Haplotype primer for identifying Q-shaped bemisia tabaci and identification method
A Bemisia tabaci, haplotype technology, applied in the field of agricultural biology
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Embodiment 3
[0031] The Q-type Bemisia tabaci described in Example 3 was collected in Shouguang City, Shandong Province in 2011; 6(10):e25579.doi:10.1371 / journal.pone.0025579.) to detect the above Q-type Bemisia tabaci, and the Q-type Bemisia tabaci collected in Shouguang City, Shandong Province were divided into haplotype 1 and haplotype 2.
Embodiment 4
[0032]The Q-type Bemisia tabaci described in Example 4 was collected in many regions of China in 2011: A: Liaocheng City, Shandong Province, B: Dezhou City, Shandong Province, C: Zaozhuang City, Shandong Province, D: Linyi City, Shandong Province, E : Beijing, F: Shanghai, G: Nanjing, Jiangsu, H: Nanchang, Jiangxi; according to (De Barro P, Ahmed MZ, 2011. Genetic Networking of the Bemisia tabaci Cryptic Species Complex Reveals Pattern of Biological Invasions.PLoS ONE, 6(10):e25579.doi:10.1371 / journal.pone.0025579.) to detect the above Q-type Bemisia tabaci, and the Q-type Bemisia tabaci collected in the above cities were divided into haplotype 1 and Haplotype 2.
[0033] The Hin1II endonuclease described in the examples was purchased from Fermentas Company, Tris-HCl, ethylenediaminetetraacetic acid, and sodium lauryl sulfate were all purchased from Shanghai Bioengineering Company, and other reagents were all commercially available products.
Embodiment 1
[0035] (1) Extraction of Q-type Bemisia tabaci genomic DNA
[0036] Place a single Q-type Bemisia tabaci in a 0.2ml centrifuge tube containing 60 μl of alkaline lysate: 50 mmol L -1 Tris-HCl (pH8.0), 20mmol·L -1 NaCl, 1mmol L -1 EDTA (ethylenediaminetetraacetic acid) and 1% SDS (sodium dodecyl sulfate) are fully ground and homogenized with a sealed gun head, placed in a water bath at 65°C for 15 minutes, and then placed in a water bath at 95°C for 10 minutes to obtain Genomic DNA solution of type Q Bemisia tabaci.
[0037] (2) PCR amplification of COI gene of Q-type Bemisia tabaci
[0038] Using the Q-type Bemisia tabaci genomic DNA solution and the Q-type Bemisia tabaci haplotype 2 genome DNA solution as templates for PCR amplification to obtain PCR amplification products;
[0039] The PCR amplification system is:
[0040] Type Q Bemisia tabaci genomic DNA solution: 3μl; 20μM primer: 0.5μl; 5U / μl Taq enzyme: 0.5μl; 10×Taq Buffer: 5μl; 10mM dNTP: 1μl; ddH 2 0 to 50μl;
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