Variant of hepatitis B virus isolated in zimbabwe

Authors

  • Michael M. Chirara,

    1. Department of Biochemistry, University of Zimbabwe, Harare, Zimbabwe
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  • Christopher J. Chetsanga

    Corresponding author
    1. Department of Biochemistry, University of Zimbabwe, Harare, Zimbabwe
    • Department of Biochemistry, University of Zimbabwe, P.O. Box MP 167, Mt Pleasant, Harare, Zimbabwe
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Abstract

The polymerase chain reaction (PCR) was used to amplify an approximately 1.2 kb DNA fragment encompassing the pre-S/S gene region of HBV DNA from serum of patients with acute hepatitis B virus infection. Nucleotide sequence analysis revealed a number of interesting features in the S gene region. Two Bam HI sites were located at nucleotide positions 557 and 872, respectively, in the S gene. Guanine (G) was found at nucleotide position 903 as part of AGA, the codon for arginine (R) corresponding to amino acid position 122 of the S protein. Ade-nine (A) was found at nucleotide position 1017 as part of AXIA, the codon for lysine (K) corresponding to amino acid position 160 of the S protein. Nucleotide sequence alignment revealed a 97% homology to the corresponding domain of an HBVadw genome (clone pFDW294). Within the second loop of the “a” determinant, two mutations resulting in substitution of serine or threonine with the hydrophobic amino acids, methio-nine at position 143 and with alanine in place of glycine at position 145, are predicted from the consensus nucleotide sequence of the PCR-derived clones. Subtyping with monoclonal antibodies showed that the HBsAg was of the ayw subtype. © 1994 Wiiey-Liss, Inc.

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