AU2014202470A1 - High titer recombinant influenza viruses for vaccines - Google Patents

Abstract

Abstract The invention provides a composition useful to prepare high titer influenza viruses, e.g., in the absence of helper virus, which includes at least five internal genes 5 from an influenza virus isolate that replicates to high titers in embryonated chicken eggs or MDCK cells. <filename>

Description

1 HIGH TITER RECOMBINANT INFLUENZA VIRUSES FOR VACCINES Cross-Reference to Related Applications The present application is a divisional application from Australian patent application number 2012204138, which is in turn a divisional application from Australia patent application number 2007245192, the entire disclosures of which are incorporated herein by reference. Government Support This invention was made with government support under Grant Number A1044386 from the National Institutes of Health. The United States Government has certain rights in the invention. Background Negative-sense RNA viruses are classified into seven families (Rhabdoviridae, Paramyxoviridae, Filoviridae, Bornaviridae, Orthomyxoviridae, Bunyaviridae, and Arenaviridae) which include common human pathogens, such as respiratory syncytial virus, influenza virus, measles virus, and Ebola virus, as well as animal viruses with major economic 5 impact on the poultry and cattle industries (e.g., Newcastle disease virus and Rinderpest virus). The first four families are characterized by nonsegmented genomes, while the latter three have genomes comprised of six-to-eight, three, or two negative-sense RNA segments, respectively. The common feature of negative-sense RNA viruses is the negative polarity of their RNA genome; i.e., the viral RNA (vRNA) is complementary to mRNA and therefore is 10 not infectious by itself. In order to initiate viral transcription and replication, the vRNA has to be transcribed into a plus-sense mRNA or cRNA, respectively, by the viral polymerase complex and the nucleoprotein; for influenza A viruses, the viral polymerase complex is comprised of the three polymerase proteins PB2, PB 1, and PA. During viral replication, cRNA serves as a template for the synthesis of new vRNA molecules. For all negative-stranded RNA 15 viruses, non-coding regions at both the 5' and 3' termini of the vRNA and cRNA are critical for transcription and replication of the viral genome. Unlike cellular or viral mRNA transcripts, both cRNA and vRNA are neither capped at the 5' end nor polyadenylated at the very 3' end. C:\poi\word\SPEC-948705.docx WO 2007/126810 PCT/US2007/007562 2 The basic functions of many viral proteins have been elucidated biochemically and/or in the context of viral infection. However, reverse genetics systems have dramatically increased our knowledge of negative-stranded segmented and non-segmented RNA viruses with respect to their viral 5 replication and pathogenicity, as well as to the development of live attenuated virus vaccines. Reverse genetics, as the term is used in molecular virology, is defined as the generation of virus possessing a genome derived from cloned cDNAs (for a review, see Neumann et al., 2002). In order to initiate viral replication of negative-stranded RNA viruses, 10 vRNA(s) or cRNA(s) must be coexpressed with the polymerase complex and the nucleoprotein. Rabies virus was the first non-segmented negative-sense RNA virus which was generated entirely from cloned cDNA: Schnell et al. (1994) generated recombinant rabies virus by cotransfection of a cDNA construct encoding the full-length cRNA and protein expression constructs for the L, P, 15 and N proteins, all under control of the T7 RNA polymerase promoter. Infection with recombinant vaccinia virus, which provided T7 RNA polymerase, resulted in the generation of infectious rabies virus. In this T7 polymerase system, the primary transcription of the full length cRNA under control of the T7 RNA polymerase resulted in a non-capped cRNA. transcript. However, three guanidine 20 nucleotides, which form the optimal initiation sequence for T7 RNA polymerase, were attached to the 5' end. In order to create an authentic 3' end of the cRNA transcript which is essential for a productive infective cycle, the hepatitis delta ribozyme (HDVRz) sequence was used for exact autocatalytic cleavage at the 3' end of the cRNA transcript. 25 Since the initial report by Schnell et al. (1994), reverse genetics systems using similar techniques led to the generation of many non-segmented negative strand RNA viruses (Conzelmann, 1996; Conzelmann, 1998; Conzelmann et al., 1996; Marriott et al., 1999; Munoz et al., 2000; Nagai, 1999; Neumann et al., 2002; Roberts et al., 1998; Rose, 1996). Refinements of the original rescue 30 procedure included the expression of T7 RNA polymerase from stably transfected cell lines (Radecke et al., 1996) or from protein expression plasmids (Lawson et al., 1995), or heat shock procedures to increase rescue efficiencies (Parks et al., 1999). Based on the T7 polymerase system, Bridgen and Elliott (1996) created Bunyamwera virus (family Bunyaviridae) from cloned cDNAs WO 2007/126810 PCT/US2007/007562 3 and demonstrated the feasibility of artificially generating a segmented negative sense RNA virus by the T7 polymerase system. In 1999, a plasmid-based reverse genetics technique was generated based on the cellular RNA polymerase I for the generation of segmented influenza A 5 virus entirely from cloned cDNAs (Fodor et al., 1999; Neumann and Kawaoka, 1999). RNA polymerase I, a nucleolar enyme, synthesizes ribosomal ANA which, like influenza virus RNA, does not contain 5' cap or 3' polyA structures. The RNA polymerase I transcription of a construct containing an influenza viral cDNA, flanked by RNA polymerase I promoter and terminator sequences, 10 resulted in influenza vRNA synthesis (Fodor et al., 1999; Neumann and Kawaoka, 1999; Neumann and Kawaoka, 2001; Pekosz et al., 1999). The system was highly efficient, producing more than 108 infectious virus particles per ml of supernatant of plasmid-transfected cells 48 hours post-transfection. What is needed is a method to prepare high titer orthomyxoviruses such 15 as influenza A virus, entirely from cloned cDNAs. Summary of the Invention The invention provides a composition comprising a plurality of influenza virus vectors of the invention, e.g., those useful to prepare reassortant viruses 20 including 7:1 reassortants, 6:1:1 reassortants, 5:1:2 reassortants, and 5:1:1:1 reassortants. In one embodiment of the invention, the composition includes vectors for vRNA production selected from a vector comprising a promoter operably linked to an influenza virus PA cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an 25 influenza virus PB I cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus PB2 cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus HA cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an 30 influenza virus NP cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus NA cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus M cDNA linked to a transcription termination sequence, and a vector comprising a operably linked to an influenza WO 2007/126810 PCT/U S2007/UU7562 4 virus NS cDNA linked to a transcription termination sequence. The composition also includes vectors for viral protein production selected from a vector encoding influenza virus PA, a vector encoding influenza virus PB 1, a vector encoding influenza virus PB2, and a vector encoding influenza virus NP, and optionally 5 one or more vectors encoding NP, NS, M, e.g., M1 and M2, HA or NA. Preferably, the vectors encoding viral proteins further comprise a transcription termination sequence. In one embodiment, the cDNAs for PB1, PB2, PA, NP, M, and NS, and optionally NA, have sequences for PBI, PB2, PA, NP, M, and NS, and 10 optionally NA, from an influenza virus that replicates to high titers in embryonated eggs, and the cDNA for HA has sequences from a different strain of influenza virus (from a heterologous influenza virus isolate with the same or a different HA subtype, i.e., a heterologous HA). For HA from pathogenic H5N1 viruses which do not grow to high titers in embryonated eggs, the cDNA for at 15 least NA has sequences from a NI influenza virus that replicates to high titers in embryonated eggs. In one embodiment, the cDNAs for PB1, PB2, PA, NP, M, and NS include a nucleic acid molecule corresponding to a sequence (polynucleotide) encoding at least one of the proteins of a high titer, e.g., titers greater than 108 20 EID 5 o/mL, e.g., 109 EIDo/mL, 1010 EID5o/mL, or more, influenza virus. Reassortants within the scope of the invention that have high titers in embyronated eggs have titers of at least about 109 EID 5 o/mL for 5:1:1:1 reassorants (with NS K55), 5:1:2 reassortants (with NS K55) and 6:1:1 reassortants (with NS K55) and at least 4 x 108 PFU/mL for 5:1:1:1 reassortants 25 (with NS K55E) or 5:1:2 reassortants (with NS K55E). Reassortants within the scope of the invention that have high titers in MDCK cells have titers of at least 0.75 x 10 8 PFU/mL, e.g., at least 2.0 x 108 PFU/mL, for 5:1:1:1 or 6:1:1. In one embodiment, the invention includes a composition comprising a plurality of influenza virus vectors for a 5:1:2 or a 6:1:1 reassortant. The 30 composition includes a vector comprising a promoter operably linked to an influenza virus PA cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus PB1 cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus PB2 cDNA linked to a transcription WO 2007/126810 PCT/US2007/007562 5 termination sequence, a vector comprising a promoter operably linked to an influenza virus HA cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus NP cDNA linked to a transcription termination sequence, a vector comprising a promoter 5 operably linked to an influenza virus NA cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus M cDNA linked to a transcription termination sequence, and a vector comprising a promoter operably linked to an influenza virus NS cDNA linked to a transcription termination sequence. The cDNAs for PB1, PB2, PA, 10 NP, and M have sequences that are from one or more influenza viruses that replicate to high titers in embryonated eggs, wherein the cDNA for NS is from the one or more influenza viruses that replicate to high titers in embryonated eggs, and the cDNA for NA is from the one or more influenza viruses that replicate to high titers in embryonated eggs or has sequences for a heterologous 15 NA. The cDNA for HA has sequences for a heterologous HA, which is heterologous to at least the viral gene segments for PB1, PB2, PA, NP, and M. In one embodiment, the cDNA for NS has a Glu at position 55. The composition also includes a vector comprising a promoter operably linked to a DNA segment encoding influenza virus PA, a vector comprising a promoter operably linked to 20 a DNA segment encoding influenza virus PB1, a vector comprising a promoter operably linked to a DNA segment encoding influenza virus PB2, and a vector comprising a promoter operably linked.to a DNA segment encoding influenza virus NP, and optionally a vector comprising a promoter operably linked to a DNA segment encoding influenza virus HA, a vector comprising a promoter 25 operably linked to a DNA segment encoding influenza virus NA, a vector comprising a promoter operably linked to a DNA segment encoding influenza virus MI, a vector comprising a promoter operably linked to a DNA segment encoding influenza virus M2, or a vector comprising a promoter operably linked to a DNA segment encoding influenza virus NS2. In one embodiment, the 30 cDNAs for PB1, PB2, PA, NP, M, and NS include a nucleic acid molecule corresponding to a sequence (polynucleotide) encoding at least one of the proteins of a high titer, e.g., titers greater than 108 EID 50 /mL, e.g., 109 EIDso/mL, 1010 EIDso/mL, or more, influenza virus.

