Abstract |
Human immunodeficiency virus type 1 (HIV-1) infectivity and cytopathic effect require proper maturation of the viral envelope glycoprotein carbohydrate moieties. We have found that fresh human serum enhances the infectivity of HIV-1 in MT-2 cell infection assays when virus is synthesized in the presence of the mannosidase I inhibitor, 1-deoxymannojirimycin, or the mannosidase II inhibitor, swainsonine, but has no enhancing effect on virus synthesized in the presence of the glucosidase I inhibitors, castanospermine and 1-deoxynojirimycin, or the glucosidase II inhibitor, bromoconduritol. Enhanced infections were characterized by cytopathic effect, antigen synthesis and reverse transcriptase release, all which occurred sooner than in control-infected cultures. This enhancement of infection was also observed in C1q-deficient serum but was not observed in serum that was heat-inactivated or depleted of complement components C3 or factor B, thus suggesting a requirement for the alternate pathway of complement.
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Authors | D C Montefiori, W E Robinson Jr, W M Mitchell |
Journal | Antiviral research
(Antiviral Res)
Vol. 11
Issue 3
Pg. 137-46
(Apr 1989)
ISSN: 0166-3542 [Print] Netherlands |
PMID | 2472115
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Alkaloids
- Complement C3
- 1-Deoxynojirimycin
- Complement System Proteins
- RNA-Directed DNA Polymerase
- Glucosidases
- Mannosidases
- mannosyl-oligosaccharide 1,2-alpha-mannosidase
- mannosyl-oligosaccharide 1,3 - 1,6-alpha-mannosidase
- Complement Factor B
- Glucosamine
- Swainsonine
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Topics |
- 1-Deoxynojirimycin
- Alkaloids
(pharmacology)
- Cells, Cultured
- Complement C3
(immunology)
- Complement Factor B
(immunology)
- Complement System Proteins
(immunology)
- Cytopathogenic Effect, Viral
(drug effects)
- Fluorescent Antibody Technique
- Glucosamine
(analogs & derivatives, pharmacology)
- Glucosidases
(antagonists & inhibitors)
- Glycosylation
- HIV-1
(drug effects, immunology, isolation & purification, pathogenicity)
- Humans
- Mannosidases
(antagonists & inhibitors)
- RNA-Directed DNA Polymerase
(metabolism)
- Swainsonine
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