Recombinant Newcastle disease virus RNA expression systems and vaccines
View Patent ↗This invention relates to genetically engineered Newcastle disease viruses and viral vectors which express heterologous genes or mutated Newcastle disease viral genes or a combination of viral genes derived from different strains of Newcastle disease virus. The invention relates to the construction and use of recombinant negative strand NDV viral RNA templates which may be used with viral RNA-directed RNA polymerase to express heterologous gene products in appropriate host cells and/or to rescue the heterologous gene in virus particles. In a specific embodiment of the invention, the heterologous gene product is a peptide or protein derived from the genome of a human immunodeficiency virus. The RNA templates of the present invention may be prepared by transcription of appropriate DNA sequences using any DNA-directed RNA polymerase such as bacteriophage T 7 , T 3 , SP 6 polymerase, or eukaryotic polymerase I.
1. A recombinant RNA molecule comprising a binding site specific for an RNA polymerase of a Newcastle disease virus and signals required for NDV mediated replication and transcription, operatively linked to a heterologous RNA sequence, wherein the signals required for NDV mediated replication and transcription is contained in the 3′ and 5′ -noncoding flanking regions of the NDV viral RNA genome.
2. A recombinant RNA molecule comprising a binding site for an RNA polymerase of a Newcastle disease virus and signals required for NDV mediated replication and transcription, operatively linked to a Newcastle disease viral gene; wherein the RNA molecule contains a mutation, wherein the signals required for NDV mediated replication and transcription is contained in the 3′ and 5′ -noncoding flanking regions of the NDV viral RNA genome.
3. A recombinant cell comprising nucleotide sequences encoding a recombinant RNA molecule Of claim 1 or 2 and NDV RNA polymersase proteins P and L.
4. The recombinant RNA molecule of claim 1 or 2 in which the polymerase binding site comprises the polymerase binding site contained in the 3′ and 5′ -noncoding flanking region of a Newcastle disease viral RNA genome.
5. The recombinant RNA molecule of claim 1 or 2 in which the 3′ and 5′ -noncoding flanking regions have a genomic NDV viral sense sequence as shown in SEQ ID NO: 2 and SEQ ID NO: 1, respectively.
6. The recombinant RNA molecule of claim 1 in which the heterologous RNA encodes a viral antigen.
7. The recombinant RNA molecule of claim 6 in which the viral antigen is derived from human immunodeficiency virus, Newcastle disease virus, influenza, respiratory syncytial virus, Marek's disease virus, infectious bursal disease virus, infectious bronchitis virus, infectious bursitis virus, chicken anemia virus, infectious laryngotracheitis virus, avian leukosis virus, reticuloendotheliosis virus, avian influenza virus, rabies virus, feline distemper virus, vesicular stomatitis virus, rinderpest virus, or swinepox virus.
8. A method for producing a chimeric negative-strand RNA virus, comprising
transfecting a host cell with nucleotide sequences encoding the recombinant RNA of claim 1 or 2 and the viral functions required for replication and transcription, and
recovering the chimeric virus from the culture.