WO 2007/126810 PCT/US2007/007562 6 In one embodiment, a composition comprising a plurality of influenza virus vectors for a 5:1:1:1 or 6:1:1 reassortant. The composition includes comprising a vector comprising a promoter operably linked to an influenza virus PA cDNA linked to a transcription termination sequence, a vector comprising a 5 promoter operably linked to an influenza virus PB11 cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus PB2 cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus HA cDNA linked to a transcription termination sequence, a vector comprising a 10 promoter operably linked to an influenza virus NP cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus NA cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus M cDNA linked to a transcription termination sequence, and a vector comprising 15 a promoter operably linked to an influenza virus NS cDNA linked to a transcription termination sequence. The cDNAs for PB1, PB2, PA, NP, and M have sequences from one or more influenza viruses that replicate to high titers in MDCK cells, wherein the cDNA for NS is from the one or more influenza viruses that replicate to high titers in MDCK cells, wherein the cDNA for NA 20 may have sequences for a heterologous NA, and wherein the cDNA for HA has sequences for a heterologous HA. The composition also includes a vector comprising a promoter operably linked to a DNA segment encoding influenza virus PA, a vector comprising a promoter operably linked to a DNA segment encoding influenza virus PB1, a vector comprising a promoter operably linked to 25 a DNA segment encoding influenza virus P132, and a vector comprising a promoter operably linked to a DNA segment encoding influenza virus NP, and optionally a vector comprising a promoter operably linked to a DNA segment encoding influenza virus HA, a vector comprising a promoter operably linked to a DNA segment encoding influenza virus NA, a vector comprising a promoter 30 operably linked to a DNA segment encoding influenza virus M1, a vector comprising a promoter operably linked to a DNA segment encoding influenza virus M2, or a vector comprising a promoter operably linked to a DNA segment encoding influenza virus NS2. In one embodiment, the cDNAs for PBl, PB2, PA, NP, M, and NS include a nucleic acid molecule corresponding to a sequence WO 2007/126810 PCT/US2007/007562 7 (polynucleotide) encoding at least one of the proteins of a high titer, e.g., titers greater than 108 EID/o/mL, e.g., 109 EIDso/mL, 10'0 EID 50 /mL, or more, influenza virus. As described herein, recombinant (6:2 reassortant) viruses grow less well 5 in eggs than does the wild-type PR8 strain, even though they possess the same PR8 "internal" genes (i.e., those other than the HA and NA). Since vigorous growth in eggs is an essential property of vaccine seed viruses used in the production of inactivated vaccines, H5N1 vaccine candidates were generated that grow as well as the PR8 donor strain in eggs. It was found that HA-NA 10 balance and PB1 function are important growth determinants. With this knowledge, a series of H5N1 viruses was produced with altered HA-NA combinations, with the PR8 background, to assess their growth in eggs against more conventional 6:2 reassortants, including the WHO-recommended NIBRG 14 virus. A 7:1 reassortant virus and one of the 6:2 reassortants showed 15 enhanced growth in eggs. Thus, for vaccine viruses that generally produce low titers in eggs, replacement of at least the NA of the vaccine virus with the NA of an influenza virus that grows well in eggs, or replacement of all but the HA and NA, or all but the HA, of the vaccine virus, with the other viral gene segments from an influenza virus that grows to high titers in eggs, can result in 20 significantly higher viral titers. The titers of the reassortant viruses of the invention may be 2-fold, 3-fold, or greater, e.g., 7-fold or greater, than the corresponding nonreassortant vaccine virus. As also described herein, the internal genes responsible for the high growth rate of reassortants in eggs having genes from two different PR8 virus isolates was determined. The highest viral 25 titers were those where the majority of internal genes were from PR8HG (PR8(UW)). In particular, 5:1:2 reassortants (PRS(UW) PB1, PB2, PA, NP and M; PR8(Cam) NS; and H5N1 HA and NA) and 6:1:1 reassortants (PR8(UW) NA, PB1, PB2, PA, NP and M; PR8(Cam) NS; and H5 HA) had high titers in eggs. 30 As also described herein, the viral genes responsible for a high growth rate in MDCK cells, cells likely to be approved as a source of vaccine virus, was assessed. The highest growth rate in MDCK cells was found with PB2 from PR8(UW), NS from PR8(Cam) or NS K55E from PR8(UW), and a NA with a long stalk, e.g., a stalk greater than 20 mino acids but less than about 100 amino WO 2007/126810 PCT/US2007/007562 8 acids, e.g., greater than about 40 and up to about 80 amino acids in length. Thus 5:1:1:1 and 6:1:1 reassortants with PR8(UW) PA, PB1, PB2, NP and M, and NS K55E from PR8(UW) or PR8(Cam), NA from PR8(UW) or a heterologous NA source, and a heterologous HA, grew to the highest titers in MDCK cells. 5 In one embodiment, the nucleic acid molecule corresponds to a sequence encoding PB1, PB2, PA, NP, M, and NS, and optionally NA, having substantially the same activity as a corresponding polypeptide encoded by one of SEQ ID NOs:1-6 or 8. As used herein, "substantially the same activity" includes an activity that is about 0.1%, 1%, 10%, 30%, 50%, 90%, e.g., up to 100% or 10 more, or detectable protein level that is about 80%, 90% or more, the activity or protein level, respectively, of the corresponding full-length polypeptide. In one embodiment, the nucleic acid molecule corresponds to a sequence encoding a polypeptide which is substantially the same as, e.g., having at least 80%, e.g., 90%, 92%, 95%, 97% or 99%, contiguous amino acid sequence identity to, a 15 polypeptide encoded by one of SEQ ID NOs:1-6 or 8. In one embodiment, the isolated and/or purified nucleic acid molecule comprises a nucleotide sequence which is substantially the same as, e.g., having at least 50%, e.g., 60%, 70%, 80% or 90% or more contiguous nucleic acid sequence identity to, one of SEQ ID NOs: 1-6, 8, or 33 to 38 and, in one embodiment, also encodes a polypeptide 20 having at least 80%, e.g., 90%, 92%, 95%, 97% or 99%, contiguous amino acid sequence identity to a polypeptide encoded by one of SEQ ID NOs:1-6, 8, or 33 to 38. In one embodiment, the isolated and/or purified nucleic acid molecule encodes a polypeptide with one or more, for instance, 2, 5, 10, 15, 20 or more, conservative amino acids substitutions, e.g., conservative substitutions of up to 25 10% or 20% of the residues, relative to a polypeptide encoded by one of SEQ ID NOs:1-6 or 8. Conservative amino acid substitutions refer to the interchangeability of residues having similar side chains. For example, a group of amino acids having aliphatic side chains is glycine, alanine, valine, leucine, and isoleucine; a group of amino acids having aliphatic-hydroxyl side chains is 30 serine and threonine; a group of amino acids having amide-containing side chains is asparagine and glutamine; a group of amino acids having aromatic side chains is phenylalanine, tyrosine and tryptophan; a group of amino acids having basic side chains is lysine, arginine and histidine; and a group of amino acids having sulfur-containing side chain is cysteine and methionine. In one WO 2007/126810 PCT/US2007/007562 9 embodiment, conservative amino acid substitution groups are: valine-leucine isoleucine; phenylalanine-tyrosine; lysine-arginine; alanine-valine; glutamic aspartic; and asparagine-glutamine. In one embodiment, the isolated and/or purified nucleic acid molecule encodes a polypeptide with one or more, for 5 instance, 2, 3 or 4, nonconservative amino acid substitutions, relative to a polypeptide encoded by one of SEQ ID NOs:1-6 or 33-38. For instance, a K55E NS and a S360Y PB2 substitution are nonconservative substitutions. In another embodiment, the nucleic acid molecule having PB1, PB2, PA, NP, M, and NS, and optionally NA, sequences, or the complement thereof, 10 hybridizes to one of SEQ ID NOs:1-6, 8, or 33 to 38, the complement thereof, under low stringency, moderate stringency or stringent conditions. For example, the following conditions may be employed: 7% sodium dodecyl sulfate (SDS), 0.5 M NaPO 4 , 1 mM EDTA at 50*C with washing in 2X SSC, 0.1% SDS at 50*C (low stringency), more desirably in 7% sodium dodecyl sulfate (SDS), 0.5 15 M NaPO 4 , 1 mM EDTA at 50*C with washing in IX SSC, 0.1% SDS at 50*C (moderate stringency), more desirably still in 7% sodium dodecyl sulfate (SDS), 0.5 M NaPO 4 , 1 mM EDTA at 50*C with washing in 0.5X SSC, 0.1% SDS at 50*C (stringent), preferably in 7% sodium dodecyl sulfate (SDS), 0.5 M NaPO 4 , 1 mM EDTA at 50*C with washing in 0.1X SSC, 0.1% SDS at 50*C (more 20 stringent), more preferably in 7% sodium dodecyl sulfate (SDS), 0.5 M NaPO 4 , 1 mM EDTA at 50*C with washing in 0.1X SSC, 0.1% SDS at 650C (very stringent). In one embodiment, the nucleic acid molecule encodes a polypeptide which is substantially the same as, e.g., having at least 50%, e.g., 60%, 70%, 80% or 90% or more contiguous nucleic acid sequence identity to, one of SEQ 25 ID NOs: 1-6, or 33 to 38, and preferably has substantially the same activity as a corresponding full-length polypeptide encoded by one of SEQ ID NOs: 1-6, 8 or 33 to 28. Those nucleic acid molecules, or nucleic acid molecules from other NI strains that grow well in eggs, may be employed with nucleic acid for any HA, e.g., H5. 30 Thus, nucleic acid molecule may be employed to express influenza proteins, to prepare chimeric genes, e.g., with other viral genes including other influenza virus genes, and/or to prepare recombinant virus. Thus, the invention WO 2007/126810 PCT/US2007/007562 10 also provides isolated polypeptides, recombinant virus, and host cells contacted with the nucleic acid molecules or recombinant virus of the invention. The invention also provides a plurality of the following isolated and/or purified vectors: a vector comprising a promoter operably linked to an influenza 5 virus PA cDNA linked to a transcription termination sequence, a vector . comprising a promoter operably linked to an influenza virus PBI cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus PB2 cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus 10 HA cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus NP cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus NA cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus 15 M cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus NS cDNA linked to a transcription termination sequence, wherein at least one vector comprises sequences corresponding to those encoding PB I, PB2, PA, NP, M, NS, and optionally NA, or a portion thereof, having substantially the same activity as a 20 corresponding polypeptide encoded by one of SEQ ID NOs:1-6 or 8, e.g., a sequence encoding a polypeptide with at least 80% amino acid identity to a polypeptide encoded by one of SEQ ID NOs:1-6, 8 or 33 to 38. Optionally, two vectors may be employed in place of the vector comprising a promoter operably linked to an influenza virus M cDNA linked to a transcription termination 25 sequence, e.g., a vector comprising a promoter operably linked to an influenza virus Ml cDNA linked to a transcription termination sequence and a vector comprising a promoter operably linked to an influenza virus M2 cDNA linked to a transcription termination sequence. The invention includes the use of isolated and purified vectors or 30 plasmids, which express or encode influenza virus proteins, or express or encode influenza vRNA, both native and recombinant vRNA. Preferably, the vectors comprise influenza cDNA, e.g., influenza A (e.g., any influenza A gene including any of the 15 HA or 9 NA subtypes), B or C DNA (see Chapters 45 and 46 of Fields Virology (Fields et al. (eds.), Lippincott-Raven Publ., WO 2007/126810 PCT/US2007/007562 11 Philadelphia, PA (1996), which are specifically incorporated by reference herein), although it is envisioned that the gene(s) of any organism may be employed in the vectors or methods of the invention. The cDNA may be in the sense or antisense orientation relative to the promoter. Thus, a vector of the 5 invention may encode an influenza virus protein (sense) or vRNA (antisense). Any suitable promoter or transcription termination sequence may be employed to express a protein or peptide, e.g., a viral protein or peptide, a protein or peptide of a nonviral pathogen, or a therapeutic protein or peptide. A composition of the invention may also comprise a gene or open 10 reading frame of interest, e.g., a foreign gene encoding an immunogenic peptide or protein useful as a vaccine. Thus, another embodiment of the invention comprises a composition of the invention as described above in which one of the vectors is replaced with, or the composition further comprises, a vector comprising a promoter linked to 5' influenza virus sequences optionally 15 including 5' influenza virus coding sequences or a portion thereof, linked to a desired nucleic acid sequence, e.g., a desired cDNA, linked to 3' influenza virus sequences optionally including 3' influenza virus coding sequences or a portion thereof, linked to a transcription termination sequence. Preferably, the desired nucleic acid sequence such as a cDNA is in an antisense orientation. The 20 introduction of such a composition to a host cell permissive for influenza virus replication results in recombinant virus comprising vRNA corresponding to sequences of the vector. The promoter in such a vector for vRNA production may be a RNA polymerase I promoter, a RNA polymerase II promoter, a RNA polymerase III promoter, a T7 promoter, and a T3 promoter, and optionally the 25 vector comprises a transcription termination sequence such as a RNA polymerase I transcription termination sequence, a RNA polymerase II transcription termination sequence, a RNA polymerase III transcription termination sequence, or a ribozyme. In one embodiment, the vector comprising the desired nucleic acid sequence comprises a cDNA of interest. The cDNA of 30 interest, whether in a vector for vRNA or protein production, may encode an immunogenic epitope, such as an epitope useful in a cancer therapy or vaccine, or a peptide or polypeptide useful in gene therapy. When preparing virus, the vector or plasmid comprising the gene or cDNA of interest may substitute for a WO 2007/126810 PCT/US2007/007562 12 vector or plasmid for an influenza viral gene or may be in addition to vectors or plasmids for all influenza viral genes. A plurality of the vectors of the invention may be physically linked or each vector may be present on an individual plasmid or other, e.g., linear, 5 nucleic acid delivery vehicle. The promoter or transcription termination sequence in a vRNA or virus protein expression vector may be the same or different relative to the promoter or any other vector. Preferably, the vector or plasmid which expresses influenza vRNA comprises a promoter suitable for expression in at least one particular 10 host cell, e.g., avian or mammalian host cells such as canine, feline, equine, bovine, ovine, or primate cells including human cells, or preferably, for expression in more than one host. In one embodiment, one or more vectors for vRNA production comprise a promoter including, but not limited to, a RNA polymerase I promoter, e.g., a 15 human RNA polymerase I promoter, a RNA polymerase II promoter, a RNA polymerase III promoter, a T7 promoter, or a T3 promoter. Preferred transcription termination sequences for the vRNA vectors include, but are not limited to, a RNA polymerase I transcription termination sequence, a RNA polymerase II transcription termination sequence, a RNA polymerase III 20 transcription termination sequence, or a ribozyme. Ribozymes within the scope of the invention include, but are not limited to, tetrahymena ribozymes, RNase P, hammerhead ribozymes, hairpin ribozymes, hepatitis ribozyme, as well as synthetic ribozymes. In one embodiment, at least one vector for vRNA comprises a RNA 25 polymerase 1H promoter linked to a ribozyme sequence linked to viral coding sequences linked to another ribozyme sequences, optionally linked to a RNA polymerase 11 transcription termination sequence. In one embodiment, at least 2 and preferably more, e.g., 3, 4, 5, 6, 7 or 8, vectors for vRNA production comprise a RNA polymerase 11 promoter, a first ribozyme sequence, which is 5' 30 to a sequence corresponding to viral sequences including viral coding sequences, which is 5' to a second ribozyme sequence, which is 5' to a transcription termination sequence. Each RNA polymerase II promoter in each vRNA vector may be the same or different as the RNA polymerase II promoter in any other vRNA vector. Similarly, each ribozyme sequence in each vRNA vector may be WO 2007/126810 FUT/U0ZUU'//UU /304 13 the same or different as the ribozyme sequences in any other vRNA vector. In one embodiment, the ribozyme sequences in a single vector are not the same. The invention also provides a method to prepare influenza virus. The method comprises contacting a cell with a plurality of the vectors of the 5 invention, e.g., sequentially or simultaneously, for example, employing a composition of the invention, in an amount effective to yield infectious influenza virus. The invention also includes isolating virus from a cell contacted with the composition. Thus, the invention further provides isolated virus, as well as a host cell contacted with the composition or virus of the invention. In another 10 embodiment, the invention includes contacting the cell with one or more vectors, either vRNA or protein production vectors, prior to other vectors, either vRNA or protein production vectors. The methods of producing virus described herein, which do not require helper virus infection, are useful in viral mutagenesis studies, and in the 15 production of vaccines (e.g., for AIDS, influenza, hepatitis B, hepatitis C, rhinovirus, filoviruses, malaria, herpes, and foot and mouth disease) and gene therapy vectors (e.g., for cancer, AIDS, adenosine deaminase, muscular dystrophy, ornithine transcarbamylase deficiency and central nervous system tumors). Thus, a virus for use in medical therapy (e.g., for a vaccine or gene 20 therapy) is provided. The invention also provides a method to immunize an individual against a pathogen, e.g., a bacteria, virus, or parasite, or a malignant tumor. The method comprises administering to the individual an amount of at least one isolated virus of the invention, optionally in combination with an adjuvant, effective to 25 immunize the individual. The virus comprises vRNA comprising a polypeptide encoded by the pathogen or a tumor-specific polypeptide. Also provided is a method to augment or increase the expression of an endogenous protein in a mammal having an indication or disease characterized by a decreased amount or a lack of the endogenous protein. The method 30 comprises administering to the mammal an amount of an isolated virus of the invention effective to augment or increase the amount of the endogenous protein in the mammal. Preferably, the mammal is a human.

WO 2007/126810 PCT/US2007/007562 14 Brief Description of the Drawings Figure 1. Titer of various influenza viruses. Figure 2. Schematic diagram of the NI NAs used to generate H5N1/PR8 reassortant viruses by reverse genetics. VN1203fill contains a 20 amino acid (aa) 5 insertion derived from the NI of the H5NI precursor strain, GsGd96. VN1203fill.N2 contains, in addition to 20 aa from GsGd96 NA, a 14-aa insertion from N2 NA, resulting in a 34-aa insertion into the stalk of VN1203 NA. VN1 202fill.N2N9 contains, in addition to 20 aa from GsGd96 NA and 14 aa from N2 NA, a 14-aa insertion from N9 NA, resulting in a 48-aa insertion into 10 the stalk of VN1203. The predicted total length of the stalk region of each NA is given beneath each molecule. Figure 3. Growth of H5Nl/PR8 reassortant viruses in chicken embryonated eggs. The titers of the reassortant viruses containing avirulent-form VNI 203 HA and either homologous NA (VN1203) or heterologous NAs 15 (VN1203fill, VN1203fill.N2, HK213, or PR8) with a PR8 background were compared by plaque titration with MDCK cells. The titereof wild-type (egg adapted) PR8 also is included for comparison. The data are reported as mean titers and standard deviations for 3 eggs inoculated with each virus. Figure 4. Growth kinetics of H5N1 reassortant viruses in chicken 20 embryonated eggs. We inoculated eggs with the same amounts (104 EIDso) of viruses containing PR8 NA (PR8), VN1203 NA (VN1203), or VN1203fill NA (VN1203fill). Mean HA titers and standard deviations for 3 eggs inoculated with each virus were determined at the indicated time points. Figure 5. Virus elution from chicken erythrobytes. Twofold dilutions of 25 each virus (HA titers of 1:1024) containing VN1203 NA with a different stalk length, or PR8 NA, were incubated with chicken erythrocytes in a microtiter plate at 4*C for 1 hour. The plate was then stored at 37*C and reductions in the HA titer were recorded for 8 hours. Figure 6. Growth comparison of H5Nl/PR8 reassortant viruses in 30 chicken embryonated eggs. Viral titers of the 6:2 and 7:1 reassortant viruses, including the WHO-recommended NIBRG-14 strain (a VN1 194/PR8 6:2 reassortant virus) were compared by plaque titration with MDCK cells. Mean titers and standard deviations of 3 eggs inoculated with each virus are shown.

WO 2007/126810 PCT/US2007/007562 15 Thus, replacing just the NA of H5N1 viruses with the NA of PR8 may improve titers in eggs. Figure 7. Growth of reassortant H5N1 viruses possessing PR8(UW) or PR8(Cambridge) internal genes in chicken embryonated eggs. Asterisks indicate 5 a significant (p<0.05, Student t-test) reduction in infectivity compared to PR8(UW)/1 194. Figure 8. The effect of the M and NS genes on the growth of viruses in chicken embryonated eggs. The asterisk indicates a significant (p<0.05, Student t-test) increase in infectivity compared to PR8(UW)/1 194. 10 Figure 9. Growth of PR8(UW)/1 194 and NIBRG-14 virus in MDCK cells. Figure 10. Identification of a gene segment responsible for the enhanced growth of PR8(UW)/1 194 relative to NIBRG-14 in MDCK cells. Figure 11. Identification of the amino acid in PB2 responsible for the 15 high growth rate of the vaccine seed virus in MDCK cells. Figure 12. Growth rates in MDCK cells of reassortants with different HA, NA, and NS genes. The asterisk indicates significantly better virus growth compared to that of PR8(UW)/1 194. Double asterisks indicate significantly better growth rates compared to viruses expressing PR8(UW) NS. 20 Figure 13. Growth in MDCK cells of the H5N1 vaccine seed virus containing a heterologous NS segment. Figure 14. Schematic of the genotype of an H5N1 vaccine seed virus with high growth capacity in chicken embryonated eggs or MDCK cells. Figure 15. Nucleotide sequence for PR8(Cambridge) genes (SEQ ID 25 Nos:28-33). Detailed Description of the Invention Definitions As used herein, the terms "isolated and/or purified" refer to in vitro 30 preparation, isolation and/or purification of a vector, plasmid or virus of the invention, so that it is not associated with in vivo substances, or is substantially purified from in vitro substances. An isolated virus preparation is generally obtained by in vitro culture and propagation, and/or via passage in eggs, and is substantially free from other infectious agents.

