Influenza viruses with mutant PB2 segment as live attenuated vaccines
The invention provides a recombinant biologically contained influenza virus that is a PB2 knockout virus, e.g., one that is useful to generate a multivalent vaccine, and methods of making and using that virus.
1. A vaccine comprising an effective amount of an isolated stable, biologically contained multivalent influenza virus comprising: i) 8 different segments including a PA viral segment, a PB1 viral segment, a mutant PB2 viral segment, a HA viral segment, a NA viral segment, a NP viral segment, a M (M1 and M2) viral segment, and a NS (NS1 and NS2) viral segment, ii) 8 different segments including a PA viral segment, a PB1 viral segment, a mutant PB2 viral segment, a HA viral segment, a NA (NA and NB) viral segment, a NP viral segment, a M (M1 and BM2) viral segment and a NS (NS1 and NS2) viral segment, or iii) 7 different segments including a PA viral segment, a PB1 viral segment, a mutant PB2 viral segment, a HEF viral segment, a NP viral segment, a M (M1 and CM2) viral segment, and a NS (NS1 and NS2) viral segment, wherein the amount per said biologically contained influenza virus isolate in the vaccine is 0.1 to 200 micrograms of influenza virus hemagglutinin;
wherein the mutant PB2 viral segment includes 5′ and 3′ incorporation sequences including 3′ or 5′ coding and non-coding incorporation sequences flanking a heterologous nucleotide sequence comprising a therapeutic or prophylactic gene and does not include contiguous sequences corresponding to sequences encoding a functional PB2, and wherein the heterologous nucleotide sequence encodes a heterologous protein that with the influenza virus HA encoded by the HA viral segment provides for the multivalency.
2. The vaccine of claim 1 wherein the heterologous protein comprises an influenza virus HA protein or an influenza NA protein from a different strain than the HA encoded by the HA viral segment or the NA encoded by the NA viral segment.
3. The vaccine of claim 1 , wherein the heterologous protein comprises a protein of a bacterium, yeast, fungus, or a virus that is not an influenza virus.
4. The vaccine of claim 1 wherein the heterologous protein comprises a cancer associated antigen.
5. The vaccine of claim 1 , wherein the heterologous nucleotide sequence is flanked by about 3 to about 400 nucleotides of the 5′ and/or 3′ PB2 coding region adjacent to non-coding sequence.
6. A vaccine comprising an effective amount of an isolated stable, biologically contained multivalent influenza virus comprising: i) 8 different segments including a PA viral segment, a PB1 viral segment, a mutant PB2 viral segment, a HA viral segment, a NA viral segment, a NP viral segment, a M (M1 and M2) viral segment, and a NS (NS1 and NS2) viral segment, ii) 8 different segments including a PA viral segment, a PB1 viral segment, a mutant PB2 viral segment, a HA viral segment, a NA (NA and NB) viral segment, a NP viral segment, a M (M1 and BM2) viral segment and a NS (NS1 and NS2) viral segment, or iii) 7 different segments including a PA viral segment, a PB1 viral segment, a mutant PB2 viral segment, a HEF viral segment, a NP viral segment, a M (M1 and CM2) viral segment, and a NS (NS1 and NS2) viral segment, wherein the amount per said biologically contained influenza virus isolate in the vaccine is 0.1 to 200 micrograms of influenza virus hemagglutinin;
wherein the mutant PB2 viral segment includes 5′ and 3′ incorporation sequences including 3′ or 5′ coding and non-coding incorporation sequences flanking a heterologous nucleotide sequence and does not include contiguous sequences corresponding to sequences encoding a functional PB2, and wherein the heterologous nucleotide sequence encodes a heterologous protein that with the influenza virus HA encoded by the HA viral segment provides for the multivalency, wherein the segments for HA and NA are from a different isolate than the PA, PB1, PB2, NP, NS, and M segments.
7. A method to immunize a vertebrate, comprising: contacting the vertebrate with the vaccine of claim 1 .
8. The method of claim 7 wherein the vertebrate is an avian or a mammal.
9. A method to prepare a biologically contained, multivalent 8 segment influenza A or B virus, comprising contacting a host cell with one or more vectors which include transcription cassettes for vRNA production and transcription cassettes for mRNA production, wherein the transcription cassettes for vRNA production are a transcription cassette comprising a Poll promoter operably linked to an influenza virus PA DNA in an orientation for vRNA production linked to a Poll transcription termination sequence, a transcription cassette comprising a Poll promoter operably linked to an influenza virus PB1 DNA in an orientation for vRNA production linked to a Poll transcription termination sequence, a transcription cassette comprising a Poll promoter operably linked to a mutant influenza virus PB2 DNA in an orientation for vRNA production linked to a Poll transcription termination sequence, a transcription cassette comprising a Poll promoter operably linked to an influenza virus HA DNA in an orientation for vRNA production linked to a Poll transcription termination sequence, a transcription cassette comprising a Poll promoter operably linked to an influenza virus NA DNA in an orientation for vRNA production linked to a Poll transcription termination sequence, a transcription cassette comprising a Poll promoter operably linked to an influenza virus NP DNA in an orientation for vRNA production linked to a Poll transcription termination sequence, a transcription cassette comprising a Poll promoter operably linked to an influenza virus M DNA in an orientation for vRNA production linked to a Poll transcription termination sequence, and a transcription cassette comprising a Poll promoter operably linked to an influenza virus NS (NS1 and NS2) DNA in an orientation for vRNA production linked to a Poll transcription termination sequence, wherein the mutant PB2 DNA includes 5′ and 3′ incorporation sequences including 3′ or 5′ coding and non-coding incorporation sequences flanking a heterologous nucleotide sequence comprising a therapeutic or prophylactic gene and does not include contiguous sequences corresponding to sequences that encode a functional PB2, and wherein the heterologous nucleotide sequence encodes a heterologous protein; and wherein the transcription cassettes for mRNA production are a transcription cassette comprising a Poll promoter operably linked to a DNA coding region for influenza virus PA linked to a Poll transcription termination sequence, a transcription cassette comprising a Poll promoter operably linked to a DNA coding region for influenza virus PB1 linked to a Poll transcription termination sequence, and a transcription cassette comprising a Poll promoter operably linked to a DNA coding region for influenza virus NP linked to a Poll transcription termination sequence, wherein the genome of host cell is stably augmented with a transcription cassette comprising a Poll promoter operably linked to a DNA coding region for influenza virus PB2 linked to a Poll transcription termination sequence, and wherein the host cell does not comprise sequences corresponding to PB2 coding sequences for vRNA production of a wild-type PB2 segment; and isolating the biologically contained virus from the host cell, and wherein the heterologous nucleotide sequence encodes a heterologous protein that with influenza virus HA encoded by the HA vRNA provides for the multivalency.
