Journal of Virology, December 2001, p. 12081-12087, Vol. 75, No. 24
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.24.12081-12087.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Department of Microbiology/Biochemistry/Immunology, Morehouse School of Medicine, Atlanta, Georgia 30310
Received 9 April 2001/Accepted 5 September 2001
Human immunodeficiency virus type 1 (HIV-1) Nef protein exerts
several effects, both on infected cells and as a virion protein, which
work together to enhance viral replication. One of these activities is
the ability to enhance infectivity and the formation of proviral DNA.
The mechanism of this enhancement remains incompletely understood. We
show that virions with nef deleted can be restored to
wild-type infectivity by stimulating intravirion reverse transcription. Particle composition and measures of reverse transcriptase activity remain the same for Nef+ and Nef
virions both
before and after natural endogenous reverse transcription (NERT)
treatment. The effect of NERT treatment on virions pseudotyped with
murine leukemia virus envelope protein was similar to that on particles
pseudotyped with HIV-1 envelope protein. However, virions pseudotyped
with vesicular stomatitis virus G envelope protein showed no influence
of Nef on NERT enhancement of infectivity. These observations suggest
that Nef may function at a level prior to reverse transcription. Since
NERT treatment results in partial disassembly of the viral core, we
speculate that Nef may function at the level of core particle disassembly.
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