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Journal of Virology, July 2000, p. 6689-6694, Vol. 74, No. 14
Laboratory of Virology, Istituto Superiore di
Sanità, Rome,1 and Department of
Histology, Microbiology and Medical Biotechnologies, University of
Padua, Padua,2 Italy
Received 30 December 1999/Accepted 24 April 2000
The infection of CD4-negative cells by variants of tissue
culture-adapted human immunodeficiency virus type 1 (HIV-1) or HIV-2 strains has been shown to be mediated by the CXCR4 coreceptor. Here we
show that two in vitro-established
CD4
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
CD4-Independent Infection of Two
CD4
/CCR5
/CXCR4+ Pre-T-Cell
Lines by Human and Simian Immunodeficiency Viruses
/CCR5
/CXCR4+ human
pre-T-cell lines (A3 and A5) can be productively infected by wild-type
laboratory-adapted T-cell-tropic HIV-1 and HIV-2 strains in a
CD4-independent, CXCR4-dependent fashion. Despite the absence of CCR5
expression, A3 and A5 cells were susceptible to infection by the simian
immunodeficiency viruses SIVmac239 and SIVmac316. Thus, at least in A3
and A5 cells, one or more of the chemokine receptors can efficiently
support the entry of HIV and SIV isolates in the absence of CD4. These
findings suggest that to infect cells of different compartments, HIV
and SIV could have evolved in vivo to bypass CD4 and to interact
directly with an alternative receptor.
*
Corresponding author. Mailing address: Laboratory of
Virology, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy. Phone: 39-06-49903321. Fax: 39-06-49387184. E-mail: borsetti{at}iss.it.
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