Previous Article | Next Article ![]()
J. Virol., Oct 1997, 7381-7386, Vol 71, No. 10
C Meyers, TJ Mayer and MA Ozbun
The lack of a permissive system for the propagation of viral stocks
containing abundant human papillomavirus (HPV) particles has hindered the
study of infectivity and the early stages of HPV replication. The
organotypic (raft) culture system has permitted the study of a number of
the differentiation-specific aspects of HPV, including amplification of
viral DNA, expression of late genes, and viral morphogenesis. However,
these investigations have been limited to a single virus type, namely, HPV
type 31 (HPV31). We have artificially introduced linearized HPV18 genomic
DNA into primary keratinocytes by electroporation, followed by clonal
expansion and induction of epithelial stratification and differentiation in
organotypic culture. We report the synthesis of infectious HPV18 virions.
Virus particles approximately 50 nm in diameter were observed by electron
microscopy. HPV18 virions purified by isopycnic gradient were capable of
infecting keratinocytes in vitro, as shown by the expression of multiple
HPV18-specific, spliced transcripts.
Copyright © 1997, American Society for Microbiology
Synthesis of infectious human papillomavirus type 18 in differentiating epithelium transfected with viral DNA
Department of Microbiology and Immunology, The Pennsylvania State University College of Medicine, Hershey 17033, USA. cmeyers@bcmic.hmc.psu.edu
This article has been cited by other articles:
| J. Bacteriol. | Mol. Cell. Biol. | Microbiol. Mol. Biol. Rev. |
|---|
| Clin. Vaccine Immunol. | ALL ASM JOURNALS |
|---|