Literature DB >> 9854066

Quantitative detection of hepatitis B virus DNA in two international reference plasma preparations. Eurohep Pathobiology Group.

K H Heermann1, W H Gerlich, M Chudy, S Schaefer, R Thomssen.   

Abstract

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 Organization reference sample.

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Year:  1999        PMID: 9854066      PMCID: PMC84170     

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  20 in total

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Journal:  Zentralbl Bakteriol Orig A       Date:  1976-08

5.  An assay for the detection of the DNA genome of hepatitis B virus in serum.

Authors:  M Berninger; M Hammer; B Hoyer; J L Gerin
Journal:  J Med Virol       Date:  1982       Impact factor: 2.327

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Authors:  W H Gerlich; W S Robinson
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9.  Genotyping by multiplex polymerase chain reaction for detection of endemic hepatitis B virus transmission.

Authors:  R Repp; S Rhiel; K H Heermann; S Schaefer; C Keller; P Ndumbe; F Lampert; W H Gerlich
Journal:  J Clin Microbiol       Date:  1993-05       Impact factor: 5.948

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Authors:  M C Kuhns; A L McNamara; R P Perrillo; C M Cabal; C R Campbel
Journal:  J Med Virol       Date:  1989-04       Impact factor: 2.327

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  25 in total

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Authors:  I J Marin; M Poljak; K Seme; J Meglic-Volkar; M Maticic; G Lesnicar; V Brinovec
Journal:  J Clin Microbiol       Date:  2001-02       Impact factor: 5.948

4.  Real Time-PCR HBV-DNA Analysis: Significance and First Experience in Armed Forces.

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5.  Enhancement of PCR Detection Limit by Single-Tube Restriction Endonuclease-PCR (RE-PCR).

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6.  Real-time PCR assay using molecular beacon for quantitation of hepatitis B virus DNA.

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Journal:  J Clin Microbiol       Date:  2004-08       Impact factor: 5.948

7.  The laboratory diagnosis of hepatitis B virus.

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8.  Nuclease-resistant double-stranded DNA controls or standards for hepatitis B virus nucleic acid amplification assays.

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9.  Pre-s1 antigen-dependent infection of Tupaia hepatocyte cultures with human hepatitis B virus.

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10.  An improved method for the isolation of hepatitis B virus DNA from human serum.

Authors:  Harish Changotra; Prabodh K Sehajpal
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