Research

Intracellular localization of Crimean-Congo Hemorrhagic Fever (CCHF) virus glycoproteins

Sebastian Haferkamp^1,2,3 , Lisa Fernando^2,4 , Tino F Schwarz³ , Heinz Feldmann^2,4 and Ramon Flick^1,2,4

¹University of Texas Medical Branch, Department of Pathology, Center for Biodefense and Emerging Infectious Diseases, 301 University Boulevard, Galveston, Texas, 77555-0609 USA

²Special Pathogens Program, National Microbiology Laboratory, Health Canada, CA-R3E 3R2 Winnipeg, Canada

³Stiftung Juliusspital Wuerzburg, 97070 Wuerzburg, Germany

⁴Department of Medical Microbiology, University of Manitoba, 543-730 William Avenue, Winnipeg, R3E 0W3 Canada

author email corresponding author email

Virology Journal 2005, 2:42doi:10.1186/1743-422X-2-42

Published:	25 April 2005

Abstract

Background

Crimean-Congo Hemorrhagic Fever virus (CCHFV), a member of the genus Nairovirus, family Bunyaviridae, is a tick-borne pathogen causing severe disease in humans. To better understand the CCHFV life cycle and explore potential intervention strategies, we studied the biosynthesis and intracellular targeting of the glycoproteins, which are encoded by the M genome segment.

Results

Following determination of the complete genome sequence of the CCHFV reference strain IbAr10200, we generated expression plasmids for the individual expression of the glycoproteins G_N and G_C, using CMV- and chicken β-actin-driven promoters. The cellular localization of recombinantly expressed CCHFV glycoproteins was compared to authentic glycoproteins expressed during virus infection using indirect immunofluorescence assays, subcellular fractionation/western blot assays and confocal microscopy. To further elucidate potential intracellular targeting/retention signals of the two glycoproteins, GFP-fusion proteins containing different parts of the CCHFV glycoprotein were analyzed for their intracellular targeting. The N-terminal glycoprotein G_N localized to the Golgi complex, a process mediated by retention/targeting signal(s) in the cytoplasmic domain and ectodomain of this protein. In contrast, the C-terminal glycoprotein G_C remained in the endoplasmic reticulum but could be rescued into the Golgi complex by co-expression of G_N.

Conclusion

The data are consistent with the intracellular targeting of most bunyavirus glycoproteins and support the general model for assembly and budding of bunyavirus particles in the Golgi compartment.