WO 2007/126810 PCT/U S2007/007562 16 As used herein, "substantially free" means below the level of detection for a particular infectious agent using standard detection methods for that agent. A "recombinant" virus is one which has been manipulated in vitro, e.g., using recombinant DNA techniques, to introduce changes to the viral genome. 5 Reassortant viruses can be prepared by recombinant or nonrecombinant techniques. As used herein, the term "recombinant nucleic acid" or "recombinant DNA sequence or segment" refers to a nucleic acid, e.g., to DNA, that has been derived or isolated from a source, that may be subsequently chemically altered in 10 vitro, so that its sequence is not naturally occurring, or corresponds to naturally occurring sequences that are not positioned as they would be positioned in the native genome. An example of DNA "derived" from a source, would be a DNA sequence that is identified as a useful fragment, and which is then chemically synthesized in essentially pure form. An example of such DNA "isolated" from 15 a source would be a useful DNA sequence that is excised or removed from said source by chemical means, e.g., by the use of restriction endonucleases, so that it can be further manipulated, e.g., amplified, for use in the invention, by the methodology of genetic engineering. As used herein, a "heterologous" influenza virus gene or gene segment is 20 from an influenza virus source that is different than a majority of the other influenza viral genes or gene segments in a reassortant influenza virus. Influenza virus replication Influenza A viruses possess a genome of eight single-stranded negative sense viral RNAs (vRNAs) that encode a total of ten proteins. The influenza 25 virus life cycle begins with binding of the hemagglutinin (HA) to sialic acid containing receptors on the surface of the host cell, followed by receptor mediated endocytosis. The low pH in late endosomes triggers a conformational shift in the HA, thereby exposing the N-terminus of the HA2 subunit (the so called fusion peptide). The fusion peptide initiates the fusion of the viral and 30 endosomal membrane, and the matrix protein (Ml) and RNP complexes are released into the cytoplasm. RNPs consist of the nucleoprotein (NP), which encapsidates vRNA, and the viral polymerase complex, which is formed by the PA, PB1, and PB2 proteins. RNPs are transported into the nucleus, where transcription and replication take place. The RNA polymerase complex WO 2007/126810 PCT/US2007/007562 17 catalyzes three different reactions: synthesis of an mRNA with a 5' cap and 3' polyA structure, of a full-length complementary RNA (cRNA), and of genomic vRNA using the cDNA as a template. Newly synthesized vRNAs, NP, and polymerase proteins are then assembled into RNPs, exported from the nucleus, 5 and transported to the plasma membrane, where budding of progeny virus particles occurs. The neuraminidase (NA) protein plays a crucial role late in infection by removing sialic acid from sialyloligosaccharides, thus releasing newly assembled virions from the cell surface and preventing the self aggregation of virus particles. Although virus assembly involves protein-protein 10 and protein-vRNA interactions, the nature of these interactions is largely unknown. Although influenza B and C viruses are structurally and functionally similar to influenza A virus, there are some differences. For example, influenza B virus does not have a M2 protein. Similarly, influenza C virus does not have a 15 M2 protein. Cell Lines and Influenza Viruses That Can Be Used in the Present Invention According to the present invention, any cell which supports efficient replication of influenza virus can be employed in the invention, including mutant cells which express reduced or decreased levels of one or more sialic acids 20 which are receptors for influenza virus. Viruses obtained by the methods can be made into a reassortant virus. Preferably, the cells are WHO certified, or certifiable, continuous cell lines. The requirements for certifying such cell lines include characterization with respect to at least one of genealogy, growth characteristics, immunological 25 markers, virus susceptibility tumorigenicity and storage conditions, as well as by testing in animals, eggs, and cell culture. Such characterization is used to confirm that the cells are free from detectable adventitious agents. In some countries, karyology may also be required. In addition, tumorigenicity is preferably tested in cells that are at the same passage level as those used for 30 vaccine production. The virus is preferably purified by a process that has been shown to give consistent results, before being inactivated or attenuated for vaccine production (see, e.g., World Health Organization, 1982). It is preferred to establish a complete characterization of the cell lines to be used, so that appropriate tests for purity of the final product can be included.

WO 2007/126810 PC/U S2007/UU7562 18 Data that can be used for the characterization of a cell to be used in the present invention includes (a) information on its origin, derivation, and passage history; (b) information on its growth and morphological characteristics; (c) results of tests of adventitious agents; (d) distinguishing features, such as biochemical, 5 immunological, and cytogenetic patterns which allow the cells to be clearly recognized among other cell lines; and (e) results of tests for tumorigenicity. Preferably, the passage level, or population doubling, of the host cell used is as low as possible. It is preferred that the virus produced in the cell is highly purified prior to 10 vaccine or gene therapy formulation. Generally, the purification procedures will result in the extensive removal of cellular DNA, other cellular components, and adventitious agents. Procedures that extensively degrade or denature DNA can also be used. See, e.g., Mizrahi, 1990. Vaccines 15 A vaccine of the invention may comprise immunogenic proteins including glycoproteins of any pathogen, e.g., an immunogenic protein from one or more bacteria, viruses, yeast or fungi. Thus, in one embodiment, the influenza viruses of the invention may be vaccine vectors for influenza virus or other viral pathogens including but not limited to lentiviruses such as HIV, 20 hepatitis B virus, hepatitis C virus, herpes viruses such as CMV or HSV or foot and mouth disease virus. A complete virion vaccine is concentrated by ultrafiltration and then purified by zonal centrifugation or by chromatography. It is inactivated before or after purification using formalin or beta-propiolactone, for instance. 25 A subunit vaccine comprises purified glycoproteins. Such a vaccine may be prepared as follows: using viral suspensions fragmented by treatment with detergent, the surface antigens are purified, by ultracentrifugation for example. The subunit vaccines thus contain mainly HA protein, and also NA. The detergent used may be cationic detergent for example, such as hexadecyl 30 trimethyl ammonium bromide (Bachmeyer, 1975), an anionic detergent such as ammonium deoxycholate (Laver & Webster, 1976); or a nonionic detergent such as that commercialized under the name TRITON X100. The hemagglutinin may also be isolated after treatment of the virions with a protease such as bromelin, then purified by a method such as that described by Grand and Skehel (1972).

WO 2007/126810 PCT/US2007/007562 19 A split vaccine comprises visions which have been subjected to treatment with agents that dissolve lipids. A split vaccine can be prepared as follows: an aqueous suspension of the purified virus obtained as above, inactivated or not, is treated, under stirring, by lipid solvents such as ethyl ether or chloroform, 5 associated with detergents. The dissolution of the viral envelope lipids results in fragmentation of the viral particles. The aqueous phase is recuperated containing the split vaccine, constituted mainly of hemagglutinin and neuraminidase with their original lipid environment removed, and the core or its degradation products. Then the residual infectious particles are inactivated if 10 this has not already been done. Inactivated Vaccines. Inactivated influenza virus vaccines of the invention are provided by inactivating replicated virus of the invention using known methods, such as, but not limited to, formalin or S-propiolactone treatment. Inactivated vaccine types that can be used in the invention can 15 include whole-virus (WV) vaccines or subvirion (SV) (split) vaccines. The WV vaccine contains intact, inactivated virus, while the SV vaccine contains purified virus disrupted with detergents that solubilize the lipid-containing viral envelope, followed by chemical inactivation of residual virus. In addition, vaccines that can be used include those containing the 20 isolated HA and NA surface proteins, which are referred to as surface antigen or subunit vaccines. In general, the responses to SV and surface antigen (i.e., purified HA or NA) vaccines are similar. An experimental inactivated WV vaccine containing an NA antigen immunologically related to the epidemic virus and an unrelated HA appears to be less effective than conventional vaccines 25 (Ogra et al., 1977). Inactivated vaccines containing both relevant surface antigens are preferred. Live Attenuated Virus Vaccines. Live, attenuated influenza virus vaccines, can also be used for preventing or treating influenza virus infection, according to known method steps. Attenuation is preferably achieved in a single 30 step by transfer of attenuated genes from an attenuated donor virus tp a replicated isolate or reassorted virus according to known methods (see, e.g., Murphy, 1993). Since resistance to influenza A virus is mediated by the development of an immune response to the HA and NA glycoproteins, the genes coding for these surface antigens must come from the reassorted viruses or high WO 2007/126810 PCT/US2007/007562 20 growth clinical isolates. The attenuated genes are derived from the attenuated parent. In this approach, genes that confer attenuation preferably do not code for the HA and NA glycoproteins. Otherwise, these genes could not be transferred to reassortants bearing the surface antigens of the clinical virus isolate. 5 Many donor viruses have been evaluated for their ability to reproducibly attenuate influenza viruses. As a non-limiting example, the A/Ann Arbor(AA)/6/60 (H2N2) cold adapted (ca) donor virus can be used for attenuated vaccine production (see, e.g., Edwards, 1994; Murphy, 1993). Additionally, live, attenuated reassortant virus vaccines can be generated by 10 mating the ca donor virus with a virulent replicated virus of the invention. Reassortant progeny are then selected at 25*C, (restrictive for replication of virulent virus), in the presence of an H2N2 antiserum, which inhibits replication of the viruses bearing the surface antigens of the attenuated A/AA/6/60 (H2N2) ca donor virus. 15 A large series of HINI and H3N2 reassortants have been evaluated in humans and found to be satisfactorily: (a) infectious, (b) attenuated for seronegative children and immunologically primed adults, (c) immunogenic and (d) genetically stable. The immunogenicity of the ca reassortants parallels their level of replication. Thus, the acquisition of the six transferable genes of the ca 20 donor virus by new wild-type viruses has reproducibly attenuated these viruses for use in vaccinating susceptible adults and children. Other attenuating mutations can be introduced into influenza virus genes by site-directed mutagenesis to rescue infectious viruses bearing these mutant genes. Attenuating mutations can be introduced into non-coding regions of the 25 genome, as well as into coding regions. Such attenuating mutations can also be introduced into genes other than the HA or NA, e.g., the PB2 polymerase gene (Subbarao et al., 1993). Thus, new donor viruses can also be generated bearing attenuating mutations introduced by site-directed mutagenesis, and such new donor viruses can be used in the reduction of live attenuated reassortants HINI 30 and H3N2 vaccine candidates in a manner analogous to that described above for the A/AA/6/60 ca donor virus. Similarly, other known and suitable attenuated donor strains can be reassorted with influenza virus of the invention to obtain attenuated vaccines suitable for use in the vaccination of manuals (Enami et al., 1990; Muster et al., 1991; Subbarao et al., 1993).

WO 2007/126810 PCT/US2007/007562 21 It is preferred that such attenuated viruses maintain the -genes from the virus that encode antigenic determinants substantially similar to those of the original clinical isolates. This is because the purpose of the attenuated vaccine is to provide substantially the same antigenicity as the original clinical isolate of 5 the virus, while at the same time lacking infectivity to the degree that the vaccine causes minimal change of inducing a serious pathogenic condition in the vaccinated mammal. The virus can thus be attenuated or inactivated, formulated and administered, according to known methods, as a vaccine to induce an immune 10 response in an animal, e.g., a mammal. Methods are well-known in the art for determining whether such attenuated or inactivated vaccines have maintained similar antigenicity to that of the clinical isolate or high growth strain derived therefrom. Such known methods include the use of antisera or antibodies to eliminate viruses expressing antigenic determinants of the donor virus; chemical 15 selection (e.g., amantadine or rimantidine); HA and NA activity and inhibition; and DNA screening (such as probe hybridization or PCR) to confirm that donor genes encoding the antigenic determinants (e.g., HA or NA genes) are not present in the attenuated viruses. See, e.g., Robertson et al., 1988; Kilbourne, 1969; Aymard-Henry et al., 1985; Robertson et al., 1992. 20 Pharmaceutical Compositions Pharmaceutical compositions of the present invention, suitable for inoculation or for parenteral or oral administration, comprise attenuated or inactivated influenza viruses, optionally further comprising sterile aqueous or non-aqueous solutions, suspensions, and emulsions. The compositions can 25 further comprise auxiliary agents or excipients, as known in the art. See, e.g., Berkow et al., 1987; Avery's Drug Treatment, 1987; Osol, 1980; Katzung, 1992. The composition of the invention is generally presented in the form of individual doses (unit doses). Conventional vaccines generally contain about 0.1 to 200 pg, preferably 30 10 to 15 pg, of hemagglutinin from each of the strains entering into their composition. The vaccine forming the main constituent of the vaccine composition of the invention may comprise a virus of type A, B or C, or any combination thereof, for example, at least two of the three types, at least two of different subtypes, at least two of the same type, at least two of the same WO 2007/126810 PCT/US2007/007562 22 subtype, or a different isolate(s) or reassortant(s). Human influenza virus type A includes HINI, H2N2 and H3N2 subtypes. Preparations for parenteral administration include sterile aqueous or non aqueous solutions, suspensions, and/or emulsions, which may contain auxiliary 5 agents or excipients known in the art. Examples of non-aqueous solvents are propylene glycol, polyethylene glycol, vegetable oils such as olive oil, and injectable organic esters such as ethyl oleate. Carriers or occlusive dressings can be used to increase skin permeability and enhance antigen absorption. Liquid dosage forms for oral administration may generally comprise a liposome 10 solution containing the liquid dosage form. Suitable forms for suspending liposomes include emulsions, suspensions, solutions, syrups, and elixirs containing inert diluents commonly used in the art, such as purified water. Besides the inert diluents, such compositions can also include adjuvants, wetting agents, emulsifying and suspending agents, or sweetening, flavoring, or 15 perfuming agents. See, e.g., Berkow et al., 1992; Avery's, 1987; Osol, 1980; and Katzung, 1992. When a composition of the present invention is used for administration to an individual, it can further comprise salts, buffers, adjuvants, or other substances which are desirable for improving the efficacy of the composition. 20 For vaccines, adjuvants, substances which can augment a specific immune response, can be used. Normally, the adjuvant and the composition are mixed prior to presentation to the immune system, or presented separately, but into the same site of the organism being immunized. Examples of materials suitable for use in vaccine compositions are provided in Osol (1980). 25 Heterogeneity in a vaccine may be provided by mixing replicated influenza viruses for at least two influenza virus strains, such as 2-50 strains or any range or value therein. Influenza A or B virus strains having a modem antigenic composition are preferred. According to the present invention, vaccines can be provided for variations in a single strain of an influenza virus, 30 using techniques known in the art. A pharmaceutical composition according to the present invention may further or additionally comprise at least one chemotherapeutic compound, for example, for gene therapy, immunosuppressants, anti-inflammatory agents or immune enhancers, and for vaccines, chemotherapeutics including, but not WO 2007/126810 PCT/US2007/007562 23 limited to, gamma globulin, amantadine, guanidine, hydroxybenzimidazole, interferon-o' interferonfl, interferon-y, tumor necrosis factor-alpha, thiosemicarbarzones, methisazone, rifampin, ribavirin, a pyrimidine analog, a purine analog, foscarnet, phosphonoacetic acid, acyclovir, dideoxynucleosides, a 5 protease inhibitor, or ganciclovir. See, e.g., Katzung (1992), and the references cited therein on pages 798-800 and 680-681, respectively. The composition can also contain variable but small quantities of endotoxin-free formaldehyde, and preservatives, which have been found safe and not contributing to undesirable effects in the organism to which the composition 10 is administered. Pharmaceutical Purposes The administration of the composition (or the antisera that it elicits) may be for either a "prophylactic" or "therapeutic" purpose. When provided prophylactically, the compositions of the invention which are vaccines, are 15 provided before any symptom of a pathogen infection becomes manifest. The prophylactic administration of the composition serves to 'prevent or attenuate any subsequent infection. When provided prophylactically, the gene therapy compositions of the invention, are provided before any symptom of a disease becomes manifest. The prophylactic administration of the composition serves to 20 prevent or attenuate one or more symptoms associated with the disease. When provided therapeutically, an attenuated or inactivated viral vaccine is provided upon the detection of a symptom of actual infection. The therapeutic administration of the compound(s) serves to attenuate any actual infection. See, e.g., Berkow et al., 1992; Avery, 1987; and Katzung, 1992. When provided 25 therapeutically, a gene therapy composition is provided upon the detection of a symptom or indication of the disease. The therapeutic administration of the compound(s) serves to attenuate a symptom or indication of that disease. Thus, an attenuated or inactivated vaccine composition of the present invention may thus be provided either before the onset of infection (so as to 30 prevent or attenuate an anticipated infection) or after the initiation of an actual infection. Similarly, for gene therapy, the composition may be provided before any symptom of a disorder or disease is manifested or after one or more symptoms are detected.

