ORCiD
Nejat Düzgüneş: 0000-0001-6159-1391
Department
Biomedical Sciences
Document Type
Article
Publication Title
Journal of General Virology
ISSN
0022-1317
Volume
71
Issue
12
DOI
10.1099/0022-1317-71-12-2899
First Page
2899
Last Page
2907
Publication Date
1-1-1990
Abstract
We have investigated the effects of the fusion of liposomes with human immunodeficiency virus type 1 (HIV-1(LVA)) on the ability of the virus to infect CD4+ and CD4- cells. Fluorescence dequenching measurements indicated that HIV-1 fuses with liposomes composed of either cardiolipin (CL) or N-[2,3-(dioleyloxy) propyl]-N,N,N-trimethyl ammonium chloride (DOTMA) but not appreciably with dioleoylphosphatidylcholine (DOPC) liposomes. Pre-incubation of HIV-1 with DOTMA liposomes enhanced virus production (measured by p24 gag antigen production in the culture medium and in situ) in CD4+ A3.01 and H9 cells in a concentration-dependent manner, but did not mediate the infection of the CD4- cell line, K562. Preincubation of HIV-1 with between 10 and 30 μM-DOTMA liposomes, and subsequent incubation with A3.01 cells, resulted in the production of about 30-fold greater levels of virus than controls. The presence of DOTMA liposomes during the incubation of A3.01 cells with HIV-1 enhanced the infectivity of the virus up to 90-fold compared to controls. Conversely, preincubation of HIV-1 with CL liposomes inhibited infection of A3.01 cells, dependent on the concentration of liposomes; DOPC liposomes did not alter the infectivity of the virus under any of the incubation conditions. Our results thus indicate that fusion of HIV-1 with liposomes alters the ability of the virus to infect its target cells.
Recommended Citation
Konopka, K.,
Davis, B. R.,
Larsen, C. E.,
Alford, D. R.,
Debs, R. J.,
&
Düzgüneş, N.
(1990).
Liposomes modulate human immunodeficiency virus infectivity.
Journal of General Virology, 71(12), 2899–2907.
DOI: 10.1099/0022-1317-71-12-2899
https://scholarlycommons.pacific.edu/dugoni-facarticles/653
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.