Gene VII type newcastle disease marker vaccine strain as well as preparation method and application thereof
A technology for Newcastle disease and vaccine strains, applied in the field of vaccine genetic engineering, can solve problems that are not involved in the development of Newcastle disease marked vaccines
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[0030] The present invention also provides a preparation method of the gene type VII Newcastle disease marker vaccine strain Paramyxovirus type II rY2-HB strain, comprising the following steps: a. Constructing the transcription plasmid of the serotype 2 avian paramyxovirus Y2 strain; b. The extracellular domains of the F and HN genes in the Y2 strain transcription plasmid were replaced with the F and HN gene extracellular domains of the gene VII type Newcastle disease virus HB0901 strain respectively; c. the transcription plasmid after the extracellular domain replacement was combined with three auxiliary plasmids The host cells were transfected to obtain the genotype VII Newcastle disease marker vaccine strain Paramyxovirus type II rY2-HB strain. The whole genome gene sequence of the avian paramyxovirus type 2 Y2 strain is SEQ ID NO:3.
[0031] The present invention also provides the application of the gene VII type Newcastle disease marker vaccine strain paramyxovirus type II ...
Embodiment 1
[0033] The whole genome transcription plasmid construction of embodiment 1 avian paramyxovirus type 2 (APMV-2) Y2 strain
[0034] Download the whole genome sequences of 12 strains of avian paramyxovirus type 2 in GenBank, the accession numbers are KT071756, KT071757, KT071755, HQ896023, HQ896024, EU338414, HM159993, HM159994, HM159995, LC187305, LC187323 and NC039. After comparing and analyzing the nucleotide sequences of these sequences, the relatively conservative F8 strain (HQ896023) was selected as a template, and 10 unique amino acids in the genome of the strain were mutated into a consensus sequence shared by other strains (T 1440 C, C 2142 T,T 2709 C, C 5552 T,A 6397 G,A 6868 G, G 7768 T,A 11753 C, G 14409 A,T 14480 C), obtaining the whole genome sequence of a new strain of paramyxovirus Y2 strain. Through the method of gene synthesis and cloning, the whole genome plasmid of Y2 strain was constructed. The plasmid contains the whole genome sequence of Y2 strain...
Embodiment 2r
[0039] Whole-genome transcription plasmid construction and virus rescue of embodiment 2rY2-HB strain
[0040] Using the recombinant plasmid pY2 as a template, the extracellular domains of the F and HN genes of the Y2 strain were replaced by the extracellular domains of the F and HN genes of the NDV gene type VII HB0901 strain by the In-fusion method. The specific replacement positions are as follows: the ectodomain (1-1506nt) of the F gene of the NDV HB0901 strain replaces the ectodomain (1-1455nt) of the F gene of the Y2 strain, and the ectodomain (139-1713nt) of the HN gene of the NDV HB0901 strain replaces the HN gene of the Y2 strain Extracellular domain of the gene (130-1740nt). See the construction diagram Figure 4 . The specific construction scheme is as follows.
[0041] 2.1 PCR amplification of extracellular domains of F and HN genes of Newcastle disease virus HB0901 strain
[0042] Taking the allantoic fluid of chicken embryos of Newcastle disease virus HB0901 s...
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