WO 2007/126810 PC/US2007/007562 24 A composition is said to be "pharmacologically acceptable" if its administration can be tolerated by a recipient patient. Such an agent is said to be administered in a "therapeutically effective amount" if the amount administered is physiologically significant. A composition of the present invention is 5 physiologically significant if its presence results in a detectable change in the physiology of a recipient patient, e.g., enhances at least one primary or secondary humoral or cellular immune response against at least one strain of an infectious influenza virus. The "protection" provided need not be absolute, i.e., the influenza 10 infection need not be totally prevented or eradicated, if there is a statistically significant improvement compared with a control population or set of patients. Protection may be limited to mitigating the severity or rapidity of onset of symptoms of the influenza virus infection. Pharmaceutical Administration 15 A composition of the present invention may confer resistance to one or more pathogens, e.g., one or more influenza virus strains, by either passive immunization or active immunization. In active immunization, an inactivated or attenuated live vaccine composition is administered prophylactically to a host (e.g., a mammal), and the host's immune response to the administration protects 20 against infection and/or disease. For passive immunization, the elicited antisera can be recovered and administered to a recipient suspected of having an infection caused by at least one influenza virus strain. A gene therapy composition of the present invention may yield prophylactic or therapeutic levels of the desired gene product by active immunization. 25 In one embodiment, the vaccine is provided to a mammalian female (at or prior to pregnancy or parturition), under conditions of time and amount sufficient to cause the production of an immune response which serves to protect both the female and the fetus or newborn (via passive incorporation of the antibodies across the placenta or in the mother's milk). 30 The present invention thus includes methods for preventing or attenuating a disorder or disease, e.g., an infection by at least one strain of pathogen. As used herein, a vaccine is said to prevent or attenuate a disease if its administration results either in the total or partial attenuation (i.e., suppression) of a symptom or condition of the disease, or in the total or partial immunity of WO 2007/126810 PCT/US2007/075362 25 the individual to the disease. As used herein, a gene therapy composition is said to prevent or attenuate a disease if its administration results either in the total or partial attenuation (i.e., suppression) of a symptom or condition of the disease, or in the total or partial immunity of the individual to the disease. 5 At least one inactivated or attenuated influenza virus, or composition thereof, of the present invention may be administered by any means that achieve the intended purposes, using a pharmaceutical composition as previously described. For example, administration of such a composition may be by various 10 parenteral routes such as subcutaneous, intravenous, intradermal, intramuscular, intraperitoneal, intranasal, oral or transdermal routes. Parenteral administration can be by bolus injection or by gradual perfusion over time. A preferred mode of using a pharmaceutical composition of the present invention is by intramuscular or subcutaneous application. See, e.g., Berkow et al., 1992; 15 Avery, 1987; and Katzung, 1992. A typical regimen for preventing, suppressing, or treating an influenza virus related pathology, comprises administration of an effective amount of a vaccine composition as described herein, administered as a single treatment, or repeated as enhancing or booster dosages, over a period up to and including 20 between one week and about 24 months, or any range or value therein. According to the present invention, an "effective amount" of a composition is one that is sufficient to achieve a desired biological effect. It is understood that the effective dosage will be dependent upon the age, sex, health, and weight of the recipient, kind of concurrent treatment, if any, frequency of 25 treatment, and the nature of the effect wanted. The ranges of effective doses provided below are not intended to limit the invention and represent preferred dose ranges. However, the most preferred dosage will be tailored to the individual subject, as is understood and determinable by one of skill in the art. See, e.g., Berkow et al., 1992; Avery's, 1987; and Katsung, 1992. 30 The dosage of an attenuated virus vaccine for a mammalian (e.g., human) or avian adult organism can be from about 10 3 _10 7 plaque forming units (PFU)/kg, or any range or value therein. The dose of inactivated vaccine can range from about 0.1 to 200, e.g., 50 pg of hemagglutinin protein. However, the WO 2007/126810 PCT/US2007/007562 26 dosage should be a safe and effective amount as determined by conventional methods, using existing vaccines as a starting point. The dosage of immunoreactive HA in each dose of replicated virus vaccine can be standardized to contain a suitable amount, e.g., 1-50 pg or any 5 range or value therein, or the amount recommended by the U.S. Public Heath Service (PHS), which is usually 15 pg, per component for older children.3 years of age, and 7.5 tg per component for older children <3 years of age. The quantity of NA can also be standardized, however, this glycoprotein can be labile during the processor purification and storage (Kendal et al., 1980). Each 10 0.5-ml dose of vaccine preferably contains approximately 1-50 billion virus particles, and preferably 10 billion particles. The invention will be further described by the following nonlimiting examples. 15 Example 1 To develop a reverse genetics system for influenza A/Puerto Rico/8/34, viral RNA was extracted from the allantoic fluid of A/Puerto Rico/8/34 (H1N1), Madison high grower variant (PR8HG), using RNeasy Mini kit (Qiagen) according to the manufacturer's protocol. cDNA was synthesized using MMLV 20 RTase (Promega) and Unil2 primer. The cDNAs were amplified overnight by PCR using the following: Primer sets PB1: 25 Ba PB1-1 and PBI-1735R (front fragment) and PB1-903 and Ba-PB1 2341R (rear fragment) Ba-PB1-1 CACACACGGTCTCCGGGAGCGAAAGCAGGCA (SEQ ID NO:9) 30 173PB1-1735R GGGTTTGTATTTGTGTGTCACC (SEQ ID NO:28) 233PB1-903 CCAGGACACTGAAATTTCTTTCAC (SEQ ID NO:10) Ba-PB1-2341R CACACAGGTCTCCTATTAGTAGAAACAAGGCATTT (SEQ ID 35 NO:11) PB2: WO 2007/126810 PCT/US2007/007562 27 Ba PB2-1 and B2 1260R (front fragment) and WSN PB2 seq-2 and Ba PB2-2341R (rear fragment) Ba-PB2-1 CACACAGGTCTCCGGGAGCGAAAGCAGGTC (SEQ 5 ID NO:12) B2 1260R CACACACGTCTCCATCATACAATCCTCTTG (SEQ ID NO:13) WSN PB2 seq-2 CTCCTCTGATGGTGGCATAC (SEQ ID NO:14) 10 Ba-PB2-2341R CACACAGGTCTCCTATTAGTAGAAACAAGGTCGTTT (SEQ ID NO:15) PA: 15 Bn-PA-1 CACACACGTCTCCGGGAGCGAAAGCAGGTAC (SEQ ID NO:16) Bm-PA-2233R CACACACGTCTCCTATTAGTAGAAACAAGGTACTT (SEQ ID NO:17) 20 HA: Bn-HA-1: CACACACGTCTCCGGGAGCAAAAGCAGGGG (SEQ ID NO:18) Bm-NS-890R: 25 CACACACGTCTCCTATTAGTAGAAACAAGGGTGTTTT (SEQ ID NO:19) NP: Bin-NP-1 CACACACGTCTCCGGGAGCAAAAGCAGGGTA (SEQ 30 ID NO:20) Bm-NP-1565R CACACACGTCTCCTATTAGTAGAAACAAGGGTATTTTT (SEQ ID NO:21) 35 NA: Ba-NA-1: CACACAGGTCTCCGGGAGCAAAAGCAGGAGT (SEQ ID NO:22) Ba-NA-1413R: CACACAGGTCTGGTATTAGTAGAAACAAGGAGTTTTTT (SEQ 40 ID NO:23) M: Bm-M-1 CACACACGTCTCCGGGAGCAAAAGCAGGTAG (SEQ ID NO:24) 45 Bm-M-1027R CACACACGTCTCCTATTAGTAGAAACAAGGTAGTTTTT (SEQ ID NO:25)

NS:

WO 2007/126810 PCT/US2007/007562 28 Bm-NS-1 CACACACGTCTCCGGGAGCAAAAGCAGGGTG (SEQ ID NO:26) Bm-NS-890R CACACACGTCTCCTATTAGTAGAAACAAGGGTGTTTT (SEQ ID 5 NO:27) DNA polymerase: pfu Native DNA polymerase (Stratagene) The PCR products were separated by gel electrophoresis and extracted 10 from the agarose gel using a gel extraction kit (Qiagen). The extracted genes were ligated into pT7Blue blunt vector (Novagen) using a Takara ligation kit ver. II (Takara). After 5 hours, the ligated genes were transformed into JM109 (PB2, M, and NS genes) or DH5alpha (PA, PBI, and NP). Six colonies for each gene were cultured in TB for 8 hours. The plasmids were extracted from the 15 bacteria culture, and four clones per gene were sequenced. The PA, NP, M, and NS genes in pT7Blue were excised by Bsm BI enzyme (New England Biolabs). The PB11 gene was excised by Bsa I (New England Biolabs). The excised genes were ligated overnight with pPolIR vector which contains the human RNA polymerase I promoter and the mouse RNA 20 polymerase I terminator which had been digested with Bsm BI. The front fragment of the PB2 gene in pT7Blue was excised by Bsr GI (New England Biolabs) and Bam HI (Roche), and the rear fragment was excised by Bsr GI (New England Biolabs) and Spe I (Roche). The excised fragments were mixed and digested by Bsa I. After 6 hours, the digested genes were purified using a 25 PCR purification kit (Qiagen) and ligated overnight between the Bsm BI sites of the pPollR vector. The ligated PB1, PA, NP, M, and NS-pPolIR genes were used to transform JM109 (M and NS genes) or DH5alpha (PB1, PA and NP genes) overnight. The colonies of transformed bacteria were cultured in LB overnight. 30 The ligated PB2-pPolIR was used to transform JM109 overnight. The plasmids were extracted from the bacterial cultures and gene inserts were confirmed by enzyme digestion. The colonies of bacteria transformed by PB2-PollR were cultured in LB for 8 hours. The plasmids were then extracted and the gene insertion was confirmed by enzyme digestion. All pPolI constructs 35 were sequenced to ensure that they did not contain unwanted mutations.

WIU 2007/126810 PCT/U S2007/UU7562 29 The pPolIR constructs for PR8HG were transfected into 293T human embryonic kidney cells with A/WSN/33(WSN)-HA and NA, A/Hong Kong/483/97(HK)-HAavir and NA, or A/Kawasaki/O1(Kawasaki)-HA and NA Poll constructs and four protein-expression constructs for the polymerase 5 proteins and NP of A/WSN/33. The supernatants from transfected 293T cells were serially diluted (undiluted to 10-7) and infected into the allantoic cavities of 9-day-old embryonated chicken eggs. The allantoic fluids of the infected eggs were harvested and their virus titers tested by HA assay (Table 1). Table 1 10 Virus possessing HA titer (HAU/nl) of allantoic fluid from eggs inoculated PRS genes with 293T supernatants diluted at: together with the undiluted 10- 10 10 4 10" 10' 1* 1 following HA and NA genes WSN-HA NA <1 <1 200 <1 <1 <1 <1 <1 HK-HAavir NA 100 <1 <1 <1 <1 <1 <1 <1 Kawasaki-HA <1 <1 <1 <1 <1 <1 <1 <1 NA HA-positive samples (virus with WSN-HA NA at 102 and virus with HK-HAavir NA at undiluted) were diluted serially from 102 to 10-8 and 100ul of 15 each dilution was infected into embryonated chicken eggs. The allantoic fluids of the infected eggs were harvested and their virus titers tested by HA assay (Table 2). The 50% egg infectious dose (EID 5 o) of A/Puerto Rico/8/34 (H1N1) prepared from plasmids was 10'0""/ml, and the HA titer was 1:3200. A recombinant virus having the HA and NA genes from A/Hong 20 Kong/213/2003 (H5N1) and the remainder of the type A influenza virus genes from PR8HG was prepared. The titer of the recombinant virus was 1010'67

EID

50 /ml, and the HA titer was 1:1600 WU 2007/126810 PC/UUS2007/UU7562 30 Table 2 rs possessing HA titer (HAU/ml) in each dilition together with the 10-2 10-3 10.4 10-5 10-6 10-7 10-8 following HA and NA genes WSN-HA NA 160 40 40 320 40 640 <1 HK-HAavir NA 400 800 400 400 400 800 Sequences of PR8 genes: 5 PA AGCGAAAGCA GGTACTGATC CAAAATGGAA GATTTTGTGC GACAATGCTT 10 CAATCCGATG ATTGTCGAGC TTGCGGAAAA AACAATGAAA GAGTATGGGG AGGACCTGAA AATCGAAACA AACAAATTTG CAGCAATATG CACTCACTTG GAAGTATGCT TCATGTATTC AGATTTTCAC TTCATCAATG 15 AGCAAGGCGA GTCAATAATC GTAGAACTTG GTGATCCAAA TGCACTTTTG AAGCACAGAT TTGAAATAAT CGAGGGAAGA GATCGCACAA TGGCCTGGAC AGTAGTAAAC 20 AGTATTTGCA ACACTACAGG GGCTGAGAAA CCAAAGTTTC TACCAGATTT GTATGATTAC AAGGAGAATA GATTCATCGA AATTGGAGTA ACAAGGAGAG AAGTTCACAT ATACTATCTG GAAAAGGCCA ATAAAATTAA 25 ATCTGAGAAA ACACACATCC ACATTTTCTC GTTCACTGGG GAAGAAATGG CCACAAAGGC AGACTACACT CTCGATGAAG AAAGCAGGGC TAGGATCAAA ACCAGACTAT 30 TCACCATAAG ACAAGAAATG GCCAGCAGAG GCCTCTGGGA TTCCTTTCGT CAGTCCGAGA GAGGAGAAGA GACAATTGAA GAAAGGTTTG AAATCACAGG AACAATGCGC AAGCTTGCCG ACCAAAGTCT CCCGCCGAAC 35 TTCTCCAGCC TTGAAAATTT TAGAGCCTAT GTGGATGGAT TCGAACCGAA CGGCTACATT GAGGGCAAGC TGTCTCAAAT GTCCAAAGAA GTAAATGCTA GAATTGAACC 40 TTTTTTGAAA ACAACACCAC GACCACTTAG ACTTCCGAAT

