Primer composition, kit and method for detecting vesicular stomatitis Indiana viruses and vesicular stomatitis New Jersey viruses
A technology of vesicular stomatitis and primer composition, which is applied in the field of primer composition for detecting vesicular stomatitis virus Indiana and New Jersey types, can solve the problems of large electrophoresis pollution, complex instruments, and low sensitivity, and achieve detection sensitivity Improvement, accurate results, and the effect of reducing pollution
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Embodiment 1
[0027] Embodiment 1, the design of primer composition
[0028] Download the registered VSV-NJ and VSV-IND NS genes (phosphoprotein) on Genebank, use MEGA5.0 for comparative analysis, and use primer 5.0 and Primer explore V5 to design 2 sets of LAMP-specific primers to form a primer composition. Each set includes 4 primers and 1 probe: outer primers F3 and B3, inner primers FIP (FIP=F1c+F2) and BIP (BIP=B1c+B2)), probe Probe. The probe Probe is designed between F1c and B1c, and the two probe Probes are respectively labeled with different fluorescent groups: IND-Probe is labeled with CY 5.5 at the 5' end of the nucleotide sequence shown in SEQ ID No: 5 in the sequence listing Fluorescence, the 3' end is labeled with the BHQ3 quencher group, and it is bright red at a wavelength of 694nm; NJ-Probe is labeled with FAM fluorescence at the 5' end of the nucleotide sequence shown in SEQ ID No: 10 in the sequence listing, and the 3' end Labeled BHQ1 quencher, yellow-green at 520nm wav...
Embodiment 2
[0031] Example 2, Verification test of vesicular stomatitis virus Indiana type and New Jersey type dual fluorescence RT-LAMP detection method
[0032] 1. Extraction of RNA / DNA template
[0033] Refer to the instructions of EasyPure RNA Kid, a full-type gold RNA extraction kit, to extract the RNA of the virus strains shown in Table 1, and store the RNA template at -70°C for later use.
[0034] 2. Dual fluorescent RT-LAMP reaction system and reaction conditions
[0035] Using VSV-NJ and VSV-IND RNA as experimental templates, the primer concentration, BstDNA 3.0 polymerase, reaction temperature and reaction time in the reaction system were optimized respectively. The optimal reaction system for dual fluorescence RT-LAMP is: 1 μL RNA template, 2×buffer 12.5 μL (composition is 40mM Tris–HCl, 20mM KCl, 16mM MgSO 4 , 20mM (NH 4 ) 2 SO 4 , 0.2% (v / v) Tween 20, 1.6M betaine, and 2.8mM dNTPs. ), Bst DNA 3.0 polymerase 15U, AMV reverse transcriptase 20U, inner primers (IND-FIP, IND...
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