2017
DOI: 10.1128/genomea.01576-16
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Complete Genome Sequence of the WHO International Standard for Hepatitis B Virus DNA

Abstract: The World Health Organization (WHO) international standard (IS) for hepatitis B virus (HBV) DNA for use in nucleic acid amplification assays was characterized by determining the complete genome sequence, which was assigned genotype A. This information will aid the design, development, and evaluation of HBV DNA amplification assays.

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Cited by 7 publications
(4 citation statements)
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“…This highlights that the assays used to detect immunity to MuV may not always detect an adequate post-vaccination response. Only a small number of serological commercial assays such as the detection of Hepatitis B surface antibody (anti-HBs) ( 221 ) and rubella IgG ( 222 ) have been designed using WHO reference material as a standard for quantification. However, even utilizing this reference standard demonstrates significant differences in the determined quantification of either anti-HBs or rubella IgG depending on the assays used; although a value for anti-HBs of 10 IU/ml is regarded as protective against significant HBV infection, the detection of this anti-HBs is significantly influenced by which anti-HBs assays is used ( 223 227 ).…”
Section: Laboratory Determinants Of An Effective Immune Response To Mmentioning
confidence: 99%
“…This highlights that the assays used to detect immunity to MuV may not always detect an adequate post-vaccination response. Only a small number of serological commercial assays such as the detection of Hepatitis B surface antibody (anti-HBs) ( 221 ) and rubella IgG ( 222 ) have been designed using WHO reference material as a standard for quantification. However, even utilizing this reference standard demonstrates significant differences in the determined quantification of either anti-HBs or rubella IgG depending on the assays used; although a value for anti-HBs of 10 IU/ml is regarded as protective against significant HBV infection, the detection of this anti-HBs is significantly influenced by which anti-HBs assays is used ( 223 227 ).…”
Section: Laboratory Determinants Of An Effective Immune Response To Mmentioning
confidence: 99%
“…We elected to target a conserved region of the HBV polymerase gene for the development of the SQLA assay using the WHO International Standard HBV genome 23 (GenBank accession no. KY003230).…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…The HBV DNA was amplified by Nested PCR of the surface antigen gene using specific primers. The sequences of the outer primers were HBV179FS, CTAG-GACCCCTGCTCGTGTT as the outer sense, and HBV704RS, CGAACCACTGAACAAATGGCACT as the outer anti-sense; 251f, GACTYGTGGTGGACTTCTC as the inner sense; 654r, GSCCCAMBCCCATAGG as the inner antisense primer 16 synthesized by Metabion Company, Germany. Concisely, Nested PCR amplification for the first round was carried out in a total volume of 25 mL, containing 2.5 mL PCR buffer, 0.5 mL dNTP, 1 mL MgCl 2 , 1 mL of outer primers, 0.8 mL DNA Taq polymerase, 2.5 mL Template DNA, and 15.7 mL nuclease-free water In the second round, 1 mL product of the first round was used as a template, 2.5 mL PCR buffer, 0.5 mL dNTP, 1 mL MgCl 2 , 1 mL of inner primers, 0.8 mL DNA Taq polymerase, and 17.2 mL nuclease-free water was mixed to reach the final 25 mL volume.…”
Section: Methodsmentioning
confidence: 99%