Typing method of resistance for resisting subgroup A avian leukosis virus by quality chicken
A technology of avian leukosis virus and subgroup, which is applied in the field of resistance typing of high-quality chicken against avian leukosis virus A subgroup, and can solve the problems of resistance gene reporting, lack of breeding methods for high-quality chicken anti-avian leukemia A resistance typing, etc. , to achieve the effect of strong purpose, eliminating the threat of large-scale outbreak, and strong operability
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Embodiment 1
[0043] The establishment of embodiment 1 PCR-RFLP
[0044] 1. PCR amplification of TVA619 fragment
[0045] According to the SNP site (C / G) at position 619 on the mRNA sequence of the known TVA gene (GenBank accession number: AY531262.1), design PCR-RFLP amplification primer TVA6195 (5'-AAA CCG ACT GCT ACC CGC TGG AGT GGC TCT T-3', SEQ ID NO:1), TVA6193 (5'-ACT CGT CCC GTC CAT CGT-3', SEQ ID NO:2), with ear I restriction site CTCTT. Chicken genomic DNA was extracted and PCR amplified with primers TVA6195 and TVA6193. The composition of the PCR reaction system is as follows: Genomic DNA template 1 μL, 10× buffer 10 μL, dNTPs 8 μL, primer TVA6195 1 μL, primer TVA6193 1 μL, Bland Taq 1 μL, ddH 2 O to make up to 100 μL. PCR reaction program: pre-denaturation at 94°C for 3min, 1 cycle; 94°C for 40s, 67°C for 40s, 72°C for 1min, 35 cycles; extension at 72°C for 10min. When the PCR product is detected by 3.5% agarose gel electrophoresis, a specific band of about 69bp can be o...
Embodiment 2
[0050] Example 2 Establishment of 4-base Pyrosequence method
[0051] 1. PCR amplification of TVA223 fragment
[0052] According to the 4-base insertion or deletion site (GCTC / ----) at position 305-308 on the mRNA sequence of the known TVA gene (GenBank accession number: AY531262.1), the PCR amplification primer TVA2235 (5 '-CATGGTGCGGTTGTTGGAGC-3', SEQ ID NO:4), TVA2233 (5'-GGGGAACGCGGGGTGC-3', SEQ ID NO:5)), TVA2233 primers were labeled with biotin. Chicken genomic DNA was extracted and PCR amplified with primers TVA2235 and TVA2233. The composition of the PCR reaction system is as follows: Genomic DNA template 1 μL, 10× buffer 10 μL, dNTPs 8 μL, primer TVA2235 1 μL, TVA2233 1 μL, Bland Taq 1 μL, ddH 2 O to make up to 100 μL. PCR reaction program: pre-denaturation at 94°C for 3min, 1 cycle; 94°C for 40s, 62°C for 40s, 72°C for 1min, 35 cycles; extension at 72°C for 10min. The PCR product fragment was 223bp in length and was directly used for pyrosequencing.
[0053] 2...
Embodiment 3
[0056] Example 3 Establishment of Judgment Criteria for TVA Genotyping
[0057] According to the results of PCR-RFLP and 4-base pyrosequence sequencing, the present invention formulates the judgment standard of chicken resistance genotyping against subgroup A avian leukemia virus (ALV-A). The TVA resistance gene defined in the present invention has three alleles, namely TVA*S, TVA*R1 and TVA*R2. There are six genotypes of TVA genes in different chicken strains, TVA*S / S, TVA*S / R1, TVA*S / R2, TVA*R1 / R1, TVA*R1 / R2, TVA*R2 / R2. The standard of genetic resistance typing is: if a chicken carries one or two TVA*S alleles, the chicken will be susceptible to ALV-A, i.e. genetic susceptibility; if a chicken carries There is one TVA*R1 and one TVA*R2, or two TVA*R1 or two TVA*R2 alleles, then this chicken is the genotype of resistance to ALV-A, that is, the genetic resistance type. The genotyping determination is shown in Table 2.
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