GGGCCTCCCT

WO 2007/126810 PC/US2007/007562 31 GTTCTCAGCG GTCCAAATTC CTGCTGATGG ATGCCTTAAA ATTAAGCATT GAGGACCCAA GTCATGAAGG AGAGGGAATA CCGCTATATG ATGCAATCAA 5 ATGCATGAGA ACATTCTTTG GATGGAAGGA ACCCAATGTT GTTAAACCAC ACGAAAAGGG AATAAATCCA AATTATCTTC TGTCATGGAA GCAAGTACTG GCAGAACTGC AGGACATTGA GAATGAGGAG AAAATTCCAA 10 AGACTAAAAA TATGAAGAAA ACAAGTCAGC TAAAGTGGGC ACTTGGTGAG AACATGGCAC CAGAAAAGGT AGACTTTGAC GACTGTAAAG ATGTAGGTGA TTTGAAGCAA 15 TATGATAGTG ATGAACCAGA ATTGAGGTCG CTTGCAAGTT GGATTCAGAA TGAGTTTAAC AAGGCATGCG AACTGACAGA TTCAAGCTGG ATAGAGCTCG ATGAGATTGG AGAAGATGTG GCTCCAATTG AACACATTGC 20 AAGCATGAGA AGGAATTATT TCACATCAGA GGTGTCTCAC TGCAGAGCCA CAGAATACAT AATGAAGGGA GTGTACATCA ATACTGCCTT GCTTAATGCA TCTTGTGCAG 25 CAATGGATGA TTTCCAATTA ATTCCAATGA TAAGCAAGTG TAGAACTAAG GAGGGAAGGC GAAAGACCAA CTTGTATGGT TTCATCATAA AAGGAAGATC CCACTTAAGG AATGACACCG ACGTGGTAAA CTTTGTGAGC 30 ATGGAGTTTT CTCTCACTGA CCCAAGACTT GAACCACATA AATGGGAGAA GTACTGTGTT CTTGAGATAG GAGATATGCT TATAAGAAGT GCCATAGGCC AGGTTTCAAG 35 GCCCATGTTC TTGTATGTGA GAACAAATGG AACCTCAAAA ATTAAAATGA AATGGGGAAT GGAGATGAGG CGTTGCCTCC TCCAGTCACT TCAACAAATT GAGAGTATGA TTGAAGCTGA GTCCTCTGTC AAAGAGAAAG 40 ACATGACCAA AGAGTTCTTT GAGAACAAAT CAGAAACATG GCCCATTGGA GAGTCCCCCA AAGGAGTGGA GGAAAGTTCC ATTGGGAAGG TCTGCAGGAC TTTATTAGCA 45 AAGTCGGTAT TCAACAGCTT GTATGCATCT CCACAACTAG AAGGATTTTC AGCTGAATCA AGAAAACTGC TTCTTATCGT TCAGGCTCTT AGGGACAACC TGGAACCTGG GACCTTTGAT CTTGGGGGGC TATATGAAGC 50 AATTGAGGAG WO 2007/126810 PCT/US2007/007562 32 TGCCTGATTA ATGATCCCTG GGTTTTGCTT AATGCTTCTT GGTTCAACTC CTTCCTTACA CATGCATTGA GTTAGTTGTG GCAGTGCTAC TATTTGCTAT 5 CCATACTGTC CAAAAAAGTA CCTTGTTTCT ACT (SEQ ID NO:1) PBI 10 AGCGAAAGCA GGCAAACCAT TTGAATGGAT GTCAATCCGA CCTTACTTTT CTTAAAAGTG CCAGCACAAA ATGCTATAAG CACAACTTTC CCTTATACTG GAGACCCTCC TTACAGCCAT GGGACAGGAA CAGGATACAC 15 CATGGATACT GTCAACAGGA CACATCAGTA CTCAGAAAAG GGAAGATGGA CAACAAACAC CGAAACTGGA GCACCGCAAC TCAACCCGAT TGATGGGCCA CTGCCAGAAG ACAATGAACC AAGTGGTTAT GCCCAAACAG 20 ATTGTGTATT GGAGGCGATG GCTTTCCTTG AGGAATCCCA TCCTGGTATT TTTGAAAACT CGTGTATTGA AACGATGGAG GTTGTTCAGC AAACACGAGT AGACAAGCTG 25 ACACAAGGCC GACAGACCTA TGACTGGACT CTAAATAGAA ACCAACCTGC TGCAACAGCA TTGGCCAACA CAATAGAAGT GTTCAGATCA AATGGCCTCA CGGCCAATGA GTCTGGAAGG CTCATAGACT TCCTTAAGGA 30 TGTAATGGAG TCAATGAACA AAGAAGAAAT GGGGATCACA ACTCATTTTC AGAGAAAGAG ACGGGTGAGA GACAATATGA CTAAGAAAAT GATAACACAG AGAACAATGG 35 GTAAAAAGAA GCAGAGATTG AACAAAAGGA GTTATCTAAT TAGAGCATTG ACCCTGAACA CAATGACCAA AGATGCTGAG AGAGGGAAGC TAAAACGGAG AGCAATTGCA ACCCCAGGGA TGCAAATAAG GGGGTTTGTA 40 TACTTTGTTG AGACACTGGC AAGGAGTATA TGTGAGAAAC TTGAACAATC AGGGTTGCCA GTTGGAGGCA ATGAGAAGAA AGCAAAGTTG GCAAATGTTG TAAGGAAGAT 45 GATGACCAAT TCTCAGGACA CCGAACTTTC TTTCACCATC ACTGGAGATA ACACCAAATG GAACGAAAAT CAGAATCCTC GGATGTTTTT GGCCATGATC ACATATATGA CCAGAAATCA GCCCGAATGG TTCAGAAATG 50 TTCTAAGTAT WO 2007/126810 PCT/US2007/007562 33 TGCTCCAATA ATGTTCTCAA ACAAAATGGC GAGACTGGGA AAAGGGTATA TGTTTGAGAG CAAGAGTATG AAACTTAGAA CTCAAATACC TGCAGAAATG 5 CTAGCAAGCA TCGATTTGAA ATATTTCAAT GATTCAACAA GAAAGAAGAT TGAAAAAATC CGACCGCTCT TAATAGAGGG GACTGCATCA TTGAGCCCTG GAATGATGAT GGGCATGTTC AATATGTTAA GCACTGTATT 10 AGGCGTCTCC ATCCTGAATC TTGGACAAAA GAGATACACC AAGACTACTT ACTGGTGGGA TGGTCTTCAA TCCTCTGACG ATTTTGCTCT GATTGTGAAT GCACCCAATC 15 ATGAAGGGAT TCAAGCCGGA GTCGACAGGT TTTATCGAAC CTGTAAGCTA CTTGGAATCA ATATGAGCAA GAAAAAGTCT TACATAAACA GAACAGGTAC ATTTGAATTC ACAAGTTTTT TCTATCGTTA TGGGTTTGTT 20 GCCAATTTCA GCATGGAGCT TCCCAGTTTT GGGGTGTCTG GGATCAACGA GTCAGCGGAC ATGAGTATTG GAGTTACTGT CATCAAAAAC AATATGATAA ACAATGATCT 25 TGGTCCAGCA ACAGCTCAAA TGGCCCTTCA GTTGTTCATC AAAGATTACA GGTACACGTA CCGATGCCAT ATAGGTGACA CACAAATACA AACCCGAAGA TCATTTGAAA TAAAGAAACT GTGGGAGCAA ACCCGTTCCA 30 AAGCTGGACT GCTGGTCTCC GACGGAGGCC CAAATTTATA CAACATTAGA AATCTCCACA TTCCTGAAGT CTGCCTAAAA TGGGAATTGA TGGATGAGGA TTACCAGGGG 35 CGTTTATGCA ACCCACTGAA CCCATTTGTC AGCCATAAAG AAATTGAATC AATGAACAAT GCAGTGATGA TGCCAGCACA TGGTCCAGCC AAAAACATGG AGTATGATGC TGTTGCAACA ACACACTCCT GGATCCCCAA 40 AAGAAATCGA TCCATCTTGA ATACAAGTCA AAGAGGAGTA CTTGAGGATG AACAAATGTA CCAAAGGTGC TGCAATTTAT TTGAAAAATT CTTCCCCAGC AGTTCATACA 45 GAAGACCAGT CGGGATATCC AGTATGGTGG AGGCTATGGT TTCCAGAGCC CGAATTGATG CACGGATTGA TTTCGAATCT GGAAGGATAA AGAAAGAAGA GTTCACTGAG ATCATGAAGA TCTGTTCCAC CATTGAAGAG 50 CTCAGACGGC WU 2007/126810 PCT/US2007/1U7562 34 AAAAATAGTG AATTTAGCTT GTCCTTCATG AAAAAATGCC TTGTTTCTAC T (SEQ ID NO:2) 5 PB2 AGCGAAAGCA GGTCAATTAT ATTCAATATG GAAAGAATAA 10 AAGAACTACG AAATCTAATG TCGCAGTCTC GCACCCGCGA GATACTCACA AAAACCACCG TGGACCATAT GGCCATAATC AAGAAGTACA CATCAGGAAG ACAGGAGAAG 15 AACCCAGCAC TTAGGATGAA ATGGATGATG GCAATGAAAT ATCCAATTAC AGCAGACAAG AGGATAACGG AAATGATTCC TGAGAGAAAT GAGCAAGGAC AAACTTTATG GAGTAAAATG AATGATGCCG GATCAGACCG 20 AGTGATGGTA TCACCTCTGG CTGTGACATG GTGGAATAGG AATGGACCAA TAACAAATAC AGTTCATTAT CCAAAAATCT ACAAAACTTA TTTTGAAAGA GTCGAAAGGC 25 TAAAGCATGG AACCTTTGGC CCTGTCCATT TTAGAAACCA AGTCAAAATA CGTCGGAGAG TTGACATAAA TCCTGGTCAT GCAGATCTCA GTGCCAAGGA GGCACAGGAT GTAATCATGG AAGTTGTTTT CCCTAACGAA 30 GTGGGAGCCA GGATACTAAC ATCGGAATCG CAACTAACGA TAACCAAAGA GAAGAAAGAA GAACTCCAGG ATTGCAAAAT TTCTCCTTTG ATGGTTGCAT ACATGTTGGA 35 GAGAGAACTG GTCCGCAAAA CGAGATTCCT CCCAGTGGCT GGTGGAACAA GCAGTGTGTA CATTGAAGTG TTGCATTTGA CTCAAGGAAC ATGCTGGGAA CAGATGTATA CTCCAGGAGG GGAAGTGAGG AATGATGATG 40 TTGATCAAAG CTTGATTATT GCTGCTAGGA ACATAGTGAG AAGAGCTGCA GTATCAGCAG ATCCACTAGC ATCTTTATTG GAGATGTGCC ACAGCACACA GATTGGTGGA 45 ATTAGGATGG TAGACATCCT TAGGCAGAAC CCAACAGAAG AGCAAGCCGT GGATATATGC AAGGCTGCAA TGGGACTGAG AATTAGCTCA TCCTTCAGTT TTGGTGGATT CACATTTAAG AGAACAAGCG GATCATCAGT 50 CAAGAGAGAG WO 2007/126810 PC'1/U2007/007562 35 GAAGAGGTGC TTACGGGCAA TCTTCAAACA TTGAAGATAA GAGTGCATGA GGGATATGAA GAGTTCACAA TGGTTGGGAG AAGAGCAACA GCCATACTCA 5 GAAAAGCAAC CAGGAGATTG ATTCAGCTGA TAGTGAGTGG GAGAGACGAA CAGTCGATTG CCGAAGCAAT AATTGTGGCC ATGGTATTTT CACAAGAGGA TTGTATGATA AAAGCAGTCA GAGGTGATCT GAATTTCGTC 10 AATAGGGCGA ATCAACGATT GAATCCTATG CATCAACTTT TAAGACATTT TCAGAAGGAT GCGAAAGTGC TTTTTCAAAA TTGGGGAGTT GAACCTATCG ACAATGTGAT 15 GGGAATGATT GGGATATTGC CCGACATGAC TCCAAGCATC GAGATGTCAA TGAGAGGAGT GAGAATCAGC AAAATGGGTG TAGATGAGTA CTCCAGCACG GAGAGGGTAG TGGTGAGCAT TGACCGTTTT TTGAGAATCC 20 GGGACCAACG AGGAAATGTA CTACTGTCTC CCGAGGAGGT CAGTGAAACA CAGGGAACAG AGAAACTGAC AATAACTTAC TCATCGTCAA TGATGTGGGA GATTAATGGT 25 CCTGAATCAG TGTTGGTCAA TACCTATCAA TGGATCATCA GAAACTGGGA AACTGTTAAA ATTCAGTGGT CCCAGAACCC TACAATGCTA TACAATAAAA TGGAATTTGA ACCATTTCAG TCTTTAGTAC CTAAGGCCAT 30 TAGAGGCCAA TACAGTGGGT TTGTAAGAAC TCTGTTCCAA CAAATGAGGG ATGTGCTTGG GACATTTGAT ACCGCACAGA TAATAAAACT TCTTCCCTTC GCAGCCGCTC 35 CACCAAAGCA AAGTAGAATG CAGTTCTCCT CATTTACTGT GAATGTGAGG GGATCAGGAA TGAGAATACT TGTAAGGGGC AATTCTCCTG TATTCAACTA TAACAAGGCC ACGAAGAGAC TCACAGTTCT CGGAAAGGAT 40 GCTGGCACTT TAACTGAAGA CCCAGATGAA GGCACAGCTG GAGTGGAGTC CGCTGTTCTG AGGGGATTCC TCATTCTGGG CAAAGAAGAC AAGAGATATG GGCCAGCACT 45 AAGCATCAAT GAACTGAGCA ACCTTGCGAA AGGAGAGAAG GCTAATGTGC TAATTGGGCA AGGAGACGTG GTGTTGGTAA TGAAACGGAA ACGGGACTCT AGCATACTTA CTGACAGCCA GACAGCGACC AAAAGAATTC 50 GGATGGCCAT WO 2007/126810 FUT / U 52UU //UU /304L 36 CAATTAGTGT CGAATAGTTT AAAAACGACC TTGTTTCTAC T (SEQ ID NO:3) 5 NP AGCAAAAGCA GGGTAGATAA TCACTCACTG AGTGACATCA AAATCATGGC GTCTCAAGGC ACCAAACGAT CTTACGAACA GATGGAGACT 10 GATGGAGAAC GCCAGAATGC CACTGAAATC AGAGCATCCG TCGGAAAAAT GATTGGTGGA ATTGGACGAT TCTACATCCA AATGTGCACC GAACTCAAAC TCAGTGATTA TGAGGGACGG TTGATCCAAA ACAGCTTAAC 15 AATAGAGAGA ATGGTGCTCT CTGCTTTTGA CGAAAGGAGA AATAAATACC TTGAAGAACA TCCCAGTGCG GGGAAAGATC CTAAGAAAAC TGGAGGACCT ATATACAGGA 20 GAGTAAACGG AAAGTGGATG AGAGAACTCA TCCTTTATGA CAAAGAAGAA ATAAGGCGAA TCTGGCGCCA AGCTAATAAT GGTGACGATG CAACGGCTGG TCTGACTCAC ATGATGATCT GGCATTCCAA TTTGAATGAT 25 GCAACTTATC AGAGGACAAG AGCTCTTGTT CGCACCGGAA TGGATCCCAG GATGTGCTCT CTGATGCAAG GTTCAACTCT CCCTAGGAGG TCTGGAGCCG CAGGTGCTGC 30 AGTCAAAGGA GTTGGAACAA TGGTGATGGA ATTGGTCAGA ATGATCAAAC GTGGGATCAA TGATCGGAAC TTCTGGAGGG GTGAGAATGG ACGAAAAACA AGAATTGCTT ATGAAAGAAT GTGCAACATT CTCAAAGGGA 35 AATTTCAAAC TGCTGCACAA AAAGCAATGA TGGATCAAGT GAGAGAGAGC CGGAACCCAG GGAATGCTGA GTTCGAAGAT CTCACTTTTC TAGCACGGTC TGCACTCATA 40 TTGAGAGGGT CGGTTGCTCA CAAGTCCTGC CTGCCTGCCT GTGTGTATGG ACCTGCCGTA GCCAGTGGGT ACGACTTTGA AAGGGAGGGA TACTCTCTAG TCGGAATAGA CCCTTTCAGA CTGCTTCAAA ACAGCCAAGT 45 GTACAGCCTA ATCAGACCAA ATGAGAATCC AGCACACAAG AGTCAACTGG TGTGGATGGC ATGCCATTCT GCCGCATTTG AAGATCTAAG AGTATTAAGC TTCATCAAAG 50 GGACGAAGGT GCTCCCAAGA GGGAAGCTTT CCACTAGAGG

AGTTCAAATT

WO 2007/126810 PCT/US2007/UU7562 37 GCTTCCAATG AAAATATGGA GACTATGGAA TCAAGTACAC TTGAACTGAG AAGCAGGTAC TGGGCCATAA GGACCAGAAG TGGAGGAAAC ACCAATCAAC 5 AGAGGGCATC TGCGGGCCAA ATCAGCATAC AACCTACGTT CTCAGTACAG AGAAATCTCC CTTTTGACAG AACAACCATT ATGGCAGCAT TCAATGGGAA TACAGAGGGG AGAACATCTG ACATGAGGAC CGAAATCATA 10 AGGATGATGG AAAGTGCAAG ACCAGAAGAT GTGTCTTTCC AGGGGCGGGG AGTCTTCGAG CTCTCGGACG AAAAGGCAGC GAGCCCGATC GTGCCTTCCT TTGACATGAG 15 TAATGAAGGA TCTTATTTCT TCGGAGACAA TGCAGAGGAG TACGACAATT AAAGAAAAAT ACCCTTGTTT CTACT (SEQ ID NO:4) 20 M . AGCAAAAGCA GGTAGATATT GAAAGATGAG TCTTCTAACC GAGGTCGAAA CGTACGTACT CTCTATCATC CCGTCAGGCC CCCTCAAAGC 25 CGAGATCGCA CAGAGACTTG AAGATGTCTT TGCAGGGAAG AACACCGATC TTGAGGTTCT CATGGAATGG CTAAAGACAA GACCAATCCT GTCACCTCTG ACTAAGGGGA 30 TTTTAGGATT TGTGTTCACG CTCACCGTGC CCAGTGAGCG AGGACTGCAG CGTAGACGCT TTGTCCAAAA TGCCCTTAAT GGGAACGGGG ATCCAAATAA CATGGACAAA GCAGTTAAAC TGTATAGGAA GCTCAAGAGG 35 GAGATAACAT TCCATGGGGC CAAAGAAATC TCACTCAGTT ATTCTGCTGG TGCACTTGCC AGTTGTATGG GCCTCATATA CAACAGGATG GGGGCTGTGA CCACTGAAGT 40 GGCATTTGGC CTGGTATGTG CAACCTGTGA ACAGATTGCT GACTCCCAGC ATCGGTCTCA TAGGCAAATG GTGACAACAA CCAATCCACT AATCAGACAT GAGAACAGAA TGGTTTTAGC CAGCACTACA GCTAAGGCTA 45 TGGAGCAAAT GGCTGGATCG AGTGAGCAAG CAGCAGAGGC CATGGAGGTT - GCTAGTCAGG CTAGACAAAT GGTGCAAGCG ATGAGAACCA TTGGGACTCA TCCTAGCTCC 50 AGTGCTGGTC TGAAAAATGA TCTTCTTGAA AATTTGCAGG

