Reassortant influenza viruses for vaccines
The invention provides compositions and methods useful to prepare segmented, negative strand RNA viruses, e.g., orthomyxoviruses such as influenza A viruses, entirely from cloned cDNAs and in the absence of helper virus.
1. A method for producing reassortant influenza virus particles for preparation of a vaccine, comprising:
i) introducing a first set of expression vectors into cells containing a nucleoprotein and an RNA dependent RNA polymerase, wherein said vectors comprise genomic influenza vRNA segments or antigenomic cRNA segments of said genomic influenza vRNA segments;
ii) culturing said cells in the absence of helper virus such that ribonucleoprotein complexes containing the genomic influenza vRNA segments are formed and reassortant influenza viral particles comprising the genomic influenza vRNA segments is assembled in said cells; and
iii) recovering said reassortant influenza viral particles from said cells.
2. The method of claim 1 , wherein the cells are from a cell line comprising a second set of vectors encoding said nucleoprotein and the subunits of said RNA-dependent RNA polymerase.
3. The method of claim 1 , wherein said virus is an influenza virus of type A, B or C.
4. The method of claim 1 , wherein said reassortant influenza virus contains vRNA segments derived from more than one parent virus.
5. The method of claim 1 , wherein the culturing step occurs in an egg.
6. The method of claim 1 , further comprising attenuating the recovered reassortant influenza viral particles.
7. The method of claim 1 , wherein the first and second set of vectors are introduced by liposomal transfection.
8. The method of claim 1 , wherein the first and second set of vectors are all plasmids.
9. The method of claim 1 , wherein each of said genomic influenza vRNA segments or antignomic cRNA segments of said genomic influenza vRNA segments are encoded on separate vectors.
10. The method of claim 1 , wherein the RNA polymerase I promoter is a human RNA polymerase I promoter.
11. The method of claim 1 , wherein a coding sequence for each genomic influenza vRNA segments or antigenomic cRNA segments of said genomic influenza vRNA segments is upstream of a transcription terminator.