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Journal of Virology, March 2004, p. 3110-3122, Vol. 78, No. 6
0022-538X/04/$08.00+0 DOI: 10.1128/JVI.78.6.3110-3122.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
Rapid Uncoating of Vector Genomes Is the Key to Efficient Liver Transduction with Pseudotyped Adeno-Associated Virus Vectors
Clare E. Thomas, Theresa A. Storm, Zan Huang, and Mark A. Kay*
Departments
of Pediatrics and Genetics, Stanford University School of Medicine,
Stanford, California 94305
Received 26 August 2003/
Accepted 21 November 2003
Transduction
of the liver with single-stranded adeno-associated virus
serotype 2 (AAV2) vectors is inefficient; less than 10% of
hepatocytes are permissive for stable transduction, and transgene
expression is characterized by a lag phase of up to 6 weeks. AAV2-based
vector genomes packaged inside AAV6 or AAV8 capsids can transduce the
liver with higher efficiency, but the molecular mechanisms underlying
this phenomenon have not been determined. We now show that the primary
barrier to transduction of the liver with vectors based on AAV2 capsids
is uncoating of vector genomes in the nucleus. The majority of AAV2
genomes persist as encapsidated single-stranded molecules within the
nucleus for as long as 6 weeks after vector administration.
Double-stranded vector genomes packaged inside AAV2 capsids are at
least 50-fold more active than single-stranded counterparts, but these
vectors also exhibit a lag phase before maximal gene expression. Vector
genomes packaged inside AAV6 or AAV8 capsids do not persist as
encapsidated molecules and are more biologically active than vector
genomes packaged inside AAV2 capsids. Our data suggest that the rate of
uncoating of vector genomes determines the ability of complementary
plus and minus single-stranded genomes to anneal together and convert
to stable, biologically active double-stranded molecular
forms.
* Corresponding
author. Mailing address: Departments of Pediatrics and Genetics, 300
Pasteur Dr., Room G305A, Stanford University, Stanford, CA 94305.
Phone: (650) 498-6531. Fax: (650) 498-6540. E-mail:
markay{at}stanford.edu.
Journal of Virology, March 2004, p. 3110-3122, Vol. 78, No. 6
0022-538X/04/$08.00+0 DOI: 10.1128/JVI.78.6.3110-3122.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
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