A kind of anti-wssv autophagy-related gene cq-atg8 and its preparation method and application
A cq-atg8, gene technology, applied in the field of antiviral active genes, can solve problems such as no effective drug for WSSV infection has been found, and achieve the effect of strong anti-WSSV activity
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Embodiment 1
[0027] Example 1 Prokaryotic Recombination-Induced Expression and Affinity Purification of Red Claw Crawfish Cq-Atg8
[0028] According to the multiple cloning site of the pGEX4T-2 vector, the open reading frame sequence of Cq-Atg8 gene of red claw crayfish was cloned into the pGEX4T-2 vector, and the pGEX4T-2 / Cq-Atg8 recombinant expression vector was constructed, which can be expressed in the recombinant strain E. coli BL21 induces expression to produce rCq-Atg8.
[0029] induced expression
[0030] 1. Transform the constructed recombinant expression vector into E.coli BL21, and induce expression with IPTG.
[0031] 2. Pick a monoclonal colony and inoculate it in 5ml containing Amp + LB medium, 37°C, 200rpm shaker culture to OD 600 0.6 to 2.0.
[0032] 3. Inoculate 20ml containing Amp at a ratio of 1:100 + LB medium, 37°C, 200rpm shaker culture to OD 600 0.1 to 0.2.
[0033] 4. Add IPTG to a final concentration of 0.1 mM, and induce at 200 rpm at 28°C for a certain per...
Embodiment 2
[0045] Example 2 Recombinant expression rCq-Atg8 anti-WSSV experiment
[0046] Anti-WSSV activity identification of rCq-Atg8: take 4 μg rCq-Atg8, mix with WSSV; after incubation for 30 minutes, add it to the cultured crayfish hematopoietic stem cells, and mix; incubate for 6 hours, collect the cells in the culture well, and extract the total RNA of Hpt cells , Total RNA was reverse-transcribed into cDNA after 1 μg DnaseI treatment.
[0047] Real-time PCR was used to detect the transcription and expression of WSSV virus genes IE1 and VP28 in the above samples, and the 16srRNA gene was used as an internal reference. The primers used are shown in Table 1.
[0048] Table 1
[0049]
[0050] The reaction system is as follows:
[0051]
[0052] Reaction conditions: polymerase activation at 95°C for 10 minutes; denaturation at 95°C for 15 seconds, annealing at 60°C for 1 minute, and 40 cycles.
[0053] Data analysis: use 7500system SDS software version1.3.1.21 software to an...
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