CCTATCAGAA

WO 2007/126810 PCT/US2007/007562 38 ACGAATGGGG GTGCAGATGC AACGGTTCAA GTGATCCTCT CACTATTGCC GCAAATATCA TTGGGATCTT GCACTTGACA TTGTGGATTC TTGATCGTCT 5 TTTTTTCAAA TGCATTTACC GTCGCTTTAA ATACGGACTG AAAGGAGGGC CTTCTACGGA AGGAGTGCCA AAGTCTATGA GGGAAGAATA TCGAAAGGAA CAGCAGAGTG CTGTGGATGC TGACGATGGT CATTTTGTCA 10 GCATAGAGCT GGAGTAAAAA ACTACCTTGT TTCTACT (SEQ ID NO:5) NS 15 AGCAAAAGCA GGGTGACAAA AACATAATGG ATCCAAACAC TGTGTCAAGC TTTCAGGTAG ATTGCTTTCT TTGGCATGTC CGCAAACGAG TTGCAGACCA 20 AGAACTAGGC GATGCCCCAT TCCTTGATCG GCTTCGCCGA GATCAGAAAT CCCTAAGAGG AAGGGGCAGT ACTCTCGGTC TGGACATCAA GACAGCCACA CGTGCTGGAA AGCAGATAGT GGAGCGGATT CTGAAAGAAG 25 AATCCGATGA GGCACTTAAA ATGACCATGG CCTCTGTACC TGCGTCGCGT TACCTAACTG ACATGACTCT TGAGGAAATG TCAAGGGACT GGTCCATGCT CATACCCAAG 30 CAGAAAGTGG CAGGCCCTCT TTGTATCAGA ATGGACCAGG CGATCATGGA TAAGAACATC ATACTGAAAG CGAACTTCAG TGTGATTTTT GACCGGCTGG AGACTCTAAT ATTGCTAAGG GCTTTCACCG AAGAGGGAGC 35 AATTGTTGGC GAAATTTCAC CATTGCCTTC TCTTCCAGGA CATACTGCTG AGGATGTCAA AAATGCAGTT GGAGTCCTCA TCGGAGGACT TGAATGGAAT GATAACACAG 40 TTCGAGTCTC TGAAACTCTA CAGAGATTCG CTTGGAGAAG CAGTAATGAG AATGGGAGAC CTCCACTCAC TCCAAAACAG AAACGAGAAA TGGCGGGAAC AATTAGGTCA GAAGTTTGAA GAAATAAGAT GGTTGATTGA 45 AGAAGTGAGA CACAAACTGA AGATAACAGA GAATAGTTTT GAGCAAATAA CATTTATGCA AGCCTTACAT CTATTGCTTG AAGTGGAGCA AGAGATAAGA ACTTTCTCGT 50 TTCAGCTTAT TTAGTACTAA AAAACACCCT TGTTTCTACT (SEQ ID NO:6) WO 2007/126810 PUT/ US2007/097162 39 HA AGCAAAAGCAGGGGAAAATAAAAACAACCAAAATGAAGGCAAACCT 5 ACTGGTCCTGTTATGTGCACTTGCAGCTGCAGAT GCAGACACAATATGTATAGGCTACCATGCGAACAATTCAACCGACAC TGTTGACACAGTACTCGAGAAGAATGTGACAGT GACACACTCTGTTAACCTGCTCGAAGACAGCCACAACGGAAAACTAT GTAGATTAAAAGGAATAGCCCCACTACAATTGG 10 GGAAATGTAACATCGCCGGATGGCTCTTGGGAAACCCAGAATGCGAC CCACTGCTTCCAGTGAGATCATGGTCCTACATT GTAGAAACACCAAACTCTGAGAATGGAATATGTTATCCAGGAGATTT CATCGACTATGAGGAGCTGAGGGAGCAATTGAG CTCAGTGTCATCATTCGAAAGATTCGAAATATTTCCCAAAGAAAGCT 15 CATGGCCCAACCACAACACAAACGGAGTAACGG CAGCATGCTCCCATGAGGGGAAAAGCAGTTTTTACAGAAATTTGCTA TGGCTGACGGAGAAGGAGGGCTCATACCCAAAG CTGAAAAATTCTTATGTGAACAAAAAAGGGAAAGAAGTCCTTGTACT GTGGGGTATTCATCACCCGCCTAACAGTAAGGA 20 ACAACAGAATCTCTATCAGAATGAAAATGCTTATGTCTCTGTAGTGA CTTCAAATTATAACAGGAGATTTACCCCGGAAA TAGCAGAAAGACCCAAAGTAAGAGATCAAGCTGGGAGGATGAACTA TTACTGGACCTTGCTAAAACCCGGAGACACAATA ATATTTGAGGCAAATGGAAATCTAATAGCACCAATGTATGCTTTCGC 25 ACTGAGTAGAGGCTTTGGGTCCGGCATCATCAC CTCAAACGCATCAATGCATGAGTGTAACACGAAGTGTCAAACACCCC TGGGAGCTATAAACAGCAGTCTCCCTTACCAGA ATATACACCCAGTCACAATAGGAGAGTGCCCAAAATACGTCAGGAGT GCCAAATTGAGGATGGTTACAGGACTAAGGAAC 30 ATTCCGTCCATTCAATCCAGAGGTCTATTTGGAGCCATTGCCGGTTTT ATTGAAGGGGGATGGACTGGAATGATAGATGG ATGGTATGGTTATCATCATCAGAATGAACAGGGATCAGGCTATGCAG CGGATCAAAAAAGCACACAAAATGCCATTAACG GGATTACAAACAAGGTGAACACTGTTATCGAGAAAATGAACATTCAA 35 TTCACAGCTGTGGGTAAAGAATTCAACAAATTA GAAAAAAGGATGGAAAATTTAAATAAAAAAGTTGATGATGGATTTCT GGACATTTGGACATATAATGCAGAATTGTTAGT TCTACTGGAAAATGAAAGGACTCTGGATTTCCATGACTCAAATGTGA AGAATCTGTATGAGAAAGTAAAAAGCCAATTAA 40 AGAATAATGCCAAAGAAATCGGAAATGGATGTTTTGAGTTCTACCAC AAGTGTGACAATGAATGCATGGAAAGTGTAAGA AATGGGACTTATGATTATCCCAAATATTCAGAAGAGTCAAAGTTGAA CAGGGAAAAGGTAGATGGAGTGAAATTGGAATC AATGGGGATCTATCAGATTCTGGCGATCTACTCAACTGTCGCCAGTTC 45 ACTGGTGCTTTTGGTCTCCCTGGGGGCAATCA GTTTCTGGATGTGTTCTAATGGATCTTTGCAGTGCAGAATATGCATCT GAGATTAGAATTTCAGAGATATGAGGAAAAAC ACCCTTGTTTCTACT (SEQ ID NO:7) 50 ]NA WO 2007/126810 PC'US2007/UU7562 40 AGCAAAAGCAGGGGTTTAAAATGAATCCAAATCAGAAAATAATAAC CATTGGATCAATCTGTCTGGTAGTCGGACTAATT AGCCTAATATTGCAAATAGGGAATATAATCTCAATATGGATTAGCCA TTCAATTCAAACTGGAAGTCAAAACCATACTGG 5 AATATGCAACCAAAACATCATTACCTATAAAAATAGCACCTGGGTAA AGGACACAACTTCAGTGATATTAACCGGCAATT CATCTCTTTGTCCCATCCGTGGGTGGGCTATATACAGCAAAGACAAT AGCATAAGAATTGGTTCCAAAGGAGACGTTTTT GTCATAAGAGAGCCCTTTATTTCATGTTCTCACTTGGAATGCAGGACC 10 TTTTTTCTGACCCAAGGTGCCTTACTGAATGA CAAGCATTCAAGTGGGACTGTTAAGGACAGAAGCCCTTATAGGGCCT TAATGAGCTGCCCTGTCGGTGAAGCTCCGTCCC CGTACAATTCAAGATTTGAATCGGTTGCTTGGTCAGCAAGTGCATGTC ATGATGGCATGGGCTGGCTAACAATCGGAATT 15 TCAGGTCCAGATAATGGAGCAGTGGCTGTATTAAAATACAACGGCAT AATAACTGAAACCATAAAAAGTTGGAGGAAGAA AATATTGAGGACACAAGAGTCTGAATGTGCCTGTGTAAATGGTTCAT GTTTTACTATAATGACTGATGGCCCGAGTGATG GGCTGGCCTCGTACAAAATTTTCAAGATCGAAAAGGGGAAGGTTACT 20 AAATCAATAGAGTTGAATGCACCTAATTCTCAC TATGAGGAATGTTCCTGTTACCCTGATACCGGCAAAGTGATGTGTGT GTGCAGAGACAATTGGCATGGTTCGAACCGGCC ATGGGTGTCTTTCGATCAAAACCTGGATTATCAAATAGGATACATCT GCAGTGGGGTTTTCGGTGACAACCCGCGTCCCG 25 AAGATGGAACAGGCAGCTGTGGTCCAGTGTATGTTGATGGAGCAAAC GGAGTAAAGGGATTTTCATATAGGTATGGTAAT GGTGTTTGGATAGGAAGGACCAAAAGTCACAGTTCCAGACATGGGTT TGAGATGATTTGGGATCCTAATGGATGGACAGA GACTGATAGTAAGTTCTCTGTGAGGCAAGATGTTGTGGCAATGACTG 30 ATTGGTCAGGGTATAGCGGAAGTTTCGTTCAAC ATCCTGAGCTGACAGGGCTAGACTGTATGAGGCCGTGCTTCTGGGTT GAATTAATCAGGGGACGACCTAAAGAAAAAACA ATCTGGACTAGTGCGAGCAGCATTTCTTTTTGTGGCGTGAATAGTGAT ACTGTAGATTGGTCTTGGCCAGACGGTGCTGA 35 GTTGCCATTCAGCATTGACAAGTAGTCTGTTCAAAAAACTCCTTGTTT CTACT (SEQ ID NO:8) Example 2 Influenza virus A/Hong Kong/213/2003 (H5NI, HK213) replicates 40 systemically in chickens, causing lethal infection. Furthermore, this virus is lethal to chicken embryos. Thus, although its surface proteins are highly related to the currently circulating pathogenic avian influenza viruses, HK213 cannot be used as a vaccine strain as attempts to grow it in embryonated chicken eggs result in the production of poor-quality allantoic fluid. Additionally, the use of 45 this highly virulent virus in the production of vaccines is unsafe for vaccine workers. To test the feasibility of using A/PR/8/34 as a master vaccine strain, WO 2007/126810 PUT/UI2UU7/UU7362 41 the cleavage site of the hernagglutinin (HA) gene of HK213 (containing multiple basic amino acids) was mutated from a virulent to an avirulent phenotype (from RERRRKKR (SEQ ID NO:29) to ---- TETR (SEQ ID NO:30)). A virus containing the mutated HA gene produced non-lethal, localized infection in 5 chickens. Additionally, the mutated virus was non-lethal to chicken embryos. Thus, growth of the mutated virus in embronated eggs yielded high-quality allantoic fluid, and in this attenuated form, the virus is safe for vaccine producers. A recombinant virus containing the neuraminidase (NA) and mutated HA 10 genes from HK213, and all the remaining genes from high-titer A/PR/8/34 (HIN1, HG-PR8) virus (Example 1), which grows 10 times better than other A/PR/8/34 PR8 strains in eggs (1010 EIDs 0 /ml; HA titer:1:8,000), was generated in embryonated chicken eggs. This recombinant virus, which expresses surface proteins related to the currently circulating pathogenic avian influenza virus, 15 grew to high titers in embryonated chicken eggs (Figure 1). Thus, replacement of the HA and NA genes of HG-PR8 with those of a currently circulating strain of influenza virus resulted in a vaccine strain that can be safely produced, and demonstrates the use of PR8-HG as a master vaccine strain. 20 Example 3 In Hong Kong in 1997, a highly pathogenic H5N1 avian influenza virus was transmitted directly from birds to humans, causing 18 confirmed infections and 6 deaths (Subbarao et al., 1998; Claas et al., 1998). In 2004-6, the geographic distribution of H5N1 viruses expanded in Asia, spreading to several 25 adjacent European countries and to Africa. Altogether, 96 people infected with the virus have died in Vietnam, Thailand, Cambodia, Indonesia, China, Turkey, and Iraq (Li et al., 2004; WHO). These fatal outbreaks and the continued threat of a pandemic have led to the development of H5N1 virus vaccines for use in humans. However, because pathogenic H5N1 viruses grow poorly in 30 embryonated chicken eggs and pose serious biosafety concerns for vaccine producers, reverse genetics has been used to generate vaccine candidates (Subbarao et al., 2003; Webby et al., 2004; Stephanson et al., 2004; Wood & Robertson, 2004).

WO 2007/126810 U/UI2007/UU/'62 42 Recombinant (6:2 reassortant) viruses that possess modified avirulent type hemagglutinin (HA) and neuraminidase (NA) genes, both derived from a pathogenic H5N1 strain, with all remaining genes from a donor virus that grows well in eggs, are among the candidates to be produced by this method. The 5 World Health Organization (WHO) recommends A/Puerto Rico/8/34 (H1N1; PR8) as a donor virus, because of its safety in humans and vigorous growth in eggs (Wood & Robertson, 2004; Webby & Webster, 2003). Recently, it was shown that such recombinant viruses grow less well in eggs than does the wild type PR8 strain, even though they possess the same PR8 "internal" genes (i.e., 10 those other than the HA and NA) (Horimoto et al., 2006). Since vigorous growth in eggs is an essential property of vaccine seed viruses used in the production of inactivated vaccines, as described below, H5N1 vaccine candidates were generated that grow as well as the PR8 donor strain in eggs. First, the molecular basis for the high growth of PR8 in eggs was 15 determined by defining the genes responsible for this property using reassortment analysis between PR8 and a WSN strain that grows poorly in eggs. It was found that HA-NA balance and PB1 function are important growth determinants. With this knowledge, a series of H5N1 viruses was produced with altered HA-NA combinations, with the PR8 background, to assess their growth 20 in eggs against more conventional 6:2 reassortants, including the WHO recommended NIBRG-14 virus. Methods Cells and viruses 293T human embryonic kidney cells were maintained in Dulbecco's 25 modified Eagle's minimal essential medium (DMEM) with 10% fetal calf serum and antibiotics. Madin-Darby canine kidney (MDCK) cells were grown in MEM with 5% newborn calf serum and antibiotics. African green monkey Vero WCB cells, which had been established after biosafety tests for use in human vaccine production (Sugawara et al., 2002), were maintained in serum-free VP-SFM 30 medium (GIBCO-BRL) with antibiotics. Cells were maintained at 37"C in 5%

CO

2 . The A/Vietnam/i 194/2004 and A/Vietnam/1203/2004 (H5N1; VNI 194 and VN1203) strains, isolated from humans, were propagated in 10-day-old embryonated chicken eggs for 2 days at 37 0 C, after which time the allantoic fluids containing virus were harvested and used for further experiments. All WO 2007/126810 PCT/US2007/007562 43 experiments with these viruses were carried out in a Biosafety Level 3 containment laboratory. The WHO-recommended vaccine seed virus, NIBRG-14 (VN1 194/PR8 6:2 reassortant virus), was kindly gifted by Drs. John Wood and Jim Robertson at the National Institute for Biological Standards and Control, 5 UK. Construction of plasmids and reverse genetics To generate reassortants of influenza A viruses, a plasmid-based reverse genetics (Neumann et al., 1999) was used. Viral RNA from VN1 194 or VN1 203 was extracted from allantoic fluid by using a commercial kit (ISOGEN LS, 10 Nippon Gene) and was converted to cDNA by using reverse transcriptase (SuperScript III; GIBCO-BRL) and primers containing the consensus sequences of the 3' ends of the RNA segments for the H5 viruses. The full-length cDNAs were then PCR-amplified with ProofStart polymerase (QIAGEN) and H5 subtype-specific primer pairs, and cloned into a plasmid under control of the 15 human polymerase I promoter and the mouse RNA polymerase I terminator (Poll plasmids), generating a PolI-VNI 194/HA or a PolI-VN1203/HA construct containing the VN1 194 or VN1203 HA gene, respectively. By inverse PCR using back-to-back primer pairs, followed by ligation, the HA cleavage site sequence of the wild-type VN1194 or VN1203 (RERRRKKR; SEQ ID NO:29) 20 virus was altered to create the avirulent-type sequence (RETR; SEQ ID NO:31) as described in Horimoto et al. (2006), the disclosure of which is incorporated by reference herein. A PolI-VN1203NA containing the VN1 203 NA gene was constructed by the RT-PCR procedure (described above) with Ni-specific primers. A series of pPolI NA mutant plasmids were prepared by inverse PCR. 25 Using the PolI-VN1203NA as a template, pPolI-NAfill was constructed, which encodes a mutant NA containing a 20-amino acid (aa) (CNQSIITYENNTWVNQTYVN; SEQ ID NO:32) insertion derived from A/goose/Guangdong/l/96 (H5N1; GsGd96) NA into the NA stalk between 48 Pro and 49-Ile. pPolI-NAfill.N2 and -NAfill.N2N9, in which N2 (12 aa) or 30 N2+N9 (12+12 aa) sequences derived from the stalk region of each NA subtype were inserted into the NA stalk between 42-Asn and 43-Gln, were constructed as described in Castrucci et al. (1993). All of these constructs were sequenced to ensure the absence of unwanted mutations.

