Detection method for infant salmonella PCR and nucleic acid and primer pair thereinto
A Salmonella and primer pair technology, which is applied in the fields of botanical equipment and methods, microorganism-based methods, biochemical equipment and methods, etc., can solve the problem of nucleic acid and primers for the detection method of Salmonella infantis serotype PCR, which has not been invented, and achieves practical application. The effect of reducing the cost of testing, the specificity of testing results, and the
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Embodiment 1
[0022] Establishment of PCR detection method for infant Salmonella serotype
[0023] Step 1, design amplification primers according to the conserved sequence in the genomic DNA sequence of Salmonella infantis
[0024] Find the specific restriction endonuclease gene from the Salmonella infantis genome DNA sequence, and use it as the detection target gene of Salmonella infantis, the gene sequence is shown in SEQ ID NO: 1;
[0025] Input the DNA sequence of the restriction endonuclease gene into the primer design software Primer Premier 5.0 to design primers, set the GC% range to 40-60%, and the product size range to 150-300bp, and select primers from the alternative primer pairs , the primer sequences are as follows (primers were synthesized by Shanghai Sangon Bioengineering Technology Service Co., Ltd.):
[0026] SIN5-L: 5'-AGCCAACGCCACCTACTACT-3' (SEQ ID NO: 2);
[0027] SIN5-R: 5'-TGAACACCATATCCATCCACAT-3' (SEQ ID NO: 3);
[0028] Step 2, DNA template preparation
[0029]...
Embodiment 2
[0042] Detection of suspected strains of Salmonella
[0043] Using the PCR detection method for infant Salmonella serotypes in Example 1, 53 suspected strains of Salmonella isolated from food samples were detected. The food samples were collected in suburban supermarkets and bazaars in Shanghai. For sample processing and isolation of suspected strains, refer to the national standard GB / T 4789.4-2008.
[0044] From it, 2 suspected strains were detected to be positive results, and these 2 suspected strains were identified as O7:Hr:5 by the Salmonella diagnostic serum (Lanzhou Institute of Biological Products), and it was determined that it was Salmonella infantis (see the product manual for the serum identification steps and National standard GB / T 4789.4-2008), other suspected strains were identified as not Salmonella infantis. This example proves that the PCR detection method for Salmonella infantis has very high reliability.
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