Mol Cell Biol. 1982 November; 2(11): 1444-1458
Uukuniemi virus maturation: accumulation of virus particles and viral antigens in the Golgi complex.
E Kuismanen,
K Hedman,
J Saraste and
R F Pettersson
ABSTRACT
We studied the maturation of Uukuniemi virus and the localization of the viral surface glycoproteins and nucleocapsid protein in infected cells by electron microscopy, indirect immunofluorescence, and immunoelectron microscopy with specific antisera prepared in rabbits against the two glycoproteins G1 and G2 and the nucleocapsid protein N. Electron microscopy of thin sections from infected cells showed virus particles maturing at smooth-surfaced membranes close to the nucleus. Localization of the G1/G2 and N proteins by indirect immunofluorescence at different stages after infection showed the antigens to be present throughout the cell interior but concentrated in the juxtanuclear region. The G1/G2 antiserum also appeared to stain the nuclear and plasma membranes. Double staining with tetramethylrhodamine isothiocyanate-conjugated wheat germ agglutinin, which preferentially stains the Golgi complex, and fluorescein isothiocyanate-conjugated anti-rabbit immunoglobulin G, which stained the G1/G2 or N proteins, showed that the staining of the juxtanuclear region coincided. Similarly, double staining for thiamine pyrophosphatase, an enzyme activity specific for the Golgi complex, showed the fluorescence and the cytochemical stain to coincide in the juxtanuclear region. Immunoperoxidase electron microscopy of cells permeabilized with saponin revealed that the viral glycoproteins were present in the rough endoplasmic reticulum and the nuclear and Golgi membranes; the latter was heavily stained. With this method, the N protein was localized to the cytoplasm, especially around smooth-surfaced vesicles in the Golgi region. Taken together, the results indicate that Uukuniemi virus and its structural proteins accumulate in the Golgi complex, supporting the idea that this compartment rather than the plasma membrane is the site of virus maturation. This raises the interesting possibility that deficient transport of the glycoproteins to the plasma membrane and hence their accumulation in the Golgi complex determines the site of virus maturation.
Mol Cell Biol. 1982 November; 2(11): 1444-1458
This article has been cited by other articles:
-
Ribeiro, D., Foresti, O., Denecke, J., Wellink, J., Goldbach, R., Kormelink, R. J. M.
(2008). Tomato spotted wilt virus glycoproteins induce the formation of endoplasmic reticulum- and Golgi-derived pleomorphic membrane structures in plant cells. J. Gen. Virol.
89: 1811-1818
[Abstract]
[Full Text]
-
Overby, A. K., Pettersson, R. F., Grunewald, K., Huiskonen, J. T.
(2008). Insights into bunyavirus architecture from electron cryotomography of Uukuniemi virus. Proc. Natl. Acad. Sci. USA
105: 2375-2379
[Abstract]
[Full Text]
-
Overby, A. K., Popov, V. L., Pettersson, R. F., Neve, E. P. A.
(2007). The Cytoplasmic Tails of Uukuniemi Virus (Bunyaviridae) GN and GC Glycoproteins Are Important for Intracellular Targeting and the Budding of Virus-Like Particles. J. Virol.
81: 11381-11391
[Abstract]
[Full Text]
-
Shi, X., Kohl, A., Li, P., Elliott, R. M.
(2007). Role of the Cytoplasmic Tail Domains of Bunyamwera Orthobunyavirus Glycoproteins Gn and Gc in Virus Assembly and Morphogenesis. J. Virol.
81: 10151-10160
[Abstract]
[Full Text]
-
Overby, A. K., Pettersson, R. F., Neve, E. P. A.
(2007). The Glycoprotein Cytoplasmic Tail of Uukuniemi Virus (Bunyaviridae) Interacts with Ribonucleoproteins and Is Critical for Genome Packaging. J. Virol.
81: 3198-3205
[Abstract]
[Full Text]
-
Connolly-Andersen, A.-M., Magnusson, K.-E., Mirazimi, A.
(2007). Basolateral Entry and Release of Crimean-Congo Hemorrhagic Fever Virus in Polarized MDCK-1 Cells. J. Virol.
81: 2158-2164
[Abstract]
[Full Text]
-
Overby, A. K., Popov, V., Neve, E. P. A., Pettersson, R. F.
(2006). Generation and Analysis of Infectious Virus-Like Particles of Uukuniemi Virus (Bunyaviridae): a Useful System for Studying Bunyaviral Packaging and Budding. J. Virol.
80: 10428-10435
[Abstract]
[Full Text]
-
Shi, X., Kohl, A., Leonard, V. H. J., Li, P., McLees, A., Elliott, R. M.
(2006). Requirement of the N-Terminal Region of Orthobunyavirus Nonstructural Protein NSm for Virus Assembly and Morphogenesis.. J. Virol.
80: 8089-8099
[Abstract]
[Full Text]
-
Shi, X., Lappin, D. F., Elliott, R. M.
(2004). Mapping the Golgi Targeting and Retention Signal of Bunyamwera Virus Glycoproteins. J. Virol.
78: 10793-10802
[Abstract]
[Full Text]
-
Ravkov, E. V., Compans, R. W.
(2001). Hantavirus Nucleocapsid Protein Is Expressed as a Membrane-Associated Protein in the Perinuclear Region. J. Virol.
75: 1808-1815
[Abstract]
[Full Text]
-
Kikkert, M., Verschoor, A., Kormelink, R., Rottier, P., Goldbach, R.
(2001). Tomato Spotted Wilt Virus Glycoproteins Exhibit Trafficking and Localization Signals That Are Functional in Mammalian Cells. J. Virol.
75: 1004-1012
[Abstract]
[Full Text]
-
Veijola, J., Pettersson, R. F.
(1999). Transient Association of Calnexin and Calreticulin with Newly Synthesized G1 and G2 Glycoproteins of Uukuniemi Virus (Family Bunyaviridae). J. Virol.
73: 6123-6127
[Abstract]
[Full Text]
-
Kikkert, M., Van Lent, J., Storms, M., Bodegom, P., Kormelink, R., Goldbach, R.
(1999). Tomato Spotted Wilt Virus Particle Morphogenesis in Plant Cells. J. Virol.
73: 2288-2297
[Abstract]
[Full Text]
-
Cluett, E. B., Kuismanen, E., Machamer, C. E.
(1997). Heterogeneous Distribution of the Unusual Phospholipid Semilysobisphosphatidic Acid through the Golgi Complex. Mol. Biol. Cell
8: 2233-2240
[Abstract]
[Full Text]
Copyright © 1982 by the American Society for Microbiology. All rights reserved.