Primer sets and kits for multiple RPA detection of brucella abortus, brucella melitensis and brucella suis
A technology of Brucella suis and primer set, applied in the direction of recombinant DNA technology, microbe-based methods, DNA/RNA fragments, etc., to achieve high sensitivity, specificity and good repeatability
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Embodiment 1
[0048] Experimental strains and cells Brucella bovis 2308, Brucella melis 16M are preserved by Changchun Military Veterinary Research Institute; Brucella suis attenuated strain S2, type strain of Escherichia coli, Salmonella, Y. enterocolitica , Vibrio parahaemolyticus and Shigella flexneri were preserved by the Laboratory of Bacterial Diseases, Institute of Zoonoses, Jilin University.
[0049] Main instruments and reagents The gel imager was purchased from UVP Company; the program-controlled metal bath was purchased from China Kayoudi Biotechnology Co., Ltd.; the bacterial genome DNA extraction kit and common DNA product purification kit were purchased from Tiangen Biochemical Technology Co., Ltd.; Twist Basic Kit was purchased from TwistDx Inc, UK; Brucella Broth Medium was purchased from Qingdao Rishui Biotechnology Co., Ltd.
[0050] The primers were designed and synthesized according to the genomes of Brucella bovis (GenBank: AM040265.1), Brucella melis (GenBank: AE00891...
Embodiment 2
[0067] The multiple RPA detection method detects the spiked sample in order to evaluate the feasibility of the method of the present invention, the cultured Brucella suis S2 is counted, the concentration of the bacterial solution is calculated, and the bacterial solution is manually added to the serum sample, beef sample, and milk sample , using the boiling method to crudely extract the genome for spike detection.
[0068] Preparation of artificially spiked serum samples: Count the Brucella S2 bacterial liquid on a plate to obtain the concentration of the bacterial liquid, mix the bacterial liquid with the serum, and make the final concentration of Brucella in the serum 2.14×10 9 CFU / mL, centrifuge at 12000 rpm for 1 min to collect the bacteria, wash twice with sterile normal saline, finally add 100 μL of normal saline to resuspend the bacteria, boil for 30 min, centrifuge to get the supernatant genome solution, and then carry out 10 times The dilution was used as a template t...
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