| Journal of General Virology |
| First posted online 19 March 2001 | ARTICLE ABSTRACT |
| Rec 8 February 2001; Acc 12 March 2001 | DOI: 10.1099/vir.0.17678-0 |
Volker Thiel, Jens Herold, Barbara Schelle and Stuart G. Siddell
Institute of Virology and Immunology, University
of Würzburg, Versbacher Straße 7, 97078 Würzburg,
Germany
The coronavirus genome is a positive-strand RNA of extraordinary size and complexity. It is composed of approximately 30000 nucleotides and it is the largest known autonomously replicating RNA. It is also remarkable in that more than two-thirds of the genome is devoted to encoding proteins involved in the replication and transcription of viral RNA. Here, a reverse-genetic system is described for the generation of recombinant coronaviruses. This system is based upon the in vitro transcription of infectious RNA from a cDNA copy of the human coronavirus 229E genome that has been cloned and propagated in vaccinia virus. This system is expected to provide new insights into the molecular biology and pathogenesis of coronaviruses and to serve as a paradigm for the genetic analysis of large RNA virus genomes. It also provides a starting point for the development of a new class of eukaryotic, multi-gene RNA vectors that are able to express several proteins simultaneously.
© 2001 SGM
This article is now available in the June 2001 print issue of JGV (vol. 82, 1273–1281). The complete issue of the journal may be seen in electronic form on JGV Online.