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Journal of Virology, December 1999, p. 10122-10128, Vol. 73, No. 12
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Subtype-Independent Immature Secretion and Subtype-Dependent
Replication Deficiency of a Highly Frequent, Naturally Occurring
Mutation of Human Hepatitis B Virus Core Antigen
Thomas Ta-Tung
Yuan,
Pei-Ching
Tai, and
Chiaho
Shih*
Center for Tropical Diseases, Department of
Pathology, University of Texas Medical Branch, Galveston, Texas
77555-0609
Received 21 June 1999/Accepted 31 August 1999
The most frequent mutation of the human hepatitis B virus (HBV)
core antigen occurs at amino acid 97. Recently, a phenylalanine (F)-to-leucine (L) mutation at this position (mutant F97L) in HBV
surface antigen subtype ayw has been shown to result in an immature secretion phenotype, which is characterized by the
nonselective export of an excessive amount of virions containing
minus-strand, single-stranded HBV DNA. While subtype ayw
mutant F97L has been found in Europe, the major reservoir of HBV
resides in Asia and Africa. We report here that the immature secretion
phenotype indeed can be found in an HBV strain (subtype
adr) prevalent in Asia, changing from an isoleucine (I) to
a leucine (mutant I97L). Despite its immature secretion phenotype, the
adr variant I97L replicates as well as its parental
adr wild-type I97I, supporting the conclusion that the
extracellular phenotype of immature secretion is not a consequence of
the intracellular HBV DNA replication defect. Further studies
demonstrated that it is the acquisition of a leucine, rather than the
loss of a wild-type amino acid at codon 97, that is important for
immature secretion. We conclude that immature secretion is a
subtype-independent phenotype and deficiency in intracellular DNA
synthesis is a subtype-dependent phenotype. The former is caused by the
trans-acting effect of a mutant core protein, while the
latter by a cis-acting effect of a mutated nucleotide on
the ayw genome. These immature secretion variants provide
an important tool for studying the regulation of HBV virion assembly
and secretion.
*
Corresponding author. Mailing address: Center for
Tropical Diseases, Department of Pathology, University of Texas Medical Branch, Galveston, TX 77555-0609. Phone: (409) 772-2563. Fax: (409)
747-2429. E-mail: cshih{at}utmb.edu.
Journal of Virology, December 1999, p. 10122-10128, Vol. 73, No. 12
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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