A kind of primer and identification method for identifying cryptid species of Bemisia tabaci and whitefly
A technology of whitefly and whitefly, applied in biochemical equipment and methods, measurement/inspection of microorganisms, DNA/RNA fragments, etc., can solve the problems of difficulty in successful amplification
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Embodiment 1
[0035] Bemisia tabaci MEAM1 cryptic species and Bemisia tabaci MED cryptic species described in Example 1 and Example 2 are populations raised in this laboratory;
Embodiment 3
[0036] Bemisia tabaci and whitefly described in Example 3 were collected from various places in Shandong Province in 2013 (Table 1).
[0037] Table 1
[0038]
[0039] The Sac II 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.
[0040] Example 1
[0041] (1) Extraction of Genomic DNA of Bemisia tabaci MEAM1 and Bemisia tabaci MED
[0042] Place a single whitefly 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 B. tabaci MEAM1 cryptic and B. t...
Embodiment 2
[0054] A method for distinguishing whitefly MEAM1 cryptic species and whitefly MED cryptic species, the steps are as follows:
[0055] (1) Put the laboratory-raised B. tabaci MEAM1 cryptic species and B. tabaci MED cryptic species as identification samples into 0.2 ml centrifuge tubes containing 60 μl of alkaline lysate: 50 mmol L -1 Tris-HCl (pH8.0), 20mmol·L - 1 NaCl, 1mmol L -1 EDTA, 1% SDS, fully grind the homogenate with a sealed pipette tip, put it in a water bath at 65°C for 15 minutes, and then put it in a water bath at 95°C for 10 minutes to obtain a genomic DNA solution;
[0056] (2) Using the genomic DNA prepared in step (1) as a template, performing PCR amplification on the mitochondrial COI gene in the genomic DNA to obtain a PCR amplification product;
[0057] The PCR amplification system is:
[0058] Genomic DNA solution 2.5μl, 20μM primer 0.5μl, 5U / μl Taq enzyme 0.25μl, 10×Taq Buffer 2.5μl, 10mM dNTP 0.5μl, ddH 2 O supplemented to 25 μl;
[0059] The prim...
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