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Distinct Particle Morphologies Revealed Through Comparative Parallel Analyses of Retrovirus-Like Particles

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Journal J Virol
Date 2016 Jul 1
PMID 27356903
Citations 24
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Abstract

Unlabelled: The Gag protein is the main retroviral structural protein, and its expression alone is usually sufficient for production of virus-like particles (VLPs). In this study, we sought to investigate-in parallel comparative analyses-Gag cellular distribution, VLP size, and basic morphological features using Gag expression constructs (Gag or Gag-YFP, where YFP is yellow fluorescent protein) created from all representative retroviral genera: Alpharetrovirus, Betaretrovirus, Deltaretrovirus, Epsilonretrovirus, Gammaretrovirus, Lentivirus, and Spumavirus. We analyzed Gag cellular distribution by confocal microscopy, VLP budding by thin-section transmission electron microscopy (TEM), and general morphological features of the VLPs by cryogenic transmission electron microscopy (cryo-TEM). Punctate Gag was observed near the plasma membrane for all Gag constructs tested except for the representative Beta- and Epsilonretrovirus Gag proteins. This is the first report of Epsilonretrovirus Gag localizing to the nucleus of HeLa cells. While VLPs were not produced by the representative Beta- and Epsilonretrovirus Gag proteins, the other Gag proteins produced VLPs as confirmed by TEM, and morphological differences were observed by cryo-TEM. In particular, we observed Deltaretrovirus-like particles with flat regions of electron density that did not follow viral membrane curvature, Lentivirus-like particles with a narrow range and consistent electron density, suggesting a tightly packed Gag lattice, and Spumavirus-like particles with large envelope protein spikes and no visible electron density associated with a Gag lattice. Taken together, these parallel comparative analyses demonstrate for the first time the distinct morphological features that exist among retrovirus-like particles. Investigation of these differences will provide greater insights into the retroviral assembly pathway.

Importance: Comparative analysis among retroviruses has been critically important in enhancing our understanding of retroviral replication and pathogenesis, including that of important human pathogens such as human T-cell leukemia virus type 1 (HTLV-1) and HIV-1. In this study, parallel comparative analyses have been used to study Gag expression and virus-like particle morphology among representative retroviruses in the known retroviral genera. Distinct differences were observed, which enhances current knowledge of the retroviral assembly pathway.

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References
1.
Gao W, Rzewski A, Sun H, Robbins P, Gambotto A . UpGene: Application of a web-based DNA codon optimization algorithm. Biotechnol Prog. 2004; 20(2):443-8. DOI: 10.1021/bp0300467. View

2.
Garbitt-Hirst R, Kenney S, Parent L . Genetic evidence for a connection between Rous sarcoma virus gag nuclear trafficking and genomic RNA packaging. J Virol. 2009; 83(13):6790-7. PMC: 2698546. DOI: 10.1128/JVI.00101-09. View

3.
Yeager M, WEINER S, Brown P, Rein A . Supramolecular organization of immature and mature murine leukemia virus revealed by electron cryo-microscopy: implications for retroviral assembly mechanisms. Proc Natl Acad Sci U S A. 1998; 95(13):7299-304. PMC: 22596. DOI: 10.1073/pnas.95.13.7299. View

4.
Johnson M, Scobie H, Vogt V . PR domain of rous sarcoma virus Gag causes an assembly/budding defect in insect cells. J Virol. 2001; 75(9):4407-12. PMC: 114187. DOI: 10.1128/JVI.75.9.4407-4412.2001. View

5.
Goldstone D, Flower T, Ball N, Sanz-Ramos M, Yap M, Ogrodowicz R . A unique spumavirus Gag N-terminal domain with functional properties of orthoretroviral matrix and capsid. PLoS Pathog. 2013; 9(5):e1003376. PMC: 3649970. DOI: 10.1371/journal.ppat.1003376. View