WU 2007/126SIO PCT/US2007/007562 44 A previously produced series of Poll constructs, derived from A/WSN/33 (HSN1; WSN) and PRS strains was used, for reverse genetics (Horimoto et al., 2006; Neumann et al., 1999). Additionally, Poll constructs containing NA genes derived from A/Hong Kong/213/03 (H5Nl; HK213), and A/Kanagawa/173/2001 5 (HINI; Kanagawa) were used in this study (Horimoto et al., 2006; Kobasa et al., 2004; Peiris et al., 2004). Plasmids expressing WSN or PR8 NP, PA, PB 1, or PB2 under control of the chicken p-actin promoter were used for all reverse genetics experiments (Horimoto et al., 2006; Neumann et al., 1999). Briefly, Poll plasmids and protein 10 expression plasmids were mixed with a transfection reagent, Trans-IT 293T (Panvera), incubated at room temperature for 15 min, and then added to 293T cells. Transfected cells were incubated in Opti-MEM I (GIBCO-BRL) for'48 hours. For reverse genetics in Vero WCB cells, an electroporator (Amaxa) was used to transfect the plasmid mixtures according to the manufacturer's 15 instructions. Sixteen hours after transfection, freshly prepared Vero WCB cells were added onto the transfected cells and TPCK-trypsin (1 pg/ml) was added to the culture 6 hours later. Transfected cells were incubated in serum-free VP SFM for a total of 4 days. Supernatants containing infectious viruses were harvested, biologically cloned by limiting dilution in embryonated eggs, and 20 used in further experiments. Properties of viral replication in eggs Virus was inoculated into the allantoic cavity of 10-day-old embryonated chicken eggs, and incubated at 37"C for 48 hours. Virus in the allantoic fluids was then titrated by HA assay using either 0.5% chicken erythrocytes or 0.8% 25 guinea pig erythrocytes or in eggs to determine the median egg infectious dose (EIDso)/ml of virus. For some viruses, plaque titration was conducted with MDCK cells and TPCK-trypsin (1 pg/ml). The growth kinetics of some viruses was assessed in eggs after inoculating 104 EID 50 of virus. Virus elution assay from chicken erythrocytes 30 Fifty p.l of twofold dilutions of virus containing the HA titers of 1:1024 were incubated with 50 pl of 0.5% chicken erythrocytes in a microtiter plate at 4*C for 1 hour. The plate was then stored at 370C, and the reduction of HA titers WO 2007/126810 PCT/US2007/007562 45 was recorded periodically. Phosphate-buffered saline with 6.8 mM CaCl2 was used as a diluent. Results Molecular basis for the high growth property of PR8 in chicken eggs 5 Although PR8 is recommended by WHO for use as a donor virus to generate reverse genetics-based H5 influenza vaccine, the molecular basis of its high growth property is not fully understood. The M gene was said to be responsible for the vigorous growth of PR8 in eggs (Subbarao et al., 2003), but this claim is apparently not found in the published original data (Kilbourne et al., 10 1969). Thus, a reassortment analysis was conducted using a WSN strain that grows poorly in eggs. Table 3 shows the compatibility between the HAs and NAs of PR8 versus the WSN strain in terms of viral growth in embryonated chicken eggs. All reassortant test viruses grew better than the wild-type WSN, but less well than the egg-adapted PR8, demonstrating that both surface 15 glycoproteins and internal proteins are responsible for the high growth property of PR8. Table 3. Compatibility between the HAs and NAs of PR8 versus WSN strains, assessed by viral growth in chicken embryonated eggs Gene constellation of reassortant HA titerb) HA NA 6 others) Chicken RBC Guinea pig RBC WSN WSN WSN 16/8 32/8 PR8 WSN WSN 64/32 64/32 WSN PR8 WSN 16/16 32/16 PR8 PR8 WSN 128/128 128/128 WSN WSN PR8 64/64 64/64 PR8 WSN PR8 64/128 64/128 WSN PR8 PR8 512/512 512/512 PR8 PR8 PR8 2048/2048 2048/2048 20 a) Genes encoding the internal proteins PB1, PB2, PA, NP, M, and NS. b) Growth of each reassortant virus in chicken eggs, assessed in HA assays with 0.5% chicken RBC and 0.8% guinea pig RBC. HA titers from two independent experiments are shown. 25 WO 2007/126810 PCT/US2007/007562 46 Since the growth of a reassortant virus containing both of the PR8 glycoproteins and all six internal proteins derived from WSN was drastically reduced in eggs, as compared with that of PR8 (Tables 3 and 4), a series of reassortant viruses was produced to define the internal proteins responsible for 5 this property. A single-gene reassortant virus containing the WSN PB1 and all remaining genes from PR8 grew poorly, at a level similar to that of a reassortant containing all of the WSN genes encoding internal proteins, whereas a reassortant containing the PR8 PBI and WSN genes encoding all remaining internal proteins replicated to a high titer (Table 4). Thus, the PR8 PBI likely 10 possesses the optimal polymerase activity for viral genome replication in eggs, in contrast to a previous report implicating the M segment in this role (Subbarao et al., 2003). Table 4 Compatibility among genes encoding internal proteins of PR8 and WSN 15 viruses, assessed by viral growth in chicken embryonated eggs Gene constellation of reassortant a HA NA PB2 PBl PA NP M NS HA titer N PR8 PR8 PR8 PR8 PR8 PR8 PR8 PR8 2048/2048/1024 PR8 PR8 PR8 PR8 PR8 PR8 PR8 WSN 1024/1024/1024 PR8 PR8 PR8 PR8 PR8 PR8 WSN PR8 2048/1024/1024 PR8 PR8 PR8 PR8 PR8 PR8 WSN WSN 1024/1024/512 PR8 PR8 PR8 PR8 PR8 WSN PR8 PR8 1024/1024/512 PR8 PR8 PR8 PR8 WSN PR8 PR8 PR8 1024/512/256 PR8 PR8 PR8 WSN PR8 PR8 PR8 PR8 128/64/64 PR8 PR8 WSN PR8 PR8 PR8 PR8 PR8 1024/1024/1024 PR8 PR8 WSN WSN WSN WSN PR8 PR8 64/64/32 PR8 PR8 WSN WSN WSN WSN WSN WSN 128/64/64 PR8 PR8 WSN PR8 WSN WSN WSN WSN 1024/512/512 ") Both the HA and NA genes were derived from PR8 in all reassortant viruses, while some of the genes encoding internal proteins were from the WSN strain. 0) Growth rate of each reassortant virus in chicken eggs was assessed with HA assays in 0.5% 20 chicken RBC. HA titers, obtained in three independent experiments, are shown. Generation of H5N1 vaccine seed candidates with enhanced growth ability in chicken eggs In an earlier study, the growth of WSN in eggs was shown to be 25 enhanced by lengthening the NA stalk to increase NA function: the longer the stalk, the better the replication of the virus (Castrucci et al., 1993). This finding prompted the production of a series of H5N1 viruses comprising mutated br heterologous Nis with the PR8 background and compare their growth in eggs. The A/Vietnam/1 203/2004 (H5N1; VN1203) NA contains a 20-amino acid (20 30 aa) deletion in its stalk region (hence, 24 aa in the stalk). Therefore, a mutant WO 2007/126810 PCI/U S2007/UU7:562 47 NA, VN1203fill, was constructed containing a 44-aa stalk like the H5N1 precursor virus A/goose/Guangdong/1/96 (H5N1) (Xu et al., 1999), as well as other NA mutants, VN1202fill.N2 and VN1203fill.N2N9 that contained longer stalks, 58- and 72-aa, respectively (Figure 2). The heterologous N1 from A/Hong 5 Kong/213/03 (H5N1; HK213) containing 44-aa in the stalk was also examined. The NAs from H1N1 strains such as PR8, A/Kanagawa/173/2001 (H1N1; Kanagawa), and WSN, all of which possess 24-aa in the stalk, were also tested. Using these NA constructs, a total of eight reassortant viruses was generated, seven 6:2 and one 7:1 with the modified avirulent-type VN1203 HA and PR8 10 background (Table 5). Another series of reassortant viruses was constructed with the modified avirulent-type A/Vietnam/1 194/2004 (H5NI; VNI 194) HA. By comparison with constructs containing the parental VN1203 NA, only the 7:1 reassortant virus and a 6:2 reassortant containing a combination of the modified VNI 194 HA and VN1203fill NA, showed enhanced growth in eggs. 15 WV LUUIIILD51UrLiuu u o 48 r- Z.n %oo q v v ;;;, - b z - *0 C-oU > z 4-) 0 %R Cl od co (DU .: mw Ii 4)) a n 00 A 9 00 iw - F9 5 ad 0 14 -n en 4) 4 c 4=i 0- - WO 2007/126810 PCT/US2007/007562 49 Further testing of selected reassortant viruses by a plaque assay of the stock viruses demonstrated a greater than 3-fold higher titer (p=0.003, Student I test) for the reassortant virus containing PR8 NA compared with the virus containing parental VN1203 NA, although it did not grow as well as egg-adapted 5 PR8 (Figure 3). Assessment of the growth kinetics of reassortant viruses with the PR8, VN1203fill or VN1203 NA in eggs revealed a superior growth rate for the virus with PR8 NA (7:1 reassortant) (Figure 4). To determine the molecular basis of the high growth property observed in the 7:1 reassortant virus, the NA function of reassortant viruses was tested by 10 an assay evaluating virus elution from chicken erythrocytes (Figure 5). Reassortant viruses containing PR8 or VN1203fill NA were eluted from erythrocytes more rapidly than those with the parental VN1203 NA, indicating greater NA activity for PR8 or VN1203fill.NA. These results support the idea that high NA function enhances viral growth in eggs (Castrucci et al., 1993). 15 Growth comparison of H5N1 vaccine seed candidates produced in this study with the WHO-recommended vaccine seed virus, NIBRG-14, in eggs To validate the potential of candidate seed viruses in the production of H5N1 vaccines, their infectivity titers were compared with that of the WHOprovided NIBRG-14 virus under the same experimental conditions. The 7:1 20 reassortant viruses containing either VN 1194 or VN1203-derived HAs and all the other genes from our PR8 strain showed significantly higher titers (p<0.05, Student t-test) than the NIBRG-14 virus in eggs, as assessed by EID 50 (Table 6) and plaque titration (Figure 6). Interestingly, even the 6:2 reassortant virus containing both its HA and NA from the VN1 194 virus grew significantly better 25 (about 7-fold, p=0.047) than NIBRG-14 (also a VN1 194/PR8 6:2 reassortant virus) by plaque titration (Figure 5). This difference in the growth of two 6:2 reassortant viruses possessing identical VN1 194 HAs and NAs indicates that the PR8 strain used in this study would be superior to the one used to generate NIBRG-14 for supporting high viral growth during vaccine production in eggs. 30 WO 2007/126810 PCT/US2007/007562 50 ON +1+1 '-h 00 0 0 4 A~a :E .

D) r 000 41 -H -I-I ~00 Z *V 00 U O +1j .. CL) -4 0 0 tf) 0 WU 2007/126810 PCI/US2U7/UU7562 51 Discussion Recombinant viruses possessing modified avirulent-type HA and NA genes, both derived from an H5NI human isolate, and all remaining genes from the PR8 strain (6:2 reassortant) have been produced and used as seed viruses for 5 inactivated influenza vaccines now being tested in human clinical trials (Wood & Robertson, 2004). Seed strains used in this way must grow well in embryonated eggs. Although egg-adapted PR8 meets this requirement, some 6:2 reassortant viruses, despite containing six internal genes from PR8, do not grow well in eggs (Tables 3 and 5). Here it is demonstrated that the growth of egg 10 adapted PR8 in chicken eggs is affected by the functional balance of the HA and NA surface glycoproteins. It is likely that low yields of some 6:2 reassortant viruses with a PR8 background and surface glycoproteins from highly pathogenic avian viruses may result not only from an HA-NA functional imbalance for growth in eggs but also 15 from genetic (and/or functional) incompatibility between the avian surface glycoprotein genes and the internal genes from PR8. Here it is shown that among the internal genes of PR8, PB1 is very important for its high growth in eggs. This information suggests another strategy for reverse genetics-based H5N1 vaccine production; that is, the PB8 PBl gene alone may be sufficient to 20 generate vigorously growing reassortants for vaccine seed viruses. Thus, by using genes that encode non-PBI internal proteins from strains other than PR8, one might avoid genetic incompatibility between avian and PR8 viruses. Studies to dissect the molecular basis for the high growth property of PR8 PBI in eggs would be of considerable interest. One could, for example, analyze the structural 25 and functional differences between the PBls or PB1-F2s of PR8 and WSN (which differ by 18 and 10 amino acids, respectively; Chen et al., 2004). The 7:1 reassortant viruses produced in this study replicated significantly better (more than 20-fold by plaque titration) than the WHO recommended 6;2 reassortant virus NIBRG-14. Even the 6:2 reassortant that was 30 identical to the NIBRG-14 except for the PR8 strain of origin replicated 7-fold better than the recommended virus. These findings suggest that the PR8 strain used in this study may be a superior donor virus for the production of reverse genetics-based pandemic vaccines.

WOU 2007/126810 PUT/ U l2U7/UU'/62 52 One could argue that the 7:1 reassortant viruses would induce a loss of protective immune response due to antigenic differences in the NA proteins (even though both PR8 and the highly pathogenic viruses contain Ni NAs) (Murphy et al., 1972; Kilbourne et al., 1968; Chen et al., 2000). However, since 5 the HA is the major protective antigen in inactivated vaccines, the higher growth property conferred by the PR8 NA would likely offset the limited antigenic mismatch in this minor protective antigen. In the event of a pandemic caused by a highly pathogenic avian influenza virus, chicken eggs will be in short supply. It is proposed that under such conditions, 7:1 reassortant-based vaccine seed 10 viruses possessing an enhanced growth property in eggs would offer an attractive option for the generation of reverse genetics-based H5 vaccine viruses. Example 4 To identify the genes responsible for the high growth rate of an H5N1 15 vaccine seed virus in chicken embryonated eggs, the growth of reassortant H5N1 viruses possessing PR8(UW) or PR8(Cambridge) internal genes in chicken embryonated eggs was assessed (Figure 7). The HA and NA genes of all of the reassortant viruses were derived from A/Vietnam/i 194/2002. All other genes were derived from either PR8(UW) or PR8(Cambridge), which also provided the 20 non-HA and -NA genes of the NIBRG-1 4 vaccine strain. Higher titers were obtained when the majority of internal genes were from PR8(UW). The effect of the M and NS genes on the growth of viruses in chicken embryonated eggs is shown in Figure 8. For PR8(UW)/1 194-CamM and PR8(UW)/ 194-CamNS, the M and NS gene segments, respectively, were 25 derived from PR8(Cambridge), while the other internal segments came from PR8(UW). The HA and NA segments were derived from A/Vietnam/1 194/2004. Highest titers were with the M gene segment of PR8(UW) and the NS gene of PR8 (Cambridge). The results in Figures 7-8 show that the polymerase subunit (PA, PB1, 30 and PB2) and NP genes of PR8(UW) enhanced the growth of an H5N1 vaccine seed virus in chicken embryonated eggs. Also, the NS gene of PR8(Cambridge) enhanced the growth of an H5N1 vaccine seed virus in chicken embryonated eggs.

