J Virol, May 1998, p. 4065-4071, Vol. 72, No. 5
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Section of Virology,
Received 29 September 1997/Accepted 21 January 1998
Like human immunodeficiency virus type 1 (HIV-1) and simian
immunodeficiency virus (SIV), HIV-2 requires a coreceptor in
addition to CD4 for entry into cells. HIV and SIV coreceptor molecules belong to a family of seven-transmembrane-domain G-protein-coupled receptors. Here we show that primary HIV-2 isolates can use a broad
range of coreceptor molecules, including CCR1, CCR2b, CCR3, CCR4, CCR5,
and CXCR4. Despite broad coreceptor use, the chemokine ligand SDF-1
substantially blocked HIV-2 infectivity of peripheral blood mononuclear
cells, indicating that its receptor, CXCR4, was the predominant
coreceptor for infection of these cells. However, expression of CXCR4
together with CD4 on some cell types did not confer susceptibility to
infection by all CXCR4-using virus isolates. These data therefore
indicate that another factor(s) influences the ability of HIV-2 to
replicate in human cell types that express the appropriate receptors
for virus entry.
*
Corresponding author. Mailing address: Section of
Virology, Chester Beatty Laboratories, Institute of Cancer Research,
London SW3 6JB, United Kingdom. Phone: 44-171-352-8133. Fax:
44-171-352-3299. E-mail: aine{at}icr.ac.uk.
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