Journal article
Characterization of a peptide domain within the GB virus C envelope glycoprotein (E2) that inhibits HIV replication
Virology (New York, N.Y.), Vol.430(1), pp.53-62
08/15/2012
DOI: 10.1016/j.virol.2012.04.019
PMCID: PMC3568392
PMID: 22608061
Abstract
GB virus C (GBV-C) infection is associated with prolonged survival in HIV-infected cohorts, and GBV-C E2 protein inhibits HIV entry when added to CD4+ T cells. To further characterize E2 effects on HIV replication, stably transfected Jurkat cell lines expressing GBV-C E2 or control sequences were infected with HIV and replication was measured. HIV replication (all 6 isolates studied) was inhibited in all cell lines expressing a region of 17 amino acids of GBV-C E2, but not in cell lines expressing E2 without this region. In contrast, mumps and yellow fever virus replication was not inhibited by E2 protein expression. Synthetic GBV-C E2 17mer peptides did not inhibit HIV replication unless they were fused to a tat-protein-transduction-domain (TAT) for cellular uptake. These data identify the region of GBV-C E2 protein involved in HIV inhibition, and suggest that this GBV-C E2 peptide must gain entry into the cell to inhibit HIV.
► GBV-C E2 expression in a CD4+ T cell line inhibits HIV entry. ► Expression of 17 amino acids of GBV-C E2 protein inhibits HIV in a CD4+ T cell line. ► Cells expressing E2 inhibit HIV in bystander cells if there is cell-to-cell contact. ► Intracellular, but not extracellular E2 peptide inhibits HIV if it gains entry.
Details
- Title: Subtitle
- Characterization of a peptide domain within the GB virus C envelope glycoprotein (E2) that inhibits HIV replication
- Creators
- Jinhua Xiang - Department of Internal Medicine, Iowa City Veterans Affairs Medical Center and the University of Iowa, IA 52242, USAJames H McLinden - Department of Internal Medicine, Iowa City Veterans Affairs Medical Center and the University of Iowa, IA 52242, USAThomas M Kaufman - Department of Internal Medicine, Iowa City Veterans Affairs Medical Center and the University of Iowa, IA 52242, USAEmma L Mohr - Department of Internal Medicine, Iowa City Veterans Affairs Medical Center and the University of Iowa, IA 52242, USANirjal Bhattarai - Department of Internal Medicine, Iowa City Veterans Affairs Medical Center and the University of Iowa, IA 52242, USAQing Chang - Department of Internal Medicine, Iowa City Veterans Affairs Medical Center and the University of Iowa, IA 52242, USAJack T Stapleton - Department of Internal Medicine, Iowa City Veterans Affairs Medical Center and the University of Iowa, IA 52242, USA
- Resource Type
- Journal article
- Publication Details
- Virology (New York, N.Y.), Vol.430(1), pp.53-62
- DOI
- 10.1016/j.virol.2012.04.019
- PMID
- 22608061
- PMCID
- PMC3568392
- NLM abbreviation
- Virology
- ISSN
- 0042-6822
- eISSN
- 1096-0341
- Publisher
- Elsevier Inc
- Grant note
- DOI: 10.13039/100000002, name: National Institutes of Health
- Language
- English
- Date published
- 08/15/2012
- Academic Unit
- Microbiology and Immunology; Infectious Diseases; Internal Medicine
- Record Identifier
- 9984094354402771
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