Abstract |
To screen for an effective antiviral compound which acts as a membrane fluidity modulator, dichotomous effects on human immunodeficiency virus type 1 (HIV-1) infection due to different treatments of several glycolipids and lipids were examined. Continuous treatment of infected cells with 40 microg ml(-1) fattiviracin FV-8, a neutral glycolipid isolated from Streptomycetes, inhibited HIV-1 infection by 96%, whereas pretreatment with 400 microg ml(-1) enhanced infectivity 4.7-fold. The glycolipid showed similar effects as glycyrrhizin; it inhibited infection by broad enveloped viruses, blocked cell-cell fusion, reduced the infectivity of treated virions and enhanced susceptibility to viral infection and cell-cell fusion of cells pretreated with high doses of the compound. Suppression and enhancement was correlated with decreased and increased fluidity of plasma membrane of the fattiviracin FV-8-treated cells. Restricted movement of membrane molecules might impede the formation of a wide fusion pore, and therefore be critical to the entry of viruses. Thus, this can be applied as a new strategy to inhibit viral infections.
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Authors | Shinji Harada, Kazumi Yokomizo, Kazuaki Monde, Yosuke Maeda, Keisuke Yusa |
Journal | Cellular microbiology
(Cell Microbiol)
Vol. 9
Issue 1
Pg. 196-203
(Jan 2007)
ISSN: 1462-5814 [Print] India |
PMID | 17222192
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Glycolipids
- HIV Fusion Inhibitors
- fattiviracin FV-8
- Glycyrrhizic Acid
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Topics |
- Animals
- COS Cells
- Cell Fusion
- Cell Line, Tumor
- Chlorocebus aethiops
- Drug Evaluation, Preclinical
- Glycolipids
(metabolism, pharmacology)
- Glycyrrhizic Acid
(pharmacology)
- HIV Fusion Inhibitors
(pharmacology)
- HIV-1
(drug effects, metabolism)
- Humans
- Membrane Fluidity
(drug effects)
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