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Published on: April 8, 2012
Analysis of HIV particle formation using transient expression of subviral constructs in mammalian cells
K Mergener1, M Fäcke, R Welker
1Angewandte Tumorvirologie, Deutsches Krebsforschungszentrum, Heidelberg, Germany.
Insights
This study shows that human immunodeficiency virus (HIV) gag and pol gene expression in mammalian cells can produce retrovirus-like particles. Particle release depends on myristoylation, and HIV protease activity influences budding and cell toxicity.
Area of Science:
- Virology
- Molecular Biology
- Cell Biology
Background:
- Understanding human immunodeficiency virus (HIV) assembly is crucial for developing antiviral therapies.
- The gag and pol genes encode essential viral structural proteins and enzymes involved in replication.
- The role of viral protease (PR) and myristoylation in HIV particle formation requires further elucidation.
Purpose of the Study:
- To investigate the expression of human immunodeficiency virus (HIV) type 1 gag and pol genes in mammalian cells.
- To characterize the formation and release of retrovirus-like particles.
- To determine the impact of mutations and proteinase activity on particle production and morphology.
Main Methods:
- Transient expression of HIV gag and pol gene segments in mammalian cells.
- Detection of protein expression using indirect immunofluorescence and Western blotting.
- Analysis of particle release, density, composition, and morphology via sucrose density gradients, reverse transcriptase (RT) activity assays, and electron microscopy.
Main Results:
- Expression of gag and pol genes resulted in the release of particles containing processed gag proteins, reverse transcriptase (RT), and RNA.
- Particle production was independent of pol or active HIV proteinase (PR), but PR deficiency led to uncleaved proteins and vacuolar budding.
- Myristoylation is essential for particle release, and PR overexpression caused cytotoxicity and aberrant particle morphology, while PR active site mutations restored release.
Conclusions:
- HIV gag and pol gene expression can lead to the formation and release of immature retrovirus-like particles.
- Myristoylation is critical for efficient particle release.
- HIV proteinase activity plays a complex role, influencing both polyprotein processing and particle release dynamics, with overexpression leading to toxicity.
Abstract:
Segments of the human immunodeficiency virus (HIV) type 1 gag and pol genes and mutants thereof were transiently expressed in mammalian cells. Expression was dependent on the presence of the rev responsive element in cis and the rev protein in trans and was readily detected by indirect immunofluorescence or Western blotting. Transfection of constructs encoding the entire gag and pol open reading frames yielded efficient release of particles banding at a density of 1.16 g of sucrose per milliliter and consisting mainly of processed gag proteins. In addition, these particles contained the p66/p51 heterodimer of reverse transcriptase (RT), had associated RT activity, and contained RNA. Electron micrographs revealed immature retrovirus-like particles budding primarily from the plasma membrane and extracellular particles with morphological characteristics of HIV. Particle production was independent of the pol open reading frame or an active HIV proteinase (PR) but without active PR, cell-associated and particle-associated proteins remained completely uncleaved and budding occurred primarily into intracellular vacuoles. A mutation preventing myristoylation of the viral polyproteins abolished particle release but did not interfere with polyprotein synthesis and did not prevent processing. Expression of gag and PR in the same reading frame yielded complete processing of polyproteins but no budding and led to increased cell toxicity. A mutation of the PR active site in this construct prevented cytotoxicity and restored particle release indicating that the observed phenotype was caused by the overexpression of PR. These particles were aberrant in size and morphology when analyzed on sucrose density gradients and by electron microscopy. Budding was arrested at an early stage and extracellular particles appeared to be released by a different mechanism. Only short C-terminal extensions were compatible with this release mechanism since expression of a similar mutant construct encoding the entire gag-pol open reading frame did not yield particles.
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