Influenza viruses with mutant PB2 gene 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 method to prepare a biologically contained 8 segment influenza A or B virus, comprising contacting a host cell with one or more vectors which include transcription cassettes for RNA production, wherein the transcription cassettes comprise a transcription cassette comprising a PolI promoter operably linked to an influenza virus PA DNA linked to a PolI transcription termination sequence, a transcription cassette comprising a PolI promoter operably linked to an influenza virus PB1 DNA linked to a PolI transcription termination sequence, a transcription cassette comprising a PolI promoter operably linked to a mutant influenza virus PB2 DNA linked to a PolI transcription termination sequence, a transcription cassette comprising a PolI promoter operably linked to an influenza virus HA DNA linked to a PolI transcription termination sequence, a transcription cassette comprising a PolI promoter operably linked to an influenza virus NA DNA linked to a PolI transcription termination sequence, a transcription cassette comprising a PolI promoter operably linked to an influenza virus NP DNA linked to a PolI transcription termination sequence, a transcription cassette comprising a PolI promoter operably linked to an influenza virus M DNA linked to a PolI transcription termination sequence, a transcription cassette comprising a PolI promoter operably linked to an influenza virus NS (NS1 and NS2) DNA linked to a PolI transcription termination sequence, a transcription cassette comprising a PolII promoter operably linked to a DNA coding region for influenza virus PA linked to a PolII transcription termination sequence, a transcription cassette comprising a PolII promoter operably linked to a DNA coding region for influenza virus PB1 linked to a PolII transcription termination sequence, and a transcription cassette comprising a PolII promoter operably linked to a DNA coding region for influenza virus NP linked to a Porn 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, wherein the genome of host cell is stably augmented with a transcription cassette comprising a PolII promoter operably linked to a DNA coding region for influenza virus PB2 linked to a PolII transcription termination sequence, and wherein the host cell does not comprise sequences corresponding to a wild-type PB2 viral segment; and isolating the biologically contained virus from the host cell.
2. The method of claim 1 wherein the HA is an influenza A virus HA and the heterologous nucleotide sequence encodes a protein of a bacterium, yeast, fungus, or a virus that is not an influenza virus.
3. The method of claim 1 wherein the HA is an influenza A virus HA and the heterologous nucleotide sequence encodes a cancer associated antigen.
4. The method of claim 1 wherein the HA viral segment encodes one of subtypes H1 to H16.
5. A method to prepare a biologically contained 8 segment influenza A or B virus, comprising contacting a host cell with one or more vectors which include transcription cassettes for RNA production, wherein the transcription cassettes include a transcription cassette comprising a PolI promoter operably linked to an influenza virus PA DNA linked to a PolI transcription termination sequence, a transcription cassette comprising a PolI promoter operably linked to an influenza virus PB1 DNA linked to a PolI transcription termination sequence, a transcription cassette comprising a PolI promoter operably linked to a mutant influenza virus PB2 DNA linked to a PolI transcription termination sequence, a transcription cassette comprising a PolI promoter operably linked to an influenza virus HA DNA linked to a PolI transcription termination sequence, a transcription cassette comprising a PolI promoter operably linked to an influenza virus NA DNA linked to a PolI transcription termination sequence, a transcription cassette comprising a PolI promoter operably linked to an influenza virus NP DNA linked to a PolI transcription termination sequence, a transcription cassette comprising a PolI promoter operably linked to an influenza virus M DNA linked to a PolI transcription termination sequence, a transcription cassette comprising a PolI promoter operably linked to an influenza virus NS (NS1 and NS2) DNA linked to a PolI transcription termination sequence, a transcription cassette comprising a PolI promoter operably linked to a DNA coding region for influenza virus PA linked to a PolII transcription termination sequence, a transcription cassette comprising a PolII promoter operably linked to a DNA coding region for influenza virus PB1 linked to a Porn transcription termination sequence, and a transcription cassette comprising a PolII promoter operably linked to a DNA coding region for influenza virus NP linked to a PolII transcription termination sequence, wherein the genome of host cell is stably augmented with a transcription cassette comprising a PolII promoter operably linked to a DNA coding region for influenza virus PB2 linked to a PolII transcription termination sequence, wherein the host cell does not comprise sequences corresponding to a wild-type PB2 viral segment; and isolating the biologically contained virus from the host cell, wherein the cell is contacted with the vector for production of PB2 before the other vectors, 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.
6. The method of claim 5 wherein the viral segments for HA and NA are from a different isolate that the PA, PB1, PB2, NP, NS, and M viral segments.
7. The method of claim 5 wherein the cell is a 293 cell, a 293T cell, a DF-1 cell, a A549 cell, a Vero cell or a MDCK cell.
8. The method of claim 5 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.
9. The method of claim 5 wherein the HA is an influenza A virus HA and the heterologous nucleotide sequence encodes a glycoprotein.
10. The method of claim 5 wherein the HA is an influenza B virus HA and the heterologous nucleotide sequence encodes a glycoprotein.
11. The method of claim 1 wherein the cell is a 293 cell, a 293T cell, a DF-1 cell, a A549 cell, a Vero cell or a MDCK cell.
12. The method of claim 1 wherein the HA is an influenza B virus HA and the heterologous nucleotide sequence encodes a protein of a bacterium, yeast, fungus, or a virus that is not an influenza virus.
13. The method of claim 1 wherein the HA is an influenza B virus HA and the heterologous nucleotide sequence encodes a cancer associated antigen.