WU 2007/126810 PUI/US2UU7/UU762 53 To identify the gene and amino acid(s) responsible for the high growth rate of the H5N1 vaccine seed virus in MDCK cells, the growth of PR8(UW)/1 194 and NIBRG-14 virus in MDCK cells was assessed. The data in Figure 9 show that the growth of PR8(UW)/1194 was significantly better than 5 that of NIBRG-14 in MDCK cells. Moreover, the PB2 segment of PR8(UW) enhanced the growth of the vaccine seed virus in MDCK cells (Figure 10). The tyrosine residue at position 360 in PB2 of PR8(UW) is likely responsible for the high growth rate of the vaccine seed virus in MDCK cells (Figure 11). To identify a combination of genes responsible for the high growth of 10 an H5N1 vaccine seed virus in MDCK cells, the growth rates in MDCK cells of reassortants with different HA, NA, and NS genes was determined. NS from PR8(Cambridge) and NA with a long stalk (e.g., from A/Hong Kong/213/2003 or VN1203Fill) enhanced virus growth in MDCK cells (Figure 12). To determine which amino acids in NS are responsible for the high 15 growth rate of the H5NI vaccine seed virus in MDCK cells, the growth in MDCK cells of the H5N1 vaccine seed virus containing a heterologous NS segment was measured. An amino acid substitution from K [PR8(UW)NS] to E [PR8(Cambridge)] at position 55 ofNS1 enhanced the growth of the H5N1 vaccine seed viruses in MDCK cells (Figure 13). 20 Figure 14 summarizes the genotype of an H5N1 seed virus with high growth capacity in chicken embryonated eggs or MDCK cells. References Avery's Drug Treatment: Principles and Practice of Clinical 25 Pharmacology and Therapeutics 3rd edition, ADIS Press, Ltd., Williams and Wilkins, Baltimore, MD (1987). Aymard-Henry et al., Virology: A Practical Approach Oxford 1RL Press, Oxford, 119-150 (1985). Bachmeyer, Intervirology, 5:260 (1975). 30 Berkow et al., eds., The Merck Manual, 16th edition, Merck & Co., Rahway, NJ (1992). Bridgen et al., Proc. Nat]. Acad. Sci. U. S. A, 93:15400 (1996). Castrucci & Kawaoka, J. Virol., 67:759 (1993). Castrucci et al., J. Virol., 69:2725 (1995).

WU 2997/12681I PC/US2U7/UU7562 54 Chen et al., Emerg. Infect. Dis., 10:630 (2004). Chen et al., Vaccine, 18:3214 (2000). Claas et al., Lancet, 351:472 (1998). Conzelmann et al., J. Gen. Virol.. 77:381 (1996). 5 Conzelmann et al., Trends Microbiol., 4:386 (1996). Conzelmann, Annu. Rev. Genet., 32:123 (1998). Cozelmann et al., J. Virol., 6:713 (1994). Edwards, J. Infect. Dis.. 169: 68 (1994). Enami et al., Proc. Natl. Acad. Sci. U.S.A.. 87:3802 (1990). 10 Enami et al., Virology. 85:291 (1991). Fodor et al., J. Virol., 73:9679 (1999). Grand and Skehel, Nature, New Biology, 238:145 (1972). Hatta et al., Science 293:1840 (2001). Horimoto et al., J. Virol., 68:3120 (1994). 15 Horimoto et al., Vaccine, 24:3669 (2006). Keitel et al., in Textbook of Influenza, eds. Nickolson, K. G., Webster, R. G., and Hay, A. (Blackwell, Oxford), pp. 373-390 (1998). Kendal et al., Infect. Immunity, 22:966 (1980). Kilbourne et al., J. Virol., 2:281 (1968). 20 Kilbourne, Bull. M2 World Health Org., 41: 653 (1969). Kilbourne, Bull. World Health Org., 41:643 (1969). Kobasa et al., Nature, 431:703 (2004). Kovesdi et al., J. Curr. Opin. Biotechnol., .:583 (1997). Laver & Webster, Virology, !:511 (1976). 25 Lawson et al., Proc. Natl. Acad. Sci. U. S. A., 92:4477 (1995). Li et al., Nature 430:209 (2004). Marriott et al., Adv. Virus Res., 53:321 (1999). Mizrahi, (ed.), Viral Vaccines, Wiley-Liss, New York, 39-67 (1990). Munoz et al., Antiviral Res., 46:91 (2000). 30 Murphy et al., New Engl. J. Med., 286:1329 (1972). Murphy, Infect. Dis. Clin. Pract., 2: 174 (1993). Muster et al., Proc. Natl. Acad. Sci. USA, 88: 5177 (1991). Nagai et al., Microbiol. Immunol., 43:613 (1999). Nagai, Rev. Med. Virol., 2:83 (1999).

WU 2007/126810 PUT/0 U N2U7/UU756 55 Neumann et al., Adv. Virus Res., 53:265 (1999). Neumann et al., J. Gen. Virol., 83:2635 (2002). Neumann et al., J. Virol., 71:9690 (1997). Neumann et al., Proc. Natl. Acad. Sci. USA, 96:9345 (1999). 5 Neumann et al., Virology 28:243 (2001). Ogra et al., J. Infect. Dis., 134: 499 (1977). Osol (ed.), Remington's Pharmaceutical Sciences, Mack Publishing Co., Easton, PA 1324-1341 (1980). Parks et al., J. Virol., 23:3560 (1999). 10 Peiris et al., Lancet, 3_6:617 (2004). Pekosz et al., Proc. Natl. Acad. Sci. U. S. A _9:8804 (1999). Radecke et al., EMBO J., 14:5773 (1995). Roberts et al., Virology, 247:1 (1998). Robertson et al., Biologicals, 20:213 (1992). 15 Robertson et al., Giomale di Igiene e Medicina Preventiva 22:4 (1988). Rose, Proc. Natl. Acad. Sci. U. S. A 93:14998 (1996). Schnell et al., EMBO J., 13:4195 (1994). Stephenson et al., Lancet Inf Dis., 4:499 (2004). Subbarao et al., J. Virol., 67:7223 (1993). 20 Subbarao et al., Science, 279:393 (1998). Subbarao et al., Virology, 305:192 (2003). Sugawara et al., Biologicals, 30:303 (2002). Webby & Webster et al., Science, 302:1519 (2003). Webby et al., Lancet, 363:1099 (2004). 25 Wood & Robertson, Nat. Rev. Microbiol., 2:842 (2004). World Health Organization TSR No. 673 (1982). World Health Organization. Confirmed human cases of avian influenza A (H5N1). http://www.who.int/csr/disease/avian influenza/country/en/index.html 30 Xu et al., Virology, 261:15 (1999). All publications, patents and patent applications are incorporated herein by reference. While in the foregoing specification this invention has been 56 described in relation to certain preferred embodiments thereof, and many details have been set forth for purposes of illustration, it will be apparent to those skilled in the art that the invention is susceptible to additional embodiments and that certain of the details described herein may be varied considerably without 5 departing from the basic principles of the invention. Throughout the description and claims of the specification, the word "comprise" and variations of the word, such as "comprising" and "comprises", is not intended to exclude other additives, components, integers or steps. 10 A reference herein to a patent document or other matter which is given as prior art is not to be taken as an admission or a suggestion that that document or matter was, known or that the information it contains was part of the common general knowledge as at the priority date of any of the claims. <filename>

Claims (29)

1. A composition comprising a plurality of influenza virus vectors for a reassortant influenza virus, comprising 5 a) a vector for vRNA production comprising a promoter operably linked to an influenza virus PA cDNA linked to a transcription termination sequence, a vector for vRNA production comprising a promoter operably linked to an influenza virus PB 1 cDNA linked to a transcription termination sequence, a vector for vRNA production comprising a promoter operably linked to an influenza virus PB2 cDNA linked to a transcription termination 10 sequence, a vector for vRNA production comprising a promoter operably linked to an influenza virus HA cDNA linked to a transcription termination sequence, a vector for vRNA production comprising a promoter operably linked to an influenza virus NP cDNA linked to a transcription termination sequence, a vector for vRNA production comprising a promoter operably linked to an influenza virus NA cDNA linked to a transcription termination 15 sequence, a vector for vRNA production comprising a promoter operably linked to an influenza virus M cDNA linked to a transcription termination sequence, and a vector for vRNA production comprising a promoter operably linked to an influenza virus NS cDNA linked to a transcription termination sequence, wherein the cDNAs for PB 1, PB2, PA, NP, and M have sequences for PB1, PB2, PA, NP, and M that encode a polypeptide having at least 20 97% contiguous amino acid sequence identity to a corresponding polypeptide encoded by SEQ ID NOs:1-5, wherein the cDNA for NS has sequences for a NS having at least 97% contiguous amino acid sequence identity to a corresponding polypeptide encoded by SEQ ID NO:6; wherein the cDNA for HA has sequences for a heterologous HA; and wherein the cDNA for NA has sequences for a heterologous NA or sequences that encode a polypeptide 25 having at least 95% contiguous amino acid sequence identity to a corresponding polypeptide encoded by SEQ ID NO:8, wherein if the HA and NA are both heterologous they are from different isolates; and b) a vector for viral protein production comprising a promoter operably linked to a DNA segment encoding influenza virus PA, a vector for viral protein production comprising a 30 promoter operably linked to a DNA segment encoding influenza virus PB 1, a vector for viral protein production comprising a promoter operably linked to a DNA segment encoding influenza virus PB2, and a vector for viral protein production comprising a promoter operably 58 linked to a DNA segment encoding influenza virus NP, and optionally a vector for viral protein production comprising a promoter operably linked to a DNA segment encoding influenza virus HA, a vector for viral protein production comprising a promoter operably linked to a DNA segment encoding influenza virus NA, a vector for viral protein production 5 comprising a promoter operably linked to a DNA segment encoding influenza virus Ml, a vector for viral protein production comprising a promoter operably linked to a DNA segment encoding influenza virus M2, or a vector for viral protein production comprising a promoter operably linked to a DNA segment encoding influenza virus NS2. 10

2. The composition of claim 1 wherein the NS has a Glu residue at position 55

3. The composition of claim 1 wherein the cDNA for NS encodes a polypeptide having substantially the same amino acid sequence as a corresponding polypeptide encoded by SEQ ID NO:38. 15

4. The composition of any one of claims 1 to 3 wherein the promoter is a RNA polymerase I promoter, a RNA polymerase II promoter, a RNA polymerase III promoter, a T3 promoter or a T7 promoter. 20

5. The composition of any one of claims 1 to 4 wherein the HA is a type A or a type B HA.

6. The composition of any one of claims 1 to 5 wherein the NA is Ni. 25

7. The composition of any one of claims 1 to 6 wherein the HA is H5.

8. The composition of any one of claims 1 to 6 wherein a plurality of the vectors of a) comprise a RNA polymerase I promoter or a RNA polymerase II promoter. 30

9. The composition of claim 8 wherein the RNA polymerase I promoter is a human RNA polymerase I promoter.

10. The composition of any one of claims 1 to 9 wherein all of the vectors of b) comprise a RNA polymerase II promoter. 59

11. The composition of any one of claims 1 to 10 wherein each vector of a) is on a separate plasmid. 5

12. The composition of any one of claims 1 to 11 wherein each vector of b) is on a separate plasmid.

13. The composition of any one of claims 1 to 12 wherein the NA or HA is a chimeric NA or HA. 10

14. The composition of claim 1 wherein the HA is an avirulent H5 HA.

15. A method to prepare influenza virus, comprising: contacting a cell with one of: a vector comprising a promoter operably linked to an influenza virus PA cDNA linked 15 to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus PB 1 cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus PB2 cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus HA cDNA linked to a transcription termination sequence, a vector comprising a promoter 20 operably linked to an influenza virus NP cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus NA cDNA linked to a transcription termination sequence, a vector comprising a promoter operably linked to an influenza virus M cDNA linked to a transcription termination sequence, and a vector comprising a promoter operably linked to an influenza virus NS cDNA linked to a 25 transcription termination sequence, wherein the cDNAs for PB1, PB2, PA, NP, and M have sequences for PB1, PB2, PA, NP, and M that encode a polypeptide having at least 97% contiguous amino acid sequence identity to a corresponding polypeptide encoded by SEQ ID NOs:1-5, wherein the cDNA for NS has sequences for a NS having at least 97% contiguous amino acid sequence identity to a corresponding polypeptide encoded by SEQ ID NO:6; 30 wherein the cDNA for HA has sequences for a heterologous HA; and wherein the cDNA for NA has sequences for a heterologous NA or encode a polypeptide having at least 95% contiguous amino acid sequence identity to a corresponding polypeptide encoded by SEQ ID NO:8, wherein if the HA and NA are both heterologous they are from different isolates; and a 60 vector comprising a promoter operably linked to a DNA segment encoding influenza virus PA, a vector comprising a promoter operably linked to a DNA segment encoding influenza virus PB 1, a vector comprising a promoter operably linked to a DNA segment encoding influenza virus PB2, and a vector comprising a promoter operably linked to a DNA segment encoding 5 influenza virus NP, and optionally a vector comprising a promoter operably linked to a DNA segment encoding influenza virus HA, a vector comprising a promoter operably linked to a DNA segment encoding influenza virus NA, a vector comprising a promoter operably linked to a DNA segment encoding influenza virus Ml, a vector comprising a promoter operably linked to a DNA segment encoding influenza virus M2, or a vector comprising a promoter 10 operably linked to a DNA segment encoding influenza virus NS2; in an amount effective to yield infectious influenza virus.

16. The method of claim 15 further comprising isolating the virus. 15

17. Virus obtained by the method of claim 15.

18. A cell infected with the virus of claim 17.

19. The cell of claim 18 which is a cell in an embryonated egg. 20

20. The cell of claim 18 which is a MDCK cell.

21. A method to immunize an individual against a pathogen, comprising administering to the individual an amount of the virus of claim 17 effective to immunize the individual. 25

22. An isolated recombinant influenza virus comprising a viral segment for PB 1, PB2, PA, NP, M, NS, and NA that is from an influenza virus that replicates to high titers in embryonated eggs, with sequences for a polypeptide having at least 97% contiguous amino acid sequence identity to a corresponding polypeptide encoded by SEQ ID NOs: 30 1-5 and 8, a viral segment for NS having at least 97% contiguous amino acid sequence identity to a corresponding polypeptide encoded by SEQ ID NO:6 and having a Glu residue at position 55, and a viral segment for a heterologous HA. 60

23. The isolated recombinant virus of claim 22 wherein the influenza virus that replicates to high titers is PR8HG. 5

24. The isolated recombinant influenza virus of claim 22 or 23 wherein the viral segment for NA is heterologous to the viral segments for PB 1, PB2, PA, NP, NS, and M.

25. The isolated recombinant influenza virus of any one of claims 22 to 24 wherein the viral segment for HA is for H5. 10

26. An inactivated influenza virus vaccine comprising the isolated recombinant virus of any one of claims 22 to 26.

27. A composition according to claim 1, substantially as hereinbefore described with 15 reference to the Examples and/or Figures.

28. A method according to claim 15, substantially as hereinbefore described with reference to the Examples and/or Figures. 20

29. An isolated recombinant influenza virus, according to claim 22, substantially as hereinbefore described with reference to the Examples and/or Figures. <filename>