
GERLICH, WH ;
ROBINSON, WS .
CELL, 1980, 21 (03) :801-809
[10]  
Gerlich WH, 1995, VIRAL HEPATITIS REV, V1, P53