10. The method of claim 9 wherein the heterologous protein comprises an influenza virus HA protein or an influenza NA protein from a different strain than the HA encoded by the HA viral segment or the NA encoded by the NA viral segment.
11. The method of claim 9 wherein the heterologous protein comprises a protein of a bacterium, yeast, fungus, or a virus that is not an influenza virus, or comprises a cancer associated antigen.
12. The method of claim 8 wherein the HA is a type A HA.
13. The method of claim 8 wherein the cell is a 293 cell, a 293T cell, a DF-1 cell, a A549 cell, a Vero cell or a MDCK cell.
14. A method to prepare a biologically contained, multivalent 8 segment influenza A or B virus, comprising contacting a host cell with one or more vectors which include transcription cassettes for vRNA production and transcription cassettes for mRNA production, wherein the transcription cassettes for vRNA production are a transcription cassette comprising a Poll promoter operably linked to an influenza virus PA DNA in an orientation for vRNA production linked to a Poll transcription termination sequence, a transcription cassette comprising a Poll promoter operably linked to an influenza virus PB1 DNA in an orientation for vRNA production linked to a Poll transcription termination sequence, a transcription cassette comprising a Poll promoter operably linked to a mutant influenza virus PB2 DNA in an orientation for vRNA production linked to a Poll transcription termination sequence, a transcription cassette comprising a Poll promoter operably linked to an influenza virus HA DNA in an orientation for vRNA production linked to a Poll transcription termination sequence, a transcription cassette comprising a Poll promoter operably linked to an influenza virus NA DNA in an orientation for vRNA production linked to a Poll transcription termination sequence, a transcription cassette comprising a Poll promoter operably linked to an influenza virus NP DNA in an orientation for vRNA production linked to a Poll transcription termination sequence, a transcription cassette comprising a Poll promoter operably linked to an influenza virus M DNA in an orientation for vRNA production linked to a Poll transcription termination sequence, and a transcription cassette comprising a Poll promoter operably linked to an influenza virus NS (NS1 and NS2) DNA in an orientation for vRNA production linked to a Poll transcription termination sequence, wherein the mutant PB2 DNA includes 5′ and 3′ incorporation sequences including 3′ or 5′ coding and non-coding incorporation sequences flanking a heterologous nucleotide sequence and does not include contiguous sequences corresponding to sequences that encode a functional PB2, and wherein the heterologous nucleotide sequence encodes a heterologous protein; and wherein the transcription cassettes for mRNA production are a transcription cassette comprising a Poll promoter operably linked to a DNA coding region for influenza virus PA linked to a Poll transcription termination sequence, a transcription cassette comprising a Poll promoter operably linked to a DNA coding region for influenza virus PB1 linked to a Poll transcription termination sequence, and a transcription cassette comprising a Poll promoter operably linked to a DNA coding region for influenza virus NP linked to a Poll transcription termination sequence, wherein the genome of host cell is stably augmented with a transcription cassette comprising a Poll promoter operably linked to a DNA coding region for influenza virus PB2 linked to a Poll transcription termination sequence, and wherein the host cell does not comprise sequences corresponding to PB2 coding sequences for vRNA production of a wild-type PB2 segment; and isolating the biologically contained virus from the host cell, wherein the cell is contacted with the vector for mRNA production of PB2 before the other vectors, and wherein the heterologous nucleotide sequence encodes a heterologous protein that with influenza virus HA encoded by the HA vRNA provides for the multivalency.
15. The method of claim 14 wherein the heterologous protein comprises an influenza virus HA protein or an influenza NA protein from a different strain than the HA encoded by the HA viral segment or the NA encoded by the NA viral segment.
16. The method of claim 14 wherein the heterologous protein comprises a protein of a bacterium, yeast, fungus, or a virus that is not an influenza virus, or comprises a cancer associated antigen.
17. The method of claim 14 wherein the heterologous protein is a glycoprotein.
18. The method of claim 14 wherein the HA is a type A HA.
19. The method of claim 14 wherein the biologically contained virus is a 6:2 reassortant.
20. The method of claim 14 wherein the cell is a 293 cell, a 293T cell, a DF-1 cell, a A549 cell, a Vero cell or a MDCK cell.