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Journal of Virology, December 1998, p. 10298-10300, Vol. 72, No. 12
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
In Vitro Construction of Pseudovirions of Human
Papillomavirus Type 16: Incorporation of Plasmid DNA into
Reassembled L1/L2 Capsids
Kei
Kawana,1,2
Hiroyuki
Yoshikawa,2
Yuji
Taketani,2
Kunito
Yoshiike,1 and
Tadahito
Kanda1,*
Division of Molecular Genetics, National
Institute of Infectious Diseases, Shinjuku-ku, Tokyo
162-8640,1 and
Department of Obstetrics
and Gynecology, Faculty of Medicine, University of Tokyo,
Bunkyo-ku, Tokyo 113-0033,2 Japan
Received 29 June 1998/Accepted 15 September 1998
Lack of permissive and productive cell cultures for the human
papillomaviruses (HPVs) has hindered the study of virus-neutralizing antibodies and infection. We developed a cell-free system generating infectious HPV16 pseudovirions. HPV16 L1/L2 capsids, which had been
self-assembled in insect cells (Sf9) expressing virion proteins L1 and
L2, were disassembled with 2-mercaptoethanol (2-ME), a reducing agent,
and reassembled by removal of 2-ME in the presence of a
-galactosidase expression plasmid. Plasmid DNA purified together
with the reassembled capsids was resistant to DNase I digestion. The
reassembled pseudovirions mediated DNA transfer to COS-1 cells, as
monitored by induced
-galactosidase activity. Transfer was inhibited
by anti-HPV16 L1 antiserum but not by antisera against L1s of HPV6 and
HPV18. Construction in vitro of HPV pseudovirions containing marker
plasmids would be potentially useful in developing methods to assay
virus-neutralizing antibodies and to transfer exogenous genes to
HPV-susceptible cells.
*
Corresponding author. Mailing address: Division of
Molecular Genetics, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo 162-8640, Japan. Phone: 81-3-5285-1111, ext. 2524. Fax: 81-3-5285-1166. E-mail: kanda{at}nih.go.jp.
Journal of Virology, December 1998, p. 10298-10300, Vol. 72, No. 12
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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