Previous Article | Next Article ![]()
Journal of Virology, February 2008, p. 1851-1859, Vol. 82, No. 4
0022-538X/08/$08.00+0 doi:10.1128/JVI.02339-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Institut für Virologie, Justus-Liebig-Universität Giessen, Giessen, Germany,1 Clinical Laboratory, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland,2 Research Department, Kantonal Hospital St. Gallen, St. Gallen, Switzerland3
Received 29 October 2007/ Accepted 28 November 2007
In this study we report the complete sequence and genome organization of the serotype I feline coronavirus (FCoV) strain Black. Furthermore, a reverse genetic system was established for this FCoV strain by cloning a full-length cDNA copy into vaccinia virus. This clone served as basis for the generation of recombinant FCoV (recFCoV) that was shown to bear the same features in vitro as the parental FCoV. Using this system, accessory 3abc genes in the FCoV genome were replaced by green fluorescent protein (recFCoV-GFP) and Renilla luciferase genes (recFCoV-RL). In addition, we showed that feline CD14+ blood monocytes and dendritic cells can be easily detected after infection with recFCoV-GFP. Thus, our established reverse genetic system provides a suitable tool to study the molecular biology of serotype I FCoV.
Published ahead of print on 12 December 2007.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»