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Journal of Virology, November 2000, p. 10790-10795, Vol. 74, No. 22
Center for Molecular Genetics and Department
of Pediatrics, University of California San Diego School of
Medicine, La Jolla, California
Received 15 May 2000/Accepted 19 August 2000
In the absence of viral envelope gene expression, cells expressing
human immunodeficiency virus type 1 (HIV-1) gag and
pol, accessory HIV functions, and a vector genome RNA
produce and secrete large amount of noninfectious virus-like particles
(VLPs) into the conditioned medium. After partial purification, such
HIV-1 VLPs can be made infectious in cell-free conditions in vitro by complex formation with lipofection reagents or with the G protein of vesicular stomatitis virus (VSV-G). The resulting in vitro-modified HIV-1 particles are able to infect nondividing cells.
Infectivity of envelope-free HIV VLPs can also be induced by prior
modification of target cells through exposure to
partially purified VSV-G vesicles. Similarly, infection can be carried
out by attachment of envelope-free noninfectious VLPs to
unmodified cells followed by subsequent treatment of cells with
VSV-G. We interpret these findings to indicate that interaction
between a viral envelope and a cell surface receptor is
not necessary for the initial virus binding to the cells but is
required for subsequent cell entry and infection.
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Separable Mechanisms of Attachment and Cell Uptake
during Retrovirus Infection

*
Corresponding author. Mailing address: Center for
Molecular Genetics and Department of Pediatrics, UCSD School of
Medicine, 9500 Gilman Dr., La Jolla, CA 92093-0634. Phone: (619)
534-4268. Fax: (619) 534-1422. E-mail: tfriedmann{at}ucsd.edu.
Present address: Department of Medicine, USC School of Medicine,
Los Angeles, CA 90033.
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