A novel primer-extension assay for the detection of a G to A mutation in the distal precore region of hepatitis B virus DNA

J. P. Chung, K. H. Han, K. S. Kim, B. I. Yeh, S. T. Kim, K. S. Lee, C. Y. Chon, Y. M. Moon, J. K. Kang, I. S. Park

Research output: Contribution to journalArticle

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Abstract

The roles of genetic heterogeneity of the hepatitis B virus (HBV) precore gene in the pathogenesis of HBV infection are unclear. Various methods have been used to detect nucleotide (nt) 1896 precore mutants. We established a new primer-extension assay to facilitate the detection of these mutants. This assay is based upon the fact that there is no adenine in the distal precore region of wild-type HBV. Polymerase chain reaction (PCR)- amplified template DNA was denatured and annealed to the [γ-32P]-labelled primer. During primer extension in the presence of DNA polymerase and dCTP, dGTP, dTTP and ddATP, the reaction terminates if there is a nucleotide A. When mixtures of different ratios of wild-type and nt 1896 precore mutants were analysed in the primer-extension assay, correlation between the percentage known amounts and the percentage measured amounts of nt 1896 precore mutants was excellent (r2 = 0.9669). When the primer-extension assay and direct sequencing were compared in hepatitis B e antigen (HBeAg)-positive and -negative chronic active hepatitis B patients, the primer-extension assay detected a greater number of nt 1896 precore mutants than direct sequencing and thus most HBV infections were found to be mixed infections. In conclusion, the primer-extension assay is a reliable and sensitive method for the detection of nt 1896 precore mutants.

Original languageEnglish
Pages (from-to)305-313
Number of pages9
JournalJournal of Viral Hepatitis
Volume6
Issue number4
DOIs
Publication statusPublished - 1999 Jul 1

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Hepatitis B virus
Nucleotides
Mutation
DNA
Virus Diseases
Hepatitis B e Antigens
Genetic Heterogeneity
Chronic Hepatitis B
Adenine
DNA-Directed DNA Polymerase
Chronic Hepatitis
Coinfection
Polymerase Chain Reaction
Genes

All Science Journal Classification (ASJC) codes

  • Hepatology
  • Infectious Diseases
  • Virology

Cite this

Chung, J. P. ; Han, K. H. ; Kim, K. S. ; Yeh, B. I. ; Kim, S. T. ; Lee, K. S. ; Chon, C. Y. ; Moon, Y. M. ; Kang, J. K. ; Park, I. S. / A novel primer-extension assay for the detection of a G to A mutation in the distal precore region of hepatitis B virus DNA. In: Journal of Viral Hepatitis. 1999 ; Vol. 6, No. 4. pp. 305-313.
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abstract = "The roles of genetic heterogeneity of the hepatitis B virus (HBV) precore gene in the pathogenesis of HBV infection are unclear. Various methods have been used to detect nucleotide (nt) 1896 precore mutants. We established a new primer-extension assay to facilitate the detection of these mutants. This assay is based upon the fact that there is no adenine in the distal precore region of wild-type HBV. Polymerase chain reaction (PCR)- amplified template DNA was denatured and annealed to the [γ-32P]-labelled primer. During primer extension in the presence of DNA polymerase and dCTP, dGTP, dTTP and ddATP, the reaction terminates if there is a nucleotide A. When mixtures of different ratios of wild-type and nt 1896 precore mutants were analysed in the primer-extension assay, correlation between the percentage known amounts and the percentage measured amounts of nt 1896 precore mutants was excellent (r2 = 0.9669). When the primer-extension assay and direct sequencing were compared in hepatitis B e antigen (HBeAg)-positive and -negative chronic active hepatitis B patients, the primer-extension assay detected a greater number of nt 1896 precore mutants than direct sequencing and thus most HBV infections were found to be mixed infections. In conclusion, the primer-extension assay is a reliable and sensitive method for the detection of nt 1896 precore mutants.",
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A novel primer-extension assay for the detection of a G to A mutation in the distal precore region of hepatitis B virus DNA. / Chung, J. P.; Han, K. H.; Kim, K. S.; Yeh, B. I.; Kim, S. T.; Lee, K. S.; Chon, C. Y.; Moon, Y. M.; Kang, J. K.; Park, I. S.

In: Journal of Viral Hepatitis, Vol. 6, No. 4, 01.07.1999, p. 305-313.

Research output: Contribution to journalArticle

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T1 - A novel primer-extension assay for the detection of a G to A mutation in the distal precore region of hepatitis B virus DNA

AU - Chung, J. P.

AU - Han, K. H.

AU - Kim, K. S.

AU - Yeh, B. I.

AU - Kim, S. T.

AU - Lee, K. S.

AU - Chon, C. Y.

AU - Moon, Y. M.

AU - Kang, J. K.

AU - Park, I. S.

PY - 1999/7/1

Y1 - 1999/7/1

N2 - The roles of genetic heterogeneity of the hepatitis B virus (HBV) precore gene in the pathogenesis of HBV infection are unclear. Various methods have been used to detect nucleotide (nt) 1896 precore mutants. We established a new primer-extension assay to facilitate the detection of these mutants. This assay is based upon the fact that there is no adenine in the distal precore region of wild-type HBV. Polymerase chain reaction (PCR)- amplified template DNA was denatured and annealed to the [γ-32P]-labelled primer. During primer extension in the presence of DNA polymerase and dCTP, dGTP, dTTP and ddATP, the reaction terminates if there is a nucleotide A. When mixtures of different ratios of wild-type and nt 1896 precore mutants were analysed in the primer-extension assay, correlation between the percentage known amounts and the percentage measured amounts of nt 1896 precore mutants was excellent (r2 = 0.9669). When the primer-extension assay and direct sequencing were compared in hepatitis B e antigen (HBeAg)-positive and -negative chronic active hepatitis B patients, the primer-extension assay detected a greater number of nt 1896 precore mutants than direct sequencing and thus most HBV infections were found to be mixed infections. In conclusion, the primer-extension assay is a reliable and sensitive method for the detection of nt 1896 precore mutants.

AB - The roles of genetic heterogeneity of the hepatitis B virus (HBV) precore gene in the pathogenesis of HBV infection are unclear. Various methods have been used to detect nucleotide (nt) 1896 precore mutants. We established a new primer-extension assay to facilitate the detection of these mutants. This assay is based upon the fact that there is no adenine in the distal precore region of wild-type HBV. Polymerase chain reaction (PCR)- amplified template DNA was denatured and annealed to the [γ-32P]-labelled primer. During primer extension in the presence of DNA polymerase and dCTP, dGTP, dTTP and ddATP, the reaction terminates if there is a nucleotide A. When mixtures of different ratios of wild-type and nt 1896 precore mutants were analysed in the primer-extension assay, correlation between the percentage known amounts and the percentage measured amounts of nt 1896 precore mutants was excellent (r2 = 0.9669). When the primer-extension assay and direct sequencing were compared in hepatitis B e antigen (HBeAg)-positive and -negative chronic active hepatitis B patients, the primer-extension assay detected a greater number of nt 1896 precore mutants than direct sequencing and thus most HBV infections were found to be mixed infections. In conclusion, the primer-extension assay is a reliable and sensitive method for the detection of nt 1896 